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Sample records for polyethylene glycol-modified proteins

  1. Characterization of Polyethylene Glycol Modified Hemoglobins

    NASA Astrophysics Data System (ADS)

    Salazar, Gil; Barr, James; Morgan, Wayne; Ma, Li

    2011-03-01

    Polyethylene glycol modified hemoglobins (PEGHbs) was characterized by liquid chromatography and fluorescence methods. We prepared four samples of two different molecular weight PEG, 5KDa and 20KDa, modified bovine and human hemoglobin. We studied the oxygen affinities, stabilities, and peroxidase activities of PEGHbs. We have related oxygen affinities with different degrees of modifications. The data showed that the modification on the beta subunits was less stable than that of the alpha subunits on the human Hb based samples especially. We also compared peroxidase activities among different modified PEGHbs.

  2. Protein adsorption to polyethylene glycol modified liposomes from fibrinogen solution and from plasma.

    PubMed

    Price, M E; Cornelius, R M; Brash, J L

    2001-06-01

    Unmodified and polyethylene glycol (PEG) modified neutral and negatively charged liposomes were prepared by freeze-thaw and extrusion followed by chromatographic purification. The effects of PEG molecular weight (PEG 550, 2000, 5000), PEG loading (0-15 mol%), and liposome surface charge on fibrinogen adsorption were quantified using radiolabeling techniques. All adsorption isotherms increased monotonically over the concentration range 0-3 mg/ml and adsorption levels were low. Negatively charged liposomes adsorbed significantly more fibrinogen than neutral liposomes. PEG modification had no effect on fibrinogen adsorption to neutral liposomes. An inverse relationship was found between PEG loading of negatively charged liposomes and fibrinogen adsorption. PEGs of all three molecular weights at a loading of 5 mol% reduced fibrinogen adsorption to negatively charged liposomes. Protein adsorption from diluted plasma (10% normal strength) to four different liposome types (neutral, PEG-neutral, negatively charged, and PEG-negatively charged) was investigated using gel electrophoresis and immunoblotting. The profiles of adsorbed proteins were similar on all four liposome types, but distinctly different from the profile of plasma itself, indicating a partitioning effect of the lipid surfaces. alpha2-macroglobulin and fibronectin were significantly enriched on the liposomes whereas albumin, transferrin, and fibrinogen were depleted compared to plasma. Apolipoprotein AI was a major component of the adsorbed protein layers. The blot of complement protein C3 adsorbed on the liposomes suggested that the complement system was activated. PMID:11406096

  3. Surface forces and protein adsorption on dextran- and polyethylene glycol-modified polydimethylsiloxane.

    PubMed

    Farrell, Megan; Beaudoin, Stephen

    2010-12-01

    Dextran and polyethylene glycol (PEG) are often covalently bound to the surface of polydimethylsiloxane (PDMS) for the purpose of modifying its hydrophilicity and biocompatibility. In this work, the effects of the dextran and PEG on the morphology, wetting, and surface charge of the resulting surfaces were quantified and correlated with changes in the amount of fibrinogen and albumin adsorbed from aqueous solution. PDMS films were functionalized in a microwave oxygen plasma to create surface hydroxyl groups that were subsequently aminated by incubation in a (3-aminopropyl)trimethoxysilane (APTES) solution. Oxidized dextran and PEG-aldehyde were linked to the surface amines via reductive amination. This process resulted in low surface coverage of immobilized PEG in the end-on conformation and a more uniform and dense distribution of side-on immobilized dextran. The immobilized dextran reduced the contact angle of the PDMS film from 109° to 80° and neutralized the zeta potential over the pH range from 3 to 11. An atomic force microscope was used to measure the interaction force between the modified PDMS and a model hydrophobic surface (polystyrene latex) and a model hydrophilic surface (silica) in aqueous solution to show that van der Waals and hydrophobic attractive forces are the dominant forces for protein adsorption in this system. The PEG- and dextran-modified PDMS were exposed to BSA and fibrinogen to test their resistance to protein adsorption. The coatings were ineffective at reducing the adsorption of either molecule, and the dextran-modification of the PDMS caused more BSA to adsorb than in the case of the unmodified PDMS. PMID:20801620

  4. Surface Forces and Protein Adsorption on Dextran- and Polyethylene Glycol-Modified Polydimethylsiloxane

    PubMed Central

    Farrell, Megan; Beaudoin, Stephen

    2010-01-01

    Dextran and polyethylene glycol (PEG) are often covalently bound to the surface of polydimethylsiloxane (PDMS) for the purpose of modifying its hydrophilicity and biocompatibility. In this work, the effects of the dextran and PEG on the morphology, wetting, and surface charge of the resulting surfaces were quantified and correlated with changes in the amount of fibrinogen and albumin adsorbed from aqueous solution. PDMS films were functionalized in a microwave oxygen plasma to create surface hydroxyl groups that were subsequently aminated by incubation in a (3-aminopropyl)trimethoxysilane (APTES) solution. Oxidized dextran and PEG-aldehyde were linked to the surface amines via reductive amination. This process resulted in low surface coverage of immobilized PEG in the end-on conformation and a more uniform and dense distribution of side-on immobilized dextran. The immobilized dextran reduced the contact angle of the PDMS film from 109° to 80° and neutralized the zeta potential over the pH range from 3 to 11. An atomic force microscope was used to measure the interaction force between the modified PDMS and a model hydrophobic surface (polystyrene latex) and a model hydrophilic surface (silica) in both water and electrolyte solutions to show that van der Waals and hydrophobic attractive forces are the dominant forces for protein adsorption in this system. The PEG- and dextran-modified PDMS were exposed to BSA and fibrinogen to test their resistance to protein adsorption. The coatings were ineffective at reducing the adsorption of either molecule, and the dextran-modification of the PDMS caused more BSA to adsorb than in the case of the unmodified PDMS. PMID:20801620

  5. Cell separation by immunoaffinity partitioning with polyethylene glycol-modified Protein A in aqueous polymer two-phase systems

    NASA Technical Reports Server (NTRS)

    Karr, Laurel J.; Van Alstine, James M.; Snyder, Robert S.; Shafer, Steven G.; Harris, J. Milton

    1988-01-01

    Previous work has shown that polyethylene glycol (PEG)-bound antibodies can be used as affinity ligands in PEG-dextran two-phase systems to provide selective partitioning of cells to the PEG-rich phase. In the present work it is shown that immunoaffinity partitioning can be simplified by use of PEG-modified Protein A which complexes with unmodified antibody and cells and shifts their partitioning into the PEG-rich phase, thus eliminating the need to prepare a PEG-modified antibody for each cell type. In addition, the paper provides a more rigorous test of the original technique with PEG-bound antibodies by showing that it is effective at shifting the partitioning of either cell type of a mixture of two cell populations.

  6. Structure of poly(ethylene glycol)-modified horseradish peroxidase in organic solvents: infrared amide I spectral changes upon protein dehydration are largely caused by protein structural changes and not by water removal per se.

    PubMed Central

    Al-Azzam, Wasfi; Pastrana, Emil A; Ferrer, Yancy; Huang, Qing; Schweitzer-Stenner, Reinhard; Griebenow, Kai

    2002-01-01

    Fourier transform infrared (FTIR) spectroscopy has emerged as a powerful tool to guide the development of stable lyophilized protein formulations by providing information on the structure of proteins in amorphous solids. The underlying assumption is that IR spectral changes in the amide I and III region upon protein dehydration are caused by protein structural changes. However, it has been claimed that amide I IR spectral changes could be the result of water removal per se. Here, we investigated whether such claims hold true. The structure of horseradish peroxidase (HRP) and poly(ethylene glycol)-modified HRP (HRP-PEG) has been investigated under various conditions (in aqueous solution, the amorphous dehydrated state, and dissolved/suspended in toluene and benzene) by UV-visible (UV-Vis), FTIR, and resonance Raman spectroscopy. The resonance Raman and UV-Vis spectra of dehydrated HRP-PEG dissolved in neat toluene or benzene were very similar to that of HRP in aqueous buffer, and thus the heme environment (heme iron spin, coordination, and redox state) was essentially the same under both conditions. Therefore, the three-dimensional structure of HRP-PEG dissolved in benzene and toluene was similar to that in aqueous solution. The amide I IR spectra of HRP-PEG in aqueous buffer and of dehydrated HRP-PEG dissolved in neat benzene and toluene were also very similar, and the secondary structure compositions (percentages of alpha-helices and beta-sheets) were within the standard error the same. These results are irreconcilable with recent claims that water removal per se could cause substantial amide I IR spectral changes (M. van de Weert, P.I. Haris, W.E. Hennink, and D.J. Crommelin. 2001. Anal. Biochem. 297:160-169). On the contrary, amide I IR spectral changes upon protein dehydration are caused by perturbations in the secondary structure. PMID:12496131

  7. Antitumor drug effect of betulinic acid mediated by polyethylene glycol modified liposomes.

    PubMed

    Liu, Yanping; Gao, Dawei; Zhang, Xuwu; Liu, Zhiwei; Dai, Kun; Ji, Bingshuo; Wang, Qianqian; Luo, Liyao

    2016-07-01

    Betulinic acid (BA), as a natural pentacyclic lupine-type triterpene, principally derives from bark of white birch, due to its potent pharmacological properties and low side-effect, which has been demonstrated a prominent efficiency on cancer therapy. However, the poor solubility and low bioavailability limit its pharmaceutical effect. Herein, we reported the rapid efficient synthesis of the polyethylene glycol modified (PEGylated) BA liposomes using ethanol injection technique for the first time. In the study, hydrophobic BA was encapsulated in the lipid bilayer of liposomes, meanwhile hydrophilic PEG layer covered the surface of liposomes. The mean diameter of PEGylated BA liposomes was 142nm, which can effectively accumulate in the tumor tissues. In vitro drug release study showed that the PEGylated BA liposomes had a better sustained drug release effect than BA liposomes. The PEGylated BA liposomes also exhibited a better tumor inhibitory effect compared with those of free BA or BA liposomes in vitro and in vivo experiments. Therefore, the PEGylated BA liposomes could serve as a better alternative for the cancer therapy in future. PMID:27127036

  8. Effect of supercritical carbon dioxide as an exfoliation aid on bio-based polyethylene terephthalate glycol-modified/clay nanocomposites

    NASA Astrophysics Data System (ADS)

    Jang, Kwangho; Lee, Jae Wook; Hong, In-Kwon; Lee, Sangmook

    2013-08-01

    Bio-based PETG (bio-based glycol modified polyethylene terephthalate, Ecozen T95) / clay (organo-modified montmorillonite, OMMT, C10A) nanocomposites were prepared by co-rotating twin screw extruder attached with supercritical carbon dioxide (scCO2) injection system. The effects of nano-clay and scCO2 on the properties of PETG/clay nanocomposites were investigated by measuring thermal, rheological, tensile, impact, and barrier properties. The thermal and mechanical properties decreased with increasing nano-clay content, but they recovered or even exceeded the properties of neat PETG as scCO2 was added. It was verified due to a good dispersion of the nano-clay in PETG matrix for PETG/clay nanocomposites by XRD, SEM, and TEM. It was thought that scCO2 could be an effective exfoliation agent for many nanocomposites systems as well as for bio-based PET/clay nanocomposites.

  9. Adsorption of poly(ethylene glycol)-modified lysozyme to silica.

    PubMed

    Daly, Susan M; Przybycien, Todd M; Tilton, Robert D

    2005-02-15

    Covalent grafting of poly(ethylene glycol) (PEG) to pharmaceutical proteins, "PEGylation", is becoming more commonplace due to improved therapeutic efficacy. As these conjugates encounter interfaces in manufacture, purification, and end use and adsorption to these interfaces may alter achievable production yields and in vivo efficacies, it is important to understand how PEGylation affects protein adsorption mechanisms. To this end, we have studied the adsorption of unmodified and PEGylated chicken egg lysozyme to silica, using optical reflectometry, total internal reflection fluorescence (TIRF) spectroscopy, and atomic force microscopy (AFM) under varying conditions of ionic strength and extent of PEG modification. PEGylation of lysozyme changes the shape of the adsorption isotherm and alters the preferred orientation of lysozyme on the surface. There is an abrupt transition in the isotherm from low to high surface excess concentrations that correlates with a change in orientation of mono-PEGylated conjugates lying with the long axis parallel to the silica surface to an orientation with the long axis oriented perpendicular to the surface. No sharp transition is observed in the adsorption isotherm for di-PEGylated lysozyme within the range of concentrations examined. The net effect of PEGylation is to decrease the number of protein molecules per unit area relative to the adsorption of unmodified lysozyme, even under conditions where the surface is densely packed with conjugates. This is due to the area sterically excluded by the PEG grafts. The other major effect of PEGylation is to make conjugate adsorption significantly less irreversible than unmodified lysozyme adsorption. PMID:15697278

  10. Poly(propylene fumarate)/Polyethylene Glycol-Modified Graphene Oxide Nanocomposites for Tissue Engineering.

    PubMed

    Díez-Pascual, Ana M; Díez-Vicente, Angel L

    2016-07-20

    Poly(propylene fumarate) (PPF)-based nanocomposites incorporating different amounts of polyethylene glycol-functionalized graphene oxide (PEG-GO) have been prepared via sonication and thermal curing, and their surface morphology, structure, thermal stability, hydrophilicity, water absorption, biodegradation, cytotoxicity, mechanical, viscoelastic and antibacterial properties have been investigated. SEM and TEM images corroborated that the noncovalent functionalization with PEG caused the exfoliation of GO into thinner flakes. IR spectra suggested the presence of strong hydrogen-bonding interactions between the nanocomposite components. A gradual rise in the level of hydrophilicity, water uptake, biodegradation rate, surface roughness, protein absorption capability and thermal stability was found upon increasing GO concentration in the composites. Tensile tests revealed improved stiffness, strength and toughness for the composites compared to unfilled PPF, ascribed to a homogeneous GO dispersion within the matrix along with a strong PPF/PEG-GO interfacial adhesion via polar and hydrogen bonding interactions. Further, the nanocomposites retained enough stiffness and strength under a biological state to provide effective support for bone tissue formation. The antibacterial activity was investigated against Gram-positive Staphylococcus aureus and Staphylococcus epidermidis as well as Gram-negative Pseudomonas aeruginosa and Escherichia coli microorganisms, and it rose sharply upon increasing GO concentration; systematically, the biocide effect was stronger versus Gram-positive bacteria. Cell viability data demonstrated that PPF/PEG-GO composites do not induce toxicity over human dermal fibroblasts. These novel materials show great potential to be applied in the bone tissue engineering field. PMID:27383639

  11. Sorption of adamantanes on polyethylene glycol-modified graphitized thermal soot

    NASA Astrophysics Data System (ADS)

    Yashkin, S. N.; Ageeva, Yu. A.

    2014-04-01

    The thermodynamic characteristics of sorption of adamantane and its functional derivatives on graphitized thermal soot (GTS) modified with polyethylene glycol Carbowax 20M were determined by equilibrium gas chromatography. The resulting thermodynamic characteristics were analyzed and compared with the data measured for adamantanes on the surface of nonmodified GTS and polyethylene glycol deposited on an inert substrate. The solid carbon substrate was shown to affect the character of intermolecular interactions in the GTS-modifier system and the retention of framework compounds under the conditions of gas, liquid, and solid-state chromatography.

  12. Capillary electrophoretic separation of poly(ethylene glycol)-modified granulocyte-colony stimulating factor.

    PubMed

    Lee, Kyung Soo; Na, Dong Hee

    2010-03-01

    We evaluated the utility of capillary electrophoretic methods for analyzing poly(ethylene glycol) (PEG)-modified granulocyte-colony stimulating factor (G-CSF), a long-acting form of GCSF for the treatment of cancer therapy-induced neutropenia. Low- and high-molecularweight PEG-G-CSF conjugates prepared with aldehyde-activated PEG-5K and PEG-20K were separated by high-performance size-exclusion chromatography (HP-SEC), capillary zone electrophoresis (CZE), and sodium dodecyl sulfate-capillary gel electrophoresis (SDS-CGE). HPSEC showed low resolution for separating mono- and di-PEG-G-CSFs. SDS-CGE had higher resolution, but required a long analysis and had low peak efficiency. CZE could successfully separate both PEG-5K- and PEG-20K-conjugated G-CSFs with a running time of 20 min and high peak efficiency. In conclusion, CZE was better than SDS-CGE for separating PEG-G-CSF conjugates and will be useful for PEGylation studies, such as reaction monitoring for optimization of the PEGylation reaction, and purity and stability tests of PEG-G-CSF. PMID:20361316

  13. Polyethylene-Glycol-Modified Single-Walled Carbon Nanotubes for Intra-Articular Delivery to Chondrocytes

    PubMed Central

    Sacchetti, Cristiano; Liu-Bryan, Ru; Magrini, Andrea; Rosato, Nicola; Bottini, Nunzio; Bottini, Massimo

    2015-01-01

    Osteoarthritis (OA) is a common and debilitating degenerative disease of articular joints for which no disease-modifying medical therapy is currently available. Inefficient delivery of pharmacologic agents into cartilage-resident chondrocytes after systemic administration has been a limitation to the development of anti-OA medications. Direct intra-articular injection enables delivery of high concentrations of agents in close proximity to chondrocytes; however, the efficacy of this approach is limited by the fast clearance of small molecules and biomacromolecules after injection into the synovial cavity. Coupling of pharmacologic agents with drug delivery systems able to enhance their residence time and cartilage penetration can enhance the effectiveness of intra-articularly injected anti-OA medications. Herein we describe an efficient intra-articular delivery nanosystem based on single-walled carbon nanotubes (SWCNTs) modified with polyethylene glycol (PEG) chains (PEG-SWCNTs). We show that PEG-SWCNTs are capable to persist in the joint cavity for a prolonged time, enter the cartilage matrix, and deliver gene inhibitors into chondrocytes of both healthy and OA mice. PEG-SWCNT nanoparticles did not elicit systemic or local side effects. Our data suggest that PEG-SWCNTs represent a biocompatible and effective nanocarrier for intra-articular delivery of agents to chondrocytes. PMID:25415768

  14. Platelet adhesion and activation on polyethylene glycol modified polyurethane surfaces. Measurement of cytoplasmic calcium.

    PubMed

    Park, K D; Suzuki, K; Lee, W K; Lee, J E; Kim, Y H; Sakurai, Y; Okano, T

    1996-01-01

    Polyurethane (PU) surfaces were modified by coupling polyethylene glycol (PEG; molecular weight, 1,000) chains carrying different terminal groups (PU-PEG1K-OH, PU-PEG1K-NH2, PU-PEG1K-SO3) and longer PEG chains (MW, 3,350; PU-PEG3.4K-OH). The modified PU surfaces have the same PEG (1K) chain density. Surface induced platelet activation was evaluated by measuring cytoplasmic free calcium concentration in platelets contacting modified surfaces, and platelet adhesion onto modified surfaces was investigated in vitro. Cytoplasmic free calcium levels in platelets contacting PU-PEG-SO3 remained relatively constant, in contrast to the significant increase observed for PU-PEG-NH2, PU-PEG-OH, and control PU surfaces. The degree of platelet adhesion clearly demonstrates that all PEG graft surfaces prevented platelet adhesion. Among PEG1K surfaces, PU-PEG-SO3 shows the lowest platelet adhesion. In the case of relatively longer PEG grafted surfaces (PU-PEG3.4K-OH and PU-PEG3.4K-Hep), both surfaces were found to prevent the increase in both cytoplasmic free calcium and platelet adhesion. These results suggest that longer PEG chain grafting is more effective than shorter grafting in preventing platelet activation and adhesion because of the highly dynamic movement of hydrated PEG chains at the interface. In addition, in vitro platelet interaction is dependent upon terminal groups of PEG chains on PEG1K series surfaces. PMID:8945010

  15. Polyethylene Glycol Modified, Cross-Linked Starch Coated Iron Oxide Nanoparticles for Enhanced Magnetic Tumor Targeting

    PubMed Central

    Cole, Adam J.; David, Allan E.; Wang, Jianxin; Galbán, Craig J.; Hill, Hannah L.; Yang, Victor C.

    2010-01-01

    While successful magnetic tumor targeting of iron oxide nanoparticles has been achieved in a number of models, the rapid blood clearance of magnetically suitable particles by the reticuloendothelial system (RES) limits their availability for targeting. This work aimed to develop a long-circulating magnetic iron oxide nanoparticle (MNP) platform capable of sustained tumor exposure via the circulation and, thus, enhanced magnetic tumor targeting. Aminated, cross-linked starch (DN) and aminosilane (A) coated MNPs were successfully modified with 5 kDa (A5, D5) or 20 kDa (A20, D20) polyethylene glycol (PEG) chains using simple N-Hydroxysuccinimide (NHS) chemistry and characterized. Identical PEG-weight analogues between platforms (A5 & D5, A20 & D20) were similar in size (140–190 nm) and relative PEG labeling (1.5% of surface amines – A5/D5, 0.4% – A20/D20), with all PEG-MNPs possessing magnetization properties suitable for magnetic targeting. Candidate PEG-MNPs were studied in RES simulations in vitro to predict long-circulating character. D5 and D20 performed best showing sustained size stability in cell culture medium at 37°C and 7 (D20) to 10 (D5) fold less uptake in RAW264.7 macrophages when compared to previously targeted, unmodified starch MNPs (D). Observations in vitro were validated in vivo, with D5 (7.29 hr) and D20 (11.75 hr) showing much longer half-lives than D (0.12 hr). Improved plasma stability enhanced tumor MNP exposure 100 (D5) to 150 (D20) fold as measured by plasma AUC0-∞ Sustained tumor exposure over 24 hours was visually confirmed in a 9L-glioma rat model (12 mg Fe/kg) using magnetic resonance imaging (MRI). Findings indicate that both D5 and D20 are promising MNP platforms for enhanced magnetic tumor targeting, warranting further study in tumor models. PMID:21176955

  16. Poly(ethylene glycol)-Modified Tapered-Slit Membrane Filter for Efficient Release of Captured Viable Circulating Tumor Cells.

    PubMed

    Kim, Young Jun; Kang, Yoon-Tae; Cho, Young-Ho

    2016-08-16

    The grafting of poly(ethylene glycol) (PEG) onto an SU8 microfilter has been demonstrated for efficient capture and release of circulating tumor cells (CTCs). Previous CTC filters showed low cell release efficiency due to hydrophobic surfaces, even though their capture efficiency was considerable. PEG, a hydrophilic polymeric compound mainly used to form nonfouling thin films on silicon surfaces, induces repulsive force so that the nonspecific adsorption of the surface is incomparably reduced in comparison with unmodified filter surfaces. The effectiveness of PEG-modified CTC filters was verified through lung (H358) and colorectal (SW620) cancer cells spiked, respectively, in phosphate-buffered saline (PBS) and unprocessed whole blood. The modified SU8 filters achieved approximately 37.7% and 22.8% improvement in release efficiency without significant changes in cell viability and capture efficiency. In order to verify the filter's potential for clinical applications, we extended our experiments using cancer patient blood samples. Six blood samples from colorectal and lung cancer patients were processed, and captured CTCs were efficiently released. From these experiments, the present PEG-modified filter captures and releases on average 14 ± 7.4 CTCs/mL, including EpCAM-negative CTCs, which could not be captured by previous single antibody-based methods. The antibody-free isolation with enhanced release efficiency facilitates viable cell retrieval, which is significant to CTC culture and comprehensive molecular study for verifying the mechanism of metastasis and cancer. PMID:27444512

  17. Pharmacokinetic properties of a 40 kDa branched polyethylene glycol-modified form of consensus interferon-alpha (PEG-CIFN) in rhesus monkeys.

    PubMed

    Du, Yu; Tian, Hong; Gao, Xiang-Dong; Yao, Wen-Bing

    2008-11-01

    The pharmacokinetic properties of a branched 40 kDa polyethylene glycol (PEG) conjugate formulation of consensus interferon-alpha (CIFN) was evaluated in rhesus monkeys following subcutaneous administration. Four groups of rhesus monkeys (n=6 per group) received 1250, 300 and 150 microg/kg of PEG-CIFN and 150 microg/kg CIFN, respectively. Serum concentrations of the interferons were measured with an antiviral activity assay at various time points after administration. The PK profiles of the pooled data were described by a noncompartmental method. Peak concentration of PEG-CIFN was observed at 27-31 h, followed by a prolonged decay in comparison with the unmodified CIFN, the PEG-CIFN had a 4-5-fold longer terminal half-life. The apparent clearance (dose(sc)/AUC) decreased from 150 mL/h/kg for CIFN to 19.0-45.5 mL/h/kg for PEG-CIFNs. The AUC was lower for PEG-CIFN than that for CIFN at the 150 microg/kg. PMID:18985796

  18. Polyethylene glycol enhanced protein refolding.

    PubMed

    Cleland, J L; Builder, S E; Swartz, J R; Winkler, M; Chang, J Y; Wang, D I

    1992-09-01

    Previous studies on the refolding of recombinant bovine carbonic anhydrase B (CAB) indicated that polyethylene glycol (PEG) significantly enhanced the recovery of active protein by reducing aggregation. To further test the ability of PEG to enhance refolding, three recombinant human proteins, deoxyribonuclease (rhDNAse), tissue plasminogen activator (rhtPA), and interferon-gamma (rhIFN-gamma) were refolded in the presence of PEG (3350 MW). rhDNAse produced from CHO cells was denatured in 7.2 M urea and refolded by rapid dilution to 4.0 M urea and 0.20 mg/ml protein. When a final PEG to rhDNAse molar ratio of 5 to 1 (0.1 milligram PEG, 3350 MW) was used in the dilution buffer, refolding was improved by 30% to yield complete recovery of active protein. Impure E. coli derived inclusion body preparations of rhDNAse were solubilized in 8 M urea and refolded by dilution to 4 M urea and 0.10 mg/ml protein. Refolding with a dilution buffer which yielded a final PEG to rhDNAse molar ratio of 10 to 1 (0.1 milligram PEG, 3350 MW) resulted in a three-fold increase in the recovery of active protein. When PEG was used in the dilution buffer, aggregation of rhDNAse did not occur during refolding in either case. rhtPA produced from CHO cells was denatured in 5 M guanidine hydrochloride (GuHCl) and refolded by rapid dilution to 0.10 M GuHCl and 0.20 mg/ml protein.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1368998

  19. Radioprotection by polyethylene glycol-protein complexes in mice

    SciTech Connect

    Gray, B.H.; Stull, R.W.

    1983-03-01

    Polyethylene glycol of about 5000 D was activated with cyanuric chloride, and the activated compound was complexed to each of three proteins. Polyethylene glycol-superoxide dismutase and polyethylene glycol-catalase were each radioprotectants when administered prophylactically to female B6CBF1 mice before irradiation. The dose reduction factor for these mice was 1.2 when 5000 units of polyethylene glycol-catalase was administered before /sup 60/Co irradiation. Female B6CBF1 mice administered prophylactic intravenous injections of catalase, polyethylene glycol-albumin, or heat-denatured polyethylene glycol-catalase had survival rates similar to phosphate-buffered saline-injected control mice following /sup 60/Co irradiation. Polyethylene glycol-superoxide dismutase and polyethylene glycol-catalase have radioprotective activity in B6CBF1 mice, which appears to depend in part on enzymatic activities of the complex. However, no radioprotective effect was observed in male C57BL/6 mice injected with each polyethylene glycol-protein complex at either 3 or 24 hr before irradiation. The mechanism for radioprotection by these complexes may depend in part on other factors.

  20. A novel preparation of milk protein/polyethylene terephthalate fabric

    NASA Astrophysics Data System (ADS)

    Zhou, J. F.; Zheng, D. D.; Zhong, L.; Zhang, F. X.; Zhang, G. X.

    2016-07-01

    In this work, -NH2 groups were introduced to polyethylene terephthalate (PET) fibers by nitration and reduction method, and then milk protein was grafted on the nitrated and reduced PET (NR PET) fibers by sucrose glycidyl ether crosslinking agent. FTIR suggested the milk protein was successfully grafted on PET fiber surface. SEM images showed a layer of substance covered on the PET fiber surface. DSC demonstrated an excellent thermal stability of milk protein/PET fiber. The moisture regain was improved by milk protein/PET fiber. Moreover, the crease recovery angle and stiffness were retained by the milk protein/PET fabric.

  1. Extrusion foaming of protein-based thermoplastic and polyethylene blends

    NASA Astrophysics Data System (ADS)

    Gavin, Chanelle; Lay, Mark C.; Verbeek, Casparus J. R.

    2016-03-01

    Currently the extrusion foamability of Novatein® Thermoplastic Protein (NTP) is being investigated at the University of Waikato in collaboration with the Biopolymer Network Ltd (NZ). NTP has been developed from bloodmeal (>86 wt% protein), a co-product of the meat industry, by adding denaturants and plasticisers (tri-ethylene glycol and water) allowing it to be extruded and injection moulded. NTP alone does not readily foam when sodium bicarbonate is used as a chemical blowing agent as its extensional viscosity is too high. The thermoplastic properties of NTP were modified by blending it with different weight fractions of linear low density polyethylene (LLDPE) and polyethylene grafted maleic anhydride (PE-g-MAH) compatibiliser. Extrusion foaming was conducted in two ways, firstly using the existing water content in the material as the blowing agent and secondly by adding sodium bicarbonate. When processed in a twin screw extruder (L/D 25 and 10 mm die) the material readily expanded due to the internal moisture content alone, with a conditioned expansion ratio of up to ± 0.13. Cell structure was non-uniform exhibiting a broad range cell sizes at various stages of formation with some coalescence. The cell size reduced through the addition of sodium bicarbonate, overall more cells were observed and the structure was more uniform, however ruptured cells were also visible on the extrudate skin. Increasing die temperature and introducing water cooling reduced cell size, but the increased die temperature resulted in surface degradation.

  2. Interfacial Protein-Protein Associations

    PubMed Central

    Langdon, Blake B.; Kastantin, Mark; Walder, Robert; Schwartz, Daniel K.

    2014-01-01

    While traditional models of protein adsorption focus primarily on direct protein-surface interactions, recent findings suggest that protein-protein interactions may play a central role. Using high-throughput intermolecular resonance energy transfer (RET) tracking, we directly observed dynamic, protein-protein associations of bovine serum albumin on poly(ethylene glycol) modified surfaces. The associations were heterogeneous and reversible, and associating molecules resided on the surface for longer times. The appearance of three distinct RET states suggested a spatially heterogeneous surface – with areas of high protein density (i.e. strongly-interacting clusters) coexisting with mobile monomers. Distinct association states exhibited characteristic behavior, i.e. partial-RET (monomer-monomer) associations were shorter-lived than complete-RET (protein-cluster) associations. While the fractional surface area covered by regions with high protein density (i.e. clusters) increased with increasing concentration, the distribution of contact times between monomers and clusters was independent of solution concentration, suggesting that associations were a local phenomenon, and independent of the global surface coverage. PMID:24274729

  3. Modulation of Protein Adsorption and Cell Proliferation on Polyethylene Immobilized Graphene Oxide Reinforced HDPE Bionanocomposites.

    PubMed

    Upadhyay, Rahul; Naskar, Sharmistha; Bhaskar, Nitu; Bose, Suryasarathi; Basu, Bikramjit

    2016-05-18

    The uniform dispersion of nanoparticles in a polymer matrix, together with an enhancement of interfacial adhesion is indispensable toward achieving better mechanical properties in the nanocomposites. In the context to biomedical applications, the type and amount of nanoparticles can potentially influence the biocompatibility. To address these issues, we prepared high-density polyethylene (HDPE) based composites reinforced with graphene oxide (GO) by melt mixing followed by compression molding. In an attempt to tailor the dispersion and to improve the interfacial adhesion, we immobilized polyethylene (PE) onto GO sheets by nucleophilic addition-elimination reaction. A good combination of yield strength (ca. 20 MPa), elastic modulus (ca. 600 MPa), and an outstanding elongation at failure (ca. 70%) were recorded with 3 wt % polyethylene grafted graphene oxide (PE-g-GO) reinforced HDPE composites. Considering the relevance of protein adsorption as a biophysical precursor to cell adhesion, the protein adsorption isotherms of bovine serum albumin (BSA) were determined to realize three times higher equilibrium constant (Keq) for PE-g-GO-reinforced HDPE composites as compared to GO-reinforced composites. To assess the cytocompatibility, we grew osteoblast cell line (MC3T3) and human mesenchymal stem cells (hMSCs) on HDPE/GO and HDPE/PE-g-GO composites, in vitro. The statistically significant increase in metabolically active cell over different time periods in culture for up to 6 days in MC3T3 and 7 days for hMSCs was observed, irrespective of the substrate composition. Such observation indicated that HDPE with GO or PE-g-GO addition (up to 3 wt %) can be used as cell growth substrate. The extensive proliferation of cells with oriented growth pattern also supported the fact that tailored GO addition can support cellular functionality in vitro. Taken together, the experimental results suggest that the PE-g-GO in HDPE can effectively be utilized to enhance both mechanical and

  4. Controlling microencapsulation and release of micronized proteins using poly(ethylene glycol) and electrospraying.

    PubMed

    Bock, Nathalie; Dargaville, Tim R; Woodruff, Maria A

    2014-07-01

    The fabrication of tailored microparticles for delivery of therapeutics is a challenge relying upon a complex interplay between processing parameters and materials properties. The emerging use of electrospraying allows better tailoring of particle morphologies and sizes than current techniques, critical to reproducible release profiles. While dry encapsulation of proteins is essential for the release of active therapeutics from microparticles, it is currently uncharacterized in electrospraying. To this end, poly(ethylene glycol) (PEG) was assessed as a micronizing and solubilizing agent for dry protein encapsulation and release from electrosprayed particles made from polycaprolactone (PCL). The physical effect of PEG in protein-loaded poly(lactic-co-glycolic acid) (PLGA) particles was also studied, for comparison. The addition of 5-15 wt% PEG 6 kDa or 35 kDa resulted in reduced PCL particle sizes and broadened distributions, which could be improved by tailoring the electrospraying processing parameters, namely by reducing polymer concentration and increasing flow rate. Upon micronization, protein particle size was reduced to the micrometer domain, resulting in homogenous encapsulation in electrosprayed PCL microparticles. Microparticle size distributions were shown to be the most determinant factor for protein release by diffusion and allowed specific control of release patterns. PMID:24657821

  5. Surface modification of polydimethylsiloxane with photo-grafted poly(ethylene glycol) for micropatterned protein adsorption and cell adhesion.

    PubMed

    Sugiura, Shinji; Edahiro, Jun-ichi; Sumaru, Kimio; Kanamori, Toshiyuki

    2008-06-01

    In this study, we applied photo-induced graft polymerization to micropatterned surface modification of polydimethylsiloxane (PDMS) with poly(ethylene glycol). Two types of monomers, polyethylene glycol monoacrylate (PEGMA) and polyethylene glycol diacrylate (PEGDA), were tested for surface modification of PDMS. Changes in the surface hydrophilicity and surface element composition were characterized by contact angle measurement and electron spectroscopy for chemical analysis. The PEGMA-grafted PDMS surfaces gradually lost their hydrophilicity within two weeks. In contrast, the PEGDA-grafted PDMS surface maintained stable hydrophilic characteristics for more than two months. Micropatterned protein adsorption and micropatterned cell adhesion were successfully demonstrated using PEGDA-micropatterned PDMS surfaces, which were prepared by photo-induced graft polymerization using photomasks. The PEGDA-grafted PDMS exhibited useful characteristics for microfluidic devices (e.g. hydrophilicity, low protein adsorption, and low cell attachment). The technique presented in this study will be useful for surface modification of various research tools and devices. PMID:18242961

  6. Rationalization of Membrane Protein Crystallization with Polyethylene Glycol Using a Simple Depletion Model

    PubMed Central

    Tanaka, Shinpei; Ataka, Mitsuo; Onuma, Kazuo; Kubota, Tomomi

    2003-01-01

    Based on the importance of crystallizing membrane proteins in a rational way, cytochrome bc1 complex (BC1) was crystallized using polyethylene glycol (PEG) as a sole crystallization agent. Interaction between protein-detergent complexes of BC1 was estimated by dynamic light scattering, and was compared with the numerical calculation using the Derjaguin-Landau-Verwey-Overbeek potential plus a depletion potential, without considering specific surface properties of the protein-detergent complexes. The experiments and calculation were found to be consistent and we obtained a relation between PEG molecular weight M and the range of depletion zone δ as δ ∼ M0.48±0.02. The stability of liquid phase of BC1 solutions was controlled by a ratio of (the range of depletion zone)/(the radius of a BC1 particle), which was consistent with recent theoretical predictions. The crystallization was most successful under a condition where the stability of the liquid phase changed from stable to unstable. The PEG molecular weight that fulfilled this condition coincided with the one used empirically to crystallize BC1 in the past by a number of groups. These results are compared to the fact that membrane proteins were often successfully crystallized close to the detergent cloud point. PMID:12719259

  7. High performance protein microarrays based on glycidyl methacrylate-modified polyethylene terephthalate plastic substrate.

    PubMed

    Liu, Yingshuai; Li, Chang Ming; Hu, Weihua; Lu, Zhisong

    2009-01-15

    There is a great challenge to immobilize high density of probe molecules for high performance protein microarrays, and this is achieved in this work by using polyethylene terephthalate (PET) plastic substrate onto which glycidyl methacrylate (GMA) photopolymer is grafted under mild conditions to introduce high density of epoxy groups for covalent immobilization of proteins. The poly(GMA)-grafted PET (PGMA-PET) surface was characterized with atomic force microscope (AFM) and attenuated total reflectance Fourier transform infra-red (ATR-FTIR) spectroscopy. For high density of protein immobilization and good quality of microspots, experiments were conducted to optimize the printing buffer, and an optimal buffer was found out to be PBS with 10% glycerol+0.003% triton X-100. According to the studies of loading capacity and immobilization kinetics, the optimal protein probe concentration and incubation time for the efficient immobilization are 200 microg mL(-1) and 8h, respectively. The performance of the PGMA-PET-based protein microarrays is evaluated with sandwich immunoassay using rat IgG and anti-rat IgG as model proteins, demonstrating a limit of detection (LOD) of 10 pg mL(-1) and a dynamic range of five orders of magnitude which are better than or very comparable with the reported or commercially available immunoassays, while providing a high-throughput approach. The work renders a simple and economic method to manufacture high performance protein microarrays and is expected to have great potentials in broad applications related to clinic diagnosis, drug discovery and proteomic research. PMID:19064107

  8. Characterizing the modification of surface proteins with poly(ethylene glycol) to interrupt platelet adhesion

    PubMed Central

    Xu, Haiyan; Kaar, Joel L.; Russell, Alan J.; Wagner, William R.

    2010-01-01

    Surface protein modification with poly(ethylene glycol) (PEG) can inhibit acute thrombosis on damaged vascular and biomaterial surfaces by blocking surface protein–platelet interactions. However, the feasibility of employing protein reactive PEGs to limit intravascular and biomaterial thrombosis in vivo is contingent upon rapid and extensive surface protein modification. To characterize the factors controlling this potential therapeutic approach, the model protein bovine serum albumin was adsorbed onto polyurethane surfaces and modified with PEG-carboxymethyl succinimidyl ester (PEG-NHS), PEG-isocyanate (PEG-ISO), or PEG-diisocyanate (PEG-DISO) in aqueous buffer at varying concentrations and contact times. It was found that up to 5 PEGs could be attached per albumin molecule within one min and that adsorbed albumin PEGylation approached maximal levels by 6 min. The lability of reactive PEGs in aqueous buffer reduced total protein modification by 50% when the PEG solution was incubated for 7 min prior to application. For fibrinogen PEGylation (performed in the solution phase), PEG-NHS was more reactive than PEG-ISO or PEG-DISO. The γ peptide of fibrinogen, which contains several key platelet-binding motifs, was highly modified. A marked reduction in platelet adhesion was observed on fibrinogen-adsorbed polyurethane treated with PEG-NHS or PEG-DISO. Relative differences in platelet adhesion on PEG-NHS and PEG-DISO modified surfaces could be attributed to differences in reactivity towards fibrinogen and the size of the polymer backbone. Taken together, these findings provide insight and guidance for applying protein reactive PEGs for the interruption of acute thrombotic deposition. PMID:16457880

  9. Durable grafting of silkworm pupa protein onto the surface of polyethylene terephthalate fibers.

    PubMed

    Zhou, Jianfeng; Zheng, Dandan; Zhang, Fengxiu; Zhang, Guangxian

    2016-12-01

    In this paper, reactive -NH2 groups (8.36×10(-6)mol/g fabric) were introduced to the surface of polyethylene terephthalate (PET) fabrics by a nitration and reduction method, and epoxy groups were introduced to silkworm pupa protein (SPP) by reaction with epoxy chloropropane. PET-SPP composite fabrics were then prepared by reaction of these two precursors. The results showed that the SPP was firmly grafted onto the PET fabric surface and that the hydrophilicity of the fabric was markedly improved by the grafting of SPP. SEM images revealed a layer of substance covering the surface of the PET fibers, and XPS investigation showed that the nitrogen content of the PET-SPP fabric was higher than that of the original PET fabric (2.32% vs 0%). ATR-FTIR adsorption bands at 1653 and 1543cm(-1) suggested the successful grafting of SPP onto the PET fabric surface. The DSC and TG of the PET fibers demonstrated that the thermal stability of the original PET fibers was maintained well by the SPP-grafted PET fibers. The breaking strength, bending rigidity, air permeability, and crease recovery angle of the original PET fabric were also retained by the SPP-grafted PET fabric. PMID:27612829

  10. Effects of maleimide-polyethylene glycol-modified human hemoglobin (MP4) on tissue necrosis in SKH1-hr hairless mice

    PubMed Central

    2009-01-01

    Objective Tissue hypoxia after blood loss, replantation and flap reperfusion remains a challenging task in surgery. Normovolemic hemodilution improves hemorheologic properties without increasing oxygen carrying capacity. Red blood cell transfusion is the current standard of treatment with its attendant risks. The aim of this study was to investigate the potential of the chemically modified hemoglobin, MP4, to reduce skin flap necrosis and its effect on selected blood markers and kidneys. Materials and methods Tissue ischemia was induced in the ear of hairless mice (n = 26). Hemodilution was performed by replacing one third of blood volume with the similar amount of MP4, dextran, or blood. The extent of non-perfused tissue was assessed by intravital fluorescent microscopy. Results Of all groups, MP4 showed the smallest area of no perfusion (in percentage of the ear ± SEM: 16.3% ± 2.4), the control group the largest (22.4% ± 3.5). Leukocytes showed a significant increase in the MP4 and dextran group (from 8.7 to 13.6 respectively 15.4*109/l). On histology no changes of the kidneys could be observed. Conclusion MP4 causes an increase of leukocytes, improves the oxygen supply of the tissue and shows no evidence of renal impairment. PMID:19380283

  11. Interrelationship between partition behavior of organic compounds and proteins in aqueous dextran-polyethylene glycol and polyethylene glycol-sodium sulfate two-phase systems.

    PubMed

    Ferreira, Luisa A; da Silva, Nuno R; Wlodarczyk, Samarina R; Loureiro, Joana A; Madeira, Pedro P; Teixeira, José A; Uversky, Vladimir N; Zaslavsky, Boris Y

    2016-04-22

    Partition behavior of adenosine and guanine mononucleotides was examined in aqueous dextran-polyethylene glycol (PEG) and PEG-sodium sulfate two-phase systems. The partition coefficients for each series of mononucleotides were analyzed as a functions of the number of phosphate groups and found to be dependent on the nature of nucleic base and on the type of ATPS utilized. It was concluded that an average contribution of a phosphate group into logarithm of partition coefficient of a mononucleotide cannot be used to estimate the difference between the electrostatic properties of the coexisting phases of ATPS. The data obtained in this study were considered together with those for other organic compounds and proteins reported previously, and the linear interrelationship between logarithms of partition coefficients in dextran-PEG, PEG-Na2SO4 and PEG-Na2SO4-0.215M NaCl (all in 0.01M Na- or K/Na-phosphate buffer, pH 7.4 or 6.8) was established. Similar relationship was found for the previously reported data for proteins in Dex-PEG, PEG-600-Na2SO4, and PEG-8000-Na2SO4 ATPS. It is suggested that the linear relationships of the kind established in ATPS may be observed for biological properties of compounds as well. PMID:27016118

  12. Wear properties of polyethylene-metal and polyethylene-ceramic bearings for hip joint replacements: The effect of temperature and protein precipitation in hip simulator tests

    NASA Astrophysics Data System (ADS)

    Liao, Yen-Shuo

    Ultra-high-molecular weight polyethylene (PE) cups bearing against metal or ceramic balls are the most commonly used combinations of materials for human hip joint replacements. The wear properties of these materials are typically evaluated in the laboratory using hip joint wear simulators, while lubricated with bovine serum. A previous test evaluating the PE cups against cobalt-chrome (CoCr), zirconia (Zr) and alumina balls demonstrated the sensitivity of serum proteins to elevated temperature; especially for Zr/PE, which showed the highest protein precipitation and bulk lubricant temperature but the lowest cup wear. In the present investigation, a temperature control system was used on a hip simulator to systematically evaluate the relationship between temperature and denaturation of the serum proteins which, in turn, affects the friction and wear properties of the prosthetic materials being tested. In order to control protein precipitation, the interface was temperature reduced by circulating coolant at 4°C through the center of the CoCr or Zr balls during a wear test. With cooling, protein assay of the serum showed 66% and 50% reductions in protein precipitation with the CoCr and Zr balls, respectively. The wear rate of the PE cups against the CoCr balls decreased by an average of 44%, whereas two of the three PE cups running against Zr balls exhibited slight increases in their wear rates, and the third showed a two fold increase. Under scanning electron microscopy, there were marked differences in the worn surfaces of the cups for the various conditions, and differences in the morphology of the PE wear debris recovered from the serum. For example, granular particles predominated without cooling, whereas fibrous particles predominated with cooling. Since particles generated in vivo (i.e., retrieved from periprosthetic tissues) typically show approximately equal proportions of granules and fibrils, the use of an intermediate coolant temperature might provide

  13. Protein adsorption and cell adhesion on nanoscale bioactive coatings formed from poly(ethylene glycol) and albumin microgels

    PubMed Central

    Scott, Evan A.; Nichols, Michael D.; Cordova, Lee H.; George, Brandon J.; Jun, Young-Shin; Elbert, Donald L.

    2008-01-01

    Late-term thrombosis on drug-eluting stents is an emerging problem that might be addressed using extremely thin, biologically-active hydrogel coatings. We report a dip-coating strategy to covalently link poly(ethylene glycol) (PEG) to substrates, producing coatings with <≈100 nm thickness. Gelation of PEG-octavinylsulfone with amines in either bovine serum albumin (BSA) or PEG-octaamine was monitored by dynamic light scattering (DLS), revealing the presence of microgels before macrogelation. NMR also revealed extremely high end group conversions prior to macrogelation, consistent with the formation of highly crosslinked microgels and deviation from Flory-Stockmayer theory. Before macrogelation, the reacting solutions were diluted and incubated with nucleophile-functionalized surfaces. Using optical waveguide lightmode spectroscopy (OWLS) and quartz crystal microbalance with dissipation (QCM-D), we identified a highly hydrated, protein-resistant layer with a thickness of approximately 75 nm. Atomic force microscopy in buffered water revealed the presence of coalesced spheres of various sizes but with diameters less than about 100 nm. Microgel-coated glass or poly(ethylene terephthalate) exhibited reduced protein adsorption and cell adhesion. Cellular interactions with the surface could be controlled by using different proteins to cap unreacted vinylsulfone groups within the coating. PMID:18771802

  14. Polyvinylpyrrolidone-Poly(ethylene glycol) Modified Silver Nanorods Can Be a Safe, Noncarrier Adjuvant for HIV Vaccine.

    PubMed

    Liu, Ye; Balachandran, Yekkuni L; Li, Dan; Shao, Yiming; Jiang, Xingyu

    2016-03-22

    One of the biggest obstacles for the development of HIV vaccines is how to sufficiently trigger crucial anti-HIV immunities via a safe manner. We herein integrated surface modification-dependent immunostimulation against HIV vaccine and shape-dependent biosafety and designed a safe noncarrier adjuvant based on silver nanorods coated by both polyvinylpyrrolidone (PVP) and polyethylene glycol (PEG). Such silver nanorods can significantly elevate crucial immunities of HIV vaccine and overcome the toxicity, which is a big problem for other existing adjuvants. This study thus provided a principle for designing a safe and high-efficacy material for an adjuvant and allow researchers to really have a safe and effective prophylaxis against HIV. We expect this material approach to be applicable to other types of vaccines, whether they are preventative or therapeutic. PMID:26844372

  15. Protein adsorption is required for stealth effect of poly(ethylene glycol)- and poly(phosphoester)-coated nanocarriers.

    PubMed

    Schöttler, Susanne; Becker, Greta; Winzen, Svenja; Steinbach, Tobias; Mohr, Kristin; Landfester, Katharina; Mailänder, Volker; Wurm, Frederik R

    2016-04-01

    The current gold standard to reduce non-specific cellular uptake of drug delivery vehicles is by covalent attachment of poly(ethylene glycol) (PEG). It is thought that PEG can reduce protein adsorption and thereby confer a stealth effect. Here, we show that polystyrene nanocarriers that have been modified with PEG or poly(ethyl ethylene phosphate) (PEEP) and exposed to plasma proteins exhibit a low cellular uptake, whereas those not exposed to plasma proteins show high non-specific uptake. Mass spectrometric analysis revealed that exposed nanocarriers formed a protein corona that contains an abundance of clusterin proteins (also known as apolipoprotein J). When the polymer-modified nanocarriers were incubated with clusterin, non-specific cellular uptake could be reduced. Our results show that in addition to reducing protein adsorption, PEG, and now PEEPs, can affect the composition of the protein corona that forms around nanocarriers, and the presence of distinct proteins is necessary to prevent non-specific cellular uptake. PMID:26878141

  16. Protein adsorption is required for stealth effect of poly(ethylene glycol)- and poly(phosphoester)-coated nanocarriers

    NASA Astrophysics Data System (ADS)

    Schöttler, Susanne; Becker, Greta; Winzen, Svenja; Steinbach, Tobias; Mohr, Kristin; Landfester, Katharina; Mailänder, Volker; Wurm, Frederik R.

    2016-04-01

    The current gold standard to reduce non-specific cellular uptake of drug delivery vehicles is by covalent attachment of poly(ethylene glycol) (PEG). It is thought that PEG can reduce protein adsorption and thereby confer a stealth effect. Here, we show that polystyrene nanocarriers that have been modified with PEG or poly(ethyl ethylene phosphate) (PEEP) and exposed to plasma proteins exhibit a low cellular uptake, whereas those not exposed to plasma proteins show high non-specific uptake. Mass spectrometric analysis revealed that exposed nanocarriers formed a protein corona that contains an abundance of clusterin proteins (also known as apolipoprotein J). When the polymer-modified nanocarriers were incubated with clusterin, non-specific cellular uptake could be reduced. Our results show that in addition to reducing protein adsorption, PEG, and now PEEPs, can affect the composition of the protein corona that forms around nanocarriers, and the presence of distinct proteins is necessary to prevent non-specific cellular uptake.

  17. Capture of Magnetic Nanoparticles in Simulated Blood Vessels: Effects of Proteins and Coating with Poly(ethylene glycol)

    NASA Astrophysics Data System (ADS)

    Robertson, Jaimee; Brazel, Christopher

    2012-11-01

    Magnetic nanoparticles (MNPs) have applications in cancer treatment as they can be captured and localized to a diseased site by use of an external magnetic field. After localization, cancer treatments such as magnetically targeted chemotherapy and localized hyperthermia can be applied. Previously, our lab has shown that the percent capture of MNPs is significantly reduced when MNPs are dispersed in protein solutions compared to water or aqueous polymer solutions. The purpose of this study was to determine the effects of proteins on capture efficiency and to investigate the ability of poly(ethylene glycol), PEG, coatings to reduce aggregation of MNPs with proteins, allowing for a greater capture of MNPs in flow. Using Tygon® tubing to simulate blood vessels, a maghemite nanoparticle solution was pumped through a capture zone, where a magnetic field was applied. After passing through the capture zone, the fluid flowed to a spectrophotometer, which measured the absorbance of the solution. The introduction of proteins into the nanoparticle solution reduced the percent capture of MNPs. However, coating the MNPs with PEG aided in preventing aggregation and led to higher capture efficiencies in protein solutions. Additionally, the effects of capture length and protein exposure time were examined. It was found that a higher percent capture is attainable with a longer capture length. Furthermore, on a scale of hours, the percent capture is not affected by the protein exposure time. Funded by NSF REU Grant 1062611 and NIH NCI R21CA 141388.

  18. Capillary isoelectric focusing and fluorometric detection of proteins and microorganisms dynamically modified by poly(ethylene glycol) pyrenebutanoate.

    PubMed

    Horka, Marie; Ruzicka, Filip; Horký, Jaroslav; Holá, Veronika; Slais, Karel

    2006-12-15

    The nonionogenic pyrene-based tenside, poly(ethylene glycol) pyrenebutanoate, was prepared and applied in capillary isoelectric focusing with fluorometric detection. This dye was used here as a buffer additive in capillary isoelectric focusing for a dynamic modification of the sample of proteins and microorganisms. The values of the isoelectric points of the labeled bioanalytes were calculated with use of the fluorescent pI markers and were found comparable with pI of the native compounds. The mixed cultures of proteins and microorganisms, Escherichia coli CCM 3954, Staphylococcus epidermidis CCM 4418, Proteus vulgaris, Enterococcus faecalis CCM 4224, and Stenotrophomonas maltophilia, the strains of the yeast cells, Candida albicans CCM 8180, Candida krusei, Candida parapsilosis, Candida glabrata, Candida tropicalis, and Saccharomyces cerevisiae were reproducibly focused and separated by the suggested technique. Using UV excitation for the on-column fluorometric detection, the minimum detectable amount was down to 10 cells injected on the separation capillary. PMID:17165837

  19. Improving biocompatibility by controlling protein adsorption: Modification and design of biomaterials using poly(ethylene glycol) microgels and microspheres

    NASA Astrophysics Data System (ADS)

    Scott, Evan Alexander

    2009-12-01

    Guided by the clinical needs of patients and developments in biology and materials science, the primary focus of the biomaterials field remains at the solid/liquid interface between biomaterial surfaces and biological fluids. For blood-contacting devices, biological responses are initially elicited and directed by proteins that adsorb from this multicomponent solution to form thin films on their surfaces. The identity, conformation, and quantity of adsorbed proteins are related to the properties of a material's surface. For example, hydrophobic surfaces tend to be thrombotic via interactions between platelets and adsorbed fibrinogen, while surface-activation of specific enzymes initiates the coagulation cascade on hydrophilic surfaces. The objective of this thesis is to improve the design of biomaterials through the analysis and control of adsorbing protein layers. This goal is approached through three separate strategies. First, a proteomics-based methodology is presented for the assessment of protein conformation at the residue level after adsorption to biomaterial surfaces. A quantitative mass spectrometric technique is additionally suggested for the identification and quantification of proteins within adsorbed protein layers. Second, a method is described for the covalent attachment of poly(ethylene glycol) (PEG)-based hydrogel coatings onto biomaterials surfaces for the minimization of protein adsorption. The coatings are applied using partially crosslinked PEG solutions containing polymer and protein oligomers and microgels that can be designed to control cell adhesion. Finally, a modular strategy is proposed for the assembly of bioactive PEG-based hydrogel scaffolds. This was accomplished using novel PEG microspheres with diverse characteristics that individually contribute to the ability of the scaffold to direct cellular infiltration. The methodologies proposed by this thesis contribute to the recent shift in biomaterials and tissue engineering strategies

  20. Protein partitioning in poly(ethylene glycol)/sodium polyacrylate aqueous two-phase systems.

    PubMed

    Johansson, Hans-Olof; Magaldi, Flavio Musa; Feitosa, Eloi; Pessoa, Adalberto

    2008-01-18

    The partition of hemoglobin, lysozyme and glucose-6-phosphate dehydrogenase (G6PDH) in a novel inexpensive aqueous two-phase system (ATPS) composed by poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) has been studied. The effect of NaCl and Na(2)SO(4), pH and PEG molecular size on the partitioning has been studied. At high pH (above 9), hemoglobin partitions strongly to the PEG-phase. Although some precipitation of hemoglobin occurs, high recovery values are obtained particularly for lysozyme and G6PDH. The partitioning forces are dominated by the hydrophobic and electrochemical (salt) effects, since the positively charged lysozyme and negatively charged G6PDH partitions to the non-charged PEG and the strongly negatively charged polyacrylate enriched phase, respectively. PMID:18078945

  1. Effects of one-seed juniper and polyethylene glycol on intake, rumen fermentation, and plasma amino acids in sheep and goats fed supplemental protein and tannins.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    We tested the effect of polyethylene glycol (PEG) on juniper and total intake, rumen fermentation, and plasma amino acids (AA) of 12 does and 12 ewes fed sudangrass and basal diets containing 10% quebracho tannins with no protein supplement (Control; 5% CP) or high rumen degradable (RDP 15% CP) or u...

  2. Protein corona over silver nanoparticles triggers conformational change of proteins and drop in bactericidal potential of nanoparticles: Polyethylene glycol capping as preventive strategy.

    PubMed

    Ban, Deependra Kumar; Paul, Subhankar

    2016-10-01

    Here, we demonstrated that starch-capped silver nanoparticles (AgNPST) with a size range of 10-15nm could readily interact with a small protein bovine α-lactalbumin (BLA) through the formation of protein corona. We further observed that such phenomena not only caused structural change of BLA but drastic drop in the bactericidal potential of AgNP. To design a strategy towards minimizing protein adsorption and maximizing the retention of bactericidal potential of AgNP, we developed stable polyethylene glycol (PEG)-capped AgNP (AgNPPEG) that clearly demonstrated reduced conformational changes of protein and retention of substantial bactericidal potential of AgNPPEG, compared to AgNPST. Moreover, AgNPPEG also showed excellent hemocompatibility. A relatively larger protein bovine serum albumin (BSA) and human blood serum solution containing serum proteins were also used in this study to validate our hypotheses. Overall, our study established that protein coated AgNP losses its inherent bactericidal potential substantially; however, when functionalized with a suitable material such as PEG, it could reduce such drop in substantial amount. Moreover, it achieved improved biocompatibility in actual physiological condition that might find a better therapeutic avenue in many bacteria-mediated disorders. PMID:27424088

  3. Polyethylenimine modified poly(ethylene terephthalate) capillary channeled-polymer fibers for anion exchange chromatography of proteins.

    PubMed

    Jiang, Liuwei; Jin, Yi; Marcus, R Kenneth

    2015-09-01

    Native poly(ethylene terephthalate) (PET) capillary-channeled polymer (C-CP) fibers have been previously studied as stationary phases for reversed phase and affinity protein separations. In this study, surface modified PET C-CP fibers were evaluated for the anion exchange separation of proteins. The native PET C-CP fibers were aminated using polyethylenimine (PEI) followed by a 1,4-butanediol diglycidyl ether (BUDGE) cross-linking step. Subsequent PEI/BUDGE treatments can be employed to further develop the polyamine layer on the fiber surfaces. The PEI densities of the modified fibers were quantified through the ninhydrin reaction, yielding values of 0.43-0.89μmolg(-1). The surface modification impact on column permeability was found to be 0.66×10(-11) to 1.33×10(-11)m(2), depending on the modification time and conditions. The dynamic binding capacities of the modified fiber media were determined to be 1.99-8.54mgmL(-1) bed volume, at linear velocities of 88-438cmmin(-1) using bovine serum albumin as the model protein. It was found that increasing the mobile phase linear velocity (up to 438cmmin(-1)) had no effect on the separation quality for a synthetic protein mixture, reflecting the lack of van Deemter C-term effects for the C-CP fiber phase. The low-cost, easy modification method and the capability of fast protein separation illustrate great potential in the use of PEI/BUDGE-modified PET C-CP fibers for high-throughput protein separation and downstream processing. PMID:26253835

  4. Using poly(ethylene glycol) silane to prevent protein adsorption in microfabricated silicon channels

    NASA Astrophysics Data System (ADS)

    Bell, Darrel J.; Brody, James P.; Yager, Paul

    1998-03-01

    Microfluidic devices fabricated in silicon are quickly finding use in many areas of technology. Exploration of new applications of this technology has shown both advantages and disadvantages to extreme miniaturization of chemical assays. While accuracy, efficiency and smaller sample volumes are among the advantages, interactions between the walls of the micro-channels and the fluid or particles it contains are among the disadvantages. Our group is applying this technology to chemical and biological warfare (CBW) agent purification and detection. We present preliminary result towards achieving a long-term antifouling surface in our detection system. A microfluidic device was anisotropically etched in a (100) silicon wafer and attached to a Pyrex glass slip to create an enclosed channel. Poly(ethylene glycol) (PEG) silane was covalently bonded to the hydroxyls of an oxide layer on the silicon device and the Pyrex cover slip. Fluorescently labeled ovalbumin, a CBW simulant, was in contact with an unmodified and PEG-modified channel. The extent of adsorption was determined using fluorescence microscopy.

  5. Surface modification of ultrahigh molecular weight polyethylene by the poly(ethylene glycol)-grafted method and its effect on the adsorption of proteins and the adhesion of blood platelets.

    PubMed

    Xia, Bing; Xie, Meiju; Yang, Bangcheng

    2013-01-01

    With the help of a silane coupling agent, poly(ethylene glycol) (PEG), a well-biocompatable agent, was grafted onto the surface of ultrahigh molecular weight polyethylene (UHMWPE) by ultraviolet initiation. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analysis proved the success of PEG grafting. Water contact angle measurement showed that the modified UHMWPE was obviously improved in surface hydrophilicity and thermogravimetric analysis result showed that its thermostability did not decline even it was pretreated by strong acids. Then, the protein adsorption of the modified UHMWPE was investigated using three model proteins including bovine serum albumin, lysozyme, and fibrinogen. Rabbit blood was used to study the platelet adhesion on the surface of modified UHMWPE. The results indicated that the quantity of protein adsorption on the modified UHMWPE grafted PEG reduced apparently for all the model proteins while there was some specific differences or exceptions among them. It was ascribed to the changed surface chemical composition, surface hydrophilicity and surface topography after modification. The adhesive ability of blood platelets on the modified surface of UHMWPE decreased after PEG grafting. Owing to the improved resistance to fibrinogen adsorption and platelet adhesion, the surface modification might endow the UHWMPE surface better anticoagulation ability according to clotting mechanism. PMID:22807149

  6. Inflammatory inert poly(ethylene glycol)--protein wound dressing improves healing responses in partial- and full-thickness wounds.

    PubMed

    Shingel, Kirill I; Di Stabile, Liliana; Marty, Jean-Paul; Faure, Marie-Pierre

    2006-12-01

    In this study, a novel soft hydrogel system based on the poly(ethylene glycol)-protein conjugates was evaluated as an occlusive wound dressing material. The hydrogel material, referred by the name of BioAquacare, contains up to 96% of the liquid and is formulated with phosphate-buffered saline and safe preservative to control bacterial load in the open wounds. Performance of the BioAquacare as a wound dressing material was assessed in partial- and full-thickness wounds in pigs. Wound analysis comprised macroscopic determination of the wound size, histological examination of the healing tissues and biochemical characterisation of wound exudates. The wounds treated with BioAquacare healed without any signs of inflammation, skin irritation, oedema or erythema. Cellular composition of the reepithelialised wounds was very similar to that of the normal skin, with a well-developed stratum corneum and epithelial layer. It was observed that BioAquacare plays the role of a liquid compartment, which provides pronounced hydration effect and helps maintain a natural moist environment of the healing tissues. BioAquacare showed relatively low protein-absorbing activity, absorbing predominantly low-molecular-weight molecules, including interleukin (IL)-1beta, IL-6, transforming growth factor-beta1 and products of haemoglobin degradation. It is concluded that application of the moist BioAquacare dressing promotes fast reepithelialisation by creating favourable environment for keratinocytes proliferation and it also reduces scarring. The results show that BioAquacare can be considered as a safe, biocompatible and inflammatory inert wound dressing material. PMID:17199768

  7. Data in support of intermolecular interactions at early stage of protein/detergent particle association induced by salt/polyethylene glycol mixtures.

    PubMed

    Odahara, Takayuki; Odahara, Koji

    2016-06-01

    The data provide information in support of the research article, "Intermolecular interactions at early stage of protein/detergent particle association induced by salt/polyethylene glycol mixtures" [1]. The data regarding variation of absorption spectra is used as an indicator of the duration of Rp. viridis PRU and RC, Rb. sphaeroides RC and LH2, and Rb. capsulatus LH2 in the native state in the presence of NaCl/polyethylene glycol (PEG) mixture. The data about minimum concentrations of salt and PEG whose aqueous phases are mutually separated presents information on additional influence of Tris buffer and N-octyl-β-d-glucoside on the salt-PEG phase separation. PMID:27135050

  8. Data in support of intermolecular interactions at early stage of protein/detergent particle association induced by salt/polyethylene glycol mixtures

    PubMed Central

    Odahara, Takayuki; Odahara, Koji

    2016-01-01

    The data provide information in support of the research article, “Intermolecular interactions at early stage of protein/detergent particle association induced by salt/polyethylene glycol mixtures” [1]. The data regarding variation of absorption spectra is used as an indicator of the duration of Rp. viridis PRU and RC, Rb. sphaeroides RC and LH2, and Rb. capsulatus LH2 in the native state in the presence of NaCl/polyethylene glycol (PEG) mixture. The data about minimum concentrations of salt and PEG whose aqueous phases are mutually separated presents information on additional influence of Tris buffer and N-octyl-β-d-glucoside on the salt–PEG phase separation. PMID:27135050

  9. High-speed separation of proteins by microchip electrophoresis using a polyethylene glycol-coated plastic chip with a sodium dodecyl sulfate-linear polyacrylamide solution.

    PubMed

    Nagata, Hideya; Tabuchi, Mari; Hirano, Ken; Baba, Yoshinobu

    2005-07-01

    In this paper, we describe a method for size-based electrophoretic separation of sodium dodecyl sulfate (SDS)-protein complexes on a polymethyl methacrylate (PMMA) microchip, using a separation buffer solution containing SDS and linear polyacrylamide as a sieving matrix. We developed optimum conditions under which protein separations can be performed, using polyethylene glycol (PEG)-coated polymer microchips and electrokinetic sample injection. We studied the performance of protein separations on the PEG-coated PMMA microchip. The electrophoretic separation of proteins (21.5-116.0 kDa) was completed with separation lengths of 3 mm, achieved within 8 s on the PEG-coated microchip. This high-speed method may be applied to protein separations over a large range of molecular weight, making the PEG-coated microchip approach applicable to high-speed proteome analysis systems. PMID:15937980

  10. pH-Responsive Polyethylene Glycol Monomethyl Ether-ε-Polylysine-G-Poly (Lactic Acid)-Based Nanoparticles as Protein Delivery Systems

    PubMed Central

    Liu, Huiqin; Li, Yijia; Yang, Rui; Gao, Xiujun; Ying, Guoguang

    2016-01-01

    The application of poly(lactic acid) for sustained protein delivery is restricted by the harsh pH inside carriers. In this study, we synthesized a pH-responsive comb-shaped block copolymer, polyethylene glycol monomethyl ether-ε-polylysine-g-poly (lactic acid) (PEP)to deliver protein (bovine serum albumin (BSA)). The PEP nanoparticles could automatically adjust the internal pH to a milder level, as shown by the quantitative ratio metric results. The circular dichroism spectra showed that proteins from the PEP nanoparticles were more stable than those from poly(lactic acid) nanoparticles. PEP nanoparticles could achieve sustained BSA release in both in vitro and in vivo experiments. Cytotoxicity results in HL-7702 cells suggested good cell compatibility of PEP carriers. Acute toxicity results showed that the PEP nanoparticles induced no toxic response in Kunming mice. Thus, PEP nanoparticles hold potential as efficient carriers for sustained protein release. PMID:27467072

  11. Polyethylene Glycol Propionaldehydes

    NASA Technical Reports Server (NTRS)

    Harris, Joe M.; Sedaghat-Herati, Mohammad R.; Karr, Laurel J.

    1992-01-01

    New class of compounds derived from polyethylene glycol (PEG's) namely, PEG-propionaldehydes, offers two important advantages over other classes of PEG aldehyde derivatives: compounds exhibit selective chemical reactivity toward amino groups and are stable in aqueous environment. PEG's and derivatives used to couple variety of other molecules, such as, to tether protein molecules to surfaces. Biotechnical and biomedical applications include partitioning of two phases in aqueous media; immobilization of such proteins as enzymes, antibodies, and antigens; modification of drugs; and preparation of protein-rejecting surfaces. In addition, surfaces coated with PEG's and derivatives used to control wetting and electroosmosis. Another potential application, coupling to aminated surfaces.

  12. Chemistry and stability of thiol based polyethylene glycol surface coatings on colloidal gold and their relationship to protein adsorption and clearance in vivo

    NASA Astrophysics Data System (ADS)

    Carpinone, Paul

    Nanomaterials have presented a wide range of novel biomedical applications, with particular emphasis placed on advances in imaging and treatment delivery. Of the many particulate nanomaterials researched for biomedical applications, gold is one of the most widely used. Colloidal gold has been of great interest due to its chemical inertness and its ability to perform multiple functions, such as drug delivery, localized heating of tissues (hyperthermia), and imaging (as a contrast agent). It is also readily functionalized through the use of thiols, which spontaneously form sulfur to gold bonds with the surface. Polyethylene glycol (PEG) is the most widely used coating material for these particles as it provides both steric stability to the suspension and protein resistance. These properties extend the circulation time of the particles in blood, and consequently the efficacy of the treatment. Despite widespread use of PEG coated gold particles, the coating chemistry and stability of these particles are largely unknown. The goal of this work was to identify the mechanisms leading to degradation and stability of thiol based polyethylene glycol coatings on gold particles and to relate this behavior to protein adsorption and clearance in vivo. The results indicate that the protective PEG coating is susceptible to sources of oxidation (including dissolved oxygen) and competing adsorbates, among other factors. The quality of commercially available thiolated PEG reagents was also found to play a key role in the quality and protein resistance of the final PEG coating. Analysis of the stability of these coatings indicated that they rapidly degrade under physiological conditions, leading to the onset of protein adsorption when exposed to plasma or blood. Paralleling the protein adsorption behavior and onset of coating degradation observed in vitro, blood clearance of parenterally administered PEG coated particles in mice began after approximately 2h of circulation time. Taken

  13. One step growth of protein antifouling surfaces: monolayers of poly(ethylene oxide) (PEO) derivatives on oxidized and hydrogen-passivated silicon surfaces.

    PubMed

    Cecchet, Francesca; De Meersman, Benoît; Demoustier-Champagne, Sophie; Nysten, Bernard; Jonas, Alain M

    2006-01-31

    We compare two routes for creating protein adsorption-resistant self-assembled monolayers (SAMs) by chemical modification of silicon surfaces with poly(ethylene oxide) (PEO) oligomeric derivatives. The first route involves the assembly of 2-methyl[(polyethyleneoxy)propyl]trichlorosilane (Cl3SiMPEO) films onto oxidized silicon surfaces (OH-SiO(x)) either by a liquid-phase process at room temperature or by a gas-phase process at 423 K, producing Si-O-Si bonds between the substrate and the organic layer. The second pathway makes use of the assembly of poly(ethylene glycol methyl ether) (MPEG) films onto hydrogen-passivated silicon surfaces (H-Si) using a liquid-phase process at 353 or 423 K, leading to the formation of Si-O-C bonds between the substrate and the organic layer. Structural investigation by X-ray reflectometry (XRR) reveals that the thickness and surface densities of the grafted PEO monolayers strongly depend on experimental conditions such as temperature and grafting time. Atomic force microscopy (AFM) shows that very smooth and homogeneous monolayers can be obtained with average roughnesses close to those measured on the corresponding bare substrates. Finally, the antifouling properties of the modified silicon surfaces were evaluated by X-ray photoelectron spectroscopy (XPS), using a membrane protein (P.69 antigen) as model protein. Both types of PEO monolayers exhibit excellent protein repellency, as soon as the grafting density is equal to or higher than 1.7 chains/nm2. PMID:16430281

  14. Polyethylene Glycol 3350

    MedlinePlus

    Polyethylene glycol 3350 is used to treat occasional constipation. Polyethylene glycol 3350 is in a class of medications ... Polyethylene glycol 3350 comes as a powder to be mixed with a liquid and taken by mouth. ...

  15. Proteomic analysis of lettuce seed germination and thermoinhibition by sampling of individual seeds at germination and removal of storage proteins by polyethylene glycol fractionation.

    PubMed

    Wang, Wei-Qing; Song, Bin-Yan; Deng, Zhi-Jun; Wang, Yue; Liu, Shu-Jun; Møller, Ian Max; Song, Song-Quan

    2015-04-01

    Germination and thermoinhibition in lettuce (Lactuca sativa 'Jianyexianfeng No. 1') seeds were investigated by a proteomic comparison among dry seeds, germinated seeds at 15°C, at 15°C after imbibition at 25°C for 48 h, or at 25°C in KNO3 (all sampled individually at germination), and ungerminated seeds at 25°C, a thermoinhibitory temperature. Before two-dimensional gel electrophoresis analysis, storage proteins (greater than 50% of total extractable protein) were removed by polyethylene glycol precipitation, which significantly improved the detection of less abundant proteins on two-dimensional gels. A total of 108 protein spots were identified to change more than 2-fold (P<0.05) in abundance in at least one germination treatment. Nineteen proteins increasing and one protein decreasing in abundance during germination had higher abundance in germinated 15°C, 15°C after imbibition at 25°C for 48 h, and 25°C in KNO3 seeds than in ungerminated 25°C seeds. Gene expression of 12 of those proteins correlated well with the protein accumulation. Methionine metabolism, ethylene production, lipid mobilization, cell elongation, and detoxification of aldehydes were revealed to be potentially related to lettuce seed germination and thermoinhibition. Accumulation of three proteins and expression of five genes participating in the mevalonate (MVA) pathway of isoprenoid biosynthesis correlated positively with seed germinability. Inhibition of this pathway by lovastatin delayed seed germination and increased the sensitivity of germination to abscisic acid. MVA pathway-derived products, cytokinins, partially reversed the lovastatin inhibition of germination and released seed thermoinhibition at 25°C. We conclude that the MVA pathway for isoprenoid biosynthesis is involved in lettuce seed germination and thermoinhibition. PMID:25736209

  16. Proteomic Analysis of Lettuce Seed Germination and Thermoinhibition by Sampling of Individual Seeds at Germination and Removal of Storage Proteins by Polyethylene Glycol Fractionation1

    PubMed Central

    Song, Bin-Yan; Deng, Zhi-Jun; Wang, Yue; Liu, Shu-Jun; Møller, Ian Max; Song, Song-Quan

    2015-01-01

    Germination and thermoinhibition in lettuce (Lactuca sativa ‘Jianyexianfeng No. 1’) seeds were investigated by a proteomic comparison among dry seeds, germinated seeds at 15°C, at 15°C after imbibition at 25°C for 48 h, or at 25°C in KNO3 (all sampled individually at germination), and ungerminated seeds at 25°C, a thermoinhibitory temperature. Before two-dimensional gel electrophoresis analysis, storage proteins (greater than 50% of total extractable protein) were removed by polyethylene glycol precipitation, which significantly improved the detection of less abundant proteins on two-dimensional gels. A total of 108 protein spots were identified to change more than 2-fold (P < 0.05) in abundance in at least one germination treatment. Nineteen proteins increasing and one protein decreasing in abundance during germination had higher abundance in germinated 15°C, 15°C after imbibition at 25°C for 48 h, and 25°C in KNO3 seeds than in ungerminated 25°C seeds. Gene expression of 12 of those proteins correlated well with the protein accumulation. Methionine metabolism, ethylene production, lipid mobilization, cell elongation, and detoxification of aldehydes were revealed to be potentially related to lettuce seed germination and thermoinhibition. Accumulation of three proteins and expression of five genes participating in the mevalonate (MVA) pathway of isoprenoid biosynthesis correlated positively with seed germinability. Inhibition of this pathway by lovastatin delayed seed germination and increased the sensitivity of germination to abscisic acid. MVA pathway-derived products, cytokinins, partially reversed the lovastatin inhibition of germination and released seed thermoinhibition at 25°C. We conclude that the MVA pathway for isoprenoid biosynthesis is involved in lettuce seed germination and thermoinhibition. PMID:25736209

  17. Involvement of 14-3-3 protein GRF9 in root growth and response under polyethylene glycol-induced water stress.

    PubMed

    He, Yuchi; Wu, Jingjing; Lv, Bing; Li, Jia; Gao, Zhiping; Xu, Weifeng; Baluška, František; Shi, Weiming; Shaw, Pang Chui; Zhang, Jianhua

    2015-04-01

    Plant 14-3-3 proteins are phosphoserine-binding proteins that regulate a wide array of targets via direct protein-protein interactions. In this study, the role of a 14-3-3 protein, GRF9, in plant response to water stress was investigated. Arabidopsis wild-type, GRF9-deficient mutant (grf9), and GRF9-overexpressing (OE) plants were treated with polyethylene glycol (PEG) to induce mild water stress. OE plant showed better whole-plant growth and root growth than the wild type under normal or water stress conditions while the grf9 mutant showed worse growth. In OE plants, GRF9 favours the allocation of shoot carbon to roots. In addition, GRF9 enhanced proton extrusion, mainly in the root elongation zone and root hair zone, and maintained root growth under mild water stress. Grafting among the wild type, OE, and grf9 plants showed that when OE plants were used as the scion and GRF9 was overexpressed in the shoot, it enhanced sucrose transport into the root, and when OE plants were used as rootstock and GRF9 was overexpressed in the root, it caused more release of protons into the root surface under water stress. Taken together, the results suggest that under PEG-induced water stress, GRF9 is involved in allocating more carbon from the shoot to the root and enhancing proton secretion in the root growing zone, and this process is important for root response to mild water stress. PMID:25873671

  18. Involvement of 14-3-3 protein GRF9 in root growth and response under polyethylene glycol-induced water stress

    PubMed Central

    He, Yuchi; Wu, Jingjing; Lv, Bing; Li, Jia; Gao, Zhiping; Xu, Weifeng; Baluška, František; Shi, Weiming; Shaw, Pang Chui; Zhang, Jianhua

    2015-01-01

    Plant 14-3-3 proteins are phosphoserine-binding proteins that regulate a wide array of targets via direct protein–protein interactions. In this study, the role of a 14-3-3 protein, GRF9, in plant response to water stress was investigated. Arabidopsis wild-type, GRF9-deficient mutant (grf9), and GRF9-overexpressing (OE) plants were treated with polyethylene glycol (PEG) to induce mild water stress. OE plant showed better whole-plant growth and root growth than the wild type under normal or water stress conditions while the grf9 mutant showed worse growth. In OE plants, GRF9 favours the allocation of shoot carbon to roots. In addition, GRF9 enhanced proton extrusion, mainly in the root elongation zone and root hair zone, and maintained root growth under mild water stress. Grafting among the wild type, OE, and grf9 plants showed that when OE plants were used as the scion and GRF9 was overexpressed in the shoot, it enhanced sucrose transport into the root, and when OE plants were used as rootstock and GRF9 was overexpressed in the root, it caused more release of protons into the root surface under water stress. Taken together, the results suggest that under PEG-induced water stress, GRF9 is involved in allocating more carbon from the shoot to the root and enhancing proton secretion in the root growing zone, and this process is important for root response to mild water stress. PMID:25873671

  19. The effects of poly(zwitterions)s versus poly(ethylene glycol) surface coatings on the biodistribution of protein nanoparticles.

    PubMed

    Wang, Jing; Yuan, Shanmei; Zhang, Yajun; Wu, Wei; Hu, Yong; Jiang, Xiqun

    2016-08-16

    Zwitterionic poly(carboxybetaine) (PCB), poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) and non-ionic poly(ethylene glycol) (PEG), which have similar degrees of polymerization, were grafted to branched polyethyleneimine (PEI) to generate PCB-grafted PEI (PEI-PCB), PMPC-grafted PEI (PEI-PMPC) and PEG-grafted PEI (PEI-PEG) copolymers, respectively. These grafted PEI copolymers with almost the same grafting number were coated on the surface of 110 nm bovine serum albumin-poly(N-3-acrylamidophenylboronic acid) (BSA-PAPBA) nanoparticles to make a comparison of the surface decoration effect on the biodistribution of nanoparticles. Compared to the nanoparticles without surface decoration, surface decoration with the copolymers significantly prolonged the circulation time of BSA-PAPBA nanoparticles, leading to remarkable enhancement of tumor uptake of the nanoparticles. The drug accumulation at the tumor site reached more than 10% injected dose per gram of tumor. Among them, the PEI-PMPC-decorated nanoparticles exhibited the best performance in tumor accumulation and anticancer ability. Thus, these surface-decorated nanoparticles may serve as a strong candidate for high tumor accumulation of drug delivery systems. PMID:27426309

  20. Two Novel Class II Hydrophobins from Trichoderma spp. Stimulate Enzymatic Hydrolysis of Poly(Ethylene Terephthalate) when Expressed as Fusion Proteins

    PubMed Central

    Espino-Rammer, Liliana; Ribitsch, Doris; Przylucka, Agnieszka; Marold, Annemarie; Greimel, Katrin J.; Herrero Acero, Enrique; Guebitz, Georg M.; Kubicek, Christian P.

    2013-01-01

    Poly(ethylene terephthalate) (PET) can be functionalized and/or recycled via hydrolysis by microbial cutinases. The rate of hydrolysis is however low. Here, we tested whether hydrophobins (HFBs), small secreted fungal proteins containing eight positionally conserved cysteine residues, are able to enhance the rate of enzymatic hydrolysis of PET. Species of the fungal genus Trichoderma have the most proliferated arsenal of class II hydrophobin-encoding genes among fungi. To this end, we studied two novel class II HFBs (HFB4 and HFB7) of Trichoderma. HFB4 and HFB7, produced in Escherichia coli as fusions to the C terminus of glutathione S-transferase, exhibited subtle structural differences reflected in hydrophobicity plots that correlated with unequal hydrophobicity and hydrophily, respectively, of particular amino acid residues. Both proteins exhibited a dosage-dependent stimulation effect on PET hydrolysis by cutinase from Humicola insolens, with HFB4 displaying an adsorption isotherm-like behavior, whereas HFB7 was active only at very low concentrations and was inhibitory at higher concentrations. We conclude that class II HFBs can stimulate the activity of cutinases on PET, but individual HFBs can display different properties. The present findings suggest that hydrophobins can be used in the enzymatic hydrolysis of aromatic-aliphatic polyesters such as PET. PMID:23645195

  1. Separating chemical and excluded volume interactions of polyethylene glycols with native proteins: Comparison with PEG effects on DNA helix formation.

    PubMed

    Shkel, Irina A; Knowles, D B; Record, M Thomas

    2015-09-01

    Small and large PEGs greatly increase chemical potentials of globular proteins (μ2), thereby favoring precipitation, crystallization, and protein-protein interactions that reduce water-accessible protein surface and/or protein-PEG excluded volume. To determine individual contributions of PEG-protein chemical and excluded volume interactions to μ2 as functions of PEG molality m3 , we analyze published chemical potential increments μ23  = dμ2/dm3 quantifying unfavorable interactions of PEG (PEG200-PEG6000) with BSA and lysozyme. For both proteins, μ23 increases approximately linearly with the number of PEG residues (N3). A 1 molal increase in concentration of PEG -CH2 OCH2 - groups, for any chain-length PEG, increases μBSA by ∼2.7 kcal/mol and μlysozyme by ∼1.0 kcal/mol. These values are similar to predicted chemical interactions of PEG -CH2 OCH2 - groups with these protein components (BSA ∼3.3 kcal/mol, lysozyme ∼0.7 kcal/mol), dominated by unfavorable interactions with amide and carboxylate oxygens and counterions. While these chemical effects should be dominant for small PEGs, larger PEGS are expected to exhibit unfavorable excluded volume interactions and reduced chemical interactions because of shielding of PEG residues in PEG flexible coils. We deduce that these excluded volume and chemical shielding contributions largely compensate, explaining why the dependence of μ23 on N3 is similar for both small and large PEGs. PMID:25924886

  2. In situ forming parenteral depot systems based on poly(ethylene carbonate): effect of polymer molecular weight on model protein release.

    PubMed

    Chu, Dafeng; Curdy, Catherine; Riebesehl, Bernd; Beck-Broichsitter, Moritz; Kissel, Thomas

    2013-11-01

    The objective of this study was to investigate the effect of molecular weight (MW) on the drug release from poly(ethylene carbonate) (PEC) based surface-eroding in situ forming depots (ISFD). In phosphate buffered saline (PBS) pH 7.4, 63.7% of bovine serum albumin BSA was released from high MW PEC of 200 kDa (PEC200) in DMSO (15%, w/w) in 2 days, while during the same time period, the release of BSA from PEC41 samples was only 22.5%. At higher concentrations of PEC41 (25%, w/w), the initial burst was further reduced, and even after 6 days, only 16.3% was released. Compared to depots based on PEC200, there was lower rate of solvent release, slower phase inversion, and a denser surface in PEC41 samples. An expansion in size of PEC41 depots suggested that the polymer barrier of PEC41 impeded the diffusion of solvent out of the samples effectively. In conclusion, the initial burst of protein from ISFD of PEC41 was significantly reduced, which would be a promising candidate as polymeric carrier. PMID:23791717

  3. Functionalized poly(ethylene glycol) diacrylate microgels by microfluidics: In situ peptide encapsulation for in serum selective protein detection.

    PubMed

    Celetti, Giorgia; Natale, Concetta Di; Causa, Filippo; Battista, Edmondo; Netti, Paolo A

    2016-09-01

    Polymeric microparticles represent a robustly platform for the detection of clinically relevant analytes in biological samples; they can be functionalized encapsulating a multiple types of biologics entities, enhancing their applications as a new class of colloid materials. Microfluidic offers a versatile platform for the synthesis of monodisperse and engineered microparticles. In this work, we report microfluidic synthesis of novel polymeric microparticles endowed with specific peptide due to its superior specificity for target binding in complex media. A peptide sequence was efficiently encapsulated into the polymeric network and protein binding occurred with high affinity (KD 0.1-0.4μM). Fluidic dynamics simulation was performed to optimize the production conditions for monodisperse and stable functionalized microgels. The results demonstrate the easy and fast realization, in a single step, of functionalized monodisperse microgels using droplet-microfluidic technique, and how the inclusion of the peptide within polymeric network improve both the affinity and the specificity of protein capture. PMID:27137799

  4. In situ immobilization of proteins and RGD peptide on polyurethane surfaces via poly(ethylene oxide) coupling polymers for human endothelial cell growth.

    PubMed

    Wang, Dong-an; Ji, Jian; Sun, Yong-hong; Shen, Jia-cong; Feng, Lin-xian; Elisseeff, Jennifer H

    2002-01-01

    A "CBABC"-type pentablock coupling polymer, mesylMPEO, was designed and synthesized to promote human endothelial cell growth on the surfaces of polyurethane biomaterials. The polymer was composed of a central 4,4'-methylenediphenyl diisocyanate (MDI) coupling unit and poly(ethylene oxide) (PEO) spacer arms with methanesulfonyl (mesyl) end groups pendent on both ends. As the presurface modifying additive (pre-SMA), the mesylMPEO was noncovalently introduced onto the poly(ether urethane) (PEU) surfaces by dip coating, upon which the protein/peptide factors (gelatin, albumin, and arginine-glycine-aspartic acid tripeptide [RGD]) were covalently immobilized in situ by cleavage of the original mesyl end groups. The pre-SMA synthesis and PEU surface modification were characterized using nuclear magnetic resonance spectroscopy ((1)H NMR), attenuated total reflection infrared spectroscopy (ATR-FTIR), and X-ray photoelectron spectroscopy (XPS). Human umbilical vein endothelial cells (HUVEC) were harvested manually by collagenase digestion and seeded on the modified PEU surfaces. Cell adhesion ratios (CAR) and cell proliferation ratios (CPR) were measured using flow cytometry, and the individual cell viability (ICV) was determined by MTT assay. The cell morphologies were investigated by optical inverted microscopy (OIM) and scanning electrical microscopy (SEM). The gelatin- and RGD-modified surfaces were HUVEC-compatible and promoted HUVEC growth. The albumin-modified surfaces were compatible but inhibited cell adhesion. The results also indicated that, for HUVEC in vitro cultivation, the cell adhesion stage was of particular importance and had a significant impact on the cell responses to the modified surfaces. PMID:12425667

  5. Resistance to moist conditions of whey protein isolate and pea starch biodegradable films and low density polyethylene nondegradable films: a comparative study

    NASA Astrophysics Data System (ADS)

    Mehyar, G. F.; Bawab, A. Al

    2015-10-01

    Biodegradable packaging materials are degraded under the natural environmental conditions. Therefore using them could alleviate the problem of plastics accumulation in nature. For effective replacement of plastics, with biodegradable materials, biodegradable packages should keep their properties under the high relative humidity (RH) conditions. Therefore the objectives of the study were to develop biodegradable packaging material based on whey protein isolate (WPI) and pea starch (PS). To study their mechanical, oxygen barrier and solubility properties under different RHs compared with those of low density polyethylene (LDPE), the most used plastic in packaging. Films of WPI and PS were prepared separately and conditioned at different RH (30-90%) then their properties were studied. At low RHs (<50%), WPI films had 2-3 times lower elongation at break (E or stretchability) than PS and LDPE. Increasing RH to 90% significantly (P<0.01) increased the elongation of PS but not WPI and LDPE films. LDPE and WPI films kept significantly (P<0.01) higher tensile strength (TS) than PS films at high RH (90%). Oxygen permeability (OP) of all films was very low (<0.5 cm3 μm m-2 d-1 kPa-1) below 40% RH but increased for PS films and became significantly (P<0.01) different than that of LDPE and WPI at > 40% RH. Oxygen permeability of WPI and LDPE did not adversely affected by increasing RH to 65%. Furthermore, WPI and LDPE films had lower degree of hydration at 50% and 90% RH and total soluble matter than PS films. These results suggest that WPI could be successfully replacing LDPE in packaging of moist products.

  6. Protein partition between the different phases comprising poly(ethylene glycol)-salt aqueous two-phase systems, hydrophobic interaction chromatography and precipitation: a generic description in terms of salting-out effects.

    PubMed

    Huddleston, J; Abelaira, J C; Wang, R; Lyddiatt, A

    1996-05-17

    The solution behaviour of selected proteins has been studied under conditions promoting precipitation, binding to mildly hydrophobic adsorbents or partition. Solvophobic theory may be used to describe these forms of protein partition. The tendency of a protein to partition therein is dependent upon surface properties of the protein solute mediated by the concentration and nature of added salts. As applied to partitioning in poly(ethylene glycol) (PEG)-salt systems this implies that linear (Brönsted) relationships apply only to proteins partitioned close to the critical point. At longer tie-line lengths protein partitioning is increasingly influenced by salting-out forces. This is confirmed by the observed behaviour of the proteins. The point at which this behaviour changes has been unambiguously defined enabling the direct comparison of phase transition of proteins during partition in all systems. The results obtained show that phase transition during adsorption and partition occur at similar concentrations of salt. This is less than that required to promote precipitation. It appears, from these limited studies, that top-phase preferring proteins are partitioned at salt concentrations above those required to cause adsorption. Proteins preferring the lower phase are partitioned at salt concentrations close to or below those required for adsorption. This raises questions regarding the solvated molecular form of the partitioned proteins and the definition of the partition coefficient. PMID:8798879

  7. Polyethylene Glycol 3350

    MedlinePlus

    Polyethylene glycol 3350 comes as a powder to be mixed with a liquid and taken by mouth. It is usually taken once a day as needed for up to ... to produce a bowel movement.To use the powder, follow these steps: If you are using polyethylene ...

  8. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... Acrylonitrile. Methacrylonitrile. Vinyl chloride. Itaconic acid. Styrene-maleic anhydride resin, partial 2... terephthalate or terephthalic acid with ethylene glycol, modified with one or more of the following: Azelaic acid, dimethyl azelate, dimethyl sebacate, sebacic acid. Ethylene terephthalate copolymers: Prepared...

  9. Polyetheylenimine-Polyplexes of Spiegelmer NOX-A50 Directed against Intracellular High Mobility Group Protein A1 (HMGA1) Reduce Tumor Growth in Vivo*

    PubMed Central

    Maasch, Christian; Vater, Axel; Buchner, Klaus; Purschke, Werner G.; Eulberg, Dirk; Vonhoff, Stefan; Klussmann, Sven

    2010-01-01

    High mobility group A1 (HMGA1) proteins belong to a group of architectural transcription factors that are overexpressed in a range of human malignancies, including pancreatic adenocarcinoma. They promote anchorage-independent growth and epithelial-mesenchymal transition and are therefore suggested as potential therapeutic targets. Employing in vitro selection techniques against a chosen fragment of HMGA1, we have generated biostable l-RNA oligonucleotides, so-called Spiegelmers, that specifically bind HMGA1b with low nanomolar affinity. We demonstrate that the best binding Spiegelmers, NOX-A50 and NOX-f33, compete HMGA1b from binding to its natural binding partner, AT-rich double-stranded DNA. We describe a formulation method based on polyplex formation with branched polyethylenimine for efficient delivery of polyethylene glycol-modified Spiegelmers and show improved tissue distribution and persistence in mice. In a xenograft mouse study using the pancreatic cancer cell line PSN-1, subcutaneous administration of 2 mg/kg per day NOX-A50 formulated in polyplexes showed an enhanced delivery of NOX-A50 to the tumor and a significant reduction of tumor volume. Our results demonstrate that intracellular targets can be successfully addressed with a Spiegelmer using polyethylenimine-based delivery and underline the importance of HMGA1 as a therapeutic target in pancreatic cancer. PMID:20961861

  10. pH-dependent immobilization of proteins on surfaces functionalized by plasma-enhanced chemical vapor deposition of poly(acrylic acid)- and poly(ethylene oxide)-like films.

    PubMed

    Belegrinou, Serena; Mannelli, Ilaria; Lisboa, Patricia; Bretagnol, Frederic; Valsesia, Andrea; Ceccone, Giacomo; Colpo, Pascal; Rauscher, Hubert; Rossi, François

    2008-07-15

    The interaction of the proteins bovine serum albumin (BSA), lysozyme (Lys), lactoferrin (Lf), and fibronectin (Fn) with surfaces of protein-resistant poly(ethylene oxide) (PEO) and protein-adsorbing poly(acrylic acid) (PAA) fabricated by plasma-enhanced chemical vapor deposition has been studied with quartz crystal microbalance with dissipation monitoring (QCM-D). We focus on several parameters which are crucial for protein adsorption, i.e., the isoelectric point (pI) of the proteins, the pH of the solution, and the charge density of the sorbent surfaces, with the zeta-potential as a measure for the latter. The measurements reveal adsorption stages characterized by different segments in the plots of the dissipation vs frequency change. PEO remains protein-repellent for BSA, Lys, and Lf at pH 4-8.5, while weak adsorption of Fn was observed. On PAA, different stages of protein adsorption processes could be distinguished under most experimental conditions. BSA, Lys, Lf, and Fn generally exhibit a rapid initial adsorption phase on PAA, often followed by slower processes. The evaluation of the adsorption kinetics also reveals different adsorption stages, whereas the number of these stages does not always correspond to the structurally different phases as revealed by the D- f plots. The results presented here, together with information obtained in previous studies by other groups on the properties of these proteins and their interaction with surfaces, allow us to develop an adsorption scenario for each of these proteins, which takes into account electrostatic protein-surface and protein-protein interaction, but also the pH-dependent properties of the proteins, such as shape and exposure of specific domains. PMID:18549295

  11. Method for casting polyethylene pipe

    NASA Technical Reports Server (NTRS)

    Elam, R. M., Jr.

    1973-01-01

    Short lengths of 7-cm ID polyethylene pipe are cast in a mold which has a core made of room-temperature-vulcanizable (RTV) silicone. Core expands during casting and shrinks on cooling to allow for contraction of the polyethylene.

  12. Method for shaping polyethylene tubing

    NASA Technical Reports Server (NTRS)

    Kramer, R. C.

    1981-01-01

    Method forms polyethylene plastic tubing into configurations previously only possible with metal tubing. By using polyethylene in place of copper or stain less steel tubing inlow pressure systems, fabrication costs are significantly reduced. Polyethylene tubing can be used whenever low pressure tubing is needed in oil operations, aircraft and space applications, powerplants, and testing laboratories.

  13. Ethylene glycol modified 2-(2‧-aminophenyl)benzothiazoles at the amino site: the excited-state N-H proton transfer reactions in aqueous solution, micelles and potential application in live-cell imaging

    NASA Astrophysics Data System (ADS)

    Liu, Bo-Qing; Chen, Yi-Ting; Chen, Yu-Wei; Chung, Kun-You; Tsai, Yi-Hsuan; Li, Yi-Jhen; Chao, Chi-Min; Liu, Kuan-Miao; Tseng, Huan-Wei; Chou, Pi-Tai

    2016-03-01

    Triethylene glycol monomethyl ether and poly(ethylene glycol) monomethyl ether modified 2-(2‧-aminophenyl)benzothiazoles, namely ABT-P3EG, ABT-P7EG and ABT-P12EG varied by different chain length of poly(ethylene glycol) at the amino site, were synthesized to probe their photophysical and bio-imaging properties. In polar, aprotic solvents such as CH2Cl2 ultrafast excited-state intramolecular proton transfer (ESIPT) takes place, resulting in a large Stokes shifted tautomer emission in the green-yellow (550 nm) region. In neutral water, ABT-P12EG forms micelles with diameters of 15  ±  3 nm under a critical micelle concentration (CMC) of ~80 μM, in which the tautomer emission is greatly enhanced free from water perturbation. Cytotoxicity experiments showed that all ABT-PnEGs have negligible cytotoxicity against HeLa cells even at doses as high as 1 mM. Live-cell imaging experiments were also performed, the results indicate that all ABT-PnEGs are able to enter HeLa cells. While the two-photon excitation emission of ABT-P3EG in cells cytoplasm shows concentration independence and is dominated by the anion blue fluorescence, ABT-P7EG and ABT-P12EG exhibit prominent green tautomer emission at  >  CMC and in part penetrate to the nuclei, adding an additional advantage for the cell imaging.

  14. Modular poly(ethylene glycol) scaffolds provide the ability to decouple the effects of stiffness and protein concentration on PC12 cells.

    PubMed

    Scott, Rebecca A; Elbert, Donald L; Willits, Rebecca Kuntz

    2011-11-01

    This research focused on developing a modular poly(ethylene glycol) (PEG) scaffold, assembled from PEG microgels and collagen I, to provide an environment to decouple the chemical and mechanical cues within a three-dimensional scaffold. We first characterized the microgel fabrication process, examining the size, polydispersity, swelling ratio, mesh size and storage modulus of the polymer particles. The resulting microgels had a low polydispersity index, PDI=1.08, and a diameter of ~1.6 μm. The mesh size of the microgels, calculated from the swelling ratio, was 47.53 Å. Modular hydrogels (modugels) were then formed by compacting N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride/N-hydroxysuccinimidyl group-activated microgels with PEG-4arm-amine and 0, 1, 10, or 100 μg ml(-1) collagen. The stiffness (G(∗)) of the modugels was not significantly altered with the addition of collagen, allowing for modification of the chemical environment independent from the mechanical properties of the scaffold. PC12 cell aggregation increased in modugels as collagen concentrations increased and cell viability in modugels was improved over bulk PEG hydrogels. Overall, these results indicate that further exploration of modular scaffolds formed from microgels could allow for a better understanding of the relationship between the chemical and mechanical properties and cellular behavior. PMID:21787889

  15. Polyethylene glycol modification decreases the cardiac toxicity of carbonaceous dots in mouse and zebrafish models

    PubMed Central

    Chen, Jian-tao; Sun, Hua-qin; Wang, Wei-liang; Xu, Wen-ming; He, Qin; Shen, Shun; Qian, Jun; Gao, Hui-le

    2015-01-01

    Aim: Carbonaceous dots (CDs), which have been used for diagnosis, drug delivery and gene delivery, are accumulated in heart at high concentrations. To improve their biocompatibility, polyethylene glycol-modified CDs (PEG-CDs) were prepared. In this study we compared the cardiac toxicity of CDs and PEG-CDs in mouse and zebrafish models. Methods: Mice were intravenously treated with CDs (size: 4.9 nm, 5 mg·kg−1·d−1) or PEG-CDs (size: 8.3 nm, 5 mg·kg−1·d−1) for 21 d. Their blood biochemistry indices, ECG, and histological examination were examined for evaluation of cardiac toxicity. CDs or PEG-CDs was added in incubator of cmlc2 transgenic Zebrafish embryos at 6 hpf, and the shape and size of embryos' hearts were observed at 48 hpf using a fluorescent microscope. Furthermore, whole-mount in situ hybridization was used to examine the expression of early cardiac marker gene (clml2) at 48 hpf. Results: Administration of CDs or PEG-CDs in mice caused mild, but statistically insignificant reduction in serum creatine kinase (CK) and lactate dehydrogenase (LDH) levels detected at 7 d, which were returned to the respective control levels at 21 d. Neither CDs nor PEG-CDs caused significant changes in the morphology of heart cells. Administration of CDs, but not PEG-CDs, in mice caused marked increase of heart rate. Both CDs and PEG-CDs did not affect other ECG parameters. In the zebrafish embryos, addition of CDs (20 μg/mL) caused heart development delay, whereas addition of CDs (80 μg/mL) led to heart malformation. In contrast, PEG-CDs caused considerably small changes in heart development, which was consistent with the results from the in situ hybridization experiments. Conclusion: CDs causes greater cardiac toxicity, especially regarding heart development. Polyethylene glycol modification can attenuate the cardiac toxicity of CDs. PMID:26456589

  16. Methoxy-poly(ethylene glycol) modified poly(L-lactide) enhanced cell affinity of human bone marrow stromal cells by the upregulation of 1-cadherin and delta-2-catenin.

    PubMed

    Mao, Xueli; Chen, Zetao; Ling, Junqi; Quan, Jingjing; Peng, Hui; Xiao, Yin

    2014-01-01

    Poly(L-lactide) (PLLA), a versatile biodegradable polymer, is one of the most commonly-used materials for tissue engineering applications. To improve cell affinity for PLLA, poly(ethylene glycol) (PEG) was used to develop diblock copolymers. Human bone marrow stromal cells (hBMSCs) were cultured on MPEG-b-PLLA copolymer films to determine the effects of modification on the attachment and proliferation of hBMSC. The mRNA expression of 84 human extracellular matrix (ECM) and adhesion molecules was analyzed using RT-qPCR to understand the underlying mechanisms. It was found that MPEG-b-PLLA copolymer films significantly improved cell adhesion, extension, and proliferation. This was found to be related to the significant upregulation of two adhesion genes, CDH1 and CTNND2, which encode 1-cadherin and delta-2-catenin, respectively, two key components for the cadherin-catenin complex. In summary, MPEG-b-PLLA copolymer surfaces improved initial cell adhesion by stimulation of adhesion molecule gene expression. PMID:24834434

  17. Solubilization of native integral membrane proteins in aqueous buffer by non-covalent chelation with monomethoxy polyethylene glycol (mPEG) polymers

    PubMed Central

    Janaratne, Thamara K.; Okach, Linda; Brock, Ansgar; Lesley, Scott A.

    2011-01-01

    Highly hydrophobic integral membrane proteins (IMPs) are typically purified in excess detergent media, often resulting in rapid inactivation and denaturation of the protein. One promising approach to solve this problem is to couple hydrophilic polymers, such as monomethoxypolyethylene glycol (mPEG) to IMPs under mild conditions in place of detergents. However, the broad application of this approach is hampered by poor reaction efficiencies, low tolerance of detergent stabilized membrane proteins to reaction conditions and a lack of proper site-specific reversible approaches. Here we have developed a straightforward, efficient and mild approach to site-specific non-covalent binding of long-chain polymers to recombinant IMPs. This method uses the hexa-histidine tag (His-Tag) often used for purification of recombinant proteins as an attachment site for mPEGs. Solubility studies performed using five different IMPs confirmed that all tested mPEG-bound IMPs were completely soluble and stable in detergent free aqueous buffer compared to their precipitated native proteins under the identical circumstances. Activity assays and circular dichroism (CD) spectroscopy confirmed the structural integrity of modified IMPs. PMID:21740061

  18. Effects of adding protein, condensed tannins, and polyethylene glycol to diets of sheep and goats fed one-seed juniper and low quality roughage

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The biochemical mechanisms that limit voluntary intake of one-seed juniper by browsing ruminants are not well understood. Twelve Rambouillet ewes (78 ± 2.3 kg BW) and 12 Boer-Spanish does (54 ± 1.4 kg BW) were used in a split-plot sequence design to investigate the effects of adding protein, quebrac...

  19. Disintegration of porous polyethylene prostheses.

    PubMed

    Kerr, A G; Riley, D N

    1999-06-01

    A Plastipore (porous polyethylene) Total Ossicular Replacement Prosthesis gave an excellent initial hearing result which was maintained for 14 years. Hearing then began to deteriorate and revision surgery showed disintegration of the prosthesis and a defect in the stapes footplate. Histological examination confirmed previous findings in porous polyethylene with multinucleated foreign body giant cells and breakdown of the material. PMID:10384839

  20. Reduction of Non-Specific Protein Adsorption Using Poly(ethylene) Glycol (PEG) Modified Polyacrylate Hydrogels In Immunoassays for Staphylococcal Enterotoxin B Detection

    PubMed Central

    Charles, Paul T.; Stubbs, Veronte R.; Soto, Carissa M.; Martin, Brett D.; White, Brandy J.; Taitt, Chris R.

    2009-01-01

    Three PEG molecules (PEG-methacrylate, -diacrylate and -dimethacrylate) were incorporated into galactose-based polyacrylate hydrogels and their relative abilities to reduce non-specific protein adsorption in immunoassays were determined. Highly crosslinked hydrogels containing amine-terminated functionalities were formed and used to covalently attach antibodies specific for staphylococcal enterotoxin B (SEB). Patterned arrays of immobilized antibodies in the PEG-modified hydrogels were created with a PDMS template containing micro-channels for use in sandwich immunoassays to detect SEB. Different concentrations of the toxin were applied to the hydrogel arrays, followed with a Cy3-labeled tracer antibody specific for the two toxins. Fluorescence laser scanning confocal microscopy of the tracer molecules provided both qualitative and quantitative measurements on the detection sensitivity and the reduction in non-specific binding as a result of PEG incorporation. Results showed the PEG-modified hydrogel significantly reduced non-specific protein binding with a detection limit for SEB of 1 ng/mL. Fluorescence signals showed a 10-fold decrease in the non-specific binding and a 6-fold increase in specific binding of SEB. PMID:22389622

  1. Preparation of hydroxylated polyethylene surfaces.

    PubMed

    Zand, A; Walter, N; Bahu, M; Ketterer, S; Sanders, M; Sikorski, Y; Cunningham, R; Beholz, L

    2008-01-01

    The surfaces of high-density or ultra-high-molecular-weight polyethylenes were hydroxylated using a two-step process. The wetting and wear properties of the untreated (virgin) and surface hydroxylated polyethylenes were compared. The introduction of hydroxyl groups provided an increase in surface hydrophilicity resulting in reduced wear. Hydrophilicity was analyzed by optical analysis of water contact angle. Wear was determined by weight loss under conditions of a reciprocating pin-on-plate apparatus with the panels immersed in water or calf serum. These results suggest that hydroxylation of polyethylene friction-bearing orthopedic surfaces may lead to a longer joint life. PMID:18318959

  2. Colonization, biofilm formation and biodegradation of polyethylene by a strain of Rhodococcus ruber.

    PubMed

    Orr, I Gilan; Hadar, Y; Sivan, A

    2004-07-01

    A two-step enrichment procedure led to the isolation of a strain of Rhodococcus ruber (C208) that utilized polyethylene films as sole carbon source. In liquid culture, C208 formed a biofilm on the polyethylene surface and degraded up to 8% (gravimetrically) of the polyolefin within 30 days of incubation. The bacterial adhesion to hydrocarbon assay and the salt aggregation test both showed that the cell-surface hydrophobicity of C208 was higher than that of three other isolates which were obtained from the same consortium but were less efficient than C208 in the degradation of polyethylene. Mineral oil, but not nonionic surfactants, enhanced the colonization of polyethylene and increased biodegradation by about 50%. Fluorescein diacetate (FDA) hydrolysis and protein content analysis were used to test the viability and biomass density of the C208 biofilm on the polyethylene, respectively. Both FDA activity and protein content of the biofilm in a medium containing mineral oil peaked 48-72 h after inoculation and then decreased sharply. This finding apparently reflected rapid utilization of the mineral oil adhering to the polyethylene. The remaining biofilm population continued to proliferate moderately and presumably played a major role in biodegradation of the polyethylene. Fourier transform infrared spectra of UV-photooxidized polyethylene incubated with C208 indicated that biodegradation was initiated by utilization of the carbonyl residues formed in the photooxidized polyethylene. PMID:15221232

  3. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph... prescribed conditions: (a) Fluorinated polyethylene food-contact articles are produced by modifying...

  4. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of... following prescribed conditions: (a) Oxidized polyethylene is the basic resin produced by the mild...

  5. Effects of Biomass in Polyethylene or Polylactic Acid Composites

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Previous studies have shown that compounding Polyethylene (PE) or Polylactic acid (PLA) with a dairy-based bioplastic resulted in composites with good mechanical properties. In this study, mass ratios of a dairy-protein-based material (DBP) ranging from 0, 5, 10 and 20 wt% replaced equivalent masse...

  6. Electromagnetic Characteristics of Thin Polyethylene-Carbon-Polyethylene Films

    NASA Astrophysics Data System (ADS)

    Volynets, N. I.; Lyubimov, A. G.; Plyushch, A. O.; Poddubskaya, O. G.; Kuzhir, P. P.; Korovin, E. Yu.; Suslyaev, V. I.; Macutkevic, J.; Pikutskaya, E. S.; Baturkin, S. A.; Klochkov, A. Ya.

    2015-09-01

    A method of manufacturing a polyethylene - expanded carbon - polyethylene layered structures which allows thin (down to 90 μm) and flexible sandwiches to be easily made, is suggested. The electromagnetic properties of the manufactured composite materials at frequencies from 1 MHz to 3 GHz, 26-37.5 GHz, and 0.1-1.4 THz are analyzed. It is established that the material so obtained is opaque for the Ka microwave band due to high reflectivity (96-97%), does not transmit electromagnetic radiation of the terahertz range, has a high conductivity (up to 1 S/m) in the frequency range from 1 MHz to 1 GHz, and retains the main physical polyethylene properties (light weight, elasticity, and flexibility).

  7. Degradable polyethylene: fantasy or reality.

    PubMed

    Roy, Prasun K; Hakkarainen, Minna; Varma, Indra K; Albertsson, Ann-Christine

    2011-05-15

    Plastic waste disposal is one of the serious environmental issues being tackled by our society today. Polyethylene, particularly in packaging films, has received criticism as it tends to accumulate over a period of time, leaving behind an undesirable visual footprint. Degradable polyethylene, which would enter the eco-cycle harmlessly through biodegradation would be a desirable solution to this problem. However, the "degradable polyethylene" which is presently being promoted as an environmentally friendly alternative to the nondegradable counterpart, does not seem to meet this criterion. This article reviews the state of the art on the aspect of degradability of polyethylene containing pro-oxidants, and more importantly the effect these polymers could have on the environment in the long run. On exposure to heat, light, and oxygen, these polymers disintegrate into small fragments, thereby reducing or increasing the visual presence. However, these fragments can remain in the environment for prolonged time periods. This article also outlines important questions, particularly in terms of time scale of complete degradation, environmental fate of the polymer residues, and possible accumulation of toxins, the answers to which need to be established prior to accepting these polymers as environmentally benign alternatives to their nondegradable equivalents. It appears from the existing literature that our search for biodegradable polyethylene has not yet been realized. PMID:21495645

  8. Profiles in garbage: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1997-11-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks -- along with salad dressing, fruit juices, peanut butter, and other household and consumer products -- use PET bottles. PET also is used for film, sheeting for cups and food trays, oven-safe trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early 1970s. Because it is an ``engineered`` resin, PET is more expensive than commodity resins such as high-density polyethylene (HDPE) and, for the same reason, it is usually the highest valued plastic recyclable.

  9. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... chlorination of polyethylene conforming to the density, maximum n-hexane extractable fraction, and maximum... polyethylene is limited to use only as a modifier admixed at levels not exceeding 15 weight percent in...

  10. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  11. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  12. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  13. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  14. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  15. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  16. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  17. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  18. Waste product profile: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1996-02-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks are the primary product packaged in PET. Salad dressing, peanut butter, and other household and consumer products also use PET bottles. PET is also used for film, sheeting for cups and food trays, ovenable trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early `70s. Because it is an ``engineered`` resin, it is more expensive than commodity resins such as high-density polyethylene (HDPE). The primary market for recycled PET is the fiber industry, which uses PET for carpet fiber, sweaters and other clothing, and for other uses. Recycled PET can also be used for food and beverage containers. Export markets, particularly Asian countries, are becoming increasingly important.

  19. Single electron states in polyethylene

    SciTech Connect

    Wang, Y.; MacKernan, D.; Cubero, D. E-mail: n.quirke@imperial.ac.uk; Coker, D. F.; Quirke, N. E-mail: n.quirke@imperial.ac.uk

    2014-04-21

    We report computer simulations of an excess electron in various structural motifs of polyethylene at room temperature, including lamellar and interfacial regions between amorphous and lamellae, as well as nanometre-sized voids. Electronic properties such as density of states, mobility edges, and mobilities are computed on the different phases using a block Lanczos algorithm. Our results suggest that the electronic density of states for a heterogeneous material can be approximated by summing the single phase density of states weighted by their corresponding volume fractions. Additionally, a quantitative connection between the localized states of the excess electron and the local atomic structure is presented.

  20. Single electron states in polyethylene

    NASA Astrophysics Data System (ADS)

    Wang, Y.; MacKernan, D.; Cubero, D.; Coker, D. F.; Quirke, N.

    2014-04-01

    We report computer simulations of an excess electron in various structural motifs of polyethylene at room temperature, including lamellar and interfacial regions between amorphous and lamellae, as well as nanometre-sized voids. Electronic properties such as density of states, mobility edges, and mobilities are computed on the different phases using a block Lanczos algorithm. Our results suggest that the electronic density of states for a heterogeneous material can be approximated by summing the single phase density of states weighted by their corresponding volume fractions. Additionally, a quantitative connection between the localized states of the excess electron and the local atomic structure is presented.

  1. Poly(ethylene oxide) functionalization

    DOEpatents

    Pratt, Russell Clayton

    2014-04-08

    A simple procedure is provided by which the hydroxyl termini of poly(ethylene oxide) can be appended with functional groups to a useful extent by reaction and precipitation. The polymer is dissolved in warmed toluene, treated with an excess of organic base and somewhat less of an excess of a reactive acylating reagent, reacted for several hours, then precipitated in isopropanol so that the product can be isolated as a solid, and salt byproducts are washed away. This procedure enables functionalization of the polymer while not requiring laborious purification steps such as solvent-solvent extraction or dialysis to remove undesirable side products.

  2. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.780 Polyethylene. (a)...

  3. Crystallization studies of polyethylene -poly(ethylene glycol) graft copolymers

    NASA Astrophysics Data System (ADS)

    Mark, P. R.; Hovey, G. E.; Murthy, N. S.; Breitenkamp, K.; Kade, M.; Emerick, T.

    2006-03-01

    Structure and crystallization behavior of three copolymers obtained by grafting poly (ethylene glycol) (PEG) chains to polyethylene (PE) main chain was investigated by variable temperature x-ray diffraction and thermal analysis. The results show that PEG side chains and PE main chains crystallize into separate domains. This is especially true when grafted chains are long (50 and 100 repeat units), in which the PEG domains are same as in PEG homopolymer both in structure and in melting behavior. In the copolymer with shorter chains (25 repeat units), the PEG crystals are not distinct and melting is broad. The PEG domains can be dissolved in water or ethanol without altering the mechanical integrity of the film. PE crystallites in both samples are similar to that in PE homopolymer. For instance, the thermal expansion of the basal cell plane (a- and b-axes) of the PE domains agrees well with that of PE homopolymer over the entire temperature range from ambient to melt. However, the chain-axis dimension PE-lattice in the copolymer is shorter by ˜ 0.05 å and the basal dimensions are larger by ˜ 0.05 å. The changes in these dimensions due to the changes in the length of the grafted PEG chains were investigated.

  4. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polyethylene has a minimum number average molecular weight of 1,200, as determined by high temperature vapor pressure osmometry; contains a maximum of 5 percent by weight of total oxygen; and has an acid value of...

  5. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... produced by the direct chlorination of polyethylene conforming to the density, maximum n-hexane extractable... percent in plastic articles prepared from polyvinyl chloride and/or from vinyl chloride...

  6. Osmotic effects of polyethylene glycol.

    PubMed

    Schiller, L R; Emmett, M; Santa Ana, C A; Fordtran, J S

    1988-04-01

    Polyethylene glycol (PEG) has been used to increase the osmotic pressure of fluids used to cleanse the gastrointestinal tract. However, little is known about its osmotic activity. To investigate this activity systematically, solutions of PEG of differing molecular weights were made and subjected to measurement of osmolality by both freezing point depression and vapor pressure osmometry. Measured osmolality was increasingly greater than predicted from average molecular weight as PEG concentration increased. Measurement of sodium activity in NaCl/PEG solutions by means of an ion-selective electrode suggested that the higher than expected osmolality could be due in part to interactions that, in effect, sequestered water from the solution. Osmolality was consistently greater by freezing point osmometry than by vapor pressure osmometry. To determine which osmometry method reflected biologically relevant osmolality, normal subjects underwent steady-state total gut perfusion with an electrolyte solution containing 105 g/L of PEG 3350. This produced rectal effluent that was hypertonic by freezing point osmometry but isotonic by vapor pressure osmometry. Assuming that luminal fluid reaches osmotic equilibrium with plasma during total gut perfusion, this result suggests that the vapor pressure osmometer accurately reflects the biologically relevant osmolality of intestinal contents. We conclude that PEG exerts more of an osmotic effect than would be predicted from its molecular weight. This phenomenon may reflect interactions between PEG and water molecules that alter the physical chemistry of the solution and sequester water from the solution. PMID:3345895

  7. Maxillofacial prostheses of chlorinated polyethylene.

    PubMed

    May, P D

    1978-05-01

    There is clearly a need for maxillofacial prosthetic materials with improved properties. The chlorinated polyethylenes are thermoplastic elastomers which have particularly promising properties, and were used by us to prepare improved maxillofacial prostheses. Suitable CPE resins were compounded with other polymers and with pigments on a heated rubber mill to form thin sheets in a variety of shades. These were heated at 190 degrees C for 10 min and placed between heated linotype mold halves. The prosthesis was formed in a hand press. Sometimes heating and pressing were repeated. After cooling in water, the prosthesis was removed and hand-shaded with oil-soluble dyes. Physical properties were evaluated using standard techniques; skin irritation studies were conducted by 14-day insult patch tests on rabbits. Clinical evaluations were conducted on human volunteers. Parallel evaluations were conducted on commerically available materials for comparison. The CPE was superior to all of the three commerical materials in most properties, and comparable to the better of the three in the remaining properties. On balance, CPE was significantly superior. Early results indicate that the materials and techniques required are easily handled in the dental lab and that the final prosthesis has excellent aesthetic and patient acceptability. PMID:670262

  8. Charge packets modeling in polyethylene

    NASA Astrophysics Data System (ADS)

    Baudoin, F.; Laurent, C.; Teyssedre, G.; Le Roy, S.

    2014-04-01

    Charge packets in insulating polymers have been reported by many groups within the last two decades, especially in polyethylene-based materials. They consist in a pulse of net charge that remains in the form of a pulse as it crosses the insulation. In spite of a variety of characteristics depending on material properties and experimental conditions, one of the puzzling aspects of the packets is their repetitive character until they eventually die away. Several theories have been proposed to explain their formation and propagation. Two of them have the advantage of simplicity and of being physically based, being the existence of an hysteresis loop in the injection mechanism or a negative differential mobility of carriers with the electric field. Based on these descriptions, some progress has been done recently by discussing the shape of the packets during their propagation but none of the concepts has been incorporated into a transport model to describe the full evolution from the packet generation to their vanishing. Here, we used a simplified transport model featuring bipolar charge injection and transport coupled to specific conditions in charge injection or carrier mobility to reproduce experimental results. One of the salient features of the results is that both models are able to reproduce the repetitive character and the dying away of the packets that appear to be linked with the internal field distribution modulated by a bipolar space charge.

  9. Interchain electron states in polyethylene

    NASA Astrophysics Data System (ADS)

    Serra, S.; Tosatti, E.; Iarlori, S.; Scandolo, S.; Santoro, G.

    2000-08-01

    We present a theoretical study of the nature of the lowest empty conduction-band states in crystalline polyethylene (PE), conducted through density-functional electronic structure calculations. Results reveal that the wave function of the conduction-band edge is of interchain character, as opposed to the intrachain character of all the filled valence-band states. Thus, while a hole added to neutral PE will mainly belong to the PE chain backbone bonds, an added electron in PE will mostly reside between the chains, and far from the existing bonds. Moreover, the added electron state charge centroid is predicted to move further out from the chain backbone towards the low-density interstitial region, if and when the chains are pried apart. This suggests that injected electrons will naturally flow to low-density regions inside real PE, and that the experimentally established propensity of PE to expel electrons out of the bulk, should be directly related to the interchain nature of the conduction states.

  10. Acute polyethylene fracture in an uncemented acetabular cup

    PubMed Central

    Gross, Allan E.; Dust, William N.

    1997-01-01

    The smaller acetabular components used in total hip replacement may have a polyethylene liner that is too thin, resulting in higher polyethylene stress and an increased potential for wear. The authors present a case that highlights the problem of acute polyethylene fracture. To compensate for the thinness of the polyethylene, the authors recommend the use of a smaller head size to allow polyethylene thickness of at least 8 mm. PMID:9267302

  11. Catastrophic Failure of the Acetabular Polyethylene Liner in Ceramic-on-Polyethylene Total Hip Arthroplasty

    PubMed Central

    Manzano, Givenchy; Levin, Rayna A. C.; Mayor, Michael B.; Schwarzkopf, Ran

    2014-01-01

    Introduction: Catastrophic polyethylene failure is a rare complication of ceramic-on-polyethylene total hip arthroplasty due to the favorable tribological characteristics of ceramic. Failure of the polyethylene liner can be disastrous, increasing periprosthetic osteolysis, metallosis, and risk of dislocation. Complications associated with ceramic-on-polyethylene articulations have been studied extensively, however, only few reports have described its catastrophic wear. We report such a case of complete wear of the acetabular liner in a ceramic-on-polyethylene prosthesis in a 57-year adult male. Case Report: A 57-year adult male with a history of bilateral total hip arthroplasty presented to our institution with bilateral hip pain worst on the right. Range of motion was limited by pain on the right hip at the extremes of motion. Radiographs revealed severe osteolysis, heterotopic ossification, complete wear of the acetabular liner, bony impingement of the femoral greater trochanter on the acetabular rim and superior migration of the femoral head. All findings were confirmed intraoperatively. Revision of the acetabular components was performed, which successfully alleviated the patient’s symptoms. Conclusion: Failure of the ceramic-on-polyethylene liner in our patient is due to the use of a non-cross linked polyethylene liner, a highly active lifestyle, and poor follow up. Arthroplasty surgeons should be aware of this complication especially in highly active patients with a conventional polyethylene liner and chronic hip pain. PMID:27298960

  12. Polymeric compositions incorporating polyethylene glycol as a phase change material

    DOEpatents

    Salyer, Ival O.; Griffen, Charles W.

    1989-01-01

    A polymeric composition comprising a polymeric material and polyethylene glycol or end-capped polyethylene glycol as a phase change material, said polyethylene glycol and said end-capped polyethylene glycol having a molecular weight greater than about 400 and a heat of fusion greater than about 30 cal/g; the composition is useful in making molded and/or coated materials such as flooring, tiles, wall panels and the like; paints containing polyethylene glycols or end-capped polyethylene glycols are also disclosed.

  13. Elongational rheology of polyethylene melts

    NASA Astrophysics Data System (ADS)

    Seyfzadeh, Bijan

    Elongational melt flow behavior is an important and fundamental concept underlying many industrial plastics operations which involve a rapid change of shape as for example fiber spinning and stretching, bottle blow molding, and film blowing and stretching. Under high process loads polymeric materials experience enormous stresses causing the molecular structure to gain considerable orientation. This event has significant effects on the melt flow behavior and can be measured in terms of elongational viscosity and changes in enthalpy and entropy. Different polymeric materials with unique molecular characteristics are expected to respond uniquely to the elongational deformation; hence, molecular parameters such as molecular weight and degree of branching were related to the measurable elongational flow variables. Elongational viscosities were measured for high and low density polyethylenes using an advanced capillary extrusion rheometer fitted with semi-hyperbolic dies. Said dies establish a purely elongational. flow field at constant elongational strain rate. The elongational viscosities were evaluated under influence of process strain rate, Hencky strain (natural logarithm of area reduction of the extrusion die), and temperature. Enthalpy and entropy changes associated with the orientation development of semi-hyperbolic processed melts were also determined. Results showed that elongational viscosities were primarily affected by differences in weight average molecular weight rather than degree of branching. This effect was process strain rate as well as temperature dependent. An investigation of melt relaxation and the associated first decay time constants revealed that with increasing strain rate the molecular field of the melt asymptotically gained orientation in approaching a limit. As a result of this behavior molecular uniqueness vanished at high process strain rates, yielding to orientation development and the associated restructuring of the melt's molecular

  14. Recent advances in polyethylene separator technology

    NASA Astrophysics Data System (ADS)

    Weighall, M. J.

    The well known technical and production benefits of polyethylene separator materials over other separator materials have prompted a dramatic increase in polyethylene separator usage in recent years. Separator trends in the United States from 1980 to 1996, and in Europe from 1987 to 1992, are shown. The manufacturing process for polyethylene separators is outlined, with particular emphasis on the latest advances in manufacturing technology. These improvements have resulted in a higher quality product, and also benefit the environment because of the sophisticated oil extraction and solvent recovery system. The product quality improvements resulting from the latest manufacturing technology include consistent conformance to dimensional specifications, low electrical resistance, close control of residual oil content, virtual elimination of pinholes, and good running properties on the battery manufacturers' plate enveloping machines. The material can also be manufactured with a very thin backweb to reduce electrical resistance still further.

  15. Relationship between interfacial forces measured by colloid-probe atomic force microscopy and protein resistance of poly(ethylene glycol)-grafted poly(L-lysine) adlayers on niobia surfaces.

    PubMed

    Pasche, Stéphanie; Textor, Marcus; Meagher, Laurence; Spencer, Nicholas D; Griesser, Hans J

    2005-07-01

    Adsorbed layers of "comb-type" copolymers consisting of PEG chains grafted onto a poly(l-lysine) (PLL) backbone on niobium oxide substrates were studied by colloid-probe AFM in order to characterize the interfacial forces associated with coatings of varying architectures (PEG/PLL ratios and PEG chain lengths) and their relevance to protein resistance. The steric and electrostatic forces measured varied substantially with the architecture of the PLL-g-PEG copolymers. Varying the ionic strength of the buffer solutions enabled discrimination between electrostatic and steric-entropic contributions to the net interfacial force. For high PEG grafting densities the steric component was most prominent, but at low ionic strengths and high grafting densities, a repulsive electrostatic surface force was also observed; its origin was assigned to the niobia charges beneath the copolymer, as insufficient protonated amine groups in the PLL backbone were available for compensation of the oxide surface charges. For lower grafting densities and lower ionic strengths there was a substantial attractive electrostatic contribution arising from interaction of the electrical double layer arising from the protonated amine groups, with that of the silica probe surface (as under low ionic strength conditions, the electrical double layer was thicker than the PEG layer). For these PLL-g-PEG coatings the net interfacial force can thus be a markedly varying superposition of electrostatic and steric-entropic contributions, depending on various factors. The force curves correlate with protein adsorption data, demonstrating the utility of AFM colloid-probe force measurements for quantitative analysis of surface forces and how they determine interfacial interactions with proteins. Such characterization of the net interfacial forces is essential to elucidate the multiple types of interfacial forces relevant to the interactions between PLL-g-PEG coatings and proteins and to advance interpretation of

  16. Tensile Deformation of Polyethylenes: Crystallinity Effects

    NASA Astrophysics Data System (ADS)

    Crist, Buckley; Metaxas, Costas

    2004-03-01

    The crystalline fraction of polyethylene can be reduced by increasing the cooling rate, the molecular weight or the fraction of comonomer. All three methods have been used in this study of tensile deformation which shows that true stress - true strain behavior depends systematically on morphology. The dependence of uniaxial yield stress on crystal thickness is well understood in terms of dislocation nucleation. Post yield flow is dominated by the strain hardening rate that is larger in polyethylenes of lower crystallinity. Noncrystalline polymer evidently reduces the plastic compliance while providing for elastic (reversible) strains. These observations are examined in terms of old and new theories for deformation of semicrystalline polymers.

  17. Polyethylene glycol-electrolyte solution (PEG-ES)

    MedlinePlus

    Polyethylene glycol-electrolyte solution (PEG-ES) is used to empty the colon (large intestine, bowel) before a ... Polyethylene glycol-electrolyte solution (PEG-ES) comes as a powder to mix with water and take by ...

  18. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  19. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  20. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  1. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  2. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene glycol (400) monolaurate. 178.3760 Section 178.3760 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400)...

  3. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  4. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  5. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface of articles intended for use in contact...

  6. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  7. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  8. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  9. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  10. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  11. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  12. Computational method for analysis of polyethylene biodegradation

    NASA Astrophysics Data System (ADS)

    Watanabe, Masaji; Kawai, Fusako; Shibata, Masaru; Yokoyama, Shigeo; Sudate, Yasuhiro

    2003-12-01

    In a previous study concerning the biodegradation of polyethylene, we proposed a mathematical model based on two primary factors: the direct consumption or absorption of small molecules and the successive weight loss of large molecules due to β-oxidation. Our model is an initial value problem consisting of a differential equation whose independent variable is time. Its unknown variable represents the total weight of all the polyethylene molecules that belong to a molecular-weight class specified by a parameter. In this paper, we describe a numerical technique to introduce experimental results into analysis of our model. We first establish its mathematical foundation in order to guarantee its validity, by showing that the initial value problem associated with the differential equation has a unique solution. Our computational technique is based on a linear system of differential equations derived from the original problem. We introduce some numerical results to illustrate our technique as a practical application of the linear approximation. In particular, we show how to solve the inverse problem to determine the consumption rate and the β-oxidation rate numerically, and illustrate our numerical technique by analyzing the GPC patterns of polyethylene wax obtained before and after 5 weeks cultivation of a fungus, Aspergillus sp. AK-3. A numerical simulation based on these degradation rates confirms that the primary factors of the polyethylene biodegradation posed in modeling are indeed appropriate.

  13. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, oxidized. 177.1620 Section 177.1620 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as...

  14. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as...

  15. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  16. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  17. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food...

  18. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food...

  19. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related...

  20. POLYETHYLENE ENCAPSULATES FOR HAZARDOUS WASTE DRUMS

    EPA Science Inventory

    This capsule report summarizes studies of the use of polyethylene (P.E.) for encapsulating drums of hazardous wastes. Flat PE sheet is welded to roto moded PE containers which forms the encapsulates. Plastic pipe welding art was used, but the prototype welding apparatus required ...

  1. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  2. DNP with Trityl Radicals in Deuterated Polyethylene

    NASA Astrophysics Data System (ADS)

    Wang, Li; Meyer, W.; Berlin, A.; Herick, J.; Hess, C.; Reicherz, G.

    2016-02-01

    Chemically doping with trityl radicals was performed in fully deuterated polyethylene. The behavior of paramagnetic centers has been investigated by ESR X-band spectrometer. The highest deuteron polarization was 8% at 2.5 T and 1 K with a spin concentration of 3 × 1019 spins/g.

  3. Herbicide dissipation from low density polyethylene mulch

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Field and laboratory studies were conducted to examine herbicide dissipation when applied to low density polyethylene (LDPE) mulch for dry scenarios vs. washing off with water. In field studies, halosulfuron, paraquat, carfentrazone, glyphosate, and flumioxazin were applied to black 1.25-mil LDPE at...

  4. Preservation of Mercury in Polyethylene Containers.

    ERIC Educational Resources Information Center

    Piccolino, Samuel Paul

    1983-01-01

    Reports results of experiments favoring use of 0.5 percent nitric acid with an oxidant (potassium dichromate or potassium permanganate) to preserve samples in polyethylene containers for mercury analysis. Includes procedures used and statistical data obtained from the experiments. (JN)

  5. STRESS CRACK TESTING OF POLYETHYLENE GEOMEMBRANES

    EPA Science Inventory

    The sensitivity of high density polyethylene (HDPE) geomembranes to stress cracking is evaluated under accelerated conditions at a constant stress. he test specimens are according to ASTM D-1822, and are of the dumbbell shape with a constant length in the central section. he acce...

  6. Macrophage phagocytosis of polyethylene particulate in vitro.

    PubMed

    Voronov, I; Santerre, J P; Hinek, A; Callahan, J W; Sandhu, J; Boynton, E L

    1998-01-01

    In this study, an in vitro model has been developed to examine the interactions of macrophages with ultrahigh molecular-weight polyethylene (UHMWPE) and high-density polyethylene (HDPE) particles. Polyethylene particles are the major constituent of the material debris formed as a result of orthopedic implant wear. However, the study of polyethylene particle interactions with cells has been limited. UHMWPE (18-20 microns) and HDPE (4-10 microns) were suspended in soluble collagen type I and subsequently solidified on glass coverslips. The particle chemistry was characterized by Fourier transform infra-red spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). Mouse cell line macrophages (IC-21) were established on the collagen-particle substrata and maintained for up to 24 h. The response of the cells to the particles was examined by light and transmission electron microscopy (LM and TEM), as well as by scanning electron microscopy (SEM), and compared to cells on control collagen surfaces without particles. Histological analysis of the samples revealed that the macrophages surrounded larger particles (18-20 microns) and the cells appeared to be attached to the surface of the particles, and the smaller particles (4-10 microns) had been phagocytosed within 2 h. Inflammatory cytokines (TNF-alpha, IL-1 alpha, IL-1 beta, and IL-6), lysosomal enzymes (beta-galactosidase and hexosaminidase), and prostaglandin E2 were released into the medium, and IL-1 alpha, IL-1 beta, PGE2, beta-galactosidase, and hexosaminidase levels were significantly increased over collagen control values. The results demonstrate active phagochemotaxis by macrophages for wear particulates and validate this model as a means of studying the specific in vitro interactions of polyethylene with cells. PMID:9429095

  7. Protein

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Proteins are the major structural and functional components of all cells in the body. They are macromolecules that comprise 1 or more chains of amino acids that vary in their sequence and length and are folded into specific 3-dimensional structures. The sizes and conformations of proteins, therefor...

  8. Proteins.

    ERIC Educational Resources Information Center

    Doolittle, Russell F.

    1985-01-01

    Examines proteins which give rise to structure and, by virtue of selective binding to other molecules, make genes. Binding sites, amino acids, protein evolution, and molecular paleontology are discussed. Work with encoding segments of deoxyribonucleic acid (exons) and noncoding stretches (introns) provides new information for hypotheses. (DH)

  9. Modeling cutinase enzyme regulation in polyethylene terepthalate plastic biodegradation

    NASA Astrophysics Data System (ADS)

    Apri, M.; Silmi, M.; Heryanto, T. E.; Moeis, M. R.

    2016-04-01

    PET (Polyethylene terephthalate) is a plastic material that is commonly used in our daily life. The high production of PET and others plastics that can be up to three hundred million tons per year, is not matched by its degradation rate and hence leads to environmental pollution. To overcome this problem, we develop a biodegradation system. This system utilizes LC Cutinase enzyme produced by engineered escherichia coli bacteria to degrade PET. To make the system works efficaciously, it is important to understand the mechanism underlying its enzyme regulation. Therefore, we construct a mathematical model to describe the regulation of LC Cutinase production. The stability of the model is analyzed. We show that the designated biodegradation system can give an oscillatory behavior that is very important to control the amount of inclusion body (the miss-folded proteins that reduce the efficiency of the biodegradation system).

  10. Fabrication of poly(ethylene glycol) hydrogel microstructures using photolithography.

    PubMed

    Revzin, A; Russell, R J; Yadavalli, V K; Koh, W G; Deister, C; Hile, D D; Mellott, M B; Pishko, M V

    2001-09-01

    The fabrication of hydrogel microstructures based upon poly(ethylene glycol) diacrylates, dimethacrylates, and tetraacrylates patterned photolithographically on silicon or glass substrates is described. A silicon/silicon dioxide surface was treated with 3-(trichlorosilyl)propyl methacrylate to form a self-assembled monolayer (SAM) with pendant acrylate groups. The SAM presence on the surface was verified using ellipsometry and time-of-flight secondary ion mass spectrometry. A solution containing an acrylated or methacrylated poly(ethylene glycol) derivative and a photoinitiator (2,2-dimethoxy-2-phenylacetophenone) was spin-coated onto the treated substrate, exposed to 365 nm ultraviolet light through a photomask, and developed with either toluene, water, or supercritical CO2. As a result of this process, three-dimensional, cross-linked PEG hydrogel microstructures were immobilized on the surface. Diameters of cylindrical array members were varied from 600 to 7 micrometers by the use of different photomasks, while height varied from 3 to 12 micrometers, depending on the molecular weight of the PEG macromer. In the case of 7 micrometers diameter elements, as many as 400 elements were reproducibly generated in a 1 mm2 square pattern. The resultant hydrogel patterns were hydrated for as long as 3 weeks without delamination from the substrate. In addition, micropatterning of different molecular weights of PEG was demonstrated. Arrays of hydrogel disks containing an immobilized protein conjugated to a pH sensitive fluorophore were also prepared. The pH sensitivity of the gel-immobilized dye was similar to that in an aqueous buffer, and no leaching of the dye-labeled protein from the hydrogel microstructure was observed over a 1 week period. Changes in fluorescence were also observed for immobilized fluorophore labeled acetylcholine esterase upon the addition of acetyl acholine. PMID:12448421

  11. Fabrication of poly(ethylene glycol) hydrogel microstructures using photolithography

    NASA Technical Reports Server (NTRS)

    Revzin, A.; Russell, R. J.; Yadavalli, V. K.; Koh, W. G.; Deister, C.; Hile, D. D.; Mellott, M. B.; Pishko, M. V.

    2001-01-01

    The fabrication of hydrogel microstructures based upon poly(ethylene glycol) diacrylates, dimethacrylates, and tetraacrylates patterned photolithographically on silicon or glass substrates is described. A silicon/silicon dioxide surface was treated with 3-(trichlorosilyl)propyl methacrylate to form a self-assembled monolayer (SAM) with pendant acrylate groups. The SAM presence on the surface was verified using ellipsometry and time-of-flight secondary ion mass spectrometry. A solution containing an acrylated or methacrylated poly(ethylene glycol) derivative and a photoinitiator (2,2-dimethoxy-2-phenylacetophenone) was spin-coated onto the treated substrate, exposed to 365 nm ultraviolet light through a photomask, and developed with either toluene, water, or supercritical CO2. As a result of this process, three-dimensional, cross-linked PEG hydrogel microstructures were immobilized on the surface. Diameters of cylindrical array members were varied from 600 to 7 micrometers by the use of different photomasks, while height varied from 3 to 12 micrometers, depending on the molecular weight of the PEG macromer. In the case of 7 micrometers diameter elements, as many as 400 elements were reproducibly generated in a 1 mm2 square pattern. The resultant hydrogel patterns were hydrated for as long as 3 weeks without delamination from the substrate. In addition, micropatterning of different molecular weights of PEG was demonstrated. Arrays of hydrogel disks containing an immobilized protein conjugated to a pH sensitive fluorophore were also prepared. The pH sensitivity of the gel-immobilized dye was similar to that in an aqueous buffer, and no leaching of the dye-labeled protein from the hydrogel microstructure was observed over a 1 week period. Changes in fluorescence were also observed for immobilized fluorophore labeled acetylcholine esterase upon the addition of acetyl acholine.

  12. Speciation of antimony in polyethylene terephthalate bottles

    SciTech Connect

    Martin, R.R.; Ablett, J.; Shotyk, W.S.; Naftel, S.; Northrup, P.

    2009-12-18

    Antimony contamination has been reported in drinking water from polyethylene terephthalate (PET) bottles. Micro-X-ray fluorescence (XRF) analysis has been used to identify the distribution and chemical form of residual antimony used as a catalyst in the manufacture of PET bottles. The results are consistent with clusters of Sb(III) having dimensions of the order of tens of micrometers, clearly showing the ability of synchrotron radiation analyses to both map elemental distribution and determine oxidation state.

  13. Greater osteoblast and endothelial cell adhesion on nanostructured polyethylene and titanium

    PubMed Central

    Raimondo, Theresa; Puckett, Sabrina; Webster, Thomas J

    2010-01-01

    Mostly due to desirable mechanical properties (such as high durability and low wear), certain synthetic polymers (such as polyethylene) and metals (such as titanium) have found numerous applications in the medical device arena from orthopedics to the vasculature, yet frequently, they do not proactively encourage desirable cell responses. In an effort to improve the efficacy of such traditional materials for various implant applications, this study used electron beam evaporation to create nanostructured surface features that mimic those of natural tissue on polyethylene and titanium. For other materials, it has been shown that the creation of nanorough surfaces increases surface energy leading to greater select protein (such as vitronectin and fibronectin) interactions to increase specific cell adhesion. Here, osteoblast (bone forming cells) and endothelial cell (cells that line the vasculature) adhesion was determined on nanostructured compared to conventional, nano-smooth polyethylene and titanium. Results demonstrated that nanorough surfaces created by electron beam evaporation increased the adhesion of both cells markedly better than conventional smooth surfaces. In summary, this study provided evidence that electron beam evaporation can modify implant surfaces (specifically, polyethylene and titanium) to have nanostructured surface features to improve osteoblast and endothelial cell adhesion. Since the adhesion of anchorage dependent cells (such as osteoblasts and endothelial cells) is a prerequisite for their long-term functions, this study suggests that electron beam evaporation should be further studied for improving materials for various biomedical applications. PMID:20856840

  14. Biodegradation of low-density polyethylene by marine bacteria from pelagic waters, Arabian Sea, India.

    PubMed

    Harshvardhan, Kumar; Jha, Bhavanath

    2013-12-15

    Sixty marine bacteria isolated from pelagic waters were screened for their ability to degrade low-density polyethylene; among them, three were positive and able to grow in a medium containing polythene as the sole carbon source. The positive isolates were identified as Kocuria palustris M16, Bacillus pumilus M27 and Bacillus subtilis H1584 based on the 16S rRNA gene sequence homology. The weight loss of polyethylene was 1%, 1.5% and 1.75% after 30 days of incubation with the M16, M27 and H1584 isolates, respectively. The maximum (32%) cell surface hydrophobicity was observed in M16, followed by the H1584 and M27 isolates. The viability of the isolates growing on the polyethylene surface was confirmed using a triphenyltetrazolium chloride reduction test. The viability was also correlated with a concomitant increase in the protein density of the biomass. Polyethylene biodegradation was further confirmed by an increase in the Keto Carbonyl Bond Index, the Ester Carbonyl Bond Index and the Vinyl Bond Index, which were calculated from FT-IR spectra. PMID:24210946

  15. Molecular mechanism of viscoelasticity in aligned polyethylene

    NASA Astrophysics Data System (ADS)

    Hammad, Ali; Hasan, Hikmatyar; Swinburne, Thomas; Del Rosso, Stefano; Iannucci, Lorenzo; Sutton, Adrian

    2014-03-01

    Aligned polyethylene is used in industrial and medical applications due to its low density and high tensile strength. Extensive experimental work has been done to determine its mechanical properties, notably its viscoelasticity. However, the molecular processes that underlie these macroscopic properties are poorly understood. We develop a united atom model of aligned chains, in which intermolecular interactions are modelled by a Lennard-Jones potential, and the elastic energy within chains is modelled with harmonic springs. Using this simple model, we demonstrate the nucleation of solitons from chain ends, as one molecular chain is stretched with respect to another, and how load is transferred between chains in disregistry by intermolecular interactions. We develop an equation of motion for the movement of solitons along molecular chains, allowing us to replace a collection of aligned chains with a gas of solitons. Although solitons have been invoked to account for dielectric relaxation in crystalline regions of polyethylene, we believe this may be the first time they are discussed in the context of mechanical properties of aligned polyethylene.

  16. Extensional Flow Induced Crystallization of Polyethylene

    NASA Astrophysics Data System (ADS)

    Nicholson, David; Locker, C. Rebecca; Tsou, Andy; Rutledge, Gregory

    2014-03-01

    The majority of manufactured polyethylene is used in films mostly through the blown film fabrication process where extensional flow induced crystallization is a critical component in affecting the development of crystalline morphology and amorphous topology. In order to optimize the blown film performance, it is critical to understand the mechanism of extensional flow induced crystallization of polyethylene. Model high density polyethylene with a Mn of 20,000 g/mol and a PDI (polydispersity) of 2 and lower were synthesized by organometallic catalysts. Extensional flow induced crystallization of these materials was measured using the SER (Sentmanat Extensional Rheometer) either at a given rate with varying temperatures or vice versa. A continuum model was applied to analyze the flow induced crystallization data. All samples after extensional flow were quenched in ice water and the resulting morphology was characterized using SAXS and WAXS. The extensional rate was found to be effective in modifying morphology whereas the temperature was not; neither temperature nor strain rate affected the final film crystallinity. With an increase in extensional rate, crystallites became thinner and narrower with potentially higher connectivity which could lead to higher toughness.

  17. Grafting functional antioxidants on highly crosslinked polyethylene

    NASA Astrophysics Data System (ADS)

    Al-Malaika, S.; Riasat, S.; Lewucha, C.

    2016-05-01

    The problem of interference of antioxidants, such as hindered phenols, with peroxide-initiated crosslinking of polyethylene was addressed through the use of functional (reactive) graftable antioxidants (g-AO). Reactive derivatives of hindered phenol and hindered amine antioxidants were synthesised, characterised and used to investigate their grafting reactions in high density polyethylene; both non-crosslinked (PE) and highly peroxide-crosslinked (PEXa). Assessment of the extent of in-situ grafting of the antioxidants, their retention after exhaustive solvent extraction in PE and PEXa, and the stabilising performance of the grafted antioxidants (g-AO) in the polymer were examined and benchmarked against conventionally stabilised crosslinked & non-crosslinked polyethylene. It was shown that the functional antioxidants graft to a high extent in PEXa, and that the level of interference of the g-AOs with the polymer crosslinking process was minimal compared to that of conventional antioxidants which bear the same antioxidant function. The much higher level of retention of the g-AOs in PEXa after exhaustive solvent extraction, compared to that of the corresponding conventional antioxidants, accounts for their superior long-term thermal stabilising performance under severe extractive conditions.

  18. Polyethylene solidification of low-level wastes

    SciTech Connect

    Kalb, P.D.; Colombo, P.

    1985-02-01

    This topical report describes the results of an investigation on the solidification of low-level radioactive waste in polyethylene. Waste streams selected for this study included those which result from advanced volume reduction technologies (dry evaporator concentrate salts and incinerator ash) and those which remain problematic for solidification using contemporary agents (ion exchange resins). Four types of commercially available low-density polyethylenes were employed which encompass a range of processing and property characteristics. Process development studies were conducted to ascertain optimal process control parameters for successful solidification. Maximum waste loadings were determined for each waste and polyethylene type. Property evaluation testing was performed on laboratory-scale specimens to assess the potential behavior of actual waste forms in a disposal environment. Waste form property tests included water immersion, deformation under compressive load, thermal cycling and radionuclide leaching. Recommended waste loadings of 70 wt % sodium sulfate, 50 wt % boric acid, 40 wt % incinerator ash, and 30 wt % ion exchange resins, which are based on process control and waste form performance considerations are reported. 37 refs., 33 figs., 22 tabs.

  19. Bisoxalamide Clarifiers to Improve Optical Performance of Polyethylene Resins

    NASA Astrophysics Data System (ADS)

    Wang, Lin; Hill, Martin; Santos, Nestor, Jr.; Banks, Andrew; Huang, Jessica; Keene, Ellen; Keaton, Rich

    The use of special nucleating agents, often referred to as clarifying agents, to improve optical performance of polyethylene is not widely used in the industry. A series of bisoxalamide compounds were synthesized and mixed with linear low density polyethylene (LLDPE) to test clarification effects. In this talk, we will discuss structure/property relationship of these molecules on optical and thermal properties of LLDPE. Bisoxalamide clarifiers to improve optical performance of polyethylene resins.

  20. The yield behavior of polyethylene tubes subjected to biaxial loadings

    NASA Technical Reports Server (NTRS)

    Semeliss, M.; Wong, R.; Tuttle, M.

    1990-01-01

    High-density polyethylene is subjected to biaxial states of stress to examine the yield behavior of the semicrystalline thermoplastic under constant octahedral shear-stress rates. Combinations of internal pressures and axial loads are applied to thin-walled tubes of polyethylene, and the strain response in the axial and hoop directions are measured. The polyethylene specimens are found to be anisotropic, and the experimental measurements are compared to yield criteria that are applicable to isotropic and anisotropic materials.

  1. Chemical interaction of polyethylene matrix with vegetable fillers in biocomposites

    NASA Astrophysics Data System (ADS)

    Pantyukhov, Petr; Monakhova, Tatiana; Popov, Anatoly; Zykova, Anna

    2016-05-01

    The paper studies the diffusion of low molecular weight components from vegetable fillers into polyethylene matrix during the preparation of biocomposites. In order to identify the diffusible substances a model experiment used where the hexadecane acted as a model of polyethylene. It was determined that polyphenolic compounds and chlorophyll penetrate from vegetable fillers to hexadecane to the maximum extent. There was found a correlation between the amount of polyphenolic compounds diffusible from the fillers to hexadecane and thermal oxidation kinetics of real biocomposites based on polyethylene and vegetable fillers. Thus, it has been assumed the diffusion of polyphenols and chlorophyll from vegetable fillers into polyethylene matrix during the preparation of biocomposites.

  2. Comparison of cross-linked polyethylene materials for orthopaedic applications.

    PubMed

    Collier, John P; Currier, Barbara H; Kennedy, Francis E; Currier, John H; Timmins, Graham S; Jackson, Simon K; Brewer, Robin L

    2003-09-01

    Cross-linked polyethylenes are being marketed by orthopaedic manufacturers to address the problem of osteolysis caused by polyethylene particulate wear debris. Wear testing of these cross-linked polyethylenes in hip simulators has shown dramatic reduction in wear rate compared with standard ultrahigh molecular weight polyethylene, either gamma irradiated in air or nitrogen - or ethylene oxide-sterilized. However, this reduction in wear rate is not without cost. The cross-linking processes can result in materials with lower mechanical properties than standard ultrahigh molecular weight polyethylene. To evaluate the effect of the various cross-linking processes on physical and mechanical properties of ultrahigh molecular weight polyethylene, commercially available cross-linked polyethylenes from six orthopaedic manufacturers were tested. This study was the culmination of collaboration with these manufacturers, who provided cross-linked polyethylene for this study, wear characteristics of the material they provided, and review of the physical and mechanical properties measure for their polyethylene. Cross-linked materials were evaluated as received and after an accelerated aging protocol. Free radical identity and concentration, oxidation, crystallinity, melt temperature, ultimate tensile strength, elongation at break, tensile stress at yield, and toughness are reported for each material. By comparing these physical and mechanical properties, surgeons can evaluate the trade-off that results from developing materials with substantially lower wear rates. PMID:12966304

  3. Mechanisms for Covalent Immobilization of Horseradish Peroxidase on Ion-Beam-Treated Polyethylene

    PubMed Central

    Kondyurin, Alexey V.; Naseri, Pourandokht; Tilley, Jennifer M. R.; Nosworthy, Neil J.; Bilek, Marcela M. M.; McKenzie, David R.

    2012-01-01

    The surface of polyethylene was modified by plasma immersion ion implantation. Structure changes including carbonization and oxidation were observed. High surface energy of the modified polyethylene was attributed to the presence of free radicals on the surface. The surface energy decay with storage time after treatment was explained by a decay of the free radical concentration while the concentration of oxygen-containing groups increased with storage time. Horseradish peroxidase was covalently attached onto the modified surface by the reaction with free radicals. Appropriate blocking agents can block this reaction. All aminoacid residues can take part in the covalent attachment process, providing a universal mechanism of attachment for all proteins. The native conformation of attached protein is retained due to hydrophilic interactions in the interface region. The enzymatic activity of covalently attached protein remained high. The long-term activity of the modified layer to attach protein is explained by stabilisation of unpaired electrons in sp2 carbon structures. A high concentration of free radicals can give multiple covalent bonds to the protein molecule and destroy the native conformation and with it the catalytic activity. The universal mechanism of protein attachment to free radicals could be extended to various methods of radiation damage of polymers. PMID:24278665

  4. Patterned functional carbon fibers from polyethylene

    SciTech Connect

    Hunt, Marcus A; Saito, Tomonori; Brown, Rebecca H; Kumbhar, Amar S; Naskar, Amit K

    2012-01-01

    Patterned, continuous carbon fibers with controlled surface geometry were produced from a novel melt-processible carbon precursor. This portends the use of a unique technique to produce such technologically innovative fibers in large volume for important applications. The novelties of this technique include ease of designing and fabricating fibers with customized surface contour, the ability to manipulate filament diameter from submicron scale to a couple of orders of magnitude larger scale, and the amenable porosity gradient across the carbon wall by diffusion controlled functionalization of precursor. The geometry of fiber cross-section was tailored by using bicomponent melt-spinning with shaped dies and controlling the melt-processing of the precursor polymer. Circular, trilobal, gear-shaped hollow fibers, and solid star-shaped carbon fibers of 0.5 - 20 um diameters, either in self-assembled bundle form, or non-bonded loose filament form, were produced by carbonizing functionalized-polyethylene fibers. Prior to carbonization, melt-spun fibers were converted to a char-forming mass by optimizing the sulfonation on polyethylene macromolecules. The fibers exhibited distinctly ordered carbon morphologies at the outside skin compared to the inner surface or fiber core. Such order in carbon microstructure can be further tuned by altering processing parameters. Partially sulfonated polyethylene-derived hollow carbon fibers exhibit 2-10 fold surface area (50-500 m2/g) compared to the solid fibers (10-25 m2/g) with pore sizes closer to the inside diameter of the filaments larger than the sizes on the outer layer. These specially functionalized carbon fibers hold promise for extraordinary performance improvements when used, for example, as composite reinforcements, catalyst support media, membranes for gas separation, CO2 sorbents, and active electrodes and current collectors for energy storage applications.

  5. Polyethylene terephthalate thin films; a luminescence study

    NASA Astrophysics Data System (ADS)

    Carmona-Téllez, S.; Alarcón-Flores, G.; Meza-Rocha, A.; Zaleta-Alejandre, E.; Aguilar-Futis, M.; Murrieta S, H.; Falcony, C.

    2015-04-01

    Polyethylene Terephthalate (PET) films doped with Rare Earths (RE3+) have been deposited on glass by spray pyrolysis technique at 240 °C, using recycled PET and (RE3+) chlorides as precursors. Cerium, terbium, dysprosium and europium were used as dopants materials, these dopants normally produce luminescent emissions at 450, 545, 573 and 612 nm respectively; the doped films also have light emissions at blue, green, yellow and red respectively. All RE3+ characteristic emissions were observed at naked eyes. Every deposited films show a high transmission in the visible range (close 80% T), films surfaces are pretty soft and homogeneous. Films thickness is around 3 μm.

  6. Nonlinear viscoelastic characterization of thin polyethylene film

    NASA Technical Reports Server (NTRS)

    Wilbeck, J. S.

    1981-01-01

    In order to understand the state of stress and strain in a typical balloon fabricated from thin polyethylene film, experiment data in the literature reviewed. It was determined that the film behaves as a nonlinear viscoelasticity material and should be characterized accordingly. A simple uniaxial, nonlinear viscoelastic model was developed for predicting stress given a certain strain history. The simple model showed good qualitative agreement with results of constant rate, uniaxial accurately predicting stresses for cyclic strain histories typical of balloon flights. A program was outlined which will result in the development of a more complex nonlinear viscoelastic model.

  7. Biocompatible composites of ultrahigh molecular weight polyethylene

    NASA Astrophysics Data System (ADS)

    Panin, S. V.; Kornienko, L. A.; Suan, T. Nguen; Ivanova, L. P.; Korchagin, M. A.; Chaikina, M. V.; Shilko, S. V.; Pleskachevskiy, Yu. M.

    2015-10-01

    Mechanical and tribotechnical characteristics of biocompatible, antifriction and extrudable composites based on ultrahigh molecular weight polyethylene (UHMWPE) as well as hybrid matrix "UHMWPE + PTFE" with biocompatible hydroxyapatite filler under the dry friction and boundary lubrication were investigated. A comparative analysis of effectiveness of adding the hydroxyapatite to improve the wear resistance of composites based on these two matrices was performed. It is shown that the wear intensity of nanocomposites based on the hybrid matrix is lower than that for the composites based on pure UHMWPE. Possibilities of using the composites of the polymer "UHMWPE-PTFE" mixture as a material for artificial joints implants are discussed.

  8. Initial Stages of the Pyrolysis of Polyethylene.

    PubMed

    Popov, Konstantin V; Knyazev, Vadim D

    2015-12-10

    An experimental study of the kinetics of the initial stages of the pyrolysis of high-density polyethylene (PE) was performed. Quantitative yields of gas-phase products (C1-C8 alkanes and alkenes) and functional groups within the remaining polyethylene melt (methyl, vinyl, vinylene, vinylidene, and branching sites) were obtained as a function of time (0-20 min) at five temperatures in the 400-440 °C range. Gas chromatography and NMR ((1)H and (13)C) were used to detect the gas- and condensed-phase products, respectively. Modeling of polyethylene pyrolysis was performed, with the primary purpose of determining the rate constants of several critical reaction types important at the initial pyrolysis stages. Detailed chemical mechanisms were created (short and extended mechanisms) and used with both the steady-state approximation and numerical integration of the differential kinetic equations. Rate constants of critical elementary reactions (C-C backbone scission, two kinds of H-atom transfer, radical addition to the double bond, and beta-scission of tertiary alkyl radicals) were adjusted, resulting in an agreement between the model and the experiment. The values of adjusted rate constants are in general agreement with those of cognate reactions of small molecules in the gas phase, with the exception of the rate constants of the backbone C-C scission, which is found to be approximately 1-2 orders of magnitude lower. This observation provides tentative support to the hypothesis that congested PE melt molecular environment impedes the tumbling motions of separating fragments in C-C bond scission, thus resulting in less "loose" transition state and lower rate constant values. Sensitivity of the calculations to selected uncertainties in model properties was studied. Values and estimated uncertainties of four combinations of rate constants are reported as derived from the experimental results via modeling. The dependence of the diffusion-limited rate constant for radical

  9. Thermoluminescence Measurements of Medical Grade Polyethylene

    NASA Astrophysics Data System (ADS)

    Lewis, Scott; Dunlap, Greg; Palmer, Jeane; Jahan, M. S.

    1999-11-01

    Ultra-high molecular weight polyethylene (UHMWPE) is a biomaterial used in hip and knee joint replacements. Because this material is implanted into the body the material must be sterilized to prevent infection after implantation. Gamma irradiation is the most common method of sterilization, but it has one drawback; it causes the formation of free radicals and subsequent oxidative degradation of PE. By using thermoluminescence (TL) technique, free radical quenching temperature can be determined. In this study, UHMWPE was X-irradiated ( ~1 MRad at 10 keV) at 32 ^oC and subsequently heated to 200 ^oC at 1 ^oC / sec. The resulting luminescence known as thermoluminescence (TL) was recorded using a commercial TL dosimeter. The TL output, known as a glow curve, consists of two glow peaks, the prominent one occurs at 70 ^oC and a second one at 120 ^oC. It is suggested that the peak at 70 ^oC results from the recombination of free radicals due to molecular motion in the amorphous region, and the 120 ^oC peak is due to the motion of crystalline medium of the polyethylene matrix. Thermal annealing of free radicals as detected by TL can be a useful technique for diagnostic test of stabilization of radiation-sterilized medical joint components. *Supported by NSF REU Program (grant number EEC9619821) at the University of Memphis.

  10. Degradation of Green Polyethylene by Pleurotus ostreatus

    PubMed Central

    da Luz, José Maria Rodrigues; Paes, Sirlaine Albino; Ribeiro, Karla Veloso Gonçalves; Mendes, Igor Rodrigues; Kasuya, Maria Catarina Megumi

    2015-01-01

    We studied the biodegradation of green polyethylene (GP) by Pleurotus ostreatus. The GP was developed from renewable raw materials to help to reduce the emissions of greenhouse gases. However, little information regarding the biodegradation of GP discarded in the environment is available. P. ostreatus is a lignocellulolytic fungus that has been used in bioremediation processes for agroindustrial residues, pollutants, and recalcitrant compounds. Recently, we showed the potential of this fungus to degrade oxo-biodegradable polyethylene. GP plastic bags were exposed to sunlight for up to 120 days to induce the initial photodegradation of the polymers. After this period, no cracks, pits, or new functional groups in the structure of GP were observed. Fragments of these bags were used as the substrate for the growth of P. ostreatus. After 30 d of incubation, physical and chemical alterations in the structure of GP were observed. We conclude that the exposure of GP to sunlight and its subsequent incubation in the presence of P. ostreatus can decrease the half-life of GP and facilitate the mineralization of these polymers. PMID:26076188

  11. Polyethylene nanofibres with very high thermal conductivities.

    PubMed

    Shen, Sheng; Henry, Asegun; Tong, Jonathan; Zheng, Ruiting; Chen, Gang

    2010-04-01

    Bulk polymers are generally regarded as thermal insulators, and typically have thermal conductivities on the order of 0.1 W m(-1) K(-1). However, recent work suggests that individual chains of polyethylene--the simplest and most widely used polymer--can have extremely high thermal conductivity. Practical applications of these polymers may also require that the individual chains form fibres or films. Here, we report the fabrication of high-quality ultra-drawn polyethylene nanofibres with diameters of 50-500 nm and lengths up to tens of millimetres. The thermal conductivity of the nanofibres was found to be as high as approximately 104 W m(-1) K(-1), which is larger than the conductivities of about half of the pure metals. The high thermal conductivity is attributed to the restructuring of the polymer chains by stretching, which improves the fibre quality toward an 'ideal' single crystalline fibre. Such thermally conductive polymers are potentially useful as heat spreaders and could supplement conventional metallic heat-transfer materials, which are used in applications such as solar hot-water collectors, heat exchangers and electronic packaging. PMID:20208547

  12. Polyethylene wear in uncemented acetabular components.

    PubMed

    Hernandez, J R; Keating, E M; Faris, P M; Meding, J B; Ritter, M A

    1994-03-01

    We measured polyethylene wear in 231 porous-coated uncemented acetabular cups. We divided the hips into two groups according to the fixation of the femoral component, by cementing (n = 97) or press-fit (n = 134). Follow-up was from three to five years. The patients in two sub-groups were matched for weight, diagnosis, sex, age and length of follow-up. The linear wear rate of cups articulated with uncemented femoral components (0.22 mm/year) was significantly higher than the wear rate (0.15 mm/year) of cups articulated within cemented femoral components (p < 0.05). These results can be compared with previously reported wear rates of 0.08 mm/year for cemented all-polyethylene cups and 0.11 mm/year for cemented metal-backed cups. The higher wear rates of uncemented arthroplasties could jeopardize the long-term results of this type of hip replacement. PMID:8113288

  13. Nanostructurization and thermal properties of polyethylenes' welds

    NASA Astrophysics Data System (ADS)

    Galchun, Anatoliy; Korab, Nikolay; Kondratenko, Volodymyr; Demchenko, Valeriy; Shadrin, Andriy; Anistratenko, Vitaliy; Iurzhenko, Maksym

    2015-03-01

    As it is known, polyethylene (PE) is one of the common materials in the modern world, and PE products take the major share on industrial and trade markets. For example, various types of technical PE like PE-63, PE-80, and PE-100 have wide industrial applications, i.e., in construction, for pipeline systems etc. A rapid development of plastics industry outstrips detailed investigation of welding processes and welds' formation mechanism, so they remain unexplored. There is still no final answer to the question how weld's microstructure forms. Such conditions limit our way to the understanding of the problem and, respectively, prevent scientific approaches to the welding of more complicated (from chemical point of view) types of polymers than PE. Taking into account state-of-the-art, the article presents results of complex studies of PE weld, its structure, thermophysical and operational characteristics, analysis of these results, and basing on that some hypotheses of welded joint and weld structure formation. It is shown that welding of dissimilar types of polyethylene, like PE-80 and PE-100, leads to the formation of better-ordered crystallites, restructuring the crystalline phase, and amorphous areas with internal stresses in the welding zone.

  14. Degradation of Green Polyethylene by Pleurotus ostreatus.

    PubMed

    da Luz, José Maria Rodrigues; Paes, Sirlaine Albino; Ribeiro, Karla Veloso Gonçalves; Mendes, Igor Rodrigues; Kasuya, Maria Catarina Megumi

    2015-01-01

    We studied the biodegradation of green polyethylene (GP) by Pleurotus ostreatus. The GP was developed from renewable raw materials to help to reduce the emissions of greenhouse gases. However, little information regarding the biodegradation of GP discarded in the environment is available. P. ostreatus is a lignocellulolytic fungus that has been used in bioremediation processes for agroindustrial residues, pollutants, and recalcitrant compounds. Recently, we showed the potential of this fungus to degrade oxo-biodegradable polyethylene. GP plastic bags were exposed to sunlight for up to 120 days to induce the initial photodegradation of the polymers. After this period, no cracks, pits, or new functional groups in the structure of GP were observed. Fragments of these bags were used as the substrate for the growth of P. ostreatus. After 30 d of incubation, physical and chemical alterations in the structure of GP were observed. We conclude that the exposure of GP to sunlight and its subsequent incubation in the presence of P. ostreatus can decrease the half-life of GP and facilitate the mineralization of these polymers. PMID:26076188

  15. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  16. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  17. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  18. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  19. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  20. SECURING CONTAINERIZED HAZARDOUS WASTES WITH POLYETHYLENE RESIN AND FIBERGLASS ENCAPSULATES

    EPA Science Inventory

    This study investigates the fabrication and use of polyethylene resin and fiberglass to encapsulate and secure containerized hazardous wastes. Laboratory-scale encapsulates of composite structure were made from powdered, high-density polyethylene (HDPE) and epoxy-resin-wetted fib...

  1. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... following prescribed conditions: (a) Polyethylene phthalate films consist of a base sheet of ethylene... as constituents of the base sheet or as constituents of coatings applied to the base sheet. (b) Polyethylene phthalate articles consist of a base polymer of ethylene terephthalate polymer, or...

  2. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene phthalate polymers. 177.1630 Section... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as... polymers. Polyethylene phthalate polymers identified in this section may be safely used as, or...

  3. The adhesion of oxygen-plasma treated poly(ethylene) and poly(ethylene terephthlate) films

    SciTech Connect

    Holton, S.L.; Kinloch, A.J.; Watts, J.F.

    1996-12-31

    The effects of low-pressure oxygen-plasma treatment on the surfaces of poly(ethylene) (PE) and poly(ethylene terephthlate) (PET) films and its influence on the adhesion of PE/PET laminates were assessed. The 90{degree} peel test was used to estimate the adhesive fracture energy, G{sub c} for the laminates. XPS, SEM and AFM were used to analyse the treated films and fracture surfaces. Significant improvements in bond strength occurred within very short treatment times (5s at 50W) with the maximum adhesion occurring after 300s. For longer treatment times the bond strengths decrease slightly. G{sub c} values were found to be low when PET was the peel arm. When PE was the peel arm, the G{sub c} values were substantially larger using the current analysis.

  4. Crosslinked polyethylene foams, via EB radiation

    NASA Astrophysics Data System (ADS)

    Cardoso, E. C. L.; Lugão, A. B.; Andrade E. Silva, L. G.

    1998-06-01

    Polyethylene foams, produced by radio-induced crosslinking, show a smooth and homogeneous surface, when compared to chemical crosslinking method using peroxide as crosslinking agent. This process fosters excellent adhesive and printability properties. Besides that, closed cells, intrinsic to theses foams, imparts opitmum mechanical, shocks and insulation resistance, indicating these foams to some markets segments as: automotive and transport; buoyancy, flotation and marine: building and insulation: packaging: domestic sports and leisure goods. We were in search of an ideal foam, by adding 5 to 15% of blowing agent in LDPE. A series of preliminary trials defined 203° C as the right blowing agent decomposition temperature. At a 22.7 kGy/dose ratio, the lowest dose for providing an efficient foam was 30 kGy, for a formulation comprising 10% of azodicarbonamide in LDPE, within a 10 minutes foaming time.

  5. Water potential of aqueous polyethylene glycol.

    PubMed

    Steuter, A A

    1981-01-01

    Water potential (Psiomega) values were determined for aqueous colloids of four molecular sizes of polyethylene glycol (PEG) using freezing-point depression and vapor-pressure deficit methods. A significant third-order interaction exists between the method used to determine Psiomega, PEG molecular size, and concentration. At low PEG concentrations, freezing-point depression measurements result in higher (less negative) values for Psiomega than do vapor-pressure deficit measurements. The reverse is true at high concentrations. PEG in water does not behave according to van't Hoff's law. Psiomega is related to molality for a given PEG but not linearly. Moreover, Psiomega varies with the molecular size of the PEG. It is suggested that the Psiomega of PEG in water may be controlled primarily by the matric forces of ethylene oxide subunits of the PEG polymer. The term matricum is proposed for PEG in soil-plant-water relation studies. PMID:16661635

  6. Depolymerization of polyethylene terephthalate in supercritical methanol

    NASA Astrophysics Data System (ADS)

    Goto, Motonobu; Koyamoto, Hiroshi; Kodama, Akio; Hirose, Tsutomu; Nagaoka, Shoji

    2002-11-01

    The degradation of polyethylene terephthalate (PET) in supercritical methanol was investigated with the aim of developing a process for chemical recycling of waste plastics. A batch reactor was used at temperatures of 573-623 K under an estimated pressure of 20 MPa for a reaction time of 2-120 min. PET was decomposed to its monomers, dimethyl terephthalate and ethylene glycol, by methanolysis in supercritical methanol. The reaction products were analysed using size-exclusion chromatography, gas chromatography-mass spectrometry, and reversed-phase liquid chromatography. The molecular weight distribution of the products was obtained as a function of reaction time. The yields of monomer components of the decomposition products including by-products were measured. Continuous kinetics analysis was performed on the experimental data.

  7. Vacuum Outgassing of High Density Polyethylene

    SciTech Connect

    Dinh, L N; Sze, J; Schildbach, M A; Chinn, S C; Maxwell, R S; Raboin, P; McLean II, W

    2008-08-11

    A combination of thermogravimetric analysis (TGA) and temperature programmed decomposition (TPD) was employed to identify the outgassing species, the total amount of outgassing, and the outgassing kinetics of high density polyethylene (HDPE) in a vacuum environment. The isoconversional kinetic analysis was then used to analyze the outgassing kinetics and to predict the long-term outgassing of HDPE in vacuum applications at ambient temperature. H{sub 2}O and C{sub n}H{sub x} with n as high as 9 and x centering around 2n are the major outgassing species from solid HDPE, but the quantities evolved can be significantly reduced by vacuum baking at 368 K for a few hours prior to device assembly.

  8. Li + grafting of ion irradiated polyethylene

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Rybka, V.; Vacík, J.; Hnatowicz, V.; Öchsner, R.; Ryssel, H.

    1999-02-01

    Foils of oriented polyethylene (PE) were irradiated with 63 keV Ar + and 155 keV Xe + ions to different fluences at room temperature and then doped from water solution of LiCl. The as irradiated and irradiated plus doped samples were examined by IR, EPR and neutron depth profiling (NDP) technique. The sheet resistance was also measured by the standard two points method. After Li salt doping of ion modified layer of PE, a reaction between degraded macromolecules and Li occur and thus a new chemical structure C-Li + is formed. Owing to the presence of these cations on the polymer chain, the irradiated plus doped layer exhibits higher electric conductivity compared to as-irradiated ones.

  9. Thermal analysis of polyethylene + X% carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Lozovyi, Fedir; Ivanenko, Kateryna; Nedilko, Sergii; Revo, Sergiy; Hamamda, Smail

    2016-02-01

    The aim of this research is to study the influence of the multi-walled carbon nanotubes (MWCNTs) on the thermomechanical and structural properties of high-density polyethylene. Several, complementary experimental techniques were used, namely, dilatometry, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Raman spectroscopy, and infrared (IR) spectroscopy. Dilatometry data showed that nanocomposites exhibit anisotropic behavior, and intensity of the anisotropy depends on the MWCNT concentration. The shapes of the dilatometric curves of the nanocomposites under study differ significantly for the radial and longitudinal directions of the samples. DSC results show that MWCNTs weekly influence calorimetry data, while Raman spectra show that the I D/ I G ratio decreases when MWCNT concentration increases. The IR spectra demonstrate improvement of the crystallinity of the samples as the content in MWCNTs rises.

  10. Polyethylene oxide hydration in grafted layers

    NASA Astrophysics Data System (ADS)

    Dormidontova, Elena; Wang, Zilu

    Hydration of water soluble polymers is one of the key-factors defining their conformation and properties, similar to biopolymers. Polyethylene oxide (PEO) is one of the most important biomedical-applications polymers and is known for its reverse temperature solubility due to hydrogen bonding with water. As in many practical applications PEO chains are grafted to surfaces, e.g. of nanoparticles or planar surfaces, it is important to understand PEO hydration in such grafted layers. Using atomistic molecular dynamic simulations we investigate the details of molecular conformation and hydration of PEO end-grafted to gold surfaces. We analyze polymer and water density distribution as a function of distance from the surface for different grafting densities. Based on a detailed analysis of hydrogen bonding between polymer and water in grafted PEO layers, we will discuss the extent of PEO hydration and its implication for polymer conformation, mobility and layer properties. This research is supported by NSF (DMR-1410928).

  11. Investigation of Raman spectra of polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Zhu, Changjun; Tong, Na; Song, Lixin; Zhang, Guoqing

    2015-08-01

    Raman spectrometry was employed to study the characteristics of Raman spectra of polyethylene terephthalate (PET), which were treated with sodium hydroxide, sulfuric acid and copper sulfate, respectively. Raman spectra under different conditions were obtained and the characteristics of the Raman spectra were analyzed. The morphology structures were observed under different conditions using Atomic Force Microscope. The results show that the spectral intensity of PET treated with sodium hydroxide is higher than that untreated between 200-1750 cm-1, while the intensity of PET treated with sodium hydroxide is lower than that untreated beyond 1750 cm-1 and the fluorescence background of Raman spectra is decreased. The spectral intensity of PET treated with sulfuric acid is remarkably reduced than that untreated, and the intensity of PET treated with copper sulphate is much higher than that untreated.

  12. Thermoviscoelastic models for polyethylene thin films

    NASA Astrophysics Data System (ADS)

    Li, Jun; Kwok, Kawai; Pellegrino, Sergio

    2016-02-01

    This paper presents a constitutive thermoviscoelastic model for thin films of linear low-density polyethylene subject to strains up to yielding. The model is based on the free volume theory of nonlinear thermoviscoelasticity, extended to orthotropic membranes. An ingredient of the present approach is that the experimentally inaccessible out-of-plane material properties are determined by fitting the model predictions to the measured nonlinear behavior of the film. Creep tests, uniaxial tension tests, and biaxial bubble tests are used to determine the material parameters. The model has been validated experimentally, against data obtained from uniaxial tension tests and biaxial cylindrical tests at a wide range of temperatures and strain rates spanning two orders of magnitude.

  13. Polyethylene welding by pulsed visible laser irradiation

    NASA Astrophysics Data System (ADS)

    Torrisi, L.; Caridi, F.; Visco, A. M.; Campo, N.

    2011-01-01

    Laser welding of plastics is a relatively new process that induces locally a fast polymer heating. For most applications, the process involves directing a pulsed beam of visible light at the weld joint by going through one of the two parts. This is commonly referred to as “through transmission visible laser welding”. In this technique, the monochromatic visible light source uses a power ns pulsed laser in order to irradiate the joint through one part and the light is absorbed in the vicinity of the other part. In order to evaluate the mechanical resistance of the welded joint, mass quadrupole spectrometry, surface profilometry, microscopy techniques and mechanical shear tests were employed. The welding effect was investigated as a function of the laser irradiation time, nature of the polyethylene materials and temperature.

  14. WAXS investigations on Polyethylene -- Carbon Nanofibers Composites

    NASA Astrophysics Data System (ADS)

    Jones, Brian; Li, Jianhua; Benitez, Rogelio; Lozano, Karen; Chipara, Mircea; Cristian Chipara, Alin; Dorina Chipara, Magdalena; Sellmyer, David J.

    2008-03-01

    Nanocomposites have been obtained by high-shear mixing of isotactic polyethylene with various amounts of purified nanofiller (vapor grown carbon nanofibers type PR-24AG from Pyrograf Products, Inc) by utilizing a HAAKE Rheomix at 65 rpm and 180 ^oC for 9 min followed by an additional mixing at 90 rpm for 5 min. Composites loaded with various amounts of vapor grown carbon nanofibers have been prepared. Various spectroscopic techniques have been used to assess the interactions between the polymeric matrix and carbon nanofibers. Wide angle X - Ray scattering investigations focused on the effect of carbon nanofibers on the crystalline phases of polypropylene and on the overall crystallinity degree of the polymeric matrix. This research aims at a better understanding of the nature and structure of the polymer -- carbon nanofibers interface.

  15. Radiation effects and crystallinity in polyethylene

    NASA Astrophysics Data System (ADS)

    Keller, A.; Ungar, G.

    A survey is presented of a series of works on the influence of crystallinity on the radiation induced effects, cross-linking in particular, in polyethylene and paraffins. The principal theme is that the usual conception of random introduction of cross-links into a random assembly of chains needs to be modified in the presence of crystallinity in general and chain folding in particular. A long series of varied investigations on polyethylene have indeed demonstrated through a series of conspicuous effects that not only the ordering intrinsic to crystals and the increased intrachain contacts due to chain folding, but the higher level morphology, the nature and mutual arrangement in particular, have a major influence on the effectivity of the radiation leading to networks. Extension of the works to paraffins identified unsuspected mobility of both the radiation precursor species and the paraffin molecule itself (cross-linked and uncross-linked) within the crystal lattice, leading to phase segregation of the cross-linked species into microscopically identifiable domains together with identifying a trend for the cross-links themselves to form non-randomly in groups. The latter phenomenon, observed also in the molten state, indicates that the departure from randomness in the cross-linking process is much more deep-rooted than originally anticipated, and calls for a general reassessment of our knowledge of cross-linking. Other topics included as part of the general enquiry are the destruction of crystallinity, the promotion of hexagonal phase through radiation, the effect of morphology on chain scission and the general, still unsolved issue of how to assess cross-links by a direct analytical method (involving NMR). The hope is expressed that the bringing together of these varied pieces of work will serve the unification of presently widely diverse areas of experience and might influence developments in the radiation studies of paraffinoid substances.

  16. Micropallet arrays with poly(ethylene glycol) walls.

    PubMed

    Wang, Yuli; Salazar, Georgina To'a; Pai, Jeng-Hao; Shadpour, Hamed; Sims, Christopher E; Allbritton, Nancy L

    2008-05-01

    Arrays of releasable micropallets with surrounding walls of poly(ethylene glycol) (PEG) were fabricated for the patterning and sorting of adherent cells. PEG walls were fabricated between the SU-8 pallets using a simple, mask-free strategy. By utilizing the difference in UV-transmittance of glass and SU-8, PEG monomer was selectively photopolymerized in the space surrounding the pallets. Since the PEG walls are composed of a cross-linked structure, the stability of the walls is independent of the pallet array geometry and the properties of the overlying solution. Even though surrounded with PEG walls, the individual pallets were detached from the array by the mechanical force generated by a focused laser pulse, with a release threshold of 6 microJ. Since the PEG hydrogels are repellent to protein adsorption and cell attachment, the walls localized cell growth to the pallet top surface. Cells grown in the microwells formed by the PEG walls were released by detaching the underlying pallet. The released cells/pallets were collected, cultured and clonally expanded. The micropallet arrays with PEG walls provide a platform for performing single cell analysis and sorting on chip. PMID:18432343

  17. Surface States and Negative Electron Affinity in Polyethylene

    SciTech Connect

    Righi, M. C.; Scandolo, S.; Serra, S.; Iarlori, S.; Tosatti, E.; Santoro, G.

    2001-08-13

    First-principles calculations are used to investigate the electronic properties of the surfaces of polyethylene. The calculations support the experimental evidence of a negative electron affinity, with calculated values of -0.17 eV and -0.10 eV for surfaces with chains perpendicular and parallel to the surface normal, respectively. Both surfaces exhibit a surface state with binding energy -1.2{+-}0.5 eV with respect to the bulk polyethylene conduction band minimum. Implications of these findings on spectroscopy, as well as on the transport and aging properties of polyethylene for high-voltage applications, are discussed.

  18. Variation of penicillin acylase partition coefficient with phase volume ratio in poly(ethylene glycol)-sodium citrate aqueous two-phase systems.

    PubMed

    Marcos, J C; Fonseca, L P; Ramalho, M T; Cabral, J M

    1998-06-26

    The influence of phase volume ratio on partition and purification of penicillin acylase from Escherichia coli on poly(ethylene glycol)-sodium citrate aqueous two-phase systems was studied. In PEG 1000 systems both partition coefficients of the enzyme and total protein increased with decreasing phase volume ratio. However, in PEG 3350 containing NaCl, penicillin acylase follows a reverse trend, while total protein behaves in the same way. Implications for protein purification designs are discussed. PMID:9699998

  19. Urinary excretion of polyethylene glycol 3350 and sulfate after gut lavage with a polyethylene glycol electrolyte lavage solution.

    PubMed

    Brady, C E; DiPalma, J A; Morawski, S G; Santa Ana, C A; Fordtran, J S

    1986-06-01

    Ingestion of an electrolyte lavage solution containing polyethylene glycol 3350 and sulfate is an effective method of cleansing the colon for diagnostic studies. Polyethylene glycol and sulfate are considered poorly absorbed from the gastrointestinal tract. Because of the quantities administered, concern exists about potential toxicity of absorption of even a small percentage, particularly for polyethylene glycol. We measured the urinary excretion of both polyethylene glycol and sulfate in normal subjects and inflammatory bowel patients. Absorption of polyethylene glycol can be assessed by measuring recovery in urine, as 85%-96% of an intravenous load is excreted in urine. Similarly, appreciable sulfate absorption would exceed renal tubular reabsorption and result in increased urinary excretion. Mean percent polyethylene glycol load recovered in urine was minimal and similar for normal (0.06%) and inflammatory bowel (0.09%) subjects. Urinary sulfate excretion after lavage was also similar for both groups and was not different from baseline. These results do not suggest the likelihood of toxicity due to polyethylene glycol 3350 or sulfate absorption during gut lavage with this solution. PMID:3699408

  20. Myocardial matrix-polyethylene glycol hybrid hydrogels for tissue engineering

    NASA Astrophysics Data System (ADS)

    Grover, Gregory N.; Rao, Nikhil; Christman, Karen L.

    2014-01-01

    Similar to other protein-based hydrogels, extracellular matrix (ECM) based hydrogels, derived from decellularized tissues, have a narrow range of mechanical properties and are rapidly degraded. These hydrogels contain natural cellular adhesion sites, form nanofibrous networks similar to native ECM, and are biodegradable. In this study, we expand the properties of these types of materials by incorporating poly(ethylene glycol) (PEG) into the ECM network. We use decellularized myocardial matrix as an example of a tissue specific ECM derived hydrogel. Myocardial matrix-PEG hybrids were synthesized by two different methods, cross-linking the proteins with an amine-reactive PEG-star and photo-induced radical polymerization of two different multi-armed PEG-acrylates. We show that both methods allow for conjugation of PEG to the myocardial matrix by gel electrophoresis and infrared spectroscopy. Scanning electron microscopy demonstrated that the hybrid materials still contain a nanofibrous network similar to unmodified myocardial matrix and that the fiber diameter is changed by the method of PEG incorporation and PEG molecular weight. PEG conjugation also decreased the rate of enzymatic degradation in vitro, and increased material stiffness. Hybrids synthesized with amine-reactive PEG had gelation rates of 30 min, similar to the unmodified myocardial matrix, and incorporation of PEG did not prevent cell adhesion and migration through the hydrogels, thus offering the possibility to have an injectable ECM hydrogel that degrades more slowly in vivo. The photo-polymerized radical systems gelled in 4 min upon irradiation, allowing 3D encapsulation and culture of cells, unlike the soft unmodified myocardial matrix. This work demonstrates that PEG incorporation into ECM-based hydrogels can expand material properties, thereby opening up new possibilities for in vitro and in vivo applications.

  1. 40 CFR 721.7255 - Polyethyleneamine crosslinked with substituted polyethylene glycol (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... substituted polyethylene glycol (generic). 721.7255 Section 721.7255 Protection of Environment ENVIRONMENTAL... substituted polyethylene glycol (generic). (a) Chemical substance and significant new uses subject to... substituted polyethylene glycol with substituted polyethylene glycol (PMN P-01-833) is subject to...

  2. 40 CFR 721.7255 - Polyethyleneamine crosslinked with substituted polyethylene glycol (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... substituted polyethylene glycol (generic). 721.7255 Section 721.7255 Protection of Environment ENVIRONMENTAL... substituted polyethylene glycol (generic). (a) Chemical substance and significant new uses subject to... substituted polyethylene glycol with substituted polyethylene glycol (PMN P-01-833) is subject to...

  3. 21 CFR 178.3750 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene glycol (mean molecular weight 200-9... Adjuvants and Production Aids § 178.3750 Polyethylene glycol (mean molecular weight 200-9,500). Polyethylene... chapter. (c) The provisions of paragraph (b) of this section are not applicable to polyethylene...

  4. 40 CFR 721.7255 - Polyethyleneamine crosslinked with substituted polyethylene glycol (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... substituted polyethylene glycol (generic). 721.7255 Section 721.7255 Protection of Environment ENVIRONMENTAL... substituted polyethylene glycol (generic). (a) Chemical substance and significant new uses subject to... substituted polyethylene glycol with substituted polyethylene glycol (PMN P-01-833) is subject to...

  5. 40 CFR 721.7255 - Polyethyleneamine crosslinked with substituted polyethylene glycol (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... substituted polyethylene glycol (generic). 721.7255 Section 721.7255 Protection of Environment ENVIRONMENTAL... substituted polyethylene glycol (generic). (a) Chemical substance and significant new uses subject to... substituted polyethylene glycol with substituted polyethylene glycol (PMN P-01-833) is subject to...

  6. 40 CFR 721.7255 - Polyethyleneamine crosslinked with substituted polyethylene glycol (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... substituted polyethylene glycol (generic). 721.7255 Section 721.7255 Protection of Environment ENVIRONMENTAL... substituted polyethylene glycol (generic). (a) Chemical substance and significant new uses subject to... substituted polyethylene glycol with substituted polyethylene glycol (PMN P-01-833) is subject to...

  7. Redox-labelled poly(ethylene glycol) used as a diffusion probe in poly(ethylene glycol) melts

    SciTech Connect

    Haas, O.; Velasquez, C.; Porat, Z.

    1995-12-01

    Ferrocene labelled monomethyl poly(ethylene glycol) MPEG with molecular weights of 1900 and 750 was prepared and used as an electrochemical diffusion probe in poly(ethylene glycol) melts. Cyclic voltammetry and chronoamperometry were used in connection with microdisk electrodes to measure the diffusion coefficient of redox tagged molecules using melted poly(ethylene glycol) as a solvent. The molecular weight of the solvent polymer was 750, 2000 and 20000. Results from the temperature dependency of the diffusion process and of the viscosity and conductivity of the polymer electrolyte are presented and discussed.

  8. Long term property prediction of polyethylene nanocomposites

    NASA Astrophysics Data System (ADS)

    Shaito, Ali Al-Abed

    The amorphous fraction of semicrystalline polymers has long been thought to be a significant contributor to creep deformation. In polyethylene (PE) nanocomposites, the semicrystalline nature of the maleated PE compatibilizer leads to a limited ability to separate the role of the PE in the nanocomposite properties. This dissertation investigates blown films of linear low-density polyethylene (LLDPE) and its nanocomposites with montmorillonite-layered silicate (MLS). Addition of an amorphous ethylene propylene copolymer grafted maleic anhydride (amEP) was utilized to enhance the interaction between the PE and the MLS. The amorphous nature of the compatibilizer was used to differentiate the effect of the different components of the nanocomposites; namely the matrix, the filler, and the compatibilizer on the overall properties. Tensile test results of the nanocomposites indicate that the addition of amEP and MLS separately and together produces a synergistic effect on the mechanical properties of the neat PE. Thermal transitions were analyzed using differential scanning calorimetry (DSC) to determine if the observed improvement in mechanical properties is related to changes in crystallinity. The effect of dispersion of the MLS in the matrix was investigated by using a combination of X-ray diffraction (XRD) and scanning electron microscopy (SEM). Mechanical measurements were correlated to the dispersion of the layered silicate particles in the matrix. The nonlinear time dependent creep of the material was analyzed by examining creep and recovery of the films with a Burger model and the Kohlrausch-Williams-Watts (KWW) relation. The effect of stress on the nonlinear behavior of the nanocomposites was investigated by analyzing creep-recovery at different stress levels. Stress-related creep constants and shift factors were determined for the material by using the Schapery nonlinear viscoelastic equation at room temperature. The effect of temperature on the tensile and creep

  9. Long-term, buffer-less, wet gel storage in non-sealed polyethylene bags.

    PubMed

    Kurien, Biji T; Scofield, R Hal

    2012-01-01

    Electrophoresed gels are normally fixed, stained, destained, and dried. Drying is normally carried out with commercial gel dryers or by drying between two cellophane sheets held together by two acrylic frames. Here, we report that stained and destained gels (7.5, 10, or 15%, denaturing or native gels; 0.4 or 1.5 mm in thickness) could be stored wet, unsealed, and without any storage buffer for several months at room temperature within flexible polyethylene bags without significant shrinking or protein diffusion. The gel remains hydrated because of the de facto sealing achieved by the polyethylene sheets (PS) adhering airtightly to the gel on either sides. The microsaturated environment generated by the thin film of water molecules trapped between the gel and the PS, along with the nonporous nature of the PS, apparently protects the gel from cracking as well as shrinking significantly. The intensity of stained proteins increased during storage probably from the slight gel shrinkage observed. Wet gel storage is useful (a) when low abundance protein spots from multiple two-dimensional electrophoresis gels have to be excised for in-gel tryptic digestion or electroelution and (b) for wet gel autoradiography. In addition to avoiding dryer contamination and saving drying time, these bags prevent the moist gel from sticking to X-ray film. Such storage could also prove useful for electrophoretic transfer of fixed and stained gels. PMID:22585508

  10. Creep behavior of 6 micrometer linear low density polyethylene film

    NASA Technical Reports Server (NTRS)

    Simpson, J. M.; Schur, W. W.

    1993-01-01

    Creep tests were performed to provide material characteristics for a 6.4-micron polyethylene film used to construct high altitude balloons. Results suggest simple power law relationships are adequate for stresses below about 4.83 MPa.

  11. Experimental study of rocket engine model with gaseous polyethylene fuel

    NASA Astrophysics Data System (ADS)

    Yemets, V. V.

    Experimental results for liquid rocket engine models with gaseous polyethylene fuel that is hard before its consumption are considered. The possibility of hard design element combustion in a liquid rocket engine is demonstrated.

  12. TECHNICAL GUIDANCE DOCUMENT: THE FABRICATION OF POLYETHYLENE FML FIELD SEAMS

    EPA Science Inventory

    This technical guidance document is meant to augment the numerous construction quality control and construction assurance (CQC and CQA) guidelines that are presently available for high density polyethylene (HDPE) liner installation and inspection.

  13. Posteromedial tibial polyethylene failure in total knee replacements.

    PubMed

    Lewis, P; Rorabeck, C H; Bourne, R B; Devane, P

    1994-02-01

    This report details 16 cases of focal posteromedial tibial polyethylene wear and failure after total knee arthroplasty. This wear phenomenon was associated with an external rotatory subluxation of the tibial component relative to the femoral component. Failure occurred in ten Miller Galante 1, three Porous Coated Anatomic, two Kinematic, and one Press-Fit Condylar knee designs at a mean time of 45 months from their implantation. With this type of failure, there did not seem to be a relationship with metal type, fixation, polyethylene manufacturing method, or polyethylene thickness. A relatively flat design of the tibial articular surface was common to all of these components. In certain patients this articular design may allow excessive component translation, which leads to polyethylene deformity, wear, and subluxation. Some methods for preventing this failure mode are reported here. PMID:8119004

  14. Mechanical Performance of Rotomoulded Wollastonite-Reinforced Polyethylene Composites

    NASA Astrophysics Data System (ADS)

    Yuan, Xiaowen; Easteal, Allan J.; Bhattacharyya, Debes

    This paper describes the development of a new processing technology for rotational moulding of wollastonite microfibre (WE) reinforced polyethylene (PE). Manufacturing wollastonite-polyethylene composites involved blending, compounding by extrusion, and granulating prior to rotational moulding. The properties of the resulting composites were characterised by tensile and impact strength measurements. The results show that tensile strength increases monotonically with the addition of wollastonite fibres, but impact strength is decreased. In addition, the processability is also decreased after adding more than 12 vol% WE because of increased viscosity. The effects of a coupling agent, maleated polyethylene (MAPE), on the mechanical performance and processability were also investigated. SEM analysis reveals good adhesion between the fibre reinforcements and polyethylene matrix at the fracture surface with the addition of MAPE. It is proposed that fillers with small particles with high aspect ratio (such as wollastonite) provide a large interfacial area between the filler and the polymer matrix, and may influence the mobility of the molecular chains.

  15. Polyethylene/Boron Composites for Radiation Shielding Applications

    SciTech Connect

    Harrison, Courtney; Grulke, Eric; Burgett, Eric; Hertel, Nolan

    2008-01-21

    Multifunctional composites made with boron are absorbers of low energy nuetrons, and could be used for structural shielding materials. Polyethylene/boron carbide composites were fabricated using conventional polymer processing techniques, and were evaluated for mechanical and radiation shielding properties. Addition of neat boron carbide (powder and nanoparticles) to an injection molding grade HPDE showed superior mechanical properties compared to neat HDPE. Radiation shielding measurements of a 2 wt% boron carbide composite were improved over those of the neat polyethylene.

  16. Polarimetric studies of polyethylene terephtalate flexible substrates

    NASA Astrophysics Data System (ADS)

    Stchakovsky, M.; Garcia-Caurel, E.; Warenghem, M.

    2008-12-01

    Polymer sheets are currently used worldwide in a wide range of applications. The manufacturing process of these sheets involves extruding machines that stretch the material in both lateral and longitudinal directions with respect to the machine direction, thus inducing birefringence. In most cases, the film obtained is optically biaxial. Polarimetric spectroscopy (Ellipsometry and Mueller Matrix) combined with conoscopic observation are the methods of choice to study these properties. In this work we report an analysis of commercially available polyethylene terephtalate (PET) films used as substrate for food packaging as well as for embedded electronic devices such as solar cells or flexible displays. Initial observation of these films through polarizing microscope in conoscopic mode reveals first the trace of optical axis plane with respect to the film surface and second, whether the optical axis is acute or not. This preliminary study allows optimal sample positioning for further polarimetric studies. The measurements and modelling are done in both reflection and transmission mode on several spectroscopic polarimetric setups from UV to NIR. The models give as a main result, the dielectric tensor of the film as well as its orientation with respect to the laboratory reference frame.

  17. Theory of the deformation of aligned polyethylene

    PubMed Central

    Hammad, A.; Swinburne, T. D.; Hasan, H.; Del Rosso, S.; Iannucci, L.; Sutton, A. P.

    2015-01-01

    Solitons are proposed as the agents of plastic and viscoelastic deformation in aligned polyethylene. Interactions between straight, parallel molecules are mapped rigorously onto the Frenkel–Kontorova model. It is shown that these molecular interactions distribute an applied load between molecules, with a characteristic transfer length equal to the soliton width. Load transfer leads to the introduction of tensile and compressive solitons at the chain ends to mark the onset of plasticity at a well-defined yield stress, which is much less than the theoretical pull-out stress. Interaction energies between solitons and an equation of motion for solitons are derived. The equation of motion is based on Langevin dynamics and the fluctuation–dissipation theorem and it leads to the rigorous definition of an effective mass for solitons. It forms the basis of a soliton dynamics in direct analogy to dislocation dynamics. Close parallels are drawn between solitons in aligned polymers and dislocations in crystals, including the configurational force on a soliton. The origins of the strain rate and temperature dependencies of the viscoelastic behaviour are discussed in terms of the formation energy of solitons. A failure mechanism is proposed involving soliton condensation under a tensile load. PMID:26339196

  18. Polyethylene degradation in a coal liquefaction environment

    SciTech Connect

    Thompson, R.L.; Rothenberger, K.S.; Cugini, A.V.

    1996-12-31

    The coprocessing of coal with waste materials such as plastic has shown promise as an economical means to recover the inherent value of the wastes while producing useful products. Polyethylene (PE) is one of the dominant plastics on the market; recent statistics indicate that low- and high-density PE together make up about half of all municipal plastic waste. However, recent studies have shown that PE is also among the most difficult plastics to convert in the traditional liquefaction environment, particularly in the presence of coal and/or donor solvents. The coal liquefaction environment is quite different than that encountered during thermal or catalytic pyrolysis. In this paper, a novel analytical method has been developed to recover incompletely reacted PE from coprocessing product streams. Once separated from the coal-derived material, gel permeation chromatography (GPC) was applied to the recovered material to ascertain the nature of the changes that occurred to the PE upon processing in a bench-scale continuous liquefaction unit. Also, 1-L semi-batch reactions were performed to investigate the reactivity of PE and coal-PE mixtures as a function of temperature.

  19. Polyethylene degradation in a coal liquefaction environment

    SciTech Connect

    Rothenberger, K.S.; Cugini, A.V.; Thompson, R.L.

    1996-12-31

    The coprocessing of coal with waste materials such as plastic has shown promise as an economical means to recover the inherent value of the wastes while producing useful products. Polyethylene (PE) is one of the dominant plastic materials; recent statistics indicate that low- and high-density PE together make up about half of all municipal plastic waste. The degradation of PE in a pyrolysis environment has been well studied, and pyrolysis-based methods for the conversion of PE to fuels have been published. However, recent studies have shown that PE is among the most difficult plastics to convert in the traditional liquefaction environment, particularly in the presence of coal and/or donor solvents. The coal liquefaction environment is quite different than that encountered during thermal or catalytic pyrolysis. Understanding the degradation behavior of PE in the liquefaction environment is important to development of a successful scheme for coprocessing coal with plastics. In this paper, a novel analytical method has been developed to recover incompletely reacted PE from coprocessing product streams. Once separated from the coal-derived material, gel permeation chromatography, a conventional polymer characterization technique, was applied to the recovered material to ascertain the nature of the changes that occurred to the PE upon processing in a bench-scale continuous liquefaction unit. In a separate phase of the project, 1-L semi-batch reactions were performed to investigate the reactivity of PE and coal-PE mixtures as a function of temperature.

  20. Fibroblasts adhesion on ion beam modified polyethylene

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Tomášová, P.; Dvořánková, B.; Hnatowicz, V.; Ochsner, R.; Ryssel, H.

    2004-02-01

    Polyethylene (PE) was irradiated with 15 keV O +, P + and Ar + ions to the fluences from 3 × 10 12 to 1 × 10 15 cm -2. The changes of surface structure and polarity and oxygen concentration were examined on pristine and as-irradiated PE. The in vitro adhesion of rat 3T3 fibroblasts on the modified PE was evaluated 24 h after inoculation. Degradation of PE is manifested by the creation of conjugated double bonds and oxidation of the PE main chain. It was proved that the implanted P atoms are chemically bound onto degraded polymer chain. Wettability of the polymer surface is affected by the structure and composition of the modified surface layer. In comparison with pristine PE (i) higher cell adhesion is observed on implanted PE and (ii) the cells cultivated on implanted PE are larger and their adherence is significantly more homogeneous. The enhancement of 3T3 cells adhesion is highest and smallest for PE implanted with O + and Ar + ions, respectively. Highest cell adhesion was observed on PE implanted to the fluence of 1 × 10 13 cm -2 regardless of the ion specie. It was shown that the cell adhesion is related to the wettability of the PE surface and that there exists an optimal wettability with respect to the cell adhesion.

  1. [Characteristics of Raman Spectra of Polyethylene Terephthalate].

    PubMed

    Tong, Na; Zhu, Chang-jun; Song, Li-xun; Zhang, Chong-hui; Zhang, Guo-qing; Zhang, Yi-xin

    2016-01-01

    Raman spectrometry was employed to study the characteristics of Raman spectra of polyethylene terephthalate (PET), which were treated with sodium hydroxide, sulfuric acid and copper sulfate, respectively. Raman spectra under different conditions were obtained and the characteristics of the Raman spectra were analyzed. The morphology structures were observed under different conditions using Atomic Force Microscope. The results show that the spectral intensity of PET treated with sodium hydroxide is higher than that untreated between 200-1 750 cm(-1), while the intensity of PET treated with sodium hydroxide is lower than that untreated beyond 1 750 cm(-1) and the fluorescence background of Raman spectra is decreased. The spectral intensity of PET treated with sulfuric acid is remarkably reduced than that untreated, and the intensity of PET treated with copper sulphate is much higher than that untreated. The research results obtained by Atomic Force Microscopy show that the variations of the Raman spectra of PET fibers are closely related to. the chemical bonds and molecular structures of PET fibers. The surface of the PET treated with sodium hydroxide is rougher than that untreated, the surface roughness of the PET treated with sulfuric acid is reduced as compared to that untreated, while the surface roughness of the PET treated with copper sulphate is increased. The results obtained by Raman spectroscopy are consistent with those by Atomic Force Microscopy, indicating that the combination of Raman spectroscopy and Atomic Force Microscopy is expected to be a promising characterization technology for polymer characteristics. PMID:27228752

  2. Organocatalytic decomposition of polyethylene terephthalate using triazabicyclodecene

    NASA Astrophysics Data System (ADS)

    Lecuyer, Julien Matsumoto

    This study focuses on the organocatalytic decomposition of polyethylene terephthalate (PET) using 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) to form a diverse library of aromatic amides. The reaction scheme was specifically designed to use low reaction temperatures (>150°C) and avoid using solvents during the reaction to provide a more environmentally friendly process. Of all the amines tested, PET aminolysis with aliphatic and aromatic amines demonstrated the best performance with yields higher than 72%. PET aminolysis with click functionalized and non-symmetric reagents facilitated attack on certain sites on the basis of reactivity. Finally, the performance of the PET degradation reactions with secondary amine and tertiary amine functionalized reagents yielded mixed results due to complications with isolating the product from the crude solution. Four of the PET-based monomers were also selected as modifiers for epoxy hardening to demonstrate the ability to convert waste into monomers for high-value applications. The glass transition temperatures, obtained using differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) of the epoxy composite samples treated with the PET-based monomers, were generally higher in comparison to the samples cured with the basic diamines due to the hydrogen bonding and added rigidity from the aromatic amide group. Developing these monomers provides a green and commercially viable alternative to eradicating a waste product that is becoming an environmental concern.

  3. Fatigue crack propagation resistance of highly crosslinked polyethylene.

    PubMed

    Bradford, Letitia; Baker, David; Ries, Michael D; Pruitt, Lisa A

    2004-12-01

    A higher degree of cross-linking has been shown to improve wear properties of ultra-high molecular weight polyethylene in laboratory studies. However, cross-linking can also affect the mechanical properties of ultra-high molecular weight polyethylene. Fatigue crack propagation resistance was determined for electron beam cross-linked ultra-high molecular weight polyethylene and compared with gamma irradiation cross-linked and noncross-linked polyethylene fatigue specimens. Crosslinking was done with different dosages of irradiation followed by melting. For one irradiation dose (50 kGy) extrusion and molding processes were compared. A fracture mechanics approach was used to determine how the degree of cross-linking affects resistance to crack propagation in ultra-high molecular weight polyethylene. Fatigue crack propagation resistance was reduced in proportion to the irradiation dose. The type of irradiation (gamma or electron beam) or manufacturing method (extrusion or molding) did not affect fatigue crack propagation resistance. The reduced fatigue strength of highly cross-linked ultra-high molecular weight polyethylene could lead to mechanical failure in conditions that are associated with cyclic local tensile stresses. PMID:15577468

  4. Launch Vehicle with Combustible Polyethylene Case Gasification Chamber Design Basis

    NASA Astrophysics Data System (ADS)

    Yemets, V.

    A single-stage launch vehicle equipped with a combustible tank shell of polyethylene and a moving propulsion plant is proposed. The propulsion plant is composed of a chamber for the gasification of the shell, a compressor of pyrolysed polyethylene and a magnetic powder obturator. It is shown that the “dental” structure of the gasification chamber is necessary to achieve the necessary contact area with the polyethylene shell. This conclusion is drawn from consideration of the thermo- physical properties of polyethylene, calculating quasisteady temperature field in the gasification chamber, estimating gasification rate of polyethylene, launch vehicle shortening rate and area of gasification. Experimental determination of the gasification rate is described. The gasification chamber specific mass as well as the propulsion plant weight-to-thrust ratio are estimated under some assumptions concerning the obturator and compressor. Combustible launch vehicles are compared with conventional launch vehicles taking into consideration their payload mass ratios. Combustible launchers are preferable as small launchers for micro and nano satellites. Reusable versions of such launchers seem suitable if polyethylene tank shells filled with metal or metal hydride fine dusts are used.

  5. Effect of sodium chloride on solute-solvent interactions in aqueous polyethylene glycol-sodium sulfate two-phase systems.

    PubMed

    da Silva, Nuno R; Ferreira, Luisa A; Madeira, Pedro P; Teixeira, José A; Uversky, Vladimir N; Zaslavsky, Boris Y

    2015-12-18

    Partition behavior of eight small organic compounds and six proteins was examined in poly(ethylene glycol)-8000-sodium sulfate aqueous two-phase systems containing 0.215M NaCl and 0.5M osmolyte (sorbitol, sucrose, TMAO) and poly(ethylene glycol)-10000-sodium sulfate-0.215M NaCl system, all in 0.01M sodium phosphate buffer, pH 6.8. The differences between the solvent properties of the coexisting phases (solvent dipolarity/polarizability, hydrogen bond donor acidity, and hydrogen bond acceptor basicity) were characterized with solvatochromic dyes using the solvatochromic comparison method. Differences between the electrostatic properties of the phases were determined by analysis of partitioning of sodium salts of dinitrophenylated (DNP-) amino acids with aliphatic alkyl side-chain. The partition coefficients of all compounds examined (including proteins) were described in terms of solute-solvent interactions. The results obtained in the study show that solute-solvent interactions of nonionic organic compounds and proteins in polyethylene glycol-sodium sulfate aqueous two-phase system change in the presence of NaCl additive. PMID:26615710

  6. Effect of amine functionalized polyethylene on clay-silver dispersion for polyethylene nanocomposites

    NASA Astrophysics Data System (ADS)

    Sánchez-Valdes, S.; Ibarra-A, M. C.; Ramírez-V, E.; Ramos-V, L. F.; Martinez-C, J. G.; Romero-G, J.; Ledezma-P, A. S.; Rodriguez-F, O. S.

    2014-08-01

    The compatibilization provided by maleic anhydride (MA) and 2-[2-(dimethylamino)-ethoxy] ethanol (DMAE) functionalized polyethylene for forming polyethylene-based nanocomposites was studied and compared. MA was grafted into PE by melt mixing to obtain PEgMA (compatibilizer 1), thereafter, PEgMA was reacted with DMAE and an antioxidant also by melt mixing to obtain PAgDMAE (compatibilizer 2). These compatibilizers were reacted using ultrasound with a solution of AgNO3 0.04 M and Ethylene glycol. Ammonium hydroxide was added in a ratio of 2:1 molar with respect to silver nitrate. These silver coated compatibilizers were mixed with PE and nano-clay (Cloisite I28E), thus forming the different hybrid PE-clay-silver nanocomposites. FTIR confirmed the formation of these two compatibilizers. All the compatibilized nanocomposites had better filler (clay and silver) dispersion and exfoliation compared to the uncompatibilized PE nanocomposites. X-ray diffraction, mechanical and antimicrobial properties attained showed that the PEgDMAE produced the better dispersed PE, clay and silver nanocomposites. The obtained nanocomposites showed outstanding antimicrobial properties against bacteria, Escherichia coli and fungus, Aspergillus niger. It is concluded that the PEgDMAE offers an outstanding capability for preparing nanocomposites with highly exfoliated and dispersed filler into the PE matrix.

  7. Remote atmospheric-pressure plasma activation of the surfaces of polyethylene terephthalate and polyethylene naphthalate.

    PubMed

    Gonzalez, E; Barankin, M D; Guschl, P C; Hicks, R F

    2008-11-01

    The surfaces of poly(ethylene terephthalate) (PET) and poly(ethylene naphthalate) (PEN) were treated with an atmospheric-pressure oxygen and helium plasma. Changes in the energy, adhesion, and chemical composition of the surfaces were determined by contact angle measurements, mechanical pull tests, and X-ray photoelectron spectroscopy (XPS). Surface-energy calculations revealed that after plasma treatment the polarity of PET and PEN increased 6 and 10 times, respectively. In addition, adhesive bond strengths were enhanced by up to 7 times. For PET and PEN, XPS revealed an 18-29% decrease in the area of the C 1s peak at 285 eV, which is attributable to the aromatic carbon atoms. The C 1s peak area due to ester carbon atoms increased by 11 and 24% for PET and PEN, respectively, while the C 1s peak area resulting from C-O species increased by about 5% for both polymers. These results indicate that oxygen atoms generated in the plasma rapidly oxidize the aromatic rings on the polymer chains. The Langmuir adsorption rate constants for oxidizing the polymer surfaces were 15.6 and 4.6 s(-1) for PET and PEN, respectively. PMID:18834154

  8. Study on ternary low density polyethylene/linear low density polyethylene/thermoplastic starch blend films.

    PubMed

    Sabetzadeh, Maryam; Bagheri, Rouhollah; Masoomi, Mahmood

    2015-03-30

    In this work, low-density polyethylene/linear low-density polyethylene/thermoplastic starch (LDPE/LLDPE/TPS) films are prepared with the aim of obtaining environmentally friendly materials containing high TPS content with required packaging properties. Blending of LDPE/LLDPE (70/30 wt/wt) with 5-20 wt% of TPS and 3 wt% of PE-grafted maleic anhydride (PE-g-MA) is performed in a twin-screw extruder, followed by the blowing process. Differential scanning calorimetric results indicate starch has more pronounced effect on crystallization of LLDPE than LDPE. Scanning electron micrograph shows a fairly good dispersion of TPS in PE matrices. Fourier transfer infrared spectra confirm compatibility between polymers using PE-g-MA as the compatibilizer. Storage modulus, loss modulus and complex viscosity increase with incorporation of starch. Tensile strength and elongation-at-break decrease from 18 to 10.5 MPa and 340 to 200%, respectively when TPS increases from 5 to 20%. However, the required mechanical properties for packaging applications are attained when 15 wt% starch is added, as specified in ASTM D4635. Finally 12% increase in water uptake is achieved with inclusion of 15 wt% starch. PMID:25563952

  9. Engineering Poly(ethylene glycol) Materials to Promote Cardiogenesis

    NASA Astrophysics Data System (ADS)

    Smith, Amanda Walker

    Heart failure is one of the leading causes of death worldwide, and the current costs of treatment put a significant economic burden on our societies. After an infarction, fibrotic tissue begins to form as part of the heart failure cascade. Current options to slow this process include a wide range of pharmaceutical agents, and ultimately the patient may require a heart transplant. Innovative treatment approaches are needed to bring down costs and improve quality of life. The possibility of regenerating or replacing damaged tissue with healthy cardiomyocytes is generating considerable excitement, but there are still many obstacles to overcome. First, while cell injections into the myocardium have demonstrated slight improvements in cardiac function, the actual engraftment of transplanted cells is very low. It is anticipated that improving engraftment will boost outcomes. Second, cellular differentiation and reprogramming protocols have not yet produced cells that are identical to adult cardiomyocytes, and immunogenicity continues to be a problem despite the advent of autologously derived induced pluripotent stem cells. This dissertation will explore biomaterials approaches to addressing these two obstacles. Tissue engineering scaffolds may improve cell engraftment by providing bioactive factors, preventing cell anoikis, and reducing cell washout by blood flow. Poly(ethylene glycol) (PEG) is often used as a coating to reduce implant rejection because it is highly resistant to protein adsorption. Because fibrosis of a material in contact with the myocardium could cause arrhythmias, PEG materials are highly relevant for cardiac tissue engineering applications. In Chapter 2, we describe a novel method for crosslinking PEG microspheres around cells to form a scaffold for tissue engineering. We then demonstrate that HL-1 cardiomyocyte viability and phenotype are retained throughout the fabrication process and during the first 7 weeks of culture. In the third chapter of the

  10. Wear of highly crosslinked polyethylene acetabular components

    PubMed Central

    Callary, Stuart A; Solomon, Lucian B; Holubowycz, Oksana T; Campbell, David G; Munn, Zachary; Howie, Donald W

    2015-01-01

    Background and purpose Wear rates of highly crosslinked polyethylene (XLPE) acetabular components have varied considerably between different published studies. This variation is in part due to the different techniques used to measure wear and to the errors inherent in measuring the relatively low amounts of wear in XLPE bearings. We undertook a scoping review of studies that have examined the in vivo wear of XLPE acetabular components using the most sensitive method available, radiostereometric analysis (RSA). Methods A systematic search of the PubMed, Scopus, and Cochrane databases was performed to identify published studies in which RSA was used to measure wear of XLPE components in primary total hip arthroplasty (THA). Results 18 publications examined 12 primary THA cohorts, comprising only 260 THAs at 2–10 years of follow-up. The mean or median proximal wear rate reported ranged from 0.00 to 0.06 mm/year. However, differences in the manner in which wear was determined made it difficult to compare some studies. Furthermore, differences in RSA methodology between studies, such as the use of supine or standing radiographs and the use of beaded or unbeaded reference segments, may limit future meta-analyses examining the effect of patient and implant variables on wear rates. Interpretation This scoping review confirmed the low wear rates of XLPE in THA, as measured by RSA. We make recommendations to enhance the standardization of reporting of RSA wear results, which will facilitate early identification of poorly performing implants and enable a better understanding of the effects of surgical and patient factors on wear. PMID:25301435

  11. Poly(ethylene glycol)-functionalized polymeric microchips for capillary electrophoresis.

    PubMed

    Sun, Xuefei; Li, Dan; Lee, Milton L

    2009-08-01

    Recently, we reported the synthesis, fabrication, and preliminary evaluation of poly(ethylene glycol) (PEG)-functionalized polymeric microchips that are inherently resistant to protein adsorption without surface modification in capillary electrophoresis (CE). In this study, we investigated the impact of cross-linker purity and addition of methyl methacrylate (MMA) as a comonomer on CE performance. Impure poly(ethylene glycol) diacrylate (PEGDA) induced electroosmotic flow (EOF) and increased the separation time, while the addition of MMA decreased the separation efficiency to approximately 25% of that obtained using microchips fabricated without MMA. Resultant improved microchips were evaluated for the separation of fluorescent dyes, amino acids, peptides, and proteins. A CE efficiency of 4.2 x 10(4) plates for aspartic acid in a 3.5 cm long microchannel was obtained. Chiral separation of 10 different D,L-amino acid pairs was obtained with addition of a chiral selector (i.e., beta-cyclodextrin) in the running buffer. Selectivity (alpha) and resolution (R(s)) for D,L-leucine were 1.16 and 1.64, respectively. Good reproducibility was an added advantage of these PEG-functionalized microchips. PMID:19572700

  12. Preparation and characterization of nonfouling polymer brushes on poly(ethylene terephthalate) film surfaces.

    PubMed

    Li, Jiehua; Tan, Dongsheng; Zhang, Xiaoqing; Tan, Hong; Ding, Mingming; Wan, Changxiu; Fu, Qiang

    2010-07-01

    In this study, a surface grafting of nonfouling poly(ethylene glycol) methyl ether acrylate (PEGMA) on poly(ethylene terephthalate) (PET) was carried out via surface-initiated atom-transfer radical polymerization (SI-ATRP) to improve hemocompatibility of polymer based biomaterials. To do this, the coupling agent with hydroxyl groups for the ATRP initiator was first anchored on the surface of PET films using photochemical method, and then these hydroxyl groups were esterified by bromoisobutyryl bromide, from which PET with various main chain lengths of PEGMA was prepared. The structures and properties of modified PET surfaces were investigated using water contact angle (WAC), ATR-FTIR, X-ray photoelectron spectroscopy (XPS) and Atomic force microscopy (AFM). The molecular weights of the free polymer from solution were determined by gel permeation chromatography (GPC). These results indicated that grafting of PEGMA on PET film is a simple way to change its surface properties. The protein adsorption resistance on the surfaces of PET was primarily evaluated by an enzyme-linked immunosorbent assay (ELISA). The result demonstrated that the protein adsorption could be well suppressed by poly(PEGMA) brush structure on the surface of PET. This work provides a new approach for polymers to enhance their biocompatibility. PMID:20399623

  13. Bactericidal activity of propylene glycol, glycerine, polyethylene glycol 400, and polyethylene glycol 1000 against selected microorganisms

    PubMed Central

    Nalawade, Triveni Mohan; Bhat, Kishore; Sogi, Suma H. P.

    2015-01-01

    Aim: The aim of the present study was to evaluate the bactericidal activity of propylene glycol, glycerine, polyethylene glycol 400 (PEG 400), and polyethylene glycol 1000 (PEG 1000) against selected microorganisms in vitro. Materials and Methods: Five vehicles, namely propylene glycol, glycerine, PEG 400, PEG 1000, and combination of propylene glycol with PEG 400, were tested for their bactericidal activity. The minimum bactericidal concentration was noted against four standard strains of organisms, i.e. Streptococcus mutans American Type Culture Collection (ATCC) 25175, Streptococcus mutans ATCC 12598, Enterococcus faecalis ATCC 35550, and Escherichia coli ATCC 25922, using broth dilution assay. Successful endodontic therapy depends upon thorough disinfection of root canals. In some refractory cases, routine endodontic therapy is not sufficient, so intracanal medicaments are used for proper disinfection of canals. Intracanal medicaments are dispensed with vehicles which aid in increased diffusion through the dentinal tubules and improve their efficacy. Among the various vehicles used, glycerine is easily available, whereas others like propylene glycol and polyethylene glycol have to be procured from appropriate sources. Also, these vehicles, being viscous, aid in sustained release of the medicaments and improve their handling properties. The most commonly used intracanal medicaments like calcium hydroxide are ineffective on many microorganisms, while most of the other medicaments like MTAD (Mixture of Tetracycline, an Acid, and a Detergent) and Triple Antibiotic Paste (TAP) consist of antibiotics which can lead to development of antibiotic resistance among microorganisms. Thus, in order to use safer and equally effective intracanal medicaments, newer alternatives like chlorhexidine gluconate, ozonized water, etc., are being explored. Similarly, the five vehicles mentioned above are being tested for their antimicrobial activity in this study. Results: All vehicles

  14. Pulmonary surfactant adsorption is increased by hyaluronan or polyethylene glycol.

    PubMed

    Taeusch, H William; Dybbro, Eric; Lu, Karen W

    2008-04-01

    In acute lung injuries, inactivating agents may interfere with transfer (adsorption) of pulmonary surfactants to the interface between air and the aqueous layer that coats the interior of alveoli. Some ionic and nonionic polymers reduce surfactant inactivation in vitro and in vivo. In this study, we tested directly whether an ionic polymer, hyaluronan, or a nonionic polymer, polyethylene glycol, enhanced adsorption of a surfactant used clinically. We used three different methods of measuring adsorption in vitro: a modified pulsating bubble surfactometer; a King/Clements device; and a spreading trough. In addition we measured the effects of both polymers on surfactant turbidity, using this assay as a nonspecific index of aggregation. We found that both hyaluronan and polyethylene glycol significantly increased the rate and degree of surfactant material adsorbed to the surface in all three assays. Hyaluronan was effective in lower concentrations (20-fold) than polyethylene glycol and, unlike polyethylene glycol, hyaluronan did not increase apparent aggregation of surfactant. Surfactant adsorption in the presence of serum was also enhanced by both polymers regardless of whether hyaluronan or polyethylene glycol was included with serum in the subphase or added to the surfactant applied to the surface. Therefore, endogenous polymers in the alveolar subphase, or exogenous polymers added to surfactant used as therapy, may both be important for reducing inactivation of surfactant that occurs with various lung injuries. PMID:18065212

  15. Volatile organic compounds in polyethylene bags-A forensic perspective.

    PubMed

    Borusiewicz, Rafał; Kowalski, Rafał

    2016-09-01

    Polyethylene bags, though not recommended, are sometimes used in some countries as improvised packaging for items sent to be analysed for the presence of volatile organic compounds, namely ignitable liquids residues. Sometimes items made of polyethylene constitute the samples themselves. It is well known what kind of volatile organic compounds are produced as a result of polyethylene thermal decomposition, but there is a lack of information relating to if some volatile compounds are present in unheated/unburned items made of polyethylene in detectable amounts and, if so, what those compounds are. The aim of this presented research was to answer these questions. 28 different bags made of polyethylene, representing 9 brands, were purchased in local shops and analysed according to the procedure routinely used for fire debris. The results proved that in almost all bags a distinctive mixture of compounds is present, comprising of n-alkanes and n-alkenes with an even number of carbon atoms in their molecules. Some other compounds (e.g., limonene, 2,2,4,6,6-pentamethylheptane) are also often present, but the presence of even n-alkanes and n-alkenes constitutes the most characteristic feature. PMID:27458996

  16. Modeling uptake of hydrophobic organic contaminants into polyethylene passive samplers.

    PubMed

    Thompson, Jay M; Hsieh, Ching-Hong; Luthy, Richard G

    2015-02-17

    Single-phase passive samplers are gaining acceptance as a method to measure hydrophobic organic contaminant (HOC) concentration in water. Although the relationship between the HOC concentration in water and passive sampler is linear at equilibrium, mass transfer models are needed for nonequilibrium conditions. We report measurements of organochlorine pesticide diffusion and partition coefficients with respect to polyethylene (PE), and present a Fickian approach to modeling HOC uptake by PE in aqueous systems. The model is an analytic solution to Fick's second law applied through an aqueous diffusive boundary layer and a polyethylene layer. Comparisons of the model with existing methods indicate agreement at appropriate boundary conditions. Laboratory release experiments on the organochlorine pesticides DDT, DDE, DDD, and chlordane in well-mixed slurries support the model's applicability to aqueous systems. In general, the advantage of the model is its application in the cases of well-agitated systems, low values of polyethylene-water partioning coefficients, thick polyethylene relative to the boundary layer thickness, and/or short exposure times. Another significant advantage is the ability to estimate, or at least bound, the needed exposure time to reach a desired CPE without empirical model inputs. A further finding of this work is that polyethylene diffusivity does not vary by transport direction through the sampler thickness. PMID:25607420

  17. Activation of Cytosolic Pyruvate Kinase by Polyethylene Glycol.

    PubMed Central

    Podesta, F. E.; Plaxton, W. C.

    1993-01-01

    Homogeneous cytosolic pyruvate kinase from endosperm of germinating castor oil (Ricinus communis L. cv Hale) seeds was potently activated by polyethylene glycol. The addition of 5% (w/v) polyethylene glycol to the pyruvate kinase reaction mixture caused a 2.6-fold increase in maximal velocity and 12.5- and 2-fold reductions in Km values for phosphoenolpyruvate and ADP, respectively. Glycerol, ethylene glycol, and bovine serum albumin also enhanced pyruvate kinase activity, albeit to a lesser extent than polyethylene glycol. The addition of 5% (w/v) polyethylene glycol to the elution buffer during high-performance gel filtration chromatography of purified cytosolic pyruvate kinase helped to stabilize the active heterotetrameric native structure of the enzyme. A higher degree of inhibition by MgATP, but lower sensitivity to the inhibitors 3-phosphoglycerate and fructose- 1,6-bisphosphate, was also observed in the presence of 5% (w/v) polyethylene glycol. It is concluded that (a) plant cytosolic pyruvate kinase activity and regulation, like that of other regulatory pyruvate kinases, is modified by extreme dilution in the assay medium, probably as a result of deaggregation of the native tetrameric enzyme, and (b) ATP is probably the major metabolic effector of germinating castor endosperm cytosolic pyruvate kinase in vivo. PMID:12231936

  18. Activation of Cytosolic Pyruvate Kinase by Polyethylene Glycol.

    PubMed

    Podesta, F. E.; Plaxton, W. C.

    1993-09-01

    Homogeneous cytosolic pyruvate kinase from endosperm of germinating castor oil (Ricinus communis L. cv Hale) seeds was potently activated by polyethylene glycol. The addition of 5% (w/v) polyethylene glycol to the pyruvate kinase reaction mixture caused a 2.6-fold increase in maximal velocity and 12.5- and 2-fold reductions in Km values for phosphoenolpyruvate and ADP, respectively. Glycerol, ethylene glycol, and bovine serum albumin also enhanced pyruvate kinase activity, albeit to a lesser extent than polyethylene glycol. The addition of 5% (w/v) polyethylene glycol to the elution buffer during high-performance gel filtration chromatography of purified cytosolic pyruvate kinase helped to stabilize the active heterotetrameric native structure of the enzyme. A higher degree of inhibition by MgATP, but lower sensitivity to the inhibitors 3-phosphoglycerate and fructose- 1,6-bisphosphate, was also observed in the presence of 5% (w/v) polyethylene glycol. It is concluded that (a) plant cytosolic pyruvate kinase activity and regulation, like that of other regulatory pyruvate kinases, is modified by extreme dilution in the assay medium, probably as a result of deaggregation of the native tetrameric enzyme, and (b) ATP is probably the major metabolic effector of germinating castor endosperm cytosolic pyruvate kinase in vivo. PMID:12231936

  19. Initial Stages of Pyrolysis of Polyethylene

    NASA Astrophysics Data System (ADS)

    Popov, Konstantin V.

    Combustion and flammability of plastics are important topics of practical interest directly related to fire safety and recycling of polymeric materials; pyrolysis of the solid is the initial step of its combustion. One of the main ways to study such complicated processes is through detailed mechanistic modeling, in which the process is represented by a set of many elementary reactions. Mechanistic modeling of combustion of plastics is considerably hindered by the lack of necessary kinetic data. In virtually all existing models of polymer pyrolysis the majority of kinetic data used are derived from the corresponding gas phase values of smaller species. The use of gas phase rate constants is, generally, not justified without an experimental justification. In the first part of the work the influence of condensed phase on the rate of scission of a carbon-carbon bond (the reaction that initiates pyrolysis and combustion) in polyethylene (PE) was studied using the method of Reactive Molecular Dynamics (RMD). A method based on a two-step kinetic mechanism was developed to decouple the cage effect from the kinetics of the reaction under study. It was observed that under the conditions of condensed phase the rate constant of C-C bond scission in PE decreased by an order of magnitude compared to that obtained in vacuum. It was also shown that under the conditions of polymer melt the rate constant does not depend on the length of the polymer chain. In the second part of the work the kinetics of liquid phase and gas phase products of PE pyrolysis were studied experimentally using Gas Chromatography and Nuclear Magnetic Resonance. Based on the assumption of applicability of gas phase kinetic data for C-C scission reaction and beta-scission reaction under the conditions of polymer melt, rate constants of hydrogen transfer, radical addition to double bonds, and radical recombination were determined via kinetic modeling of the experimental results. The obtained values of the rate

  20. Hydration of polyethylene glycol-grafted liposomes.

    PubMed

    Tirosh, O; Barenholz, Y; Katzhendler, J; Priev, A

    1998-03-01

    This study aimed to characterize the effect of polyethylene glycol of 2000 molecular weight (PEG2000) attached to a dialkylphosphatidic acid (dihexadecylphosphatidyl (DHP)-PEG2000) on the hydration and thermodynamic stability of lipid assemblies. Differential scanning calorimetry, densitometry, and ultrasound velocity and absorption measurements were used for thermodynamic and hydrational characterization. Using a differential scanning calorimetry technique we showed that each molecule of PEG2000 binds 136 +/- 4 molecules of water. For PEG2000 covalently attached to the lipid molecules organized in micelles, the water binding increases to 210 +/- 6 water molecules. This demonstrates that the two different structural configurations of the PEG2000, a random coil in the case of the free PEG and a brush in the case of DHP-PEG2000 micelles, differ in their hydration level. Ultrasound absorption changes in liposomes reflect mainly the heterophase fluctuations and packing defects in the lipid bilayer. The PEG-induced excess ultrasound absorption of the lipid bilayer at 7.7 MHz for PEG-lipid concentrations over 5 mol % indicates the increase in the relaxation time of the headgroup rotation due to PEG-PEG interactions. The adiabatic compressibility (calculated from ultrasound velocity and density) of the lipid bilayer of the liposome increases monotonically with PEG-lipid concentration up to approximately 7 mol %, reflecting release of water from the lipid headgroup region. Elimination of this water, induced by grafted PEG, leads to a decrease in bilayer defects and enhanced lateral packing of the phospholipid acyl chains. We assume that the dehydration of the lipid headgroup region in conjunction with the increase of the hydration of the outer layer by grafting PEG in brush configuration are responsible for increasing thermodynamic stability of the liposomes at 5-7 mol % of PEG-lipid. At higher PEG-lipid concentrations, compressibility and partial volume of the lipid phase

  1. Optimizing the surface density of polyethylene glycol chains by grafting from binary solvent mixtures

    NASA Astrophysics Data System (ADS)

    Arcot, Lokanathan; Ogaki, Ryosuke; Zhang, Shuai; Meyer, Rikke L.; Kingshott, Peter

    2015-06-01

    Polyethylene glycol (PEG) brushes are very effective at controlling non-specific deposition of biological material onto surfaces, which is of paramount importance to obtaining successful outcomes in biomaterials, tissue engineered scaffolds, biosensors, filtration membranes and drug delivery devices. We report on a simple 'grafting to' approach involving binary solvent mixtures that are chosen based on Hansen's solubility parameters to optimize the solubility of PEG thereby enabling control over the graft density. The PEG thiol-gold model system enabled a thorough characterization of PEG films formed, while studies on a PEG silane-silicon system examined the versatility to be applied to any substrate-head group system by choosing an appropriate solvent pair. The ability of PEG films to resist non-specific adsorption of proteins was quantitatively assessed by full serum exposure studies and the binary solvent strategy was found to produce PEG films with optimal graft density to efficiently resist protein adsorption.

  2. The Use of an Enzyme-based Sensor Array to Fingerprint Proteomic Signatures of Sera from Different Mammalian Species.

    PubMed

    Tomita, Shunsuke; Yokoyama, Saki; Kurita, Ryoji; Niwa, Osamu; Yoshimoto, Keitaro

    2016-01-01

    A cross-reactive sensor array consisting of polyion complexes (PICs) between anionic enzymes and poly(ethylene glycol)-modified (PEGylated) polyamines has been used to identify the source of mammalian sera. Although the catalytic activity of enzymes was inhibited by PIC formation with PEGylated polyamines, the subsequent addition of sera caused enzyme releases from PICs through competitive interactions between PICs and serum proteins, generating unique response patterns of changes in the enzyme activity. Linear discriminant analysis of the obtained patterns enabled the discrimination of five sera from different mammalian sources. PMID:26860572

  3. Friction and wear of hydroxyapatite reinforced high density polyethylene against the stainless steel counterface.

    PubMed

    Wang, M; Chandrasekaran, M; Bonfield, W

    2002-06-01

    Hydroxyapatite (HA) reinforced high density polyethylene (HDPE) was invented as a biomaterial for skeletal applications. In this investigation, tribological properties (e.g. wear rate and coefficient of friction) of unfilled HDPE and HA/HDPE composites were evaluated against the duplex stainless steel in dry and lubricated conditions, with distilled water or aqueous solutions of proteins (egg albumen or glucose) being lubricants. Wear tests were conducted in a custom-built test rig for HDPE and HA/HDPE containing up to 40 vol % of HA. It was found that HA/HDPE composites had lower coefficients of friction than unfilled HDPE under certain conditions. HA/HDPE also exhibited less severe fatigue failure marks than HDPE. The degradation and fatigue failure of HDPE due to the presence of proteins were severe for low speed wear testing (100 rpm) as compared to high speed wear testing (200 rpm). This was due possibly to the high shear rate at the contact which could remove any degraded film instantaneously at high sliding speed, while with a low sliding speed the build-up of a degraded layer of protein could occur. The degraded protein layer would stay at the contact for a longer time and mechanical activation would induce adverse reactions, weakening the surface layer of HDPE. Both egg albumen and glucose were found to be corrosive to steel and adversely reactive for HDPE and HA/HDPE composites. The wear modes observed were similar to that of ultra-high molecular weight polyethylene. Specimens tested with egg albumen also displayed higher wear rates, which was again attributed to corrosion accelerated wear. PMID:15348592

  4. Versatile ferrofluids based on polyethylene glycol coated iron oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Brullot, W.; Reddy, N. K.; Wouters, J.; Valev, V. K.; Goderis, B.; Vermant, J.; Verbiest, T.

    2012-06-01

    Versatile ferrofluids based on polyethylene glycol coated iron oxide nanoparticles were obtained by a facile protocol and thoroughly characterized. Superparamagnetic iron oxide nanoparticles synthesized using a modified forced hydrolysis method were functionalized with polyethylene glycol silane (PEG silane), precipitated and dried. These functionalized particles are dispersable in a range of solvents and concentrations depending on the desired properties. Examples of tunable properties are magnetic behavior, optical and magneto-optical response, thermal features and rheological behavior. As such, PEG silane functionalized particles represent a platform for the development of new materials that have broad applicability in e.g. biomedical, industrial or photonic environments. Magnetic, optical, magneto-optical, thermal and rheological properties of several ferrofluids based on PEG coated particles with different concentrations of particles dispersed in low molecular mass polyethylene glycol were investigated, establishing the applicability of such materials.

  5. Conventional Versus Cross-Linked Polyethylene for Total Hip Arthroplasty.

    PubMed

    Surace, Michele F; Monestier, Luca; Vulcano, Ettore; Harwin, Steven F; Cherubino, Paolo

    2015-09-01

    The clinical and radiographic outcomes of 88 patients who underwent primary total hip arthroplasty with either conventional polyethylene or cross-linked polyethylene (XLPE) from the same manufacturer were compared. There were no significant differences between the 2 subpopulations regarding average age, gender, side affected, or prosthetic stem and cup size. The average follow-up was 104 months (range, 55 to 131 months). To the authors' knowledge, this is the longest follow-up for this particular insert. Clinical and radiographic evaluations were performed at 1, 3, 6, and 12 months and then annually. Results showed that XLPE has a significantly greater wear reduction than that of standard polyethylene in primary total hip arthroplasty. At the longest available follow-up for these specific inserts, XLPE proved to be effective in reducing wear. PMID:26375527

  6. Space radiation transport properties of polyethylene-based composites.

    PubMed

    Kaul, R K; Barghouty, A F; Dahche, H M

    2004-11-01

    Composite materials that can serve as both effective shielding materials against cosmic-ray and energetic solar particles in deep space, as well as structural materials for habitat and spacecraft, remain a critical and mission enabling component in mission planning and exploration. Polyethylene is known to have excellent shielding properties due to its low density, coupled with high hydrogen content. Polyethylene-fiber reinforced composites promise to combine this shielding effectiveness with the required mechanical properties of structural materials. Samples of polyethylene-fiber reinforced epoxy matrix composite 1-5 cm thick were prepared at the NASA Marshall Space Flight Center and tested against a 500 MeV/nucleon Fe beam at the HIMAC facility of NIRS in Chiba, Japan. This paper presents measured and calculated results for the radiation transport properties of these samples. PMID:15644352

  7. Radiation Transport Properties of Polyethylene-Fiber Composites

    NASA Technical Reports Server (NTRS)

    Kaul, Raj K.; Barghouty, A. F.; Dahche, H. M.

    2003-01-01

    Composite materials that can both serve as effective shielding materials against cosmic-ray and energetic solar particles in deep space as well as structural materials for habitat and spacecraft remain a critical and mission enabling piece in mission planning and exploration. Polyethylene is known to have excellent shielding properties due to its low density coupled with high hydrogen content. Polyethylene fiber reinforced composites promise to combine this shielding effectiveness with the required mechanical properties of structural materials. Samples of Polyethylene-fiber reinforced epoxy matrix composite 1-5 cm thick were prepared at NASA's Marshall Space Flight Center and tested against 500 MeV/nucleon Fe beam at the HIMAC facility of NIRS in Chiba, Japan. This paper presents measured and calculated results for the radiation transport properties of these samples.

  8. Space radiation transport properties of polyethylene-based composites

    NASA Technical Reports Server (NTRS)

    Kaul, R. K.; Barghouty, A. F.; Dahche, H. M.

    2004-01-01

    Composite materials that can serve as both effective shielding materials against cosmic-ray and energetic solar particles in deep space, as well as structural materials for habitat and spacecraft, remain a critical and mission enabling component in mission planning and exploration. Polyethylene is known to have excellent shielding properties due to its low density, coupled with high hydrogen content. Polyethylene-fiber reinforced composites promise to combine this shielding effectiveness with the required mechanical properties of structural materials. Samples of polyethylene-fiber reinforced epoxy matrix composite 1-5 cm thick were prepared at the NASA Marshall Space Flight Center and tested against a 500 MeV/nucleon Fe beam at the HIMAC facility of NIRS in Chiba, Japan. This paper presents measured and calculated results for the radiation transport properties of these samples.

  9. Polyethylene Wear in Retrieved Reverse Total Shoulder Components

    PubMed Central

    Day, Judd S; MacDonald, Daniel W; Olsen, Madeline; Getz, Charles; Williams, Gerald R; Kurtz, Steven M

    2011-01-01

    Background Reverse total shoulder arthroplasty has been used to treat rotator cuff tear arthropathy, proximal humeral fractures and for failed conventional total shoulder prostheses. It has been suggested that polyethylene wear is potentially higher in reverse shoulder replacements than in conventional shoulder replacements. The modes and degree of polyethylene wear have not been completely elucidated. The purpose of this study was to evaluate polyethylene wear patterns in seven specimens retrieved at revision arthroplasty and identify factors that may be associated with increased wear. Methods Reverse total shoulder components were retrieved from 7 patients during revision arthroplasty for loosening and/or pain. Pre-operative glenoid tilt and placement, and scapular notching were evaluated using pre-operative radiographs. Polyethylene wear was evaluated using microCT and optical microscopy. Results Wear on the rim of the polyethylene humeral cup, was identified on all retrieved components. The extent of rim wear varied from a penetration depth of 0.1 to 4.7 mm. We could not demonstrate a correlation between scapular notching and rim wear. However, rim wear was more extensive when the inferior screw had made contact with the liner. Metal on metal wear between the humeral component and the inferior screw of one component was also observed. Wear of the intended bearing surface was minimal. Discussion Rim damage was the predominant cause of polyethylene wear in our retrieved specimens. Direct contact between the humeral component and inferior metaglene screws is concerning because this could lead to accelerated UHMWPE wear and also induce mechanical loosening of the glenoid component. PMID:21724419

  10. Molecularly uniform poly(ethylene glycol) certified reference material

    NASA Astrophysics Data System (ADS)

    Takahashi, Kayori; Matsuyama, Shigetomo; Kinugasa, Shinichi; Ehara, Kensei; Sakurai, Hiromu; Horikawa, Yoshiteru; Kitazawa, Hideaki; Bounoshita, Masao

    2015-02-01

    A certified reference material (CRM) for poly(ethylene glycol) with no distribution in the degree of polymerization was developed. The degree of polymerization of the CRM was accurately determined to be 23. Supercritical fluid chromatography (SFC) was used to separate the molecularly uniform polymer from a standard commercial sample with wide polydispersity in its degree of polymerization. Through the use of a specific fractionation system coupled with SFC, we are able to obtain samples of poly(ethylene glycol) oligomer with exact degrees of polymerization, as required for a CRM produced by the National Metrology Institute of Japan.

  11. High Thermal Conductivity Aligned Polyethylene-Graphene Nanocomposites

    NASA Astrophysics Data System (ADS)

    Garg, Jivtesh; Saeidijavash, Mortaza

    We investigate enhancement of thermal conductivity in polyethylene-graphene nanocomposites. The effect of alignment of both the polymer chains and the dispersed graphene flakes on thermal conductivity enhancement will be reported. In this work nanocomposites are prepared through microextrusion of polyethylene pellets and graphene nanopowder. Alignment is achieved through mechanical stretching of the nanocomposites. Thermal conductivity is measured using both Angstrom method and Laser flash. Variables involved in the study are the draw ratio and the weight percentage of graphene nanopowder. Results will shed light on the role of alignment of graphene flakes on enhancing thermal transport and provide new avenues to achieve ultra-high thermal conductivity in polymeric materials.

  12. Irradiation of linear polyethylene - Partitioning between sol and gel.

    NASA Technical Reports Server (NTRS)

    Rijke, A. M.; Mandelkern, L.

    1971-01-01

    Investigation of the importance of chain-scission processes and of the applicability of the general theory of network formation to polyethylene with respect to critical conditions for gelation, using molecular weight fractions of linear polyethylene irradiated at 133 C. The partitioning between sol and gel was found to adhere to the theory just beyond the gel point. Deviations from theory occurred as the irradiation dosage was increased. It was concluded that main-chain scission at the temperatures concerned is not a significant process.

  13. Molecular order, miscibility, and rheology of molten polyethylenes

    NASA Astrophysics Data System (ADS)

    Hussein, Ibnelwaleed Ali

    New evidence of high-temperature transitions and molecular order in molten polyethylenes is presented, and its influence on the miscibility of polyethylenes is discussed. Thermal and rheological techniques were used to investigate commercial HDPE, LDPE and Ziegler-Natta and Metallocene LLDPEs. Adequate amounts of extra antioxidants were added to the polyethylenes during melt conditioning, following a separate investigation. Polystyrene was utilized to demonstrate the typical behavior of isotropic polymer melts. Temperature sweeps during torque measurements in a melt blender, and when using a rheometer and DSC, showed thermal transitions at about 208°C and 227°C. Torque in the blender over the temperature range 208°--227°C showed a flat profile or an increase in torque near 227°C, unique behavior associated with thermotropic liquid crystal polymers (LCP). Additional support for the liquid-state order that agree with theoretical predictions for a LCP is found. These include indications of an approach to a sign change in the first normal stress difference, N1( ġ ), at low values of the steady shear rate, ġ , and a kink in the non-Newtonian viscosity eta( ġ ). A rheological investigation found no evidence of the attainment of the isotropic state at high temperature and suggested the persistence of order above these transitions. However, highly branched metallocene LLDPE ( ˜ 40 CH3/1000 C) did not show transitions or any evidence of molecular order. It is suggested that polyethylenes possess different molecular conformation in the melt state ranging from the chain-folded HDPE to the amorphous highly-branched LLDPE. It is this molecular order and mismatch of the molecular conformations of different polyethylene structures that provide an explanation for the immiscibility of polyethylenes, as revealed by the dependence of their rheological properties on blend composition. The influence of molecular weight, comonomer type, and mixing temperature on the miscibility

  14. Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions.

    PubMed

    Norsic, Sebastien; Thomas, Coralie; D'Agosto, Franck; Boisson, Christophe

    2015-04-01

    Telechelic α,ω-iodo-vinyl-polyethylenes (Vin-PE-I) were obtained by catalytic ethylene polymerization in the presence of [(C5 Me5 )2 NdCl2 Li(OEt2 )2 ] in combination with a functionalized chain-transfer agent, namely, di(10-undecenyl)magnesium, followed by treatment of the resulting di(vinylpolyethylenyl)magnesium compounds ((vinyl-PE)2 Mg) with I2 . The iodo-functionalized vinylpolyethylenes (Vin-PE-I) were transformed into unique divinyl-functionalized polyethylenes (Vin-PE-Vin) by simple treatment with tBuOK in toluene at 95 °C. Thiol-ene reactions were then successfully performed on Vin-PE-Vin with functionalized thiols in the presence of AIBN. A range of homobifunctional telechelic polyethylenes were obtained on which a hydroxy, diol, carboxylic acid, amine, ammonium chloride, trimethoxysilyl, chloro, or fluoroalkyl group was installed quantitatively at each chain end. PMID:25688747

  15. The measurement of creep in ultrahigh molecular weight polyethylene: a comparison of conventional versus highly cross-linked polyethylene.

    PubMed

    Estok, Daniel M; Bragdon, Charles R; Plank, Gordon R; Huang, Anna; Muratoglu, Orhun K; Harris, William H

    2005-02-01

    Quantification of creep of highly cross-linked polyethylene would enable separation of creep from wear when evaluating femoral head penetration into polyethylene. We compared creep magnitude of a highly cross-linked versus conventional polyethylene in the laboratory. Twelve acetabular liners of each material were tested, 6 of which had a 32-mm inner diameter (ID) and 6 had 28-mm ID. Creep was measured using coordinate measuring machines during loading at 2 Hz without motion to 4 million cycles. Penetration into 32-mm ID conventional liners reached 97 microm versus 107 microm for highly cross-linked material, not significant. Penetration into 28-mm conventional liners was 132 microm versus 155 microm for highly cross-linked material (P = .017). Ninety percent of the creep had occurred by 2.5 million cycles. PMID:15902864

  16. Polyethylene composites containing a phase change material having a C14 straight chain hydrocarbon

    DOEpatents

    Salyer, Ival O.

    1987-01-01

    A composite useful in thermal energy storage, said composite being formed of a polyethylene matrix having a straight chain alkyl hydrocarbon incorporated therein, said polyethylene being crosslinked to such a degree that said polyethylene matrix is form stable and said polyethylene matrix is capable of absorbing at least 10% by weight of said straight chain alkyl hydrocarbon; the composite is useful in forming pellets or sheets having thermal energy storage characteristics.

  17. Recent advances in crosslinking chemistry of biomimetic poly(ethylene glycol) hydrogels

    PubMed Central

    Lin, Chien-Chi

    2015-01-01

    The design and application of biomimetic hydrogels have become an important and integral part of modern tissue engineering and regenerative medicine. Many of these hydrogels are prepared from synthetic macromers (e.g., poly(ethylene glycol) or PEG) as they provide high degrees of tunability for matrix crosslinking, degradation, and modification. For a hydrogel to be considered biomimetic, it has to recapitulate key features that are found in the native extracellular matrix, such as the appropriate matrix mechanics and permeability, the ability to sequester and deliver drugs, proteins, and or nucleic acids, as well as the ability to provide receptor-mediated cell-matrix interactions and protease-mediated matrix cleavage. A variety of chemistries have been employed to impart these biomimetic features into hydrogel crosslinking. These chemistries, such as radical-mediated polymerizations, enzyme-mediated crosslinking, bio-orthogonal click reactions, and supramolecular assembly, may be different in their crosslinking mechanisms but are required to be efficient for gel crosslinking and ligand bioconjugation under aqueous reaction conditions. The prepared biomimetic hydrogels should display a diverse array of functionalities and should also be cytocompatible for in vitro cell culture and/or in situ cell encapsulation. The focus of this article is to review recent progress in the crosslinking chemistries of biomimetic hydrogels with a special emphasis on hydrogels crosslinked from poly(ethylene glycol)-based macromers. PMID:26029357

  18. Hydrophilic polysulfone film prepared from polyethylene glycol monomethylether via coupling graft

    NASA Astrophysics Data System (ADS)

    Du, Ruikui; Gao, Baojiao; Li, Yanbin

    2013-06-01

    In the presence of acid-acceptor Na2CO3, the nucleophilic substitution between chloromethylated polysulfone (CMPSF) and polyethylene glycol monomethylether (PEGME) was conducted. Polyethylene glycol (PEG) was coupling-grafted onto the side chains of polysulfone (PSF) so that the graft copolymer PSF-g-PEG was prepared and the hydrophilic modification of polysulfone membrane material was realized. The chemical structure of PSF-g-PEG was characterized by FTIR and 1H NMR. The influence of the main factors on the coupling graft reaction was investigated. The water static contact angle of PSF-g-PEG membrane was determined and its property of resisting protein pollution was examined by using bovine serum albumin (BSA) as a model protein. The experimental results show that the coupling graft reaction between CMPSF and PEGME can proceed successfully, and the reaction of chloromethyl groups of CMPSF with the hydroxyl end groups of PEGME is a typical SN1 nucleophilic substitution reaction. The polarity of the solvents and the reaction temperature greatly influence the reaction. The suitable solvent is dimethyl acetamide with stronger polarity and 70 °C is a suitable reaction temperature. After reaction of 36 h, the grafting degree of PEG can reach 48 g/100 g and the product yield is about 73.6%. The contact angle of PSF-g-PEG membrane declines rapidly with the increase of PEG grafting degree, displaying the obvious enhancement of the hydrophilicity. The adsorption capacity of BSA on PSF-g-PEG membrane decreases remarkably with the increase of PEG grafting degree, showing excellent antifouling ability of PSF-g-PEG membrane for proteins.

  19. Complement activation on poly(ethylene oxide)-like RFGD-deposited surfaces

    PubMed Central

    Szott, Luisa Mayorga; Stein, M. Jeanette; Ratner, Buddy D.; Horbett, Thomas A.

    2010-01-01

    Non-specific protein adsorption, particularly fibrinogen (Fg), is thought to be an initiating step in the foreign body response (FBR) to biomaterials by promoting phagocyte attachment. In previous studies, we therefore prepared radio frequency glow discharge (RFGD) polyethylene oxide (PEO)-like tetraglyme coatings (CH3O(CH2CH2O)4CH3) adsorbing less than 10 ng/cm2 Fg and showed that they had the expected low monocyte adhesion in vitro. However, when these were implanted in vivo, many adherent inflammatory cells and a fibrous capsule were found, suggesting the role of alternative proteins, such as activated complement proteins, in the FBR to these materials. We therefore investigated complement interactions with the tetraglyme surfaces. First, because of its well known role in complement C3 activation, we measured the hydroxyl group (-OH) content of tetraglyme, but found it to be very low. Second, we measured C3 adsorption to tetraglyme from plasma. Low amounts of C3 adsorbed on tetraglyme, though it displayed higher binding strength than the control surfaces. Finally, complement activation was determined by measuring C3a and SC5b-9 levels in serum after incubating with tetraglyme, as well as other surfaces that served as positive and negative controls, namely poly(vinyl alcohol) hydrogels, Silastic sheeting, and poly(ethylene glycol) self-assembled monolayers with different end groups. Despite displaying low hydroxyl group concentration, relatively high C3a and SC5b-9 levels were found in serum exposed to tetraglyme, similar to the values due to our positive control, PVA. Our results support the conclusion that complement activation by tetraglyme is a possible mechanism involved in the FBR to these biomaterials. PMID:21105163

  20. 75 FR 52717 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-27

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... polyethylene terephthalate film, sheet and strip from India for the period January 1, 2009 through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping...

  1. 21 CFR 178.3750 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene glycol (mean molecular weight 200-9..., PRODUCTION AIDS, AND SANITIZERS Certain Adjuvants and Production Aids § 178.3750 Polyethylene glycol (mean molecular weight 200-9,500). Polyethylene glycol identified in this section may be safely used as...

  2. 21 CFR 178.3750 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene glycol (mean molecular weight 200-9..., PRODUCTION AIDS, AND SANITIZERS Certain Adjuvants and Production Aids § 178.3750 Polyethylene glycol (mean molecular weight 200-9,500). Polyethylene glycol identified in this section may be safely used as...

  3. 21 CFR 573.800 - Polyethylene glycol (400) mono- and dioleate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Polyethylene glycol (400) mono- and dioleate. 573... DRINKING WATER OF ANIMALS Food Additive Listing § 573.800 Polyethylene glycol (400) mono- and dioleate. (a) The food additive polyethylene glycol (400) mono- and dioleate meets the following...

  4. 21 CFR 573.800 - Polyethylene glycol (400) mono- and dioleate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Polyethylene glycol (400) mono- and dioleate. 573... DRINKING WATER OF ANIMALS Food Additive Listing § 573.800 Polyethylene glycol (400) mono- and dioleate. (a) The food additive polyethylene glycol (400) mono- and dioleate meets the following...

  5. 21 CFR 573.800 - Polyethylene glycol (400) mono- and dioleate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Polyethylene glycol (400) mono- and dioleate. 573... DRINKING WATER OF ANIMALS Food Additive Listing § 573.800 Polyethylene glycol (400) mono- and dioleate. (a) The food additive polyethylene glycol (400) mono- and dioleate meets the following...

  6. Study On Temperature Distribution In T Fittings - Polyethylene Natural Gas Pipes Assemblies

    NASA Astrophysics Data System (ADS)

    Avrigean, Eugen

    2015-09-01

    The present paper intends to approach theoretically and experimentally an important topic concerning the operational safety of the polyethylene pipes used in natural gas distribution. We discuss the influence of temperature in the high density polyethylene elbows during welding to the polyethylene pipes.

  7. Proteomic Analysis of Lonicera japonica Thunb. Immature Flower Buds Using Combinatorial Peptide Ligand Libraries and Polyethylene Glycol Fractionation.

    PubMed

    Zhu, Wei; Xu, Xiaobao; Tian, Jingkui; Zhang, Lin; Komatsu, Setsuko

    2016-01-01

    Lonicera japonica Thunb. flower is a well-known medicinal plant that has been widely used for the treatment of human disease. To explore the molecular mechanisms underlying the biological activities of L. japonica immature flower buds, a gel-free/label-free proteomic technique was used in combination with combinatorial peptide ligand libraries (CPLL) and polyethylene glycol (PEG) fractionation for the enrichment of low-abundance proteins and removal of high-abundance proteins, respectively. A total of 177, 614, and 529 proteins were identified in crude protein extraction, CPLL fractions, and PEG fractions, respectively. Among the identified proteins, 283 and 239 proteins were specifically identified by the CPLL and PEG methods, respectively. In particular, proteins related to the oxidative pentose phosphate pathway, signaling, hormone metabolism, and transport were highly enriched by CPLL and PEG fractionation compared to crude protein extraction. A total of 28 secondary metabolism-related proteins and 25 metabolites were identified in L. japonica immature flower buds. To determine the specificity of the identified proteins and metabolites for L. japonica immature flower buds, Cerasus flower buds were used, which resulted in the abundance of hydroxymethylbutenyl 4-diphosphate synthase in L. japonica immature flower buds being 10-fold higher than that in Cerasus flower buds. These results suggest that proteins related to secondary metabolism might be responsible for the biological activities of L. japonica immature flower buds. PMID:26573373

  8. APPLICATION OF HYDROPHILIC STARCH-BASED COATINGS TO POLYETHYLENE SURFACES

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Coatings were applied to polyethylene film surfaces by spraying formulations prepared from a jet cooked dispersion of waxy cornstarch, a water-based epoxy resin, a wax emulsion, and a surfactant. Although the starch component separated rapidly from the coating when the film was placed in water at r...

  9. Adsorption of Polyethylene from Solution onto Starch Film Surfaces

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Since starch adsorbs onto polyethylene (PE) surfaces from cooled solutions of jet cooked starch, this study was carried out to determine whether adsorption of PE onto hydrophilic starch film surfaces would also take place if starch films were placed in hot solutions of PE in organic solvents, and th...

  10. SECURING CONTAINERIZED HAZARDOUS WASTES WITH WELDED POLYETHYLENE ENCAPSULATES

    EPA Science Inventory

    Full-scale encapsulation of 208-liter (55-gal) drums was studied as a means for managing corroding containers of hazardous wastes in the field and rendering them suitable for transport and safe deposit within a final disposal site such as a landfill. Polyethylene (PE) receivers w...

  11. Dissociation of a polyethylene liner from an acetabular cup.

    PubMed

    Cameron, H U

    1993-10-01

    A polyethylene linear dissociated from a metal acetabular shell that could not be removed at the time of hip revision because the hexagonal hole in its screw head had become rounded off. A high-speed metal cutting burr was used to remove the screw and allow cup revision. PMID:8265224

  12. Long-term Radiographic Assessment of Cemented Polyethylene Acetabular Cups

    PubMed Central

    Isaac, Graham; Porter, Neil; Fisher, John; Older, John

    2008-01-01

    In vitro studies demonstrating excessive wear in polyethylene cups sterilized using gamma irradiation and stored in air led to the abandonment of this sterilization technique. We evaluated the clinical wear performance of a metal femoral component on a polyethylene cup in a hip prosthesis from a selected subset of implants in a group of patients followed for at least 20 years and assessed the time dependency of variation in penetration rates. We measured penetration in 33 polyethylene cups in 25 patients who had a Charnley low-friction arthroplasty between 1982 and 1984. All patients had Charnley Ogee® cups implanted for more than 20 years and sterilized using the gamma irradiation in air technique. If degradation occurred over time in vivo, it was not reflected by an increased penetration rate with increasing time in vivo; even after 20 years of implantation, the degree of wear remained low. This suggests gamma irradiation affects wear on ultra-high-molecular-weight polyethylene by reducing wear secondary to the crosslinking, by increasing wear as shown through in vitro studies of heavily oxidized samples, or by oxidation resulting from prolonged shelf life. The effect of progressive oxidation in vivo does not appear to affect wear in vivo. Level of Evidence: Level IV, therapeutic study. See the Guidelines for Authors for a complete description of levels of evidence. PMID:18196419

  13. Neutron production from polyethylene and common spacecraft materials.

    PubMed

    Maurer, R H; Roth, D R; Kinnison, J D; Jordan, T M; Heilbronn, L H; Miller, J; Zeitlin, C J

    2001-12-01

    We report experimental measurements of neutron production from collisions of neutron beams with polyethylene blocks simulating tissue at the Los Alamos National Laboratory Neutron Science Center and 1 GeV/amu iron nuclei with spacecraft shielding materials at the Brookhaven National Laboratory AGS. PMID:12033226

  14. Herbicide dissipation from low density polyethylene mulch utilizing analytical techniques

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In Georgia, most of the low density polyethylene mulch (LDPM) is laid for spring vegetable production followed by a second crop in the autumn, with a potential third crop the following spring. Between these vegetable plantings, farmers often use contact and residual herbicides to control weeds that ...

  15. Attachment of human primary osteoblast cells to modified polyethylene surfaces.

    PubMed

    Poulsson, Alexandra H C; Mitchell, Stephen A; Davidson, Marcus R; Johnstone, Alan J; Emmison, Neil; Bradley, Robert H

    2009-04-01

    Ultra-high-molecular-weight polyethylene (UHMWPE) has a long history of use in medical devices, primarily for articulating surfaces due to its inherent low surface energy which limits tissue integration. To widen the applications of UHMWPE, the surface energy can be increased. The increase in surface energy would improve the adsorption of proteins and attachment of cells to allow tissue integration, thereby allowing UHMWPE to potentially be used for a wider range of implants. The attachment and function of human primary osteoblast-like (HOB) cells to surfaces of UHMWPE with various levels of incorporated surface oxygen have been investigated. The surface modification of the UHMWPE was produced by exposure to a UV/ozone treatment. The resulting surface chemistry was studied using X-ray photoelectron spectroscopy (XPS), and the topography and surface structure were probed by atomic force microscopy (AFM) and scanning electron microscopy (SEM), which showed an increase in surface oxygen from 11 to 26 atom % with no significant change to the surface topography. The absolute root mean square roughness of both untreated and UV/ozone-treated surfaces was within 350-450 nm, and the water contact angles decreased with increasing oxygen incorporation, i.e., showing an increase in surface hydrophilicity. Cell attachment and functionality were assessed over a 21 day period for each cell-surface combination studied; these were performed using SEM and the alamarBlue assay to study cell attachment and proliferation and energy-dispersive X-ray (EDX) analysis to confirm extracellular mineral deposits, and total protein assay to examine the intra- and extracellular protein expressed by the cells. HOB cells cultured for 21 days on the modified UHMWPE surfaces with 19 and 26 atom % oxygen incorporated showed significantly higher cell densities compared to cells cultured on tissue culture polystyrene (TCPS) from day 3 onward. This indicated that the cells attached and proliferated more

  16. The study of compatibility of polyethylene and polypropylene by using irradiated polyethylene wax

    NASA Astrophysics Data System (ADS)

    El-Nahas, H. H.; Gad, Y. H.; El-Hady, M. A.; Ramadan, A. B.

    2012-05-01

    The modification of the compatibility between polyethylene (PE) and polypropylene (PP) by using irradiated PE wax (PE wax) is the purpose of this study. In this part, polymer blends based on various ratios of PE and PP were blended with 2.5% PE wax in all the blend ratios to determine the optimum ratio of the blend to be compatabilized. The influence of PE wax as a compatibilizing agent for PE and PP blend was investigated through the measurements of thermal, mechanical and morphological properties. The PP/PE blends modified by this method showed higher mechanical properties than those of the unmodified blends. Also, stress and strain of the modified blend having ratio (60/40) PP/PE blend recorded the maximum mechanical behavior. Scanning electron microscopy (SEM) micrographs of modified blends showed an indication of strong interfacial adhesion and a smooth continuous surface in which giving a support to the effect of irradiated PE wax as a tool for improving the compatibility.

  17. DELIVERY OF THERAPEUTIC PROTEINS

    PubMed Central

    Pisal, Dipak S.; Kosloski, Matthew P.; Balu-Iyer, Sathy V.

    2009-01-01

    The safety and efficacy of protein therapeutics are limited by three interrelated pharmaceutical issues, in vitro and in vivo instability, immunogenicity and shorter half-lives. Novel drug modifications for overcoming these issues are under investigation and include covalent attachment of poly(ethylene glycol) (PEG), polysialic acid, or glycolic acid, as well as developing new formulations containing nanoparticulate or colloidal systems (e.g. liposomes, polymeric microspheres, polymeric nanoparticles). Such strategies have the potential to develop as next generation protein therapeutics. This review includes a general discussion on these delivery approaches. PMID:20049941

  18. Comparison of Polyethylene Glycol-Electrolyte Solution vs Polyethylene Glycol-3350 for the Treatment of Fecal Impaction in Pediatric Patients

    PubMed Central

    Boles, Erin E.; Gaines, Cameryn L.

    2015-01-01

    OBJECTIVES: The objective of this study was to evaluate the safety and efficacy of polyethylene glycol-electrolyte solution vs polyethylene glycol-3350 for the treatment of fecal impaction in pediatric patients. METHODS: A retrospective, observational, institutional review board–approved study was conducted over a 1-year time period. Patients were included in the study if they were admitted to the hospital with a diagnosis of fecal impaction or constipation and were treated with either polyethylene glycol-electrolyte solution (PEG-ES) or polyethylene glycol-3350 (PEG-3350). Patients were excluded if they were discharged prior to resolution of treatment and/or did not receive PEG-ES or PEG-3350. RESULTS: Fifty-one patients (ranging in age from 1 month to 15 years) were evaluated: 23 patients received PEG-ES and 28 patients received PEG-3350. Sex, race, age, and weight were not statistically different between the 2 groups. Resolution of fecal impaction was not significantly different between PEG-ES vs PEG-3350 (87% and 86%, respectively; p = 0.87). There was only 1 reported side effect with PEG-3350, vs 11 reported side effects with PEG-ES (p < 0.01). CONCLUSIONS: Theses results suggest that PEG-3350 is as effective as PEG-ES for the treatment of fecal impaction in pediatric patients and is associated with fewer side effects. PMID:26170773

  19. Solvent effect in the polyethylene recovery from multilayer postconsumer aseptic packaging.

    PubMed

    Cervantes-Reyes, Alejandro; Núñez-Pineda, Alejandra; Barrera-Díaz, Carlos; Varela-Guerrero, Víctor; Martínez-Barrera, Gonzalo; Cuevas-Yañez, Erick

    2015-04-01

    Polyethylene films were separated and recovered from polyethylene-aluminum composites derived from recycling multilayer postconsumer aseptic packaging. A brief study about the separation process by dissolving PE-aluminum (PE-Al) composites into a series of organic solvents with a combination of time and temperature is presented. Through this procedure, 56% polyethylene is recovered from this kind of composites in optimized conditions. DSC and TGA studies were performed to determine the thermal stability of recovered polyethylene films and to establish a comparison with a PE reference commercial product, demonstrating that recovered polyethylene films kept their thermal properties. PMID:25681948

  20. Heteromerous interactions among glycolytic enzymes and of glycolytic enzymes with F-actin: effects of poly(ethylene glycol).

    PubMed

    Walsh, J L; Knull, H R

    1988-01-01

    Interactions of glucose-6-phosphate isomerase (D-glucose-6-phosphate ketol-isomerase, EC 5.3.1.9), aldolase (D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate lyase, EC 4.1.2.13), glyceraldehyde-3-phosphate dehydrogenase (D-glyceraldehyde-3-phosphate:NAD+ oxidoreductase (phosphorylating), EC 1.2.1.12), triose-phosphate isomerase (D-glyceraldehyde-3-phosphate ketol-isomerase, EC 5.3.1.1), phosphoglycerate mutase (D-phosphoglycerate 2,3-phosphomutase, EC 5.4.2.1), phosphoglycerate kinase (ATP:3-phospho-D-glycerate 1-phosphotransferase, EC 2.7.3), enolase (2-phospho-D-glycerate hydro-lyase, EC 4.2.1.11), pyruvate kinase (ATP:Pyruvate O2-phosphotransferase, EC 2.7.1.40) and lactate dehydrogenase [S)-lactate:NAD+ oxidoreductase, EC 1.1.1.27) with F-actin, among the glycolytic enzymes listed above, and with phosphofructokinase (ATP:D-fructose-6-phosphate 1-phosphotransferase, EC 2.7.1.11) were studied in the presence of poly(ethylene glycol). Both purified rabbit muscle enzymes and rabbit muscle myogen, a high-speed supernatant fraction containing the glycolytic enzymes, were used to study enzyme-F-actin interactions. Following ultracentrifugation, F-actin and poly(ethylene glycol) tended to increase and KCl to decrease the pelleting of enzymes. In general, the greater part of the pelleting occurred in the presence of both F-actin and poly(ethylene glycol) and the absence of KCl. Enzymes that pelleted more in myogen preparations than as individual purified enzymes in the presence of poly(ethylene glycol) and the absence of F-actin were tested for specific enzyme-enzyme associations, several of which were observed. Such interactions support the view that the internal cell structure is composed of proteins that interact with one another to form the microtrabecular lattice. PMID:3334856

  1. Modification of macroporous silica gel with polyethylene glycol by exposure to radiation

    SciTech Connect

    Garkavenko, L.G.; Kiselev, A.V.; Nikitin, Yu.S.; Topchieva, I.N.

    1986-11-01

    Samples of KSK-1 macroporous silica gel with a surface modified by different amounts of polyethylene glycol (PEG) have been prepared by exposure to radiation. The influence of the method of coating with 20,000 PEG, the nature of the solvent used, and the radiation dose on its content in the modified samples after prolonged washing with water has been studied. The modified samples have been used to investigate the adsorption of serum albumin from aqueous solutions. The adsorption of albumin on silica gel coated with 1.2-1.5 mg/m/sup 2/ of polymer is significantly reduced in comparison with the untreated silica gel; no adsorption of protein occurs at PEG contents of > 1.6 mg/m/sup 2/.

  2. Poly(ethylene glycol)-Prodrug Conjugates: Concept, Design, and Applications

    PubMed Central

    Banerjee, Shashwat S.; Aher, Naval; Patil, Rajesh; Khandare, Jayant

    2012-01-01

    Poly(ethylene glycol) (PEG) is the most widely used polymer in delivering anticancer drugs clinically. PEGylation (i.e., the covalent attachment of PEG) of peptides proteins, drugs, and bioactives is known to enhance the aqueous solubility of hydrophobic drugs, prolong circulation time, minimize nonspecific uptake, and achieve specific tumor targetability through the enhanced permeability and retention effect. Numerous PEG-based therapeutics have been developed, and several have received market approval. A vast amount of clinical experience has been gained which has helped to design PEG prodrug conjugates with improved therapeutic efficacy and reduced systemic toxicity. However, more efforts in designing PEG-based prodrug conjugates are anticipated. In light of this, the current paper highlights the synthetic advances in PEG prodrug conjugation methodologies with varied bioactive components of clinical relevance. In addition, this paper discusses FDA-approved PEGylated delivery systems, their intended clinical applications, and formulations under clinical trials. PMID:22645686

  3. Preventing corona effects: multiphosphonic acid poly(ethylene glycol) copolymers for stable stealth iron oxide nanoparticles.

    PubMed

    Torrisi, V; Graillot, A; Vitorazi, L; Crouzet, Q; Marletta, G; Loubat, C; Berret, J-F

    2014-08-11

    When dispersed in biological fluids, engineered nanoparticles are selectively coated with proteins, resulting in the formation of a protein corona. It is suggested that the protein corona is critical in regulating the conditions of entry into the cytoplasm of living cells. Recent reports describe this phenomenon as ubiquitous and independent of the nature of the particle. For nanomedicine applications, however, there is a need to design advanced and cost-effective coatings that are resistant to protein adsorption and that increase the biodistribution in vivo. In this study, phosphonic acid poly(ethylene glycol) copolymers were synthesized and used to coat iron oxide particles. The copolymer composition was optimized to provide simple and scalable protocols as well as long-term stability in culture media. It is shown that polymers with multiple phosphonic acid functionalities and PEG chains outperform other types of coating, including ligands, polyelectrolytes, and carboxylic acid functionalized PEG. PEGylated particles exhibit moreover exceptional low cellular uptake, of the order of 100 femtograms of iron per cell. The present approach demonstrates that the surface chemistry of engineered particles is a key parameter in the interactions with cells. It also opens up new avenues for the efficient functionalization of inorganic surfaces. PMID:25046557

  4. Controlling Affinity Binding with Peptide-Functionalized Poly(ethylene glycol) Hydrogels**

    PubMed Central

    Lin, Chien-Chi; Anseth, Kristi S.

    2009-01-01

    Poly(ethylene glycol) (PEG) hydrogels functionalized with peptide moieties have been widely used in regenerative medicine applications. While many studies have suggested the importance of affinity binding within PEG hydrogels, the relationships between the structures of the peptide motifs and their binding to protein therapeutics remain largely unexplored, especially in the recently developed thiol-acrylate photopolymerization systems. Herein, we employ Förster resonance energy transfer (FRET) and thiol-acrylate photopolymerizations to investigate how the architectures of affinity peptides in crosslinked hydrogels affect their binding to diffusible proteins. The binding between diffusible streptavidin and biotinylated peptide immobilized to PEG hydrogel network was used as a model system to reveal the interplay between affinity binding and peptide sequences/architectures. In addition, we design peptides with different structures to enhance affinity binding within PEG hydrogels and to provide tunable affinity-based controlled delivery of basic fibroblast growth factor (bFGF). This study demonstrates the importance of affinity binding in controlling the availability of hydrogel-encapsulated proteins and provides strategies for enhancing affinity binding of protein therapeutics to bound peptide moieties in thiol-acrylate photopolymerized PEG hydrogels. The results presented herein should find useful on the design and fabrication of hydrogels to retain and sustained release of growth factors for promoting tissue regeneration. PMID:20148198

  5. Preferences for foods varying in macronutrients and tannins by lambs supplemented with polyethylene glycol.

    PubMed

    Titus, C H; Provenza, F D; Perevolotsky, A; Silanikove, N

    2000-06-01

    Supplemental polyethylene glycol (PEG) increases intake when animals eat foods high in tannins, but little is known about how PEG affects preference for foods that vary in concentrations of macronutrients and tannin. We investigated how varying macronutrients and tannins (commercially available extracts from quebracho trees) affected food intake, and we assessed the degree to which PEG (MW 3350) affected intake of tannin-rich foods by sheep. From 0715 to 1800 daily, lambs were offered diets that varied in concentrations of macronutrients: high energy/low protein (75% barley/25% alfalfa), medium energy/medium protein (35% barley/65% alfalfa), and low energy/high protein (100% alfalfa). Preference for these diets was determined in the absence of tannin, and then, in Trials 1 to 3, tannin was added in increasing concentrations (from 5 to 20%) to the diets with high and medium levels of energy. In Trial 4, tannin (10%) also was added to the low-energy diet. Lambs were supplemented with either 50 g of PEG mixed with 50 g of ground barley or 50 g of ground barley alone from 0700 to 1715 daily; lambs always consumed all of these supplements. In the absence of added tannins, all lambs preferred high energy/low protein > medium energy/medium protein > low energy/high protein. As tannin levels increased, preference for the high- and medium-energy foods decreased, and all lambs preferred foods that were lower in tannins and higher in protein. Lambs supplemented with PEG ate more macronutrients and tannins than unsupplemented lambs, and the effect became increasingly apparent as tannin levels increased from Trials 1 to 4. We conclude that the effectiveness of supplemental PEG may be low if alternative forages are equal or superior in nutritional quality and contain fewer metabolites with adverse effects. In such cases, animals would likely prefer alternatives to high-tannin foods. PMID:10875625

  6. Synergistic effect of polyethylene glycol with arginine on the prevention of heat-induced aggregation of lysozyme

    NASA Astrophysics Data System (ADS)

    Tomita, S.; Hamada, H.; Nagasaki, Y.; Shiraki, K.

    2008-03-01

    . Arginine (Arg) is a commonly used additive to prevent protein aggregation and inactivation in denaturing solutions. This paper presents new findings on the synergistic effect on the prevention of heat-induced aggregation of lysozyme using Arg in combination with polyethylene glycol (PEG). The synergistic enhancement was observed in the presence of Arg with amphiphilic polymers, such as PEG6000, PEG20000, and poly(vinyl pyrrolidone), while it was not observed with hydrophilic polymers, such as PEG200, Poly(acrylic acid), poly(vinyl alcohol), dextran, and Ficoll 70.

  7. Radiation grafting of styrene and acrylonitrile to cellulose and polyethylene

    NASA Astrophysics Data System (ADS)

    Hassanpour, S.

    1999-06-01

    Radiation induced graft polymerization is one of the best methods for obtaining material with new properties. In this work, radiation grafting of styrene, mixture of styrene and acrylonitrile to cellulose and polyethylene in the presence of methanol as a solvent by mutual method is discussed. At a low dose rate, high grafting yields were obtained from the two systems used, due to lesser termination of free radicals with the polymer growing radicals and recombination of primary radicals, resulting in a longer chain length of the grafted copolymer. In the system of styrene and acrylonitrile, comonomer technique was used and the styrene controlled the homopolymer formation during graft polymerization. Water uptake of cellulose decreased by increasing the grafting yields. Grafted cellulose can be molded to some extent and in a high percent of grafting, a new transparent material was obtained. By radiation grafting of styrene-acrylonitrile to low density polyethylene a high degree of crosslinking was observed.

  8. Strength of polyethylene, polypropylene and polystyrene behind a shock front

    SciTech Connect

    Tyler, C. E.; Bourne, N. K.; Millett, J. C. F.

    2007-12-12

    There is a recent interest in the response of thermoplastics to shock. Previous work on three simple hydrocarbons has indicated that the shear strength increases with the complexity of the side group. Strength values have been calculated using lateral stress measurements with manganin gauges that have been recalibrated for use in the low stress regime. The present work aims to investigate the effect of the configuration of the thermoplastic's chain when side groups are added. Results show that whilst polyethylene has the lowest shear strength, polypropylene and polystyrene have similar values. In all cases the strength of polymer increases with time after the shock has past. As the applied stress increases, polystrene and polypropylene strengthen to a higher degree when compared with polyethylene. Explanations are offered in terms of microstructure and tacticity of the chain.

  9. Product analysis for polyethylene degradation by radiation and thermal ageing

    NASA Astrophysics Data System (ADS)

    Sugimoto, Masaki; Shimada, Akihiko; Kudoh, Hisaaki; Tamura, Kiyotoshi; Seguchi, Tadao

    2013-01-01

    The oxidation products in crosslinked polyethylene for cable insulation formed during thermal and radiation ageing were analyzed by FTIR-ATR. The products were composed of carboxylic acid, carboxylic ester, and carboxylic anhydride for all ageing conditions. The relative yields of carboxylic ester and carboxylic anhydride increased with an increase of temperature for radiation and thermal ageing. The carboxylic acid was the primary oxidation product and the ester and anhydride were secondary products formed by the thermally induced reactions of the carboxylic acids. The carboxylic acid could be produced by chain scission at any temperature followed by the oxidation of the free radicals formed in the polyethylene. The results of the analysis led to formulation of a new oxidation mechanism which was different from the chain reactions via peroxy radicals and peroxides.

  10. MOBILE TIBIAL POLYETHYLENE BEARING IN TOTAL KNEE ARTHROPLASTY

    PubMed Central

    de Araújo Barros Cobra, Hugo Alexandre; da Palma, Idemar Monteiro

    2015-01-01

    Debris of polyethylene tibial bearings have been recognized as a major cause for the onset of the cascade of biological events leading to osteolysis and loosening of prosthetic components after total knee arthroplasty. Since then, research has been focused on alternative bearing surfaces in order to minimize the amount and rate of polyethylene wear off and, in doing so, increasing the survivorship rate for knee arthroplasties. One such option is to have a mobile tibial bearing allowing more conformity and rotational self-alignment of the components, improving kinetics and kinematics of the prosthesis. The authors present a resumed but throughout and comprehensive review of the rationale, biomechanics fundamentals, indications, pitfalls, outcomes and complications for the use of mobile tibial bearings in total knee replacement. PMID:27077055

  11. Polyethylene encapsulation full-scale technology demonstration. Final report

    SciTech Connect

    Kalb, P.D.; Lageraaen, P.R.

    1994-10-01

    A full-scale integrated technology demonstration of a polyethylene encapsulation process, sponsored by the US Department of Energy (DOE) Office of Technology Development (OTD), was conducted at the Environmental & Waste Technology Center at Brookhaven National Laboratory (BNL.) in September 1994. As part of the Polymer Solidification National Effort, polyethylene encapsulation has been developed and tested at BNL as an alternative solidification technology for improved, cost-effective treatment of low-level radioactive (LLW), hazardous and mixed wastes. A fully equipped production-scale system, capable of processing 900 kg/hr (2000 lb/hr), has been installed at BNL. The demonstration covered all facets of the integrated processing system including pre-treatment of aqueous wastes, precise feed metering, extrusion processing, on-line quality control monitoring, and process control.

  12. Hyperthermal atomic oxygen reactions with kapton and polyethylene. [in LEO

    NASA Technical Reports Server (NTRS)

    Cross, J. B.; Koontz, S. L.; Gregory, J. C.; Edgell, M. J.

    1990-01-01

    Gas phase reaction products produced by the interaction of high kinetic energy (1-3 eV) 3p ground state atomic oxygen (AO) with polyethylene and kapton were found to be H2, H2O, CO, and CO2 with NO being a possible secondary product from kapton. Hydrogen abstraction at high AO kinetic energy is postulated to be the key reaction controlling the erosion rate of kapton and polyethylene. An Arrhenius-like expression having an activation barrier of 0.4 eV can be fit to the data, which suggests that the rate limiting step in the AO/kapton reaction mechanism can be overcome by translational energy.

  13. Study of the Auger line shape of polyethylene and diamond

    NASA Technical Reports Server (NTRS)

    Dayan, M.; Pepper, S. V.

    1984-01-01

    The KVV Auger electron line shapes of carbon in polyethylene and diamond have been studied. The spectra were obtained in derivative form by electron beam excitation. They were treated by background subtraction, integration and deconvolution to produce the intrinsic Auger line shape. Electron energy loss spectra provided the response function in the deconvolution procedure. The line shape from polyethylene is compared with spectra from linear alkanes and with a previous spectrum of Kelber et al. Both spectra are compared with the self-convolution of their full valence band densities of states and of their p-projected densities. The experimental spectra could not be understood in terms of existing theories. This is so even when correlation effects are qualitatively taken into account account to the theories of Cini and Sawatzky and Lenselink.

  14. DSC melting behavior of irradiated low density polyethylenes containing antioxidants

    NASA Astrophysics Data System (ADS)

    Gal, O.; Kostoski, D.; Babić, D.; Stannett, V. T.

    The effect of antioxidants (0.5 wt% content) on the melting behaviour of low density polyethylenes, one branched and one linear, was examined with data obtained by DSC. The two polyethylenes exhibit noticeable differences in pure form; LLDPE has a higher melting point, lower heat of fusion and a more complex fusion endotherm than LDPE. The addition of antioxidants has a scarcely noticeable influence on the melting behaviour of LDPE whether irradiated or not, while in the case of LLDPE the effect is more visible. However, a careful analysis of the observed characteristics, peak temperatures and lamellae thickness distribution as well as heat of fusion, show that the observed effects are appearing as the consequence of chemical processes, scission and crosslinking, which occur in PE under either thermomechanical action (mixing in the course of the sample preparation), or radiation.

  15. Void morphology in polyethylene/carbon black composites

    SciTech Connect

    Marr, D.W.M.; Wartenberg, M.; Schwartz, K.B.

    1996-12-31

    A combination of small angle neutron scattering (SANS) and contrast matching techniques is used to determine the size and quantity of voids incorporated during fabrication of polyethylene/carbon black composites. The analysis used to extract void morphology from SANS data is based on the three-phase model of microcrack determination via small angle x-rayscattering (SAXS) developed by W.Wu{sup 12} and applied to particulate reinforced composites.

  16. The Structural Dilemma of Bulk Polyethylene: An Intermediary Structure

    PubMed Central

    Laridjani, Morteza; Leboucher, Pierre

    2009-01-01

    Background The Fourier space (reciprocal space) image of bulk polyethylene consists of lines superimposed on the coherent diffuse background. The mixed character of the image indicates the complex nature of these compounds. The inability in detecting full images of reciprocal space of polymeric substances without Compton radiation and the other undesirable diffuse scatterings has misled the structural analysis (structural characterisation) of these materials. Principal Findings We propose the use of anomalous diffractometry where, it is possible to obtain a real image of reciprocal space without Compton radiation and other undesirable scatterings. By using classical diffractometry techniques this procedure is not possible. This methodology permitted us to obtain the “Direct Delta function”, in the case of polycrystalline substances that was not previously detected. A new procedure was proposed to interpret the image of reciprocal space of bulk polyethylene. The results show the predominance of the geometry of local order determination compared to the crystal unit cell. The analysis of x-ray diffraction images illustrates that the elementary structural unit is a tetrahedron. This structural unit illustrates the atoms in the network scatter in a coherent diffuse manner. Moreover, the interference function derived from the coherent diffuse scattering dampens out quickly and the degree of randomness is superior to a liquid state. The radial distribution function derived from this interference function shows bond shortening in the tetrahedron configuration. It is this particular effect, which stabilises polyethylene. Conclusion Here we show by anomalous diffractometry that the traditional concept of the two-phase or the crystal-defect model is an oversimplification of the complex reality. The exploitation of anomalous diffractometry has illustrated that polyethylene has an intermediate ordered structure. PMID:19597553

  17. Critical experiment with uranium diluted with concrete and polyethylene

    SciTech Connect

    Sanchez, R.; Loaiza, D.; Kimpland, R.

    2006-07-01

    An experiment has been performed combining highly enriched uranium, a hydrogenous moderator (polyethylene), and concrete. The purpose of the experiment was to provide additional criticality data that can be used to verify and validate criticality safety evaluations in support of the decommissioning of nuclear facilities throughout the Dept. of Energy complex. In this experiment, criticality was observed as a function time due to the curing and drying processes that occurred in the concrete. (authors)

  18. Polyethylene Glycol (PEG)-Induced Anaphylactic Reaction During Bowel Preparation

    PubMed Central

    2015-01-01

    Barium enema is used to screen patients with gastrointestinal bleeding who do not want to undergo colonoscopy. Polyethylene glycol (PEG) is usually the bowel preparation of choice. Few allergic reactions from this product have been reported; these include urticaria, angioedema, and anaphylaxis. Reactions are thought to result from a small amount of PEG crossing the intestinal mucosa, which, in some patients, is sufficient to provoke an anaphylactic reaction. PMID:26203443

  19. Do Polyethylene Plastic Covers Affect Smoke Emissions from Debris Piles?

    NASA Astrophysics Data System (ADS)

    Weise, D. R.; Jung, H.; Cocker, D.; Hosseini, E.; Li, Q.; Shrivastava, M.; McCorison, M.

    2010-12-01

    Shrubs and small diameter trees exist in the understories of many western forests. They are important from an ecological perspective; however, this vegetation also presents a potential hazard as “ladder fuels” or as a heat source to damage the overstory during prescribed burns. Cutting and piling of this material to burn under safe conditions is a common silvicultural practice. To improve ignition success of the piled debris, polyethylene plastic is often used to cover a portion of the pile. While burning of piled forest debris is an acceptable practice in southern California from an air quality perspective, inclusion of plastic in the piles changes these debris piles to rubbish piles which should not be burned. With support from the four National Forests in southern California, we conducted a laboratory experiment to determine if the presence of polyethylene plastic in a pile of burning wood changed the smoke emissions. Debris piles in southern California include wood and foliage from common forest trees such as sugar and ponderosa pines, white fir, incense cedar, and California black oak and shrubs such as ceanothus and manzanita in addition to forest floor material and dirt. Manzanita wood was used to represent the debris pile in order to control the effects of fuel bed composition. The mass of polyethylene plastic incorporated into the pile was 0, 0.25 and 2.5% of the wood mass—a range representative of field conditions. Measured emissions included NOx, CO, CO2, SO2, polycyclic and light hydrocarbons, carbonyls, particulate matter (5 to 560 nm), elemental and organic carbon. The presence of polyethylene did not alter the emissions composition from this experiment.

  20. Post-irradiation effects in polyethylenes irradiated under various atmospheres

    NASA Astrophysics Data System (ADS)

    Suljovrujic, E.

    2013-08-01

    If a large amount of polymer free radicals remain trapped after irradiation of polymers, the post-irradiation effects may result in a significant alteration of physical properties during long-term shelf storage and use. In the case of polyethylenes (PEs) some failures are attributed to the post-irradiation oxidative degradation initiated by the reaction of residual free radicals (mainly trapped in crystal phase) with oxygen. Oxidation products such as carbonyl groups act as deep traps and introduce changes in carrier mobility and significant deterioration in the PEs electrical insulating properties. The post-irradiation behaviour of three different PEs, low density polyethylene (LDPE), linear low density polyethylene (LLDPE) and high density polyethylene (HDPE) was studied; previously, the post-irradiation behaviour of the PEs was investigated after the irradiation in air (Suljovrujic, 2010). In this paper, in order to investigate the influence of different irradiation media on the post-irradiation behaviour, the samples were irradiated in air and nitrogen gas, to an absorbed dose of 300 kGy. The annealing treatment of irradiated PEs, which can substantially reduce the concentration of free radicals, is used in this study, too. Dielectric relaxation behaviour is related to the difference in the initial structure of PEs (such as branching, crystallinity etc.), to the changes induced by irradiation in different media and to the post-irradiation changes induced by storage of the samples in air. Electron spin resonance (ESR), differential scanning calorimetry (DSC), infra-red (IR) spectroscopy and gel measurements were used to determine the changes in the free radical concentration, crystal fraction, oxidation and degree of network formation, respectively.

  1. Ultrasound-enhanced enzymatic hydrolysis of poly(ethylene terephthalate).

    PubMed

    Pellis, Alessandro; Gamerith, Caroline; Ghazaryan, Gagik; Ortner, Andreas; Herrero Acero, Enrique; Guebitz, Georg M

    2016-10-01

    The application of ultrasound was found to enhance enzymatic hydrolysis of poly(ethylene terephthalate) (PET). After a short activation phase up to 6.6times increase in the amount of released products was found. PET powder with lower crystallinity of 8% was hydrolyzed faster when compared to PET with 28% crystallinity. Ultrasound activation was found to be around three times more effective on powders vs. films most likely due to a larger surface area accessible to the enzyme. PMID:27481467

  2. Porous polyethylene implants in facial reconstruction: Outcome and complications.

    PubMed

    Ridwan-Pramana, Angela; Wolff, Jan; Raziei, Ashkan; Ashton-James, Claire E; Forouzanfar, Tymour

    2015-10-01

    The aim of the present study was to assess the indications, results and complications of patients treated with porous polyethylene (Medpor(®)) implants in the Department of Oral and Maxillofacial Surgery of VU Medical Centre, Amsterdam over 17 years. A total of 69 high-density porous polyethylene implants (Medpor(®) Biomaterial; Porex Surgical, Newman, GA) were used in forty patients (22 males, 18 females). All patients were analysed for gender, age, diagnosis, indications for surgery, follow-up period and postoperative complications. A mean age of 34.1 years was observed. The main reason for implant surgery was post-traumatic functional impairment (27.5%). Most implants were placed at the mandibular angel and the orbital floor. Unsatisfactory appearance scored the highest in postoperative complications (10.1%) followed by infection rate (7.2%). Comparing the number of implants placed over the years and the incidence of complications, makes the overall complications rate of porous polyethylene very low. A consensus about antibiotic prophylaxis is needed. The objective measurements in patient satisfaction and proper implant design would be of great use. PMID:26276064

  3. Impact resistance and fractography in ultra high molecular weight polyethylenes.

    PubMed

    Puértolas, J A; Pascual, F J; Martínez-Morlanes, M J

    2014-02-01

    Highly crosslinked ultra high molecular weight polyethylenes (UHMWPE) stabilized by a remelting process or by the addition of an antioxidant are highly wear resistant and chemically stable. However, these polyethylenes currently used in total joint replacements suffer a loss of mechanical properties, especially in terms of fracture toughness. In this study we analyze the impact behavior of different polyethylenes using an instrumented double notch Izod test. The materials studied are three resins: GUR1050, GUR1020 with 0.1wt% of vitamin E, and MG003 with 0.1wt% of vitamin E. These resins were gamma irradiated at 90kGy, and pre and post-irradiation remelting processes were applied to GUR1050 for two different time periods. Microstructural data were determined by means of differential scanning calorimetry and transmission electron microscopy. Fractography carried out on the impact fracture surfaces and images obtained by scanning electron microscopy after etching indicated the existence of a fringe structure formed by consecutive ductile-brittle and brittle-ductile transitions, which is related to the appearance of discontinuities in the load-deflection curves. A correlation has been made of the macroscopic impact strength results and the molecular chain and microstructural characteristics of these aforementioned materials, with a view to designing future resins with improved impact resistance. The use of UHMWPE resins with low molecular weight or the application of a remelting treatment could contribute to obtain a better impact strength behavior. PMID:24275347

  4. Testing and evaluation of polyethylene and sulfur cement waste forms

    SciTech Connect

    Franz, E.M.; Kalb, P.D.; Colombo, P.

    1985-01-01

    This paper discusses the results of recent studies related to the use of polyethylene and modified sulfur cement as new binder materials for the improved solidification of low-level wastes. Waste streams selected for this study include those which result from advanced volume reduction technologies (dry evaporator concentrate salts and incinerator ash) and those that remain problematic for solidification using contemporary agents (ion-exchange resins). Maximum waste loadings were determined for each waste type. Recommended waste loadings of 70 wt % sodium sulfate, 50 wt % boric acid, 40 wt % incinerator ash and 30 wt % ion exchange resins, which are based on process control and waste form performance considerations are reported for polyethylene. For sulfur cement the recommended waste loadings of 40 wt % sodium sulfate and boric acid salts and 43 wt % incinerator ash are reported. However, incorporation of ion-exchange resin waste in modified sulfur cement is not recommended due to poor waste form performance. The work presented in this paper will, in part, present data that can be used to assess the acceptability of polyethylene and modified sulfur cement waste forms to meet the requirements of 10 CFR 61. 8 refs., 10 figs., 6 tabs.

  5. Polyethylene macroencapsulation - mixed waste focus area. OST reference No. 30

    SciTech Connect

    1998-02-01

    The lead waste inventory throughout the US Department of Energy (DOE) complex has been estimated between 17 million and 24 million kilograms. Decontamination of at least a portion of the lead is viable but at a substantial cost. Because of various problems with decontamination and its limited applicability and the lack of a treatment and disposal method, the current practice is indefinite storage, which is costly and often unacceptable to regulators. Macroencapsulation is an approved immobilization technology used to treat radioactively contaminated lead solids and mixed waste debris. (Mixed waste is waste materials containing both radioactive and hazardous components). DOE has funded development of a polyethylene extrusion macroencapsulation process at Brookhaven National Laboratory (BNL) that produces a durable, leach-resistant waste form. This innovative macroencapsulation technology uses commercially available single-crew extruders to melt, convey, and extrude molten polyethylene into a waste container in which mixed waste lead and debris are suspended or supported. After cooling to room temperature, the polyethylene forms a low-permeability barrier between the waste and the leaching media.

  6. Wear Analysis in THA Utilizing Oxidized Zirconium and Crosslinked Polyethylene

    PubMed Central

    Garvin, Kevin L.; Mangla, Jimmi; Murdoch, Nathan; Martell, John M.

    2008-01-01

    Oxidized zirconium, a material with a ceramic surface on a metal substrate, and highly cross-linked polyethylene are two materials developed to reduce wear. We measured in vivo femoral head penetration in patients with these advanced bearings. We hypothesized the linear wear rates would be lower than those published for cobalt-chrome and standard polyethylene. We retrospectively reviewed a select series of 56 THAs in a relatively young, active patient population utilizing oxidized zirconium femoral heads and highly cross-linked polyethylene acetabular liners. Femoral head penetration was determined using the Martell computerized edge-detection method. All patients were available for 2-year clinical and radiographic followup. True linear wear was 4 μm/year (95% confidence intervals, ± 59 μm/year). The early wear rates in this cohort of relatively young, active patients were low and we believe justify the continued study of these alternative bearing surfaces. Level of Evidence: Level IV, therapeutic study. See the Guidelines for Authors for a complete description of levels of evidence. PMID:18946711

  7. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Boric acid (H3BO3), mixed esters with... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol... NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.1729...

  8. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Boric acid (H3BO3), mixed esters with... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol... NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.1729...

  9. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Boric acid (H3BO3), mixed esters with... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol... NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.1729...

  10. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Boric acid (H3BO3), mixed esters with... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol... NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.1729...

  11. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Boric acid (H3BO3), mixed esters with... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol... NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.1729...

  12. On the spectral behavior of an ionic styryl dye: effect of micelle-polyethylene-block-polyethylene glycol diblock copolymer assembly.

    PubMed

    Sahoo, Dibakar; Bhattacharya, Prosenjit; Chakravorti, Sankar

    2009-10-15

    The interaction of anionic micelle sodium dodecyl sulfate (SDS) and amphiphilic block copolymers polyethylene-b-polyethylene glycol (PE-b-PEG) and the sharp change of excited-state charge-transfer complex photophysics of 2-(4-(dimethylamino)styryl)-1-methylpyridinium iodide (DASPMI) inside of the supramolecular assembly have been addressed in the paper. The dramatic enhancement of emission intensity of DASPMI incorporated inside of the nanostructure formed by micellar and polymeric chains indicates a completely different environment compared to that in the water and micellar system. A huge increase in the rotational relaxation time obtained from time-resolved anisotropy decay and the value of the order parameter is indicative of a very restrictive regime in the self-assembly system. The wobbling and translational motion of the probe is also restricted inside of the micelle-polymer aggregate due to the presence of polymer chains. The translational diffusion coefficient is drastically reduced due to the aggregation. PMID:19761273

  13. Dense Poly(ethylene glycol) Brushes Reduce Adsorption and Stabilize the Unfolded Conformation of Fibronectin.

    PubMed

    Faulón Marruecos, David; Kastantin, Mark; Schwartz, Daniel K; Kaar, Joel L

    2016-03-14

    Polymer brushes, in which polymers are end-tethered densely to a grafting surface, are commonly proposed for use as stealth coatings for various biomaterials. However, although their use has received considerable attention, a mechanistic understanding of the impact of brush properties on protein adsorption and unfolding remains elusive. We investigated the effect of the grafting density of poly(ethylene glycol) (PEG) brushes on the interactions of the brush with fibronectin (FN) using high-throughput single-molecule tracking methods, which directly measure protein adsorption and unfolding within the brush. We observed that, as grafting density increased, the rate of FN adsorption decreased; however, surface-adsorbed FN unfolded more readily, and unfolded molecules were retained on the surface for longer residence times relative to those of folded molecules. These results, which are critical for the rational design of PEG brushes, suggest that there is a critical balance between protein adsorption and conformation that underlies the utility of such brushes in physiological environments. PMID:26866385

  14. Grafting of poly(ethylene glycol) on click chemistry modified Si(100) surfaces.

    PubMed

    Flavel, Benjamin S; Jasieniak, Marek; Velleman, Leonora; Ciampi, Simone; Luais, Erwann; Peterson, Joshua R; Griesser, Hans J; Shapter, Joe G; Gooding, J Justin

    2013-07-01

    Poly(ethylene glycol) (PEG) is one of the most extensively studied antifouling coatings due to its ability to reduce protein adsorption and improve biocompatibility. Although the use of PEG for antifouling coatings is well established, the stability and density of PEG layers are often inadequate to provide optimum antifouling properties. To improve on these shortcomings, we employed the stepwise construction of PEG layers onto a silicon surface. Acetylene-terminated alkyl monolayers were attached to nonoxidized crystalline silicon surfaces via a one-step hydrosilylation procedure with 1,8-nonadiyne. The acetylene-terminated surfaces were functionalized via a copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of the surface-bound alkynes with an azide to produce an amine terminated layer. The amine terminated layer was then further conjugated with PEG to produce an antifouling surface. The antifouling surface properties were investigated by testing adsorption of human serum albumin (HSA) and lysozyme (Lys) onto PEG layers from phosphate buffer solutions. Detailed characterization of protein fouling was carried out with X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) combined with principal component analysis (PCA). The results revealed no fouling of albumin onto PEG coatings whereas the smaller protein lysozyme adsorbed to a very low extent. PMID:23790067

  15. Nanostructured antifouling poly(ethylene glycol) films for silicon-based microsystems.

    PubMed

    Sharma, Sadhana; Desai, Tejal A

    2005-02-01

    The creation of antifouling surfaces is one of the major prerequisites for silicon-based micro-electrical-mechanical systems for biomedical and analytical applications (known as BioMEMS). Poly(ethylene glycol) (PEG), a water-soluble, nontoxic, and nonimmunogenic polymer has the unique ability to reduce nonspecific protein adsorption and cell adhesion and, therefore, is generally coupled with a wide variety of surfaces to improve their biocompatibility. To this end, we have analyzed PEG thin films of various grafting densities (i.e., number of PEG chains per unit area) coupled to silicon using a single-step PEG-silane coupling reaction scheme using variable-angle ellipsometry. Initial PEG concentration and coupling time were varied to attain different grafting densities. These data were theoretically analyzed to understand the phenomenon of PEG film formation. Furthermore, all the PEG films were evaluated for their ability to control biofouling using albumin and fibrinogen as the model proteins. PEG thin films formed by using higher PEG concentrations ( > or = 10 mM PEG) or coupling time ( > or = 1 h) demonstrated enhanced protein fouling resistance behavior. This analysis is expected to be useful to form PEG films of desired grafting density on silicon substrates for appropriate application. PMID:15853141

  16. Polyethylene glycol rinse solution: An effective way to prevent ischemia-reperfusion injury

    PubMed Central

    Zaouali, Mohamed Amine; Bejaoui, Mohamed; Calvo, Maria; Folch-Puy, Emma; Pantazi, Eirini; Pasut, Gianfranco; Rimola, Antoni; Ben Abdennebi, Hassen; Adam, René; Roselló-Catafau, Joan

    2014-01-01

    AIM: To test whether a new rinse solution containing polyethylene glycol 35 (PEG-35) could prevent ischemia-reperfusion injury (IRI) in liver grafts. METHODS: Sprague-Dawley rat livers were stored in University of Wisconsin preservation solution and then washed with different rinse solutions (Ringer’s lactate solution and a new rinse solution enriched with PEG-35 at either 1 or 5 g/L) before ex vivo perfusion with Krebs-Heinseleit buffer solution. We assessed the following: liver injury (transaminase levels), mitochondrial damage (glutamate dehydrogenase activity), liver function (bile output and vascular resistance), oxidative stress (malondialdehyde), nitric oxide, liver autophagy (Beclin-1 and LCB3) and cytoskeleton integrity (filament and globular actin fraction); as well as levels of metalloproteinases (MMP2 and MMP9), adenosine monophosphate-activated protein kinase (AMPK), heat shock protein 70 (HSP70) and heme oxygenase 1 (HO-1). RESULTS: When we used the PEG-35 rinse solution, reduced hepatic injury and improved liver function were noted after reperfusion. The PEG-35 rinse solution prevented oxidative stress, mitochondrial damage, and liver autophagy. Further, it increased the expression of cytoprotective heat shock proteins such as HO-1 and HSP70, activated AMPK, and contributed to the restoration of cytoskeleton integrity after IRI. CONCLUSION: Using the rinse solution containing PEG-35 was effective for decreasing liver graft vulnerability to IRI. PMID:25473175

  17. Mechanical, rheological, and bioactivity properties of ultra high-molecular-weight polyethylene bioactive composites containing polyethylene glycol and hydroxyapatite.

    PubMed

    Ahmad, Mazatusziha; Uzir Wahit, Mat; Abdul Kadir, Mohammed Rafiq; Mohd Dahlan, Khairul Zaman

    2012-01-01

    Ultrahigh-molecular-weight polyethylene/high-density polyethylene (UHMWPE/HDPE) blends prepared using polyethylene glycol PEG as the processing aid and hydroxyapatite (HA) as the reinforcing filler were found to be highly processable using conventional melt blending technique. It was demonstrated that PEG reduced the melt viscosity of UHMWPE/HDPE blend significantly, thus improving the extrudability. The mechanical and bioactive properties were improved with incorporation of HA. Inclusion of HA from 10 to 50 phr resulted in a progressive increase in flexural strength and modulus of the composites. The strength increment is due to the improvement on surface contact between the irregular shape of HA and polymer matrix by formation of mechanical interlock. The HA particles were homogenously distributed even at higher percentage showed improvement in wetting ability between the polymer matrix and HA. The inclusion of HA enhanced the bioactivity properties of the composite by the formation of calcium phosphate (Ca-P) precipitates on the composite surface as proven from SEM and XRD analysis. PMID:22666129

  18. Mechanical, Rheological, and Bioactivity Properties of Ultra High-Molecular-Weight Polyethylene Bioactive Composites Containing Polyethylene Glycol and Hydroxyapatite

    PubMed Central

    Ahmad, Mazatusziha; Wahit, Mat Uzir; Abdul Kadir, Mohammed Rafiq; Mohd Dahlan, Khairul Zaman

    2012-01-01

    Ultrahigh-molecular-weight polyethylene/high-density polyethylene (UHMWPE/HDPE) blends prepared using polyethylene glycol PEG as the processing aid and hydroxyapatite (HA) as the reinforcing filler were found to be highly processable using conventional melt blending technique. It was demonstrated that PEG reduced the melt viscosity of UHMWPE/HDPE blend significantly, thus improving the extrudability. The mechanical and bioactive properties were improved with incorporation of HA. Inclusion of HA from 10 to 50 phr resulted in a progressive increase in flexural strength and modulus of the composites. The strength increment is due to the improvement on surface contact between the irregular shape of HA and polymer matrix by formation of mechanical interlock. The HA particles were homogenously distributed even at higher percentage showed improvement in wetting ability between the polymer matrix and HA. The inclusion of HA enhanced the bioactivity properties of the composite by the formation of calcium phosphate (Ca-P) precipitates on the composite surface as proven from SEM and XRD analysis. PMID:22666129

  19. The Use of Polyethylene Glycol in Mammalian Herbivore Diet Studies: What Are We Measuring?

    PubMed

    Windley, Hannah R; Wigley, Hannah J; Ruscoe, Wendy A; Foley, William J; Marsh, Karen J

    2016-06-01

    Polyethylene glycol (PEG) has been used to study the intake and digestion of tannin-rich plants by mammalian herbivores because it preferentially binds to tannins. However, it is not clear whether the responses of herbivores to dietary PEG is due to increased protein availability from the release of tannin-bound protein, amelioration of tannin effects, or whether PEG also may bind to other compounds and change their activity in the gut. We used three native New Zealand tree species to measure the effect of PEG on the amount of foliage eaten by invasive common brushtail possums (Trichosurus vulpecula) and on in vitro digestible nitrogen (available N). The addition of PEG increased the in vitro available N content of Weinmannia racemosa foliage, and possums ate significantly more PEG-treated foliage than untreated foliage. However, possums also ate more PEG-treated Fuchsia excorticata foliage, even though PEG did not increase in vitro available N in this species. Possums ate very little Melicytus ramiflorus, regardless of PEG treatment, even though M. ramiflorus contained the highest concentration of in vitro available N. These results prompted us to use PEG and a protein supplement, casein, to manipulate the available N concentration of diets containing ground eucalypt foliage, a well-studied food species for possums. Again, the response of possums to PEG was independent of changes in in vitro available N. In addition, altering the protein content of the diet via the addition of casein did not affect how much food the possums consumed. We conclude that the effects of PEG on dry matter intake by mammalian herbivores are not due solely to the release of tannin-bound protein. There is need for a better understanding of PEG-tannin interactions in order to ensure that the use of PEG in nutritional studies does not outstrip an understanding of its mechanisms of action. PMID:27256074

  20. Adhesion, Growth, and Maturation of Vascular Smooth Muscle Cells on Low-Density Polyethylene Grafted with Bioactive Substances

    PubMed Central

    Parizek, Martin; Slepickova Kasalkova, Nikola; Bacakova, Lucie; Bacakova, Marketa; Lisa, Vera; Svorcik, Vaclav

    2013-01-01

    The attractiveness of synthetic polymers for cell colonization can be affected by physical, chemical, and biological modification of the polymer surface. In this study, low-density polyethylene (LDPE) was treated by an Ar+ plasma discharge and then grafted with biologically active substances, namely, glycine (Gly), polyethylene glycol (PEG), bovine serum albumin (BSA), colloidal carbon particles (C), or BSA+C. All modifications increased the oxygen content, the wettability, and the surface free energy of the materials compared to the pristine LDPE, but these changes were most pronounced in LDPE with Gly or PEG, where all the three values were higher than in the only plasma-treated samples. When seeded with vascular smooth muscle cells (VSMCs), the Gly- or PEG-grafted samples increased mainly the spreading and concentration of focal adhesion proteins talin and vinculin in these cells. LDPE grafted with BSA or BSA+C showed a similar oxygen content and similar wettability, as the samples only treated with plasma, but the nano- and submicron-scale irregularities on their surface were more pronounced and of a different shape. These samples promoted predominantly the growth, the formation of a confluent layer, and phenotypic maturation of VSMC, demonstrated by higher concentrations of contractile proteins alpha-actin and SM1 and SM2 myosins. Thus, the behavior of VSMC on LDPE can be regulated by the type of bioactive substances that are grafted. PMID:23586032

  1. Plasmid DNA partitioning and separation using poly(ethylene glycol)/poly(acrylate)/salt aqueous two-phase systems.

    PubMed

    Johansson, Hans-Olof; Matos, Tiago; Luz, Juliana S; Feitosa, Eloi; Oliveira, Carla C; Pessoa, Adalberto; Bülow, Leif; Tjerneld, Folke

    2012-04-13

    Phase diagrams of poly(ethylene glycol)/polyacrylate/Na(2)SO(4) systems have been investigated with respect to polymer size and pH. Plasmid DNA from Escherichia coli can depending on pH and polymer molecular weight be directed to a poly(ethylene glycol) or to a polyacrylate-rich phase in an aqueous two-phase system formed by these polymers. Bovine serum albumin (BSA) and E. coli homogenate proteins can be directed opposite to the plasmid partitioning in these systems. Two bioseparation processes have been developed where in the final step the pDNA is partitioned to a salt-rich phase giving a total process yield of 60-70%. In one of them the pDNA is partitioned between the polyacrylate and PEG-phases in order to remove proteins. In a more simplified process the plasmid is partitioned to a PEG-phase and back-extracted into a Na(2)SO(4)-rich phase. The novel polyacrylate/PEG system allows a strong change of the partitioning between the phases with relatively small changes in composition or pH. PMID:22391492

  2. Proteomic and phosphoproteomic analysis of polyethylene glycol-induced osmotic stress in root tips of common bean (Phaseolus vulgaris L.)

    PubMed Central

    Horst, Walter Johannes

    2013-01-01

    Previous studies have shown that polyethylene glycol (PEG)-induced osmotic stress (OS) reduces cell-wall (CW) porosity and limits aluminium (Al) uptake by root tips of common bean (Phaseolus vulgaris L.). A subsequent transcriptomic study suggested that genes related to CW processes are involved in adjustment to OS. In this study, a proteomic and phosphoproteomic approach was applied to identify OS-induced protein regulation to further improve our understanding of how OS affects Al accumulation. Analysis of total soluble proteins in root tips indicated that, in total, 22 proteins were differentially regulated by OS; these proteins were functionally categorized. Seventy-seven per- cent of the total expressed proteins were involved in metabolic pathways, particularly of carbohydrate and amino acid metabolism. An analysis of the apoplastic proteome revealed that OS reduced the level of five proteins and increased that of seven proteins. Investigation of the total soluble phosphoproteome suggested that dehydrin responded to OS with an enhanced phosphorylation state without a change in abundance. A cellular immunolocalization analysis indicated that dehydrin was localized mainly in the CW. This suggests that dehydrin may play a major protective role in the OS-induced physical breakdown of the CW structure and thus maintenance of the reversibility of CW extensibility during recovery from OS. The proteomic and phosphoproteomic analyses provided novel insights into the complex mechanisms of OS-induced reduction of Al accumulation in the root tips of common bean and highlight a key role for modification of CW structure. PMID:24123251

  3. Polyethylene glycol plus ascorbic acid for bowel preparation in chronic kidney disease.

    PubMed

    Lee, Jae Min; Keum, Bora; Yoo, In Kyung; Kim, Seung Han; Choi, Hyuk Soon; Kim, Eun Sun; Seo, Yeon Seok; Jeen, Yoon Tae; Chun, Hoon Jai; Lee, Hong Sik; Um, Soon Ho; Kim, Chang Duck; Kim, Myung Gyu; Jo, Sang Kyung

    2016-09-01

    The safety of polyethylene glycol plus ascorbic acid has not been fully investigated in patients with renal insufficiency. High-dose ascorbic acid could induce hyperoxaluria, thereby causing tubule-interstitial nephritis and renal failure. This study aims to evaluate the safety and efficacy of polyethylene glycol plus ascorbic acid in patients with chronic kidney disease.We retrospectively reviewed prospectively collected data on colonoscopy in patients with impaired renal function. Patients were divided into 2 groups: 2 L polyethylene glycol plus ascorbic acid (n = 61) and 4 L polyethylene glycol (n = 80). The safety of the 2 groups was compared by assessing the differences in laboratory findings before and after bowel cleansing.The laboratory findings were not significantly different before and after the administration of 2 L polyethylene glycol plus ascorbic acid or 4 L polyethylene glycol. In both groups, the estimated glomerular filtration rate was not influenced by the administration of the bowel-cleansing agent. Patients' reports on tolerance and acceptability were better in the 2 L polyethylene glycol plus ascorbic acid group than in the 4 L polyethylene glycol group.The 2 L polyethylene glycol plus ascorbic acid solution is a safe choice for bowel preparation before colonoscopy in patients with impaired renal function. PMID:27603372

  4. Cementitious building material incorporating end-capped polyethylene glycol as a phase change material

    DOEpatents

    Salyer, Ival O.; Griffen, Charles W.

    1986-01-01

    A cementitious composition comprising a cementitious material and polyethylene glycol or end-capped polyethylene glycol as a phase change material, said polyethylene glycol and said end-capped polyethylene glycol having a molecular weight greater than about 400 and a heat of fusion greater than about 30 cal/g; the compositions are useful in making pre-formed building materials such as concrete blocks, brick, dry wall and the like or in making poured structures such as walls or floor pads; the glycols can be encapsulated to reduce their tendency to retard set.

  5. Durability of highly cross-linked polyethylene in total hip and total knee arthroplasty.

    PubMed

    Dion, Neil T; Bragdon, Charles; Muratoglu, Orhun; Freiberg, Andrew A

    2015-07-01

    This article reviews the history of the development of highly cross-linked polyethylene and provides an in-depth review of the clinical results regarding the durability of highly cross-linked polyethylene (HXLPE) used in total hip arthroplasty (THA) and total knee arthroplasty (TKA). The use of polyethylene as a bearing surface has contributed to the success of THA and TKA; however, polyethylene wear and osteolysis can lead to failure. Ongoing clinical and retrieval studies are required to analyze outcomes at longer-term follow-up. PMID:26043046

  6. Deuterated polyethylene coatings for ultra-cold neutron applications

    NASA Astrophysics Data System (ADS)

    Brenner, Th.; Fierlinger, P.; Geltenbort, P.; Gutsmiedl, E.; Hollering, A.; Lauer, T.; Petzoldt, G.; Ruhstorfer, D.; Schroffenegger, J.; Seemann, K. M.; Soltwedel, O.; Stuiber, St.; Taubenheim, B.; Windmayer, D.; Zechlau, T.

    2015-09-01

    We report on the fabrication and use of deuterated polyethylene as a coating material for ultra-cold neutron (UCN) storage and transport. The Fermi potential has been determined to be 214 neV, and the wall loss coefficient η is 1.3 × 104 per wall collision. The coating technique allows for a wide range of applications in this field of physics. In particular, flexible and quasi-massless UCN guides with slit-less shutters and seamless UCN storage volumes become possible. These properties enable the use in next-generation measurements of the electric dipole moment of the neutron.

  7. Pyrolysis Pathways of Sulfonated Polyethylene, an Alternative Carbon Fiber Precursor

    SciTech Connect

    Younker, Jarod M; Saito, Tomonori; Hunt, Marcus A; Beste, Ariana; Naskar, Amit K

    2013-01-01

    Sulfonated polyethylene is an emerging precursor for the production of carbon fibers. Pyrolysis of sulfonated polyethylene was characterized by thermogravimetric analysis (TGA). n-heptane-4-sulfonic acid (H4S) was selected as a model compound for the study of sulfonated polyethylene. Density functional theory and conventional transition state theory were used to determine the rate constants of pyrolysis for H4S from 300-1000 K. Multiple reaction channels from two different mechanisms were explored: 1) internal five-centered elimination (Ei 5) and 2) radical chain reaction. The pyrolysis of H4S was simulated with kinetic Monte Carlo (kMC) to obtain TGA plots that compared favorably to experiment. We observed that at tem- peratures < 550 K, the radical mechanism was dominant and yielded the trans-alkene, whereas cis-alkene was formed at higher temperatures from the internal elimination. The maximum rates of % mass loss became independent of initial OH radical concentration at 440-480 K. Experimentally, the maximum % mass loss occurred from 440-460 K (heating rate dependent). Activation energies derived from the kMC-simulated TGAs of H4S (26-29 kcal/mol) agreed with experiment for sulfonated polyethylene ( 31 kcal/mol). The simulations revealed that in this region, decomposition of radical HOSO2 became competitive to H abstraction by HOSO2, making OH the carrying radical for the reaction chain. The maximum rate of % mass loss for internal elimination was observed at temperatures > 600 K. Low-scale carbonization utilizes temperatures < 620 K; thus, internal elimination will not be competitive. Ei5 elimination has been studied for sulfoxides and sulfones, but this represents the first study of internal elimination in sulfonic acids. Nonlinear Arrhenius plots were found for all bimolecular reactions. The most significant nonlinear behavior was observed for reactions where the barrier was small. For reactions with low activation barriers, nonlinearity was traced to

  8. Effective UV radiation dose in polyethylene exposed to weather

    NASA Astrophysics Data System (ADS)

    González-Mota, R.; Soto-Bernal, J. J.; Rosales-Candelas, I.; Calero Marín, S. P.; Vega-Durán, J. T.; Moreno-Virgen, R.

    2009-09-01

    In this work we quantified the effective UV radiation dose in orange and colorless polyethylene samples exposed to weather in the city of Aguascalientes, Ags. Mexico. The spectral distribution of solar radiation was calculated using SMART 2.9.5.; the samples absorption properties were measured using UV-Vis spectroscopy and the quantum yield was calculated using samples reflectance properties. The determining factor in the effective UV dose is the spectral distribution of solar radiation, although the chemical structure of materials is also important.

  9. Progress in polyethylene separators for lead-acid batteries

    NASA Astrophysics Data System (ADS)

    Wada, T.; Hirashima, T.

    The types and properties of separators used for lead-acid batteries are reviewed. Attention is focused on the pocket-type polyethylene (PE) separator as this is widely used in present-day automotive batteries, i.e. in low-maintenance batteries with expanded lead-calcium grids. An improved PE separator has been developed by using a PE resin of high molecular weight. The resistance of the separator to attack by hot sulphuric acid is increased by a factor of 1.5. Batteries using the improved separator show a 40% increase in lifetime under the SAE 75 °C life-cycle test.

  10. Effective Antisense Gene Regulation via Noncationic, Polyethylene Glycol Brushes.

    PubMed

    Lu, Xueguang; Jia, Fei; Tan, Xuyu; Wang, Dali; Cao, Xueyan; Zheng, Jiamin; Zhang, Ke

    2016-07-27

    Negatively charged nucleic acids are often complexed with polycationic transfection agents before delivery. Herein, we demonstrate that a noncationic, biocompatible polymer, polyethylene glycol, can be used as a transfection vector by forming a brush polymer-DNA conjugate. The brush architecture provides embedded DNA strands with enhanced nuclease stability and improved cell uptake. Because of the biologically benign nature of the polymer component, no cytotoxicity was observed. This approach has the potential to address several long-lasting challenges in oligonucleotide therapeutics. PMID:27420413

  11. Deuterated polyethylene coatings for ultra-cold neutron applications

    SciTech Connect

    Brenner, Th.; Geltenbort, P.; Fierlinger, P.; Gutsmiedl, E.; Hollering, A.; Petzoldt, G.; Ruhstorfer, D.; Stuiber, St.; Taubenheim, B.; Windmayer, D.; Lauer, T.; Schroffenegger, J.; Zechlau, T.; Seemann, K. M.; Soltwedel, O.

    2015-09-21

    We report on the fabrication and use of deuterated polyethylene as a coating material for ultra-cold neutron (UCN) storage and transport. The Fermi potential has been determined to be 214 neV, and the wall loss coefficient η is 1.3 × 10{sup 4} per wall collision. The coating technique allows for a wide range of applications in this field of physics. In particular, flexible and quasi-massless UCN guides with slit-less shutters and seamless UCN storage volumes become possible. These properties enable the use in next-generation measurements of the electric dipole moment of the neutron.

  12. THz-Spectroscopy on High Density Polyethylene with Different Crystallinity

    NASA Astrophysics Data System (ADS)

    Sommer, Stefan; Raidt, Thomas; Fischer, Bernd M.; Katzenberg, Frank; Tiller, Jörg C.; Koch, Martin

    2016-02-01

    The different crystallinity states of high density polyethylene (PE-HD) are investigated using THz time-domain spectroscopy by exploiting the complex permittivity at a frequency range from 0.5 up to 3.5 THz. We found that samples with different crystallinity can be distinguished by comparing the material specific refractive index ( n) or rather the linked complex part of the permittivity (∈ ' '). Correlating the calorimetrically determined degrees of crystallinity with the absolute values of the refractive index and the specific absorption peak at 2.18 THz, respectively, suggests in both cases a linear correlation.

  13. Theoretical study on mechanical properties of polyethylene-SWCNT complexes

    NASA Astrophysics Data System (ADS)

    Petrushenko, Igor K.

    2016-01-01

    This paper studies the mechanical properties of polyethylene (PE)-Single-walled carbon nanotube (SWCNT) complexes by using density functional theory (DFT). At the PBE/SVP level, the Young’s modulus of the complexes is obtained as a function of PE content. It is established that, with increasing number of PE chains attached to the SWCNTs, the Young’s modulus monotonically decreases. The density of states (DOS) results show that no orbital hybridization exists between the PE chains and nanotubes. The results of this work are of importance for the design of composite materials employing SWCNTs.

  14. Polyethylene glycol-based homologated ligands for nicotinic acetylcholine receptors☆

    PubMed Central

    Scates, Bradley A.; Lashbrook, Bethany L.; Chastain, Benjamin C.; Tominaga, Kaoru; Elliott, Brandon T.; Theising, Nicholas J.; Baker, Thomas A.; Fitch, Richard W.

    2010-01-01

    A homologous series of polyethylene glycol (PEG) monomethyl ethers were conjugated with three ligand series for nicotinic acetylcholine receptors. Conjugates of acetylaminocholine, the cyclic analog 1-acetyl-4,4-dimethylpiperazinium, and pyridyl ether A-84543 were prepared. Each series was found to retain significant affinity at nicotinic receptors in rat cerebral cortex with tethers of up to six PEG units. Such compounds are hydrophilic ligands which may serve as models for fluorescent/affinity probes and multivalent ligands for nAChR. PMID:19006672

  15. Catalytic degradation of high density polyethylene using zeolites.

    PubMed

    Zaggout, F R; al Mughari, A R; Garforth, A

    2001-01-01

    Plastic wastes, which cause a serious environmental problem in urban areas, can serve as sources of energy. Catalytic treatment of High Density Polyethylene (HDPE) has shown that the degradation of HDPE resulted in the production of a stream of gaseous hydrocarbons varied in the range C1-C8. The degradation was carried out using diluted forms of zeolites ZSM-5, USY and Mordenite (MORD) using a fluidized bed reactor (FBR). Effect of coke formation on the activity of the catalysts was screened by thermogravimetric (TGA). ZSM-5 showed a significant resistance to deactivation because of the nature of its small pore size compared with USY and MORD. PMID:11382018

  16. The use of poly(ethylene oxide) for the efficient stabilization of entrapped alpha-chymotrypsin in silicone elastomers: a chemometric study.

    PubMed

    Ragheb, Amro M; Hileman, Oliver E; Brook, Michael

    2005-12-01

    The enzyme alpha-chymotrypsin, a model for catalytic proteins, was entrapped in different silicone elastomers that were formed via the condensation-cure room temperature vulcanization (CC-RTV) of silanol terminated poly(dimethylsiloxane) with tetraethyl orthosilicate as a crosslinker, in the presence of different poly(ethylene oxide) oligomers that were functionalized with triethoxysilyl groups. The effects of various chemical factors on both the activity and entrapping efficiency of proteins (leaching) were studied using a 2-level fractional factorial design--a chemometrics approach. The factors studied include the concentration and chain length of poly(ethylene oxide), enzyme content, and crosslinker (TEOS) concentration. The study indicated that poly(ethylene oxide) can stabilize the entrapped alpha-chymotrypsin in silicone rubber: the specific activity can be maximized by incorporating a relatively high content of short chain, functional PEO. Increased enzyme concentration was found to adversely affect the specific activity. The effect of TEOS was found to be insignificant when PEO was present in the elastomer, however, it does affect the activity positively in the case of simple elastomers. PMID:15992922

  17. Visualization of O-GlcNAc Glycosylation Stoichiometry and Dynamics using Resolvable Poly(ethylene glycol) Mass Tags

    PubMed Central

    Clark, Peter M.; Rexach, Jessica E.; Hsieh-Wilson, Linda C.

    2014-01-01

    O -GlcNAc glycosylation is a dynamic protein posttranslational modification with roles in processes such as transcription, cell cycle regulation, and metabolism. Detailed mechanistic studies of O-GlcNAc have been hindered by a lack of methods for measuring O-GlcNAc stoichiometries and the interplay of glycosylation with other posttranslational modifications. We recently developed a method for labeling O-GlcNAc-modified proteins with resolvable poly(ethylene glycol) mass tags. This mass tagging approach enables the direct measurement of glycosylation stoichiometries and the visualization of distinct O-GlcNAc-modified subpopulations. Here, we describe protocols for labeling O-GlcNAc glycoproteins in cell lysates with mass tags. PMID:24391098

  18. Polyethylene glycol (PEG)-Poly(N-isopropylacrylamide) (PNIPAAm) based thermosensitive injectable hydrogels for biomedical applications.

    PubMed

    Alexander, Amit; Ajazuddin; Khan, Junaid; Saraf, Swarnlata; Saraf, Shailendra

    2014-11-01

    Protein and peptide delivery by the use of stimuli triggered polymers remains to be the area of interest among the scientist and innovators. In-situ forming gel for the parenteral route in the form of hydrogel and implants are being utilized for various biomedical applications. The formulation of gel depends upon factors such as temperature modulation, pH changes, the presence of ions and ultra-violet irradiation, from which drug is released in a sustained and controlled manner. Among various stimuli triggered factors, thermoresponsive is the most potential one for the delivery of protein and peptides. Poly(ethylene glycol) (PEG) based copolymers play a crucial role as a biomedical material for biomedical applications, because of its biocompatibility, biodegradability, thermosensitivity and easy controlled characters. This review, stresses on the physicochemical property, stability and compositions prospects of smart thermoresponsive polymer specifically, PEG/Poly(N-isopropylacrylamide) (PNIPAAm) based thermoresponsive injectable hydrogels, recently utilized for biomedical applications. PEG-PNIPAAm based hydrogel exhibits good gelling mechanical strength and minimizes the initial burst effect of the drug. In addition, upon changing the composition and proportion of the copolymer molecular weight and ratio, the gelling time can be reduced to a great extent providing better sol-gel transition. The hydrogel formed by the same is able to release the drug over a long duration of time, meanwhile is also biocompatible and biodegradable. Manuscript will give the new researchers an idea about the potential and benefits of PNIPAAm based thermoresponsive hydrogels for the biomedical application. PMID:25092423

  19. An Improved Cryosection Method for Polyethylene Glycol Hydrogels Used in Tissue Engineering

    PubMed Central

    Ruan, Jia-Ling; Tulloch, Nathaniel L.; Muskheli, Veronica; Genova, E. Erin; Mariner, Peter D.; Anseth, Kristi S.

    2013-01-01

    The high water content of hydrogels allows these materials to closely mimic the native biological extracellular conditions, but it also makes difficult the histological preparation of hydrogel-based bioengineered tissue. Paraffin-embedding techniques require dehydration of hydrogels, resulting in substantial collapse and deformation, whereas cryosectioning is hampered by the formation of ice crystals within the hydrogel material. Here, we sought to develop a method to obtain good-quality cryosections for the microscopic evaluation of hydrogel-based tissue-engineered constructs, using polyethylene glycol (PEG) as a test hydrogel. Conventional sucrose solutions, which dehydrate cells while leaving extracellular water in place, produce a hydrogel block that is brittle and difficult to section. We therefore replaced sucrose with multiple protein-based and nonprotein-based solutions as cryoprotectants. Our analysis demonstrated that overnight incubation in bovine serum albumin (BSA), fetal bovine serum (FBS), polyvinyl alcohol (PVA), optimum cutting temperature (OCT®) compound, and Fisher HistoPrep frozen tissue-embedding media work well to improve the cryosectioning of hydrogels. The protein-based solutions give background staining with routine hematoxylin and eosin, but the use of nonprotein-based solutions PVA and OCT reduces this background by 50%. These methods preserve the tissue architecture and cellular details with both in vitro PEG constructs and in constructs that have been implanted in vivo. This simple hydrogel cryosectioning technique improves the methodology for creation of good-quality histological sections from hydrogels in multiple applications. PMID:23448137

  20. Preparation and characterization of a microencapsulated polyethylene glycol cross-linked polyhemoglobin.

    PubMed

    Knirsch, Marcos C; Dell'Anno, Filippo; Chicoma, Dennis; Stephano, Marco Antonio; Bou-Chacra, Nádia A; Palombo, Domenico; Converti, Attilio; Polakiewicz, Bronislaw

    2015-11-01

    Many complications are associated to the therapeutic use of blood, among which are not only transfusion adverse events but also other issues such as lack of donors and high costs for collecting, testing, preserving, and distributing blood packages. Therefore, a clinically viable "blood substitute" is considered the holy grail of traumatology and may greatly benefit medicine. One of the most successful approaches to date is conjugating hemoglobin with polyethylene glycol (PEG). This conjugation aims mainly at overcoming free cell hemoglobin toxicity, which makes its use as oxygen carrier in pure form unfeasible. To improve PEG-hemoglobin conjugates feasibility, we propose applying dual functional PEG cross-linking hemoglobin molecules encapsulated by a protein carrier. The new oxygen carrier showed mean values of the hydrodynamic diameter, dispersity, and zeta potential of 1370 nm, 0.029 and -36 mV, respectively, evidencing the successful synthesis of PEG bis(N-succinimidyl succinate) and polyhemoglobin as well as the structuring of protein carrier. PMID:26314399

  1. Effect of tocopheryl polyethylene glycol succinate on the percutaneous penetration of minoxidil from water/ethanol/polyethylene glycol 400 solutions.

    PubMed

    Sheu, Ming-Thau; Wu, An-Bang; Lin, Keng-Ping; Shen, Chao-Hui; Ho, Hsiu-O

    2006-06-01

    We described to achieve the local retention of minoxidil which has penetrated the skin with minimization of its absorption into the general circulation and elimination of local irritation induced by propylene glycol. The effect of tocopheryl polyethylene glycol succinate (TPGS) on the penetration flux of minoxidil and its retention in the skin from topical minoxidil formulations consisting of water, alcohol, and polyethylene glycol 400 was characterized by an experimental design of ten solvent formulations in this study. Results show that the addition of TPGS was only able to improve the solubility of minoxidil in those solvent systems containing higher proportions of water and PEG 400, and the extent of improvement was also more profound with the addition of TPGS at concentrations higher than 5%. For those solvent systems containing a higher fraction of alcohol, an insignificant change in minoxidil solubility with increasing added amounts of TPGS was noted even with the tendency to decrease the solubility of minoxidil with higher amounts of TPGS. Increasing the amount of TPGS added gradually increased the flux and the corrected flux from solvent formulations with a lower solubility parameter, but decreased those from solvent systems with a higher solubility parameter. With the addition of TPGS, solvent formulation F6 (alcohol:PEG 400 of 50:50) was demonstrated to be the optimal choice by having an improved local effect and a reduced systemic effect compared to the reference of 2% Regaine((R)). Tocopheryl polyethylene glycol succinate (TPGS) was mainly retained locally in the stratum corneum, and the amount was proportional to the increase in the amount of TPGS added to these ten solvent formulations. PMID:16720414

  2. Lipoprotein interactions with a polyurethane and a polyethylene oxide-modified polyurethane at the plasma-material interface.

    PubMed

    Cornelius, Rena M; Macri, Joseph; Cornelius, Katherine M; Brash, John L

    2016-01-01

    Lipoproteins [high density lipoprotein (HDL), low density lipoprotein (LDL), and very low density lipoprotein (VLDL)] are present in blood in relatively high concentrations, and, given their importance in cardiovascular disease, the interactions of these species with blood contacting biomaterials and their possible role in thrombogenesis is of interest. In the present communication, quantitative data on the adsorption of apolipoprotein AI, apolipoprotein AII (the main protein components of HDL), and apolipoprotein B (the main protein component of LDL and VLDL), as well as the lipoproteins themselves from plasma to a biomedical grade polyurethane (PU) with and without a copolymer additive that contains polyethylene oxide (PEO) segments, were investigated. Adsorption from some binary solutions was also studied. Significant quantities of the apolipoproteins were found to adsorb from plasma to the PU, while adsorption to the PEO material was more than 90% lower, demonstrating strong protein resistance of the latter material. In contrast, significant quantities of the lipoproteins were found to adsorb to the PEO as well as to the PU material. From these and previously published results, it is concluded that the protein layer formed on the PU surface from plasma (and by extension from blood) contains apolipoproteins and lipoproteins in addition to other plasma proteins; the layer formed on the PEO surface, however, appears to contain minimal quantities of plasma proteins (including free apolipoproteins) but significant quantities of lipoproteins. PMID:27306077

  3. Effective isolation of exosomes with polyethylene glycol from cell culture supernatant for in-depth proteome profiling.

    PubMed

    Weng, Yejing; Sui, Zhigang; Shan, Yichu; Hu, Yechen; Chen, Yuanbo; Zhang, Lihua; Zhang, Yukui

    2016-08-01

    Exosomes are secreted nanovesicles shed by almost all kinds of cells. Recently, increased interest has been focused on these extracellular vesicles as natural carriers transporting biological contents for intercellular communication. However, current isolation techniques, such as ultracentrifugation, are not convenient and often require specialized equipment. Herein, we describe a polyethylene glycol (PEG)-based approach, which could permit facile, low-cost and effective isolation of exosomes from cell culture supernatant. High-resolution electron microscopes clearly visualized the size and morphology of isolated exosome aggregates, implying the mechanism of PEG-based precipitation. Combined with tandem mass spectrometry analysis, 6299 protein groups encoded by 5120 genes were successfully characterized from HeLa cell culture supernatant, including numerous exosome proteins which could overlap 97% of the Top 100 exosome marker proteins recorded in the ExoCarta database, as well as a series of low-abundance cytokines and biomarkers. Furthermore, we found a higher ratio of neo-cleavage sites in proteins identified from exosomes compared with cellular proteins, revealing the potential roles of exosomes in accumulation and transportation of protein degradation intermediates. PMID:27229443

  4. Medium density polyethylene composites with functionalized carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Pulikkathara, Merlyn X.; Kuznetsov, Oleksandr V.; Peralta, Ivana R. G.; Wei, Xin; Khabashesku, Valery N.

    2009-05-01

    A strong interface between the single-walled carbon nanotubes (SWNTs) and polymer matrix is necessary to achieve enhanced mechanical properties of composites. In this work a series of sidewall-functionalized SWNTs have been investigated in order to evaluate the effect of functionalization on SWNT aspect ratio and composite interfacial chemistry and their role on mechanical properties of a medium density polyethylene (MDPE) matrix. Fluorinated nanotubes (F-SWNTs) were used as precursors for subsequent sidewall functionalization with long chain alkyl groups to produce an F-SWNT- C11H23 derivative. The latter was refluorinated to yield a new perfluorinated derivative, F-SWNT- C11FxHy. The functionalized SWNTs as well as the pristine SWNTs were integrated into an MDPE matrix at a 1 wt% loading. The nanotubes and composite materials were characterized with FTIR, Raman spectroscopy, NMR, XPS, AFM, SEM, TGA, DSC and tensile tests. When incorporated into polyethylene, the new perfluorinated derivative, F-SWNT- C11FxHy, yielded the highest tensile strength value among all nanotube/MDPE composite samples, showing a 52% enhancement in comparison with the neat MDPE. The 1 wt% SWNT/MDPE composite contained nanotubes with a larger aspect ratio but, due to a lack of interfacial chemistry, it resulted in less improvement in mechanical properties compared to the composites made with the fluorinated SWNT derivatives.

  5. Medium density polyethylene composites with functionalized carbon nanotubes.

    PubMed

    Pulikkathara, Merlyn X; Kuznetsov, Oleksandr V; Peralta, Ivana R G; Wei, Xin; Khabashesku, Valery N

    2009-05-13

    A strong interface between the single-walled carbon nanotubes (SWNTs) and polymer matrix is necessary to achieve enhanced mechanical properties of composites. In this work a series of sidewall-functionalized SWNTs have been investigated in order to evaluate the effect of functionalization on SWNT aspect ratio and composite interfacial chemistry and their role on mechanical properties of a medium density polyethylene (MDPE) matrix. Fluorinated nanotubes (F-SWNTs) were used as precursors for subsequent sidewall functionalization with long chain alkyl groups to produce an F-SWNT- C(11)H(23) derivative. The latter was refluorinated to yield a new perfluorinated derivative, F-SWNT- C(11)F(x)H(y). The functionalized SWNTs as well as the pristine SWNTs were integrated into an MDPE matrix at a 1 wt% loading. The nanotubes and composite materials were characterized with FTIR, Raman spectroscopy, NMR, XPS, AFM, SEM, TGA, DSC and tensile tests. When incorporated into polyethylene, the new perfluorinated derivative, F-SWNT- C(11)F(x)H(y), yielded the highest tensile strength value among all nanotube/MDPE composite samples, showing a 52% enhancement in comparison with the neat MDPE. The 1 wt% SWNT/MDPE composite contained nanotubes with a larger aspect ratio but, due to a lack of interfacial chemistry, it resulted in less improvement in mechanical properties compared to the composites made with the fluorinated SWNT derivatives. PMID:19420641

  6. Polyethylene encapsulation of single shell tank low-level wastes

    SciTech Connect

    Kalb, P.D.; Fuhrmann, M.; Colombo, P.

    1993-01-01

    Polyethylene encapsulation is being explored for potential use in treating nitrate salts and sludges at US Department of Energy (US DOE) underground storage tank facilities. Some of these wastes contain high concentrations of fission products and are expected to maintain equilibrium temperatures of 50--70[degrees]C for many years. The potential effects of elevated temperature and high radiation conditions on key waste form properties (e.g., mechanical integrity, leachability) are examined. After 6 months of thermal conditioning, waste form tests specimens show no degradation in mechanical integrity. Leaching at elevated temperature resulted in a small increase in leach rate (a factor of less than two), while diffusion remained the dominant mechanism of release. Full-scale polyethylene waste forms containing 50--70 wt % nitrate salt can be expected to leach a total of 5--17% of the original contaminant source term after 300 years of leaching under worst-case conditions (fully saturated at 70[degrees]C).

  7. Polyethylene encapsulation of single shell tank low-level wastes

    SciTech Connect

    Kalb, P.D.; Fuhrmann, M.; Colombo, P.

    1993-04-01

    Polyethylene encapsulation is being explored for potential use in treating nitrate salts and sludges at US Department of Energy (US DOE) underground storage tank facilities. Some of these wastes contain high concentrations of fission products and are expected to maintain equilibrium temperatures of 50--70{degrees}C for many years. The potential effects of elevated temperature and high radiation conditions on key waste form properties (e.g., mechanical integrity, leachability) are examined. After 6 months of thermal conditioning, waste form tests specimens show no degradation in mechanical integrity. Leaching at elevated temperature resulted in a small increase in leach rate (a factor of less than two), while diffusion remained the dominant mechanism of release. Full-scale polyethylene waste forms containing 50--70 wt % nitrate salt can be expected to leach a total of 5--17% of the original contaminant source term after 300 years of leaching under worst-case conditions (fully saturated at 70{degrees}C).

  8. Effect of thermal modification on rheological properties of polyethylene blends

    SciTech Connect

    Siriprumpoonthum, Monchai; Nobukawa, Shogo; Yamaguchi, Masayuki; Satoh, Yasuo; Sasaki, Hiroko

    2014-03-15

    We examined the effects of thermal modification under flow field on the rheological properties of linear low-density polyethylene (LLDPE) with high molecular weight, low-density polyethylene (LDPE), and their blends, without thermal stabilizer. Although structural changes during processing are not detected by size extrusion chromatography or nuclear magnetic resonance spectroscopy, linear viscoelastic properties changed greatly, especially for the LLDPE. A cross-linking reaction took place, leading to, presumably, star-shaped long-chain branches. Consequently, the modified LLDPE, having high zero-shear viscosity, became a thermorheologically complex melt. Moreover, it should be noted that the drawdown force, defined as the uniaxial elongational force at a constant draw ratio, was significantly enhanced for the blends. Enhancement of elongational viscosity was also detected. The drawdown force and elongational viscosity are marked for the thermally modified blend as compared with those for the blend of thermally modified pure components. Intermolecular cross-linking reactions between LDPE and LLDPE, yielding polymers with more than two branch points per chain, result in marked strain-hardening in the elongational viscosity behavior even at small strain. The recovery curve of the oscillatory modulus after the shear modification is further evidence of a branched structure.

  9. Probing polyethylene crystallization via simultaneous Raman scattering, rheology and microscopy

    NASA Astrophysics Data System (ADS)

    Migler, Kalman; Kotula, Anthony; Hight Walker, Angela

    The structure and rheology of polyolefins during crystallization is of critical importance to the polymer processing industry. Here we present simultaneous Raman scattering, rheological and optical microscopy measurements of crystallizing high density polyethylenes during quiescent and slow flow conditions. Raman scattering measurements during quiescent crystallization allow us to quantify three different mass fractions of chain conformers: an amorphous fraction, an orthorhombic crystalline fraction, and a fraction of chains that contain many consecutive trans bonds but are not part of the orthorhombic crystal. These non-crystalline consecutive trans (NCCT) conformers are generated as a precursor to crystallinity. Slow steady shear rates (1 s 1) applied during isothermal crystallization experiments dramatically increase the crystallization rate as well as the amount of NCCT conformers produced. Optical measurements of sheared samples during crystallization reveal the formation of fiber structures that compositionally contain more NCCT conformers than the surrounding melt. The increase in the complex shear modulus commonly measured for crystallizing polyethylenes correlates with the growth of chain conformers and the appearance of spherulites within the melt.

  10. Analyzing and improving viscoelastic properties of high density polyethylene

    NASA Astrophysics Data System (ADS)

    Ahmed, Reaj Uddin

    2011-12-01

    High Density Polyethylene (HDPE) is closely packed, less branched polyethylene having higher mechanical properties, chemical resistance, and heat resistance than Low Density Polyentylene (LDPE). Better properties and cost effectiveness make it an important raw material over LDPE in packaging industries. Stacked containers made of HDPE experience static loading and deformation strain during their storage period in a warehouse. As HDPE is a viscoelastic material, dimensional stability of stacked HDPE containers depends on time dependent properties such as creep and stress relaxation. Now, light weighting is a driving force in packaging industries, which results in lower production costs but performance of the product becomes a challenge. Proper understanding of the viscoelastic properties of HDPE, with relevant FE simulation can facilitate improved designs. This research involves understanding and improving viscoelastic properties, creep behavior, and stress relaxation of HDPE. Different approaches were carried out to meet the objectives. Organic filler CaCO3 was added to HDPE at increasing weight fractions and corresponding property changes were investigated. Annealing heat treatments were also carried out for potential property improvements. The effect of ageing was also investigated on both annealed and non annealed HDPE. The related performance of different water bottles against squeeze pressure was also characterized. Both approaches, incorporation of CaCO3 and annealing, showed improvements in the properties of HDPE over neat HDPE. This research aids finding the optimum solution for improving viscoelastic properties, stress relaxation, and creep behavior of HDPE in manufacturing.

  11. Reduced Water Density in a Poly(ethylene oxide) Brush

    SciTech Connect

    Lee, Hoyoung; Kim, Dae Hwan; Park, Hae-Woong; Mahynski, Nathan A.; Kim, Kyungil; Meron, Mati; Lin, Binhua; Won, You-Yeon

    2012-09-05

    A model poly(ethylene oxide) (PEO) brush system, prepared by spreading a poly(ethylene oxide)-poly(n-butyl acrylate) (PEO-PnBA) amphiphilic diblock copolymer onto an air-water interface, was investigated under various grafting density conditions by using the X-ray reflectivity (XR) technique. The overall electron density profiles of the PEO-PnBA monolayer in the direction normal to the air-water interface were determined from the XR data. From this analysis, it was found that inside of the PEO brush, the water density is significantly lower than that of bulk water, in particular, in the region close to the PnBA-water interface. Separate XR measurements with a PnBA homopolymer monolayer confirm that the reduced water density within the PEO-PnBA monolayer is not due to unfavorable contacts between the PnBA surface and water. The above result, therefore, lends support to the notion that PEO chains provide a hydrophobic environment for the surrounding water molecules when they exist as polymer brush chains.

  12. Particle Size Control of Polyethylene Glycol Coated Fe Nanoparticles

    NASA Astrophysics Data System (ADS)

    Srinivasan, B.; Bonder, M. J.; Zhang, Y.; Gallo, D.; Hadjipanayis, G. C.

    2006-03-01

    Recent interest in Fe nanoparticles with high magnetization is driven by their potential use in biomedical applications such as targeted drug delivery, MRI contrast enhancement and hyperthermia treatment of cancer. This study looks at the use of a polyethylene glycol (PEG) solution to mediate the particle size and therefore control the coercivity of the resulting nanoparticles. Iron nanoparticles were synthesized using an aqueous sodium borohydride reduction of ferrous chloride by a simultaneous introduction of reagents in a Y- junction. The resulting product was collected in a vessel containing a 15 mg/ml carboxyl terminated polyethylene glycol (cPEG) in ethyl alcohol solution located under the Y junction. By varying the length of tubing below the Y junction, the particle size was varied from 5-25 nm. X-ray diffraction data indicates the presence of either amorphous Fe-B or crystalline alpha Fe, depending on the molar ratio of reagents. Magnetic measurements indicate the particles are ferromagnetic with values of coercivity ranging from 200-500 Oe and a saturation magnetization in range of 70-110 emu/g. The XRD shows that the particles are not affected by the polymer coating.

  13. Properties of high density polyethylene – Paulownia wood flour composites via injection molding

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Paulownia wood (PW) flour is evaluated as a bio-based fiber reinforcement. Composites of high density polyethylene (HDPE), 25% by weight of PW, and either 0% or 5% by weight of maleated polyethylene (MAPE) were produced by twin screw compounding followed by injection molding. Molded test composite...

  14. 75 FR 22842 - Polyethylene Retail Carrier Bags From Indonesia, Taiwan, and Vietnam

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-30

    ... publishing the notice in the Federal Register of December 3, 2009 (74 FR 63410). The hearing was held in... COMMISSION Polyethylene Retail Carrier Bags From Indonesia, Taiwan, and Vietnam Determinations On the basis... imports from Vietnam of polyethylene retail carrier bags (PRCBs), provided for in subheading 3923.21.00...

  15. 21 CFR 573.800 - Polyethylene glycol (400) mono- and dioleate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.800 Polyethylene glycol (400) mono- and dioleate. (a) The food additive polyethylene glycol (400) mono- and dioleate meets the following...

  16. 21 CFR 573.800 - Polyethylene glycol (400) mono- and dioleate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.800 Polyethylene glycol (400) mono- and dioleate. (a) The food additive polyethylene glycol (400) mono- and dioleate meets the following...

  17. Mechanical and thermal properties of high density polyethylene – dried distillers grains with solubles composites

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Dried Distillers Grain with Solubles (DDGS) is evaluated as a bio-based fiber reinforcement. Injection molded composites of high density polyethylene (HDPE), 25% by weight of DDGS, and either 5% of 0% by weight of maleated polyethylene (MAPE) were produced by twin screw compounding and injection mo...

  18. 21 CFR 178.3750 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene glycol (mean molecular weight 200-9... molecular weight 200-9,500). Polyethylene glycol identified in this section may be safely used as a... conditions: (a) The additive is an addition polymer of ethylene oxide and water with a mean molecular...

  19. 21 CFR 178.3750 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene glycol (mean molecular weight 200-9... molecular weight 200-9,500). Polyethylene glycol identified in this section may be safely used as a... conditions: (a) The additive is an addition polymer of ethylene oxide and water with a mean molecular...

  20. 76 FR 75870 - Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice of Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-05

    ..., 76 FR 45227 (July 28, 2011) (Initiation Notice). \\2\\ See Polyethylene Terephthalate Film, Sheet, and Strip from Korea: Final Results of Antidumping Duty Administrative Review and Revocation in Part, 76 FR... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice...

  1. 75 FR 10758 - Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping Duty and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-09

    ... Order: Polyethylene Terephthalate Film, Sheet and Strip (PET Film) from India, 67 FR 44179 (July 1, 2002... India, 67 FR 44175 (July 1, 2002) (Antidumping Duty Order). The notice announcing the countervailing... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation...

  2. 78 FR 79400 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Initiation...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-30

    ... and Amended Final Determination of Sales at Less Than Fair Value for the United Arab Emirates, 73 FR... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... a request for a new shipper review of the antidumping duty order on polyethylene terephthalate...

  3. 78 FR 2365 - Polyethylene Terephthalate Film, Sheet and Strip From India: Partial Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... Administrative Review, 77 FR 39216, 39217 (July 2, 2012). \\2\\ Petitioners are DuPont Teijin Films, Mitsubishi..., 77 FR 52688 (August 30, 2012). \\6\\ See Polyethylene Terephthalate (PET) Film, Sheet, and Strip from... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India:...

  4. 78 FR 42105 - Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-15

    ... COMMISSION Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission... countervailing duty order on polyethylene terephthalate film, sheet, and strip (``PET'' film) from India and the antidumping duty orders on PET film from India and Taiwan would be likely to lead to continuation...

  5. 78 FR 47276 - Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India: Final Results of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-05

    ...: Polyethylene Terephthalate Film, Sheet, and Strip From India, 67 FR 44179 (July 1, 2002). On April 2, 2012, the... 1930, as amended (the Act). See Initiation of Five-Year (``Sunset'') Reviews, 78 FR 19647 (April 2... International Trade Administration Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India:...

  6. 75 FR 34699 - Polyethylene Retail Carrier Bags from Thailand: Rescission of Antidumping Duty Administrative...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-18

    ..., 74 FR 48224 (September 22, 2009). On April 19, 2010, the petitioners withdrew their request for an... International Trade Administration Polyethylene Retail Carrier Bags from Thailand: Rescission of Antidumping... order on polyethylene retail carrier bags from Thailand. The period of review is August 1, 2008,...

  7. 75 FR 36359 - Polyethylene Retail Carrier Bags From Thailand: Extension of Time Limit for Preliminary Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-25

    ... Thailand. See Antidumping Duty Order: Polyethylene Retail Carrier Bags From Thailand, 69 FR 48204 (August 9... of Sales at Less Than Fair Value: Polyethylene Retail Carrier Bags From Thailand, 69 FR 34122, 34123... Administrative Reviews and Request for Revocation in Part, 74 FR 48224, 48226 (September 22, 2009).\\1\\ The...

  8. 76 FR 26241 - Polyethylene Retail Carrier Bags From Thailand: Extension of Time Limit for Preliminary Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-06

    ..., 75 FR 60076 (September 29, 2010). The preliminary results of this administrative review are currently... International Trade Administration Polyethylene Retail Carrier Bags From Thailand: Extension of Time Limit for... polyethylene retail carrier bags from Thailand for the period August 1, 2009, through July 31, 2010....

  9. 21 CFR 172.820 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ethylene oxide and water with a mean molecular weight of 200 to 9,500. (2) It contains no more than 0.2... the total ethylene and diethylene glycol content of polyethylene glycols having mean molecular weights... and diethylene glycol content of polyethylene glycols having mean molecular weights below...

  10. 21 CFR 172.820 - Polyethylene glycol (mean molecular weight 200-9,500).

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ethylene oxide and water with a mean molecular weight of 200 to 9,500. (2) It contains no more than 0.2... the total ethylene and diethylene glycol content of polyethylene glycols having mean molecular weights... and diethylene glycol content of polyethylene glycols having mean molecular weights below...

  11. 40 CFR 721.3900 - Alkyl polyethylene glycol phosphate, potassium salt.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., potassium salt. 721.3900 Section 721.3900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3900 Alkyl polyethylene glycol phosphate, potassium salt. (a) Chemical... as alkyl polyethylene glycol phosphate, potassium salt (P-90-481), is subject to reporting under...

  12. 40 CFR 721.3900 - Alkyl polyethylene glycol phosphate, potassium salt.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., potassium salt. 721.3900 Section 721.3900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3900 Alkyl polyethylene glycol phosphate, potassium salt. (a) Chemical... as alkyl polyethylene glycol phosphate, potassium salt (P-90-481), is subject to reporting under...

  13. 40 CFR 721.3900 - Alkyl polyethylene glycol phosphate, potassium salt.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., potassium salt. 721.3900 Section 721.3900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3900 Alkyl polyethylene glycol phosphate, potassium salt. (a) Chemical... as alkyl polyethylene glycol phosphate, potassium salt (P-90-481), is subject to reporting under...

  14. 40 CFR 721.3900 - Alkyl polyethylene glycol phosphate, potassium salt.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., potassium salt. 721.3900 Section 721.3900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3900 Alkyl polyethylene glycol phosphate, potassium salt. (a) Chemical... as alkyl polyethylene glycol phosphate, potassium salt (P-90-481), is subject to reporting under...

  15. 40 CFR 721.3900 - Alkyl polyethylene glycol phosphate, potassium salt.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., potassium salt. 721.3900 Section 721.3900 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Specific Chemical Substances § 721.3900 Alkyl polyethylene glycol phosphate, potassium salt. (a) Chemical... as alkyl polyethylene glycol phosphate, potassium salt (P-90-481), is subject to reporting under...

  16. 40 CFR 721.10360 - 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene glycol mono...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-(triethoxysilyl)-, reaction products with polyethylene glycol mono-(branched tridecyl) ether (generic). 721.10360... CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10360 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene...

  17. 40 CFR 721.10360 - 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene glycol mono...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-(triethoxysilyl)-, reaction products with polyethylene glycol mono-(branched tridecyl) ether (generic). 721.10360... CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10360 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene...

  18. 40 CFR 721.10360 - 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene glycol mono...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-(triethoxysilyl)-, reaction products with polyethylene glycol mono-(branched tridecyl) ether (generic). 721.10360... CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10360 1-Substituted propane, 3-(triethoxysilyl)-, reaction products with polyethylene...

  19. Experimental investigation of laboratory-scale rocket engine fed on solid polyethylene rod as fuel

    NASA Astrophysics Data System (ADS)

    Yemets, V. V.; Sanin, F. P. Dzhur, Ye. O.; Masliany, M. V.; Kostritsyn, O. Yu.; Minteev, G. V.; Ushkanov, V. M.

    Fire testing of the laboratory-scale rocket engine with the consumable solid polyethylene rod as fuel is described. The experimental data on heat flows, gasification rate and heat transfer coefficient are presented. Results of the testing may be useful for designing launch vehicles with combustible polyethylene tank shells.

  20. Complete genome sequence of Bacillus sp. YP1, a polyethylene-degrading bacterium from waxworm's gut.

    PubMed

    Yang, Yu; Chen, Jianwei; Wu, Wei-Min; Zhao, Jiao; Yang, Jun

    2015-04-20

    Bacillus sp. strain YP1, isolated from the gut of waxworm (the larvae of Plodia interpunctella) which ate polyethylene (PE) plastic, is capable of degrading PE and utilizing PE as sole carbon source. Here we report the complete genome sequence of strain YP1, which is relevant to polyethylene depolymerization and biodegradation. PMID:25795022

  1. 40 CFR 721.10546 - Pentenylated polyethylene glycol sulfate salt (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... sulfate salt (generic). 721.10546 Section 721.10546 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10546 Pentenylated polyethylene glycol sulfate salt... identified generically as pentenylated polyethylene glycol sulfate salt (PMN P-04-340) is subject...

  2. 40 CFR 721.10546 - Pentenylated polyethylene glycol sulfate salt (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... sulfate salt (generic). 721.10546 Section 721.10546 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10546 Pentenylated polyethylene glycol sulfate salt... identified generically as pentenylated polyethylene glycol sulfate salt (PMN P-04-340) is subject...

  3. 75 FR 38978 - Polyethylene Retail Carrier Bags From the People's Republic of China, Malaysia, and Thailand...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-07

    ... Polyethylene Retail Carrier Bags From China, Malaysia, and Thailand, 74 FR 31750 (July 2, 2009). \\1\\ On August... Duty Order: Polyethylene Retail Carrier Bags From Malaysia, 69 FR 48203 (August 9, 2004); Antidumping..., Malaysia, and Thailand: Continuation of Antidumping Duty Orders AGENCY: Import...

  4. Glass transition dynamics and cooperativity length of poly(ethylene 2,5-furandicarboxylate) compared to poly(ethylene terephthalate).

    PubMed

    Codou, Amandine; Moncel, Matthieu; van Berkel, Jesper Gabriël; Guigo, Nathanaël; Sbirrazzuoli, Nicolas

    2016-06-22

    The glass transition of poly(ethylene 2,5-furandicarboxylate) (PEF), an emergent bio-based polyester, was investigated in comparison to one of its chemical analogues: poly(ethylene terephthalate) (PET). These investigations were conducted at different crystallinities by means of stochastic modulated differential scanning calorimetry (stochastic TMDSC) and dynamic mechanical analysis (DMA). Amorphous PEF presents a higher ΔCp at the glass transition and a broader relaxation spectrum attributed to a higher free volume. The higher Tg of PEF is then purely related to segmental mobility and specific interactions in PEF. The length of cooperative rearranging regions (CRR) was similar for both materials. Additionally, the variations of the effective activation energy E of PEF and PET at glass transitions were determined by isoconversional kinetic analysis. The rate of decrease in E was similar for the two amorphous polyesters. Upon crystallization, the glass transition of PEF is broadened but its temperature range is not increased as with PET. The creation of the rigid amorphous fraction (RAF) with crystallinity is lower in PEF than in PET. The difference in free volume also explains the lower coupling between the crystalline phase and the amorphous phase in PEF. PMID:27067510

  5. Nd:Yag laser irradiation of single lap joints made by polyethylene and polyethylene doped by carbon nanomaterials

    NASA Astrophysics Data System (ADS)

    Visco, A. M.; Brancato, V.; Cutroneo, M.; Torrisi, L.

    2014-04-01

    Thermoplastic polyethylene can be welded by the transmission laser welding technique (TTLW) that exhibits some process related benefits with respect other conventional joining methods. This justifies its large use in wide fields, from the automotive to medical or domestic appliances. In this research, we studied single lap joints made by polyethylene pure and filled with carbon nanomaterials (0.2% in weight) to make the polymer laser absorbent. The joints were irradiated by a Nd:YAG laser operating at 1064 nm (first harmonic) with an intensity of 107 W/cm2 and 1 ÷ 30Hz, a maximum pulse energy of 300mJ and a laser spot of ≈ 1 cm2 (no focusing lens were employed). The joints were characterized by morphological analysis, mechanical shear tests and calorimetric analysis. The results suggested that the laser exposition time must be opportunely balanced in order to avoid a poor adhesion between the polymer sheets and to realized efficient joints. In particular the mechanical test showed that the laser exposition time of 40 seconds is the best conditions to obtain the highest shear strength of the joints of 140 N. After too prolonged laser exposure times, degrading phenomena starts.

  6. Effect of nanoclay on the properties of low density polyethylene/linear low density polyethylene/thermoplastic starch blend films.

    PubMed

    Sabetzadeh, Maryam; Bagheri, Rouhollah; Masoomi, Mahmood

    2016-05-01

    The aim of this work is to study effect of nanoclay (Cloisite(®)15A) on morphology and properties of low-density polyethylene/linear low-density polyethylene/thermoplastic starch (LDPE/LLDPE/TPS) blend films. LDPE/LLDPE blend (70/30wt/wt) containing 15wt.% TPS in the presence of PE-grafted maleic anhydride (PE-g-MA, 3wt.%) with 1, 3 and 5phr of nanoclay are compounded in a twin-screw extruder and then film blown using a blowing machine. Nanocomposites with intercalated structures are obtained, based on the X-ray diffraction (XRD) and transmission electron microscopy (TEM) studies. However, some exfoliated single platelets in the samples are also observable. Scanning electron microscopic (SEM) images confirm the ability of both exfoliated nanoclay and PE-g-MA to reduce the size of TPS domains and deform their particles within the PE matrices. As the nanoclay content increases from 1 to 5phr, the tensile strength, tear resistance and impact strength of the films increase, whereas a slight decrease in the elongation at break is observed. The film samples with 5phr nanoclay possess the required packaging properties, as specified by ASTM D4635. These films provide desired optical transparency and surface roughness which are more attractive for packaging applications. PMID:26876998

  7. Double-concave deformity of the polyethylene tibial post in posterior stabilized total knee arthroplasty.

    PubMed

    Niki, Yasuo; Matsumoto, Hideo; Yoshimine, Fumihiro; Toyama, Yoshiaki; Suda, Yasunori; Banks, Scott A

    2010-04-01

    This report describes a unique case of bilateral total knee arthroplasty necessitating revision of the polyethylene insert, which showed prominent marks on the tibial post resulting from repeated seiza-style sitting. The patient presented 7 years postoperatively with knee pain and flexion disturbance due to continuous joint effusion persisting for more than 4 months. Proliferating synovia throughout the joint revealed reactive synovitis to polyethylene particles. The retrieved polyethylene inserts displayed double-concave deformity of the tibial post with burnishing and creep in tibiofemoral articulation. The damage pattern of retrieved polyethylene inserts reflected the data from tibiofemoral contact location obtained using a shape-matching technique in the early postoperative phase. This case provides an example of damage to the polyethylene tibial post caused by a floor-sitting lifestyle and the potential clinical sequelae. PMID:19261434

  8. Degradation of degradable starch-polyethylene plastics in a compost environment

    SciTech Connect

    Johnson, K.E.; Pometto, A.L. III; Nikolov, Z.L. )

    1993-04-01

    Degradable plastics have differing degradation rates. Three types of degradation of polyethylene in the starch-polyethylene polymers can occur: chemical degradation, photodegradation, and biological degradation. This study examines all three types of degradation in 11 commercially produced degradable starch-polyethylene bags. Different rates for chemical and photo-degradation were found within a 20 day or an 8-week period. Results indicated that both the 70[degree]C oven and HT-HH film treatments were appropriate methods to evaluate oxidative degradation. In a compost environment, oxygen tension on the surface of the film appears to be the rate-limiting component for both chemical and biological degradation. Levels of starch in all bags was similar, so the prooxidant additive was critical in promoting the oxidative degradation of polyethylene. The Fe-Mn additive displayed the best catalytic activity. This study overall confirms degradation of starch-polyethylene plastics in a natural environment. 17 refs., 6 figs., 2 tabs.

  9. Effect of chain architecture on the compression behavior of nanoscale polyethylene particles

    PubMed Central

    2013-01-01

    Polymeric particles with controlled internal molecular architectures play an important role as constituents in many composite materials for a number of emerging applications. In this study, classical molecular dynamics techniques are employed to predict the effect of chain architecture on the compression behavior of nanoscale polyethylene particles subjected to simulated flat-punch testing. Cross-linked, branched, and linear polyethylene chain architectures are each studied in the simulations. Results indicate that chain architecture has a significant influence on the mechanical properties of polyethylene nanoparticles, with the network configuration exhibiting higher compressive strengths than the branched and linear architectures. These findings are verified with simulations of bulk polyethylene. The compressive stress versus strain profiles of particles show four distinct regimes, differing with that of experimental micron-sized particles. The results of this study indicate that the mechanical response of polyethylene nanoparticles can be custom-tailored for specific applications by changing the molecular architecture. PMID:23855722

  10. Tribo-biological deposits on the articulating surfaces of metal-on-polyethylene total hip implants retrieved from patients

    PubMed Central

    Cui, Zhiwei; Tian, Yi-Xing; Yue, Wen; Yang, Lei; Li, Qunyang

    2016-01-01

    Artificial total hip arthroplasty (THA) is one of the most effective orthopaedic surgeries that has been used for decades. However, wear of the articulating surfaces is one of the key failure causes limiting the lifetime of total hip implant. In this paper, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) were employed to explore the composition and formation mechanism of the tribo-layer on the articulating surfaces of metal-on-polyethylene (MoPE) implants retrieved from patients. Results showed that, in contrast to conventional understanding, the attached tribo-layer contained not only denatured proteins but also a fraction of polymer particles. The formation of the tribo-layer was believed to relate to lubrication regime, which was supposed to be largely affected by the nature of the ultra-high-molecule-weight-polyethylene (UHMWPE). Wear and formation of tribo-layer could be minimized in elasto-hydrodynamic lubrication (EHL) regime when the UHMWPE was less stiff and have a morphology containing micro-pits; whereas the wear was more severe and tribo-layer formed in boundary lubrication. Our results and analyses suggest that enhancing interface lubrication may be more effective on reducing wear than increasing the hardness of material. This finding may shed light on the design strategy of artificial hip joints. PMID:27345704

  11. Tribo-biological deposits on the articulating surfaces of metal-on-polyethylene total hip implants retrieved from patients

    NASA Astrophysics Data System (ADS)

    Cui, Zhiwei; Tian, Yi-Xing; Yue, Wen; Yang, Lei; Li, Qunyang

    2016-06-01

    Artificial total hip arthroplasty (THA) is one of the most effective orthopaedic surgeries that has been used for decades. However, wear of the articulating surfaces is one of the key failure causes limiting the lifetime of total hip implant. In this paper, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) were employed to explore the composition and formation mechanism of the tribo-layer on the articulating surfaces of metal-on-polyethylene (MoPE) implants retrieved from patients. Results showed that, in contrast to conventional understanding, the attached tribo-layer contained not only denatured proteins but also a fraction of polymer particles. The formation of the tribo-layer was believed to relate to lubrication regime, which was supposed to be largely affected by the nature of the ultra-high-molecule-weight-polyethylene (UHMWPE). Wear and formation of tribo-layer could be minimized in elasto-hydrodynamic lubrication (EHL) regime when the UHMWPE was less stiff and have a morphology containing micro-pits; whereas the wear was more severe and tribo-layer formed in boundary lubrication. Our results and analyses suggest that enhancing interface lubrication may be more effective on reducing wear than increasing the hardness of material. This finding may shed light on the design strategy of artificial hip joints.

  12. Tribo-biological deposits on the articulating surfaces of metal-on-polyethylene total hip implants retrieved from patients.

    PubMed

    Cui, Zhiwei; Tian, Yi-Xing; Yue, Wen; Yang, Lei; Li, Qunyang

    2016-01-01

    Artificial total hip arthroplasty (THA) is one of the most effective orthopaedic surgeries that has been used for decades. However, wear of the articulating surfaces is one of the key failure causes limiting the lifetime of total hip implant. In this paper, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) were employed to explore the composition and formation mechanism of the tribo-layer on the articulating surfaces of metal-on-polyethylene (MoPE) implants retrieved from patients. Results showed that, in contrast to conventional understanding, the attached tribo-layer contained not only denatured proteins but also a fraction of polymer particles. The formation of the tribo-layer was believed to relate to lubrication regime, which was supposed to be largely affected by the nature of the ultra-high-molecule-weight-polyethylene (UHMWPE). Wear and formation of tribo-layer could be minimized in elasto-hydrodynamic lubrication (EHL) regime when the UHMWPE was less stiff and have a morphology containing micro-pits; whereas the wear was more severe and tribo-layer formed in boundary lubrication. Our results and analyses suggest that enhancing interface lubrication may be more effective on reducing wear than increasing the hardness of material. This finding may shed light on the design strategy of artificial hip joints. PMID:27345704

  13. Elaboration et caracterisation de nanocomposites polyethylene/montmorillonite

    NASA Astrophysics Data System (ADS)

    Stoeffler, Karen

    This research project consists in preparing polyethylene/montmorillonite nanocomposites for film packaging applications. Montmorillonite is a natural clay with an exceptional aspect ratio. In recent years, its incorporation in polymer matrices has attracted great interest. The pioneer work from Toyota on polyamide-6/montmorillonite composites has shown that it was possible to disperse the clay at a nanometric scale. Such a structure, so-called exfoliated, leads to a significant increase in mechanical, barrier and fire retardant properties, even at low volumetric fractions of clay. This allows a valorization of the polymeric material at moderate cost. Due to its high polarity, montmorilloite exfoliation in polymeric matrices is problematic. In the particular case of polyolefin matrices, the platelets dispersion remains limited: most frequently, the composites obtained exhibit conventional structures (microcomposites) or intercalated structures. To solve this problem, two techniques are commonly employed: the surface treatment of the clay, which allows the expansion of the interfoliar gallery while increasing the affinity between the clay and the polymer, and the use of a polar compatibilizing agent (grafted polyolefin). The first part of this thesis deals with the preparation and the characterization of highly thermally stable organophilic montmorillonites. Commercial organophilic montmorillonites are treated with quaternary ammonium intercalating agents. However, those intercalating agents present a poor thermal stability and are susceptible to decompose upon processing, thus affecting the clay dispersion and the final properties of the nanocomposites. In this work, it was proposed to modify the clay with alkyl pyridinium, alkyl imidazolium and alkyl phosphonium intercalating agents, which are more stable than ammonium based cations. Organophilic montmorillonites with enhanced thermal stabilites compared to commercial organoclays (+20°C to +70°C) were prepared

  14. Physiological Investigation and Transcriptome Analysis of Polyethylene Glycol (PEG)-Induced Dehydration Stress in Cassava

    PubMed Central

    Fu, Lili; Ding, Zehong; Han, Bingying; Hu, Wei; Li, Yajun; Zhang, Jiaming

    2016-01-01

    Cassava is an important tropical and sub-tropical root crop that is adapted to drought environment. However, severe drought stress significantly influences biomass accumulation and starchy root production. The mechanism underlying drought-tolerance remains obscure in cassava. In this study, changes of physiological characters and gene transcriptome profiles were investigated under dehydration stress simulated by polyethylene glycol (PEG) treatments. Five traits, including peroxidase (POD) activity, proline content, malondialdehyde (MDA), soluble sugar and soluble protein, were all dramatically induced in response to PEG treatment. RNA-seq analysis revealed a gradient decrease of differentially expressed (DE) gene number in tissues from bottom to top of a plant, suggesting that cassava root has a quicker response and more induced/depressed DE genes than leaves in response to drought. Overall, dynamic changes of gene expression profiles in cassava root and leaves were uncovered: genes related to glycolysis, abscisic acid and ethylene biosynthesis, lipid metabolism, protein degradation, and second metabolism of flavonoids were significantly induced, while genes associated with cell cycle/organization, cell wall synthesis and degradation, DNA synthesis and chromatin structure, protein synthesis, light reaction of photosynthesis, gibberelin pathways and abiotic stress were greatly depressed. Finally, novel pathways in ABA-dependent and ABA-independent regulatory networks underlying PEG-induced dehydration response in cassava were detected, and the RNA-Seq results of a subset of fifteen genes were confirmed by real-time PCR. The findings will improve our understanding of the mechanism related to dehydration stress-tolerance in cassava and will provide useful candidate genes for breeding of cassava varieties better adapted to drought environment. PMID:26927071

  15. Physiological Investigation and Transcriptome Analysis of Polyethylene Glycol (PEG)-Induced Dehydration Stress in Cassava.

    PubMed

    Fu, Lili; Ding, Zehong; Han, Bingying; Hu, Wei; Li, Yajun; Zhang, Jiaming

    2016-01-01

    Cassava is an important tropical and sub-tropical root crop that is adapted to drought environment. However, severe drought stress significantly influences biomass accumulation and starchy root production. The mechanism underlying drought-tolerance remains obscure in cassava. In this study, changes of physiological characters and gene transcriptome profiles were investigated under dehydration stress simulated by polyethylene glycol (PEG) treatments. Five traits, including peroxidase (POD) activity, proline content, malondialdehyde (MDA), soluble sugar and soluble protein, were all dramatically induced in response to PEG treatment. RNA-seq analysis revealed a gradient decrease of differentially expressed (DE) gene number in tissues from bottom to top of a plant, suggesting that cassava root has a quicker response and more induced/depressed DE genes than leaves in response to drought. Overall, dynamic changes of gene expression profiles in cassava root and leaves were uncovered: genes related to glycolysis, abscisic acid and ethylene biosynthesis, lipid metabolism, protein degradation, and second metabolism of flavonoids were significantly induced, while genes associated with cell cycle/organization, cell wall synthesis and degradation, DNA synthesis and chromatin structure, protein synthesis, light reaction of photosynthesis, gibberelin pathways and abiotic stress were greatly depressed. Finally, novel pathways in ABA-dependent and ABA-independent regulatory networks underlying PEG-induced dehydration response in cassava were detected, and the RNA-Seq results of a subset of fifteen genes were confirmed by real-time PCR. The findings will improve our understanding of the mechanism related to dehydration stress-tolerance in cassava and will provide useful candidate genes for breeding of cassava varieties better adapted to drought environment. PMID:26927071

  16. Physiological, Ultrastructural and Proteomic Responses in the Leaf of Maize Seedlings to Polyethylene Glycol-Stimulated Severe Water Deficiency

    PubMed Central

    Shao, Ruixin; Xin, Longfei; Mao, Jun; Li, Leilei; Kang, Guozhang; Yang, Qinghua

    2015-01-01

    After maize seedlings grown in full-strength Hoagland solution for 20 days were exposed to 20% polyethylene glycol (PEG)-stimulated water deficiency for two days, plant height, shoot fresh and dry weights, and pigment contents significantly decreased, whereas malondialdehyde (MDA) content greatly increased. Using transmission electron microscopy, we observed that chloroplasts of mesophyll cells in PEG-treated maize seedlings were swollen, with a disintegrating envelope and disrupted grana thylakoid lamellae. Using two-dimensional gel electrophoresis (2-DE) method, we were able to identify 22 protein spots with significantly altered abundance in the leaves of treated seedlings in response to water deficiency, 16 of which were successfully identified. These protein species were functionally classified into signal transduction, stress defense, carbohydrate metabolism, protein metabolism, and unknown categories. The change in the abundance of the identified protein species may be closely related to the phenotypic and physiological changes due to PEG-stimulated water deficiency. Most of the identified protein species were putatively located in chloroplasts, indicating that chloroplasts may be prone to damage by PEG stimulated-water deficiency in maize seedlings. Our results help clarify the molecular mechanisms of the responses of higher plants to severe water deficiency. PMID:26370980

  17. Physiological, Ultrastructural and Proteomic Responses in the Leaf of Maize Seedlings to Polyethylene Glycol-Stimulated Severe Water Deficiency.

    PubMed

    Shao, Ruixin; Xin, Longfei; Mao, Jun; Li, Leilei; Kang, Guozhang; Yang, Qinghua

    2015-01-01

    After maize seedlings grown in full-strength Hoagland solution for 20 days were exposed to 20% polyethylene glycol (PEG)-stimulated water deficiency for two days, plant height, shoot fresh and dry weights, and pigment contents significantly decreased, whereas malondialdehyde (MDA) content greatly increased. Using transmission electron microscopy, we observed that chloroplasts of mesophyll cells in PEG-treated maize seedlings were swollen, with a disintegrating envelope and disrupted grana thylakoid lamellae. Using two-dimensional gel electrophoresis (2-DE) method, we were able to identify 22 protein spots with significantly altered abundance in the leaves of treated seedlings in response to water deficiency, 16 of which were successfully identified. These protein species were functionally classified into signal transduction, stress defense, carbohydrate metabolism, protein metabolism, and unknown categories. The change in the abundance of the identified protein species may be closely related to the phenotypic and physiological changes due to PEG-stimulated water deficiency. Most of the identified protein species were putatively located in chloroplasts, indicating that chloroplasts may be prone to damage by PEG stimulated-water deficiency in maize seedlings. Our results help clarify the molecular mechanisms of the responses of higher plants to severe water deficiency. PMID:26370980

  18. The Differential Response of Proteins to Macromolecular Crowding

    PubMed Central

    Candotti, Michela; Orozco, Modesto

    2016-01-01

    The habitat in which proteins exert their function contains up to 400 g/L of macromolecules, most of which are proteins. The repercussions of this dense environment on protein behavior are often overlooked or addressed using synthetic agents such as poly(ethylene glycol), whose ability to mimic protein crowders has not been demonstrated. Here we performed a comprehensive atomistic molecular dynamic analysis of the effect of protein crowders on the structure and dynamics of three proteins, namely an intrinsically disordered protein (ACTR), a molten globule conformation (NCBD), and a one-fold structure (IRF-3) protein. We found that crowding does not stabilize the native compact structure, and, in fact, often prevents structural collapse. Poly(ethylene glycol) PEG500 failed to reproduce many aspects of the physiologically-relevant protein crowders, thus indicating its unsuitability to mimic the cell interior. Instead, the impact of protein crowding on the structure and dynamics of a protein depends on its degree of disorder and results from two competing effects: the excluded volume, which favors compact states, and quinary interactions, which favor extended conformers. Such a viscous environment slows down protein flexibility and restricts the conformational landscape, often biasing it towards bioactive conformations but hindering biologically relevant protein-protein contacts. Overall, the protein crowders used here act as unspecific chaperons that modulate the protein conformational space, thus having relevant consequences for disordered proteins. PMID:27471851

  19. 75 FR 75454 - Polyethylene Retail Carrier Bags From Thailand: Extension of Time Limit for the Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-03

    ... polyethylene retail carrier bags from Thailand. See Polyethylene Retail Carrier Bags From Thailand: Preliminary Results of Antidumping Duty Administrative Review, 75 FR 53953 (September 2, 2010). The administrative... International Trade Administration Polyethylene Retail Carrier Bags From Thailand: Extension of Time Limit...

  20. Enhancement of the predicted drug hepatotoxicity in gel entrapped hepatocytes within polysulfone-g-poly (ethylene glycol) modified hollow fiber

    SciTech Connect

    Shen Chong; Zhang Guoliang; Meng Qin

    2010-12-01

    Collagen gel-based 3D cultures of hepatocytes have been proposed for evaluation of drug hepatotoxicity because of their more reliability than traditional monolayer culture. The collagen gel entrapment of hepatocytes in hollow fibers has been proven to well reflect the drug hepatotoxicity in vivo but was limited by adsorption of hydrophobic drugs onto hollow fibers. This study aimed to investigate the impact of hollow fibers on hepatocyte performance and drug hepatotoxicity. Polysulfone-g-poly (ethylene glycol) (PSf-g-PEG) hollow fiber was fabricated and applied for the first time to suppress the drug adsorption. Then, the impact of hollow fibers was evaluated by detecting the hepatotoxicity of eight selected drugs to gel entrapped hepatocytes within PSf and PSf-g-PEG hollow fibers, or without hollow fibers. The hepatocytes in PSf-g-PEG hollow fiber showed the highest sensitivity to drug hepatotoxicity, while those in PSf hollow fiber and cylindrical gel without hollow fiber underestimated the hepatotoxicity due to either drug adsorption or low hepatic functions. Therefore, the 3D culture of gel entrapped hepatocytes within PSf-g-PEG hollow fiber would be a promising tool for investigation of drug hepatotoxicity in vitro.

  1. Role of Side-Chain Molecular Features in Tuning Lower Critical Solution Temperatures (LCSTs) of Oligoethylene Glycol Modified Polypeptides.

    PubMed

    Gharakhanian, Eric G; Deming, Timothy J

    2016-07-01

    A series of thermoresponsive polypeptides has been synthesized using a methodology that allowed facile adjustment of side-chain functional groups. The lower critical solution temperature (LCST) properties of these polymers in water were then evaluated relative to systematic molecular modifications in their side-chains. It was found that in addition to the number of ethylene glycol repeats in the side-chains, terminal and linker groups also have substantial and predictable effects on cloud point temperatures (Tcp). In particular, we found that the structure of these polypeptides allowed for inclusion of polar hydroxyl groups, which significantly increased their hydrophilicity and decreased the need to use long oligoethylene glycol repeats to obtain LCSTs. The thioether linkages in these polypeptides were found to provide an additional structural feature for reversible switching of both polypeptide conformation and thermoresponsive properties. PMID:27102972

  2. Scoping study. High density polyethylene (HDPE) in salstone service

    SciTech Connect

    Phifer, Mark A.

    2005-02-18

    An evaluation of the use of high density polyethylene (HDPE) geomembranes in Saltstone service has been conducted due to the potential benefits that could be derived from such usage. HDPE is one of the simplest hydrocarbon polymers and one of the most common polymers utilized in the production of geomembranes, which means that its costs are relatively low. Additionally, HDPE geomembranes have an extremely low permeability and an extremely low water vapor diffusional flux, which means that it is a good barrier to contaminant transport. The primary consideration in association with HDPE geomembranes in Saltstone service is the potential impact of Saltstone on the degradation of the HDPE geomembranes. Therefore, the evaluation documented herein has primarily focused upon the potential HDPE degradation in Saltstone service.

  3. Electrospun Polyaniline/Polyethylene Oxide Nanofiber Field Effect Transistor

    NASA Technical Reports Server (NTRS)

    Pinto, N. J.; Johnson, A. T.; MacDiarmid, A. G.; Mueller, C. H.; Theofylaktos, N.; Robinson, D. C.; Miranda, F. A.

    2003-01-01

    We report on the observation of field effect transistor (FET) behavior in electrospun camphorsulfonic acid doped polyaniline(PANi)/polyethylene oxide(PE0) nanofibers. Saturation channel currents are observed at surprisingly low source/drain voltages. The hole mobility in the depletion regime is 1.4 x 10(exp -4) sq cm/V s while the 1-D charge density (at zero gate bias) is calculated to be approximately 1 hole per 50 two-ring repeat units of polyaniline, consistent with the rather high channel conductivity (approx. 10(exp -3) S/cm). Reducing or eliminating the PEO content in the fiber is expected to enhance device parameters. Electrospinning is thus proposed as a simple method of fabricating 1-D polymer FET's.

  4. A bacterium that degrades and assimilates poly(ethylene terephthalate).

    PubMed

    Yoshida, Shosuke; Hiraga, Kazumi; Takehana, Toshihiko; Taniguchi, Ikuo; Yamaji, Hironao; Maeda, Yasuhito; Toyohara, Kiyotsuna; Miyamoto, Kenji; Kimura, Yoshiharu; Oda, Kohei

    2016-03-11

    Poly(ethylene terephthalate) (PET) is used extensively worldwide in plastic products, and its accumulation in the environment has become a global concern. Because the ability to enzymatically degrade PET has been thought to be limited to a few fungal species, biodegradation is not yet a viable remediation or recycling strategy. By screening natural microbial communities exposed to PET in the environment, we isolated a novel bacterium, Ideonella sakaiensis 201-F6, that is able to use PET as its major energy and carbon source. When grown on PET, this strain produces two enzymes capable of hydrolyzing PET and the reaction intermediate, mono(2-hydroxyethyl) terephthalic acid. Both enzymes are required to enzymatically convert PET efficiently into its two environmentally benign monomers, terephthalic acid and ethylene glycol. PMID:26965627

  5. Horseradish Peroxidase Inactivation: Heme Destruction and Influence of Polyethylene Glycol

    PubMed Central

    Mao, Liang; Luo, Siqiang; Huang, Qingguo; Lu, Junhe

    2013-01-01

    Horseradish peroxidase (HRP) mediates efficient conversion of many phenolic contaminants and thus has potential applications for pollution control. Such potentially important applications suffer however from the fact that the enzyme becomes quickly inactivated during phenol oxidation and polymerization. The work here provides the first experimental data of heme consumption and iron releases to support the hypothesis that HRP is inactivated by heme destruction. Product of heme destruction is identified using liquid chromatography with mass spectrometry. The heme macrocycle destruction involving deprivation of the heme iron and oxidation of the 4-vinyl group in heme occurs as a result of the reaction. We also demonstrated that heme consumption and iron releases resulting from HRP destruction are largely reduced in the presence of polyethylene glycol (PEG), providing the first evidence to indicate that heme destruction is effectively suppressed by co-dissolved PEG. These findings advance a better understanding of the mechanisms of HRP inactivation. PMID:24185130

  6. Evaluation of polyethylene oxide compacts as gastroretentive delivery systems.

    PubMed

    Mahalingam, Ravichandran; Jasti, Bhaskara; Birudaraj, Raj; Stefanidis, Dimitrios; Killion, Robert; Alfredson, Tom; Anne, Pratap; Li, Xiaoling

    2009-01-01

    Compacts containing selected bioadhesive polymers, fillers, and binders were investigated for their potential as a bioadhesive gastroretentive delivery system to deliver water soluble and water insoluble compounds in the stomach. Compacts with 90:10, 75:25, and 60:40 of polyvinylpyrrolidone (PVP) and polyethylene oxide (PEO) were evaluated for swelling, dissolution, bioadhesion, and in vitro gastric retention. Compacts containing higher PEO showed higher swelling (111.13%) and bioadhesion (0.62 +/- 0.03 N/cm(2)), and retained their integrity and adherence onto gastric mucosa for about 9 h under in vitro conditions. In vivo gastroretentive property of compacts were evaluated in Yorkshire cross swine. Compacts containing 58% PVP, 40% PEO and 2% of water soluble or water insoluble marker compounds showed gastroadhesive and retentive properties in vivo. It is concluded that PEO in combination with PVP yields a non disintegrating type bioadhesive dosage form which is suitable for gastroretentive applications. PMID:19148757

  7. Immobilization of bacteria in microgel grafted onto macroporous polyethylene

    NASA Astrophysics Data System (ADS)

    Trelles, J. A.; Quiroga, F.; Britos, C.; Smolko, Eduardo E.; Grasselli, Mariano

    2010-03-01

    The development of " Green Chemistry" requires new materials to replace the conventional organic chemistry by biological catalysts, to produce fine chemicals in an environmentally friendly manner. Microbial whole cells can be directly used as biocatalysts, providing a simple and cheap methodology since enzyme isolation and purification are avoided. High-density polyethylene (HDPE) is a very stable polymer though it can be activated by gamma radiation to induce grafting. Glycidyl methacrylate was grafted onto macroporous HDPE and PP in the range of 1-6%, proportional to the initial monomer concentration. Grafted polymers were further chemically modified with ethylenediamine to generate a cationic hydrogel of micron-size thickness onto the internal polymer surfaces. Modified polymers were able to immobilize Gram-positive and Gram-negative bacteria that can catalyze a chemical reaction as efficient as free cells do.

  8. AFM surface investigation of polyethylene modified by ion bombardment

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Arenholz, E.; Hnatowicz, V.; Rybka, V.; Öchsner, R.; Ryssel, H.

    1998-07-01

    Polyethylene (PE) was irradiated with 63 keV Ar + and 155 keV Xe + ions to fluences of 1 × 10 13 to 3 × 10 15 cm -2 with ion energies being chosen in order to achieve approximately the same penetration depth for both species. The PE surface morphology was examined by means of atomic force microscopy (AFM), whereas the concentration of free radicals and conjugated double bonds, both created by the ion irradiation, were determined using electron paramagnetic resonance (EPR) and UV-VIS spectroscopy, respectively. As expected, the degradation of PE was higher after irradiation with heavier Xe + ions but the changes in the PE surface morphology were more pronounced for Ar + ions. This newly observed effect can be explained by stronger compaction of the PE surface layer in the case of the Xe + irradiation, connected with a reduction of free volume available.

  9. Oxidation-Enhanced TSC and TSSP of Polyethylene

    NASA Astrophysics Data System (ADS)

    Mizutani, Teruyoshi; Ikeda, Seita; Ieda, Masayuki

    1986-01-01

    The conduction, TSC and TSSP of both low-density and high-density polyethylene (LDPE and HDPE) were found to be strongly enhanced by oxidation. Oxidized PE showed two TSC peaks, P1 and P2. Peak P1 was caused by the depolarization of C{=}0 dipoles and peak P2 originated from injected homo space charge. Thermal pulse experiments revealed the existence of negative and positive homo space charges in oxidized PE polarized at high fields. VTSSP(T) increased in the temperature regions of peaks P1 and P2, and TSSP and TSC were found to be closely related to each other. Peak P1 and VTSSP(T) at room temperature were proportional to the concentration of C{=}0 groups and can be utilized for diagnosing the degradation of PE accompanied by oxidation.

  10. Modeling polyethylene wear acceleration due to femoral head dislocation damage.

    PubMed

    Kruger, Karen M; Tikekar, Nishant M; Heiner, Anneliese D; Lannutti, John J; Callaghan, John J; Brown, Thomas D

    2014-08-01

    Scratching, scraping, and metal transfer to femoral heads commonly accompany acetabular shell contact during dislocation and closed reduction maneuvers. While head damage conceptually leads to accelerated wear, reports on this subject are mainly anecdotal, and differ widely on the potency of such effect. Towards better understanding this relationship, a physically validated finite element (FE) model was used to compute polyethylene wear acceleration propensity of specific head damage patterns on thirteen retrievals. These FE models estimated wear increases averaging half an order of magnitude when compared to simulations for undamaged heads. There was no correlation between the number of dislocations sustained and wear acceleration. These results underscore the importance of implant-gentle closed reduction, and heightened wear monitoring of successfully reduced dislocation patients. PMID:24851789

  11. Direct Synthesis of Imidazolium-Functional Polyethylene by Insertion Copolymerization.

    PubMed

    Jian, Zhongbao; Leicht, Hannes; Mecking, Stefan

    2016-06-01

    Cationic imidazolium-functionalized polyethylene is accessible by insertion copolymerization of ethylene and allyl imidazolium tetrafluoroborate (AIm-BF4 ) with phosphinesulfonato palladium(II) catalyst precursors. Imidazolium-substituted repeat units are incorporated into the main chain and the initiating saturated chain end of the linear polymers, rather than the terminating unsaturated chain end. The counterion of the allyl imidazolium monomer is decisive, with the chloride analogue (AIm-Cl) no polymerization is observed. Stoichiometric studies reveal the formation of an inactive chloride complex from the catalyst precursor. An effect of moderate densities (0.5 mol%) of ionic groups on the copolymers' physical properties is exemplified by an enhanced wetting by water. PMID:27111477

  12. Hydrophobic composition based on mixed-molecular weight polyethylene

    NASA Astrophysics Data System (ADS)

    Gorlenko, Nikolay; Debelova, Natalya; Sarkisov, Yuriy; Volokitin, Gennadiy; Zavyalova, Elena; Lapova, Tatyana

    2016-01-01

    The paper presents investigations of compositions based on low and high molecular weight polyethylene so as to synthesize a hydrophobic composition for moisture protection of timber. X-ray phase analysis and measurements of the tear-off force of hydrophobic coating needed to apply to the timber surface and the limiting wetting angle are carried out to detect the hydrophobic, adhesive, electrophysical, and physicochemical properties of compositions. Kinetic dependencies are given for moisture absorption of timber specimens. It is shown that the preliminary formation of the texture by the surface patterning or its treatment with low-temperature plasma with the following protective coating results in the improvement of hydrophobic properties of the suggested compositions. These compositions can be used in the capacity of water repellents to protect building materials from moisture including restoration works.

  13. The effect of polyethylene glycol on shellac stability

    NASA Astrophysics Data System (ADS)

    Khairuddin; Pramono, Edi; Budi Utomo, Suryadi; Wulandari, Viki; A'an Zahrotul, W.; Clegg, Francis

    2016-02-01

    The effect of polyethylene glycol (PEG) having amolecular weight of 1000 and 2000 on shellac stability has been investigated in this research. The shellac was shellac wax free, and the solvent was ethanol 96%. Shellac films were prepared by solventevaporationmethod. The stability of shellac was investigated using insoluble solid test, Fourier Transform Infra Red (FTIR), Thermogravimetry Analyzer (TGA), and Water Vapour Transmission Rate (WVTR). The results showed that stability of shellac decreased after heating at 125oC for 10,30,90,and 180 minutes, and storing for 1 month at 27 oC and 85 relative humidity (RH). PEG improved the stability, and the most stable effect was achieved through PEG1000.

  14. Antibacterial Performance of Alginic Acid Coating on Polyethylene Film

    PubMed Central

    Karbassi, Elika; Asadinezhad, Ahmad; Lehocký, Marian; Humpolíček, Petr; Vesel, Alenka; Novák, Igor; Sáha, Petr

    2014-01-01

    Alginic acid coated polyethylene films were examined in terms of surface properties and bacteriostatic performance against two most representative bacterial strains, that is, Escherichia coli and Staphylococcus aureus. Microwave plasma treatment followed by brush formation in vapor state from three distinguished precursors (allylalcohol, allylamine, hydroxyethyl methacrylate) was carried out to deposit alginic acid on the substrate. Surface analyses via various techniques established that alginic acid was immobilized onto the surface where grafting (brush) chemistry influenced the amount of alginic acid coated. Moreover, alginic acid was found to be capable of bacterial growth inhibition which itself was significantly affected by the brush type. The polyanionic character of alginic acid as a carbohydrate polymer was assumed to play the pivotal role in antibacterial activity. The cell wall composition of two bacterial strains along with the substrates physicochemical properties accounted for different levels of bacteriostatic performance. PMID:25196604

  15. Laser-generated plasma by carbon nanoparticles embedded into polyethylene

    NASA Astrophysics Data System (ADS)

    Torrisi, L.; Ceccio, G.; Cutroneo, M.

    2016-05-01

    Carbon nanoparticles have been embedded into polyethylene at different concentrations by using chemical-physical processes. The synthesized material was characterized in terms of physical modifications concerning the mechanical, compositional and optical properties. Obtained flat targets have been irradiated by Nd:YAG laser at intensities of the order of 1010 W/cm2 in order to generate non-equilibrium plasma in vacuum. The laser-matter interaction produces charge separation effects with consequent acceleration of protons and carbon ions. Plasma was characterized using time-of-flight measurements of the accelerated ions. Applications of the produced targets in order to generate carbon ion beams from laser-generated plasma are presented and discussed.

  16. Irradiation of linear polyethylene - Partitioning between sol and gel.

    NASA Technical Reports Server (NTRS)

    Rijke, A. M.; Mandelkern, L.

    1971-01-01

    Molecular weight fractions of linear polyethylene were irradiated at 133 C, in the completely molten and highly crystalline states, for the purpose of assessing the importance of chain-scission processes and establishing the critical conditions for gelation. The partitioning between sol and gel in either state was found to adhere to the theory for the intermolecular cross-linking of monodisperse species for dosages just beyond the gel point. Deviations from theory occurred as the dosage was increased further. It was concluded that main-chain scission, at these temperatures, is not a significant process. High molecular weight samples in the completely molten state obeyed the Flory-Stockmayer condition for critical gelation.

  17. Simulation of polyethylene glycol and calcium-mediated membrane fusion

    SciTech Connect

    Pannuzzo, Martina; De Jong, Djurre H.; Marrink, Siewert J.; Raudino, Antonio

    2014-03-28

    We report on the mechanism of membrane fusion mediated by polyethylene glycol (PEG) and Ca{sup 2+} by means of a coarse-grained molecular dynamics simulation approach. Our data provide a detailed view on the role of cations and polymer in modulating the interaction between negatively charged apposed membranes. The PEG chains cause a reduction of the inter-lamellar distance and cause an increase in concentration of divalent cations. When thermally driven fluctuations bring the membranes at close contact, a switch from cis to trans Ca{sup 2+}-lipid complexes stabilizes a focal contact acting as a nucleation site for further expansion of the adhesion region. Flipping of lipid tails induces subsequent stalk formation. Together, our results provide a molecular explanation for the synergistic effect of Ca{sup 2+} and PEG on membrane fusion.

  18. RAPID COMMUNICATION: Pressure effect on the electrical ageing of polyethylene

    NASA Astrophysics Data System (ADS)

    Lalam, F.-Benlizidia; Hoang-The-Giam

    2000-11-01

    The purpose of this study is to show the effect of hydrostatic pressure on the electrical ageing, by a dc voltage, on polyethylene used in submarine cables. Experimental results are obtained at 1 and 300 bar, for a temperature of 70 °C in the range of an electrical field of 1.1-4.5 MV cm-1 and for up to 1500 h of ageing. By using the Weibull statistic and the estimation of confidence bounds of 90%, the results have shown an increase of lifetime with pressure. The time dependence of the breakdown behaviour of the two materials (HDPE and XLPE) is consistent with the inverse power law model. The pressure effect may be explained by changes in the activation free energy for the formation of submicrocavities.

  19. Modification of surface properties of polyethylene by Ar plasma discharge

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Kotál, V.; Slepička, P.; Bláhová, O.; Špírková, M.; Sajdl, P.; Hnatowicz, V.

    2006-03-01

    Polyethylene (PE) surface was modified by Ar plasma discharge. The changes of surface morphology and surface wettability (characterized by contact angle) were followed using AFM microscopy and standard goniometry, respectively. The changes of chemical structure of PE polymeric chain were characterized by FTIR and XPS techniques. A nanoindenter was used to study mechanical properties (microhardness, elasticity module and microscratch test) of modified PE. After exposition to the plasma discharge a fast decline of the contact angle is observed. The decline depends on the discharge power and the time elapsed from the plasma exposition. FTIR and XPS measurements indicate an oxidation of degraded polymeric chains and creation of hydroxyl, carbonyl, ether, ester and carboxyl groups. Surface morphology of modified PE depends on the plasma discharge power and exposure time. Maximum microhardness and elastic module, observed on PE specimens exposed to plasma discharge for 240 s, may be connected with PE crosslinking initiated by plasma discharge.

  20. Production and characterization of polyethylene/organoclay oriented fiber

    NASA Astrophysics Data System (ADS)

    Coppola, B.; Di Maio, L.; Scarfato, P.; Incarnato, L.

    2016-05-01

    The aim of this work was to study the influence of drawing process on the mechanical properties of polyethylene/clay fibers. To this extent, three different PE/clay blends (3, 5 and 10 wt.%) were prepared by melt compounding in a twin-screw extruder. The investigated clay was a commercial organically modified montmorillonite (Dellite 67G). After compounding fibers were produced by a single-screw extruder and drawn at different draw ratios. At increasing draw ratio an increase of elastic modulus and tensile strength was attained. The presence of clay layers increases fibers ductility hindering fibrils formation during the drawing process. Moreover, at increasing clay contents a decrease of tensile strength for high draw ratios was observed. These results demonstrated that the dispersed clay layers can be re-aggregated by the uniaxial flow induced by the drawing process resulting in a decay of mechanical properties at high draw ratios.

  1. The characterisation of two different degradable polyethylene (PE) sacks

    SciTech Connect

    Davis, G. . E-mail: gudavis@cytanet.com.cy

    2006-12-15

    The compostability of two different polyethylene (PE) products on the UK market under open-windrow composting conditions is explored within this paper. Chemical analysis of the PE bags has established their constituents in order to examine how the PE bags have an increased degradability depending on additives. Weight loss of the two different PE products within open-windrow composting conditions was recorded in order to establish the percentage weight loss as an indication of the degradability of the two products and their relative suitability for open-windrow composting. Scanning electron microscopy (SEM) of the PE products over the composting duration established the degradation processes for the PE products within the compost. These analyses concluded that one of the PE product mixes was more degradable than the other. However, neither product completed degraded within the timeframe of 12-14 weeks generally accepted for open-windrow composting in the UK.

  2. Dimensionally stable PET fibers for tire reinforcement. [Polyethylene terephthalate (POLYESTERS)

    SciTech Connect

    Rim, P.B.; Nelson, C.J.

    1991-05-01

    High-modulus, high-tenacity polyethylene terephthalate (PET) fibers have gained wide acceptance in reinforcement for rubber products such as tires and hoses; in geotextiles, and in ropes and cordage. Accordingly, a great deal of fundamental research has been conducted on how the processing and resulting morphology of these thermoplastic fibers affect their physical properties. The translation of these starting fiber properties to those in the final end-use product has received much less attention. This article compares the structure-property relationships of recently-developed PET yarns possessing high dimensional stability (i.e., high modulus and low shrinkage) with conventional PET tire yarn. Interest in these materials is stimulated by their ability to improve tire uniformity and, for some tire manufacturers, eliminate the need for post-cure inflation during tire manufacturing. Where possible, cause and effect relationships will be developed.

  3. Texturation and superhydrophobicity of polyethylene terephthalate thanks to plasma technology

    NASA Astrophysics Data System (ADS)

    Tarrade, Jeanne; Darmanin, Thierry; Taffin de Givenchy, Elisabeth; Guittard, Frédéric; Debarnot, Dominique; Poncin-Epaillard, Fabienne

    2014-02-01

    Anti-bioadhesive surfaces were designed from polyethylene terephthalate (PET) by three steps plasma-treatment. First, the nano-pattern is created by oxygen plasma-treatment with controlled dimensions. Then, the plasma-treated polymeric surface was hydrophobized with a tetrafluorocarbon plasma, allowing to obtain a water contact angle of 145 ± 4°. However, the SEM pictures give evidence to show the degradation of the structuration caused by the CF4-plasma and consequently, the superhydrophobicity was not reached. Thus, a plasma-polypyrrole layer was deposited before the plasma-fluorination, which has a protective role against the degradation generated by fluorinated species, preserving the structuration and improving the fluorination rate. Therefore, the obtained surfaces are superhydrophobic with water contact angle of 157 ± 2° and a hysteresis of 65 ± 3°. The ability of these surfaces to reduce bioadhesion will be performed in further work.

  4. Gel permeation chromatography (GPC) of repeatedly extruded polyethylene terephthalate (PET).

    PubMed

    Milana, M R; Denaro, M; Arrivabene, L; Maggio, A; Gramiccioni, L

    1998-04-01

    The paper deals with gel permeation chromatography (GPC) monitoring of the behaviour of PET (polyethylene terephthalate) after repeated extrusions. Virgin PET was submitted to three successive extrusion/drying cycles and then the samples were swelled with hexafluoroisopropanol and treated with chloroform. GPC analysis was carried out at room temperature on a B.C.S. Serial LC 2000 GPC system equipped with a series of four GPC columns with UV detection at 254 nm and chloroform as eluent. GPC results showed that after each extrusion step the molecular weight distribution of the PET was different and Mw, Mn and Mz decreased. These findings suggest that during each extrusion degradation occurs and that repeated extrusions, as in the case of the recycling PET, may cause an alteration of the molecular weight distribution of the original PET. PMID:9666895

  5. Textural changes in metallurgical coke prepared with polyethylene

    NASA Astrophysics Data System (ADS)

    Gornostayev, Stanislav S.; Heino, Jyrki J.; Kokkonen, Tommi M. T.; Makkonen, Hannu T.; Huttunen, Satu M. M.; Fabritius, Timo M. J.

    2014-10-01

    The effect of high-density polyethylene (HDPE) on the textural features of experimental coke was investigated using polarized-light optical microscopy and wavelet-based image analysis. Metallurgical coke samples were prepared in a laboratory-scale furnace with 2.5%, 5.0%, 7.5%, 10.0%, and 12.5% HDPE by mass, and one sample was prepared by 100% coal. The amounts and distribution of textures (isotropic, mosaic and banded) and pores were obtained. The calculations reveal that the addition of HDPE results in a decrease of mosaic texture and an increase of isotropic texture. Ethylene formed from the decomposition of HDPE is considered as a probable reason for the texture modifications. The approach used in this study can be applied to indirect evaluation for the reactivity and strength of coke.

  6. Polyethylene glycol diffusion in ex vivo skin tissue

    NASA Astrophysics Data System (ADS)

    Genin, V. D.; Tuchina, D. K.; Bashkatov, A. N.; Genina, E. A.; Tuchin, V. V.

    2015-11-01

    Optical clearing of the rat skin under the action of polyethylene glycol (PEG) with molecular weight 300 and 400 Dalton was studied ex vivo. The collimated transmittance was measured at the wavelength range 500-900 nm. It was found that collimated transmittance of skin samples increased, whereas weight, thickness and area of the samples decreased during PEG penetration in skin tissue. A mechanism of the optical clearing under the action of PEG is discussed. Taking into account the kinetics of volume and thickness of the skin samples, diffusion coefficient of PEGs in skin tissue has been estimated as (1.83±2.22)×10-6 cm2/s and (1.70±1.47)×10-6 cm2/s for PEG-300 and PEG-400, respectively. The presented results can be useful for enhancement of many methods of laser therapy and optical diagnostics of skin diseases and localization of subcutaneous neoplasms.

  7. Hybrid estimation technique for predicting butene concentration in polyethylene reactor

    NASA Astrophysics Data System (ADS)

    Mohd Ali, Jarinah; Hussain, M. A.

    2016-03-01

    A component of artificial intelligence (AI), which is fuzzy logic, is combined with the so-called conventional sliding mode observer (SMO) to establish a hybrid type estimator to predict the butene concentration in the polyethylene production reactor. Butene or co-monomer concentration is another significant parameter in the polymerization process since it will affect the molecular weight distribution of the polymer produced. The hybrid estimator offers straightforward formulation of SMO and its combination with the fuzzy logic rules. The error resulted from the SMO estimation will be manipulated using the fuzzy rules to enhance the performance, thus improved on the convergence rate. This hybrid estimation is able to estimate the butene concentration satisfactorily despite the present of noise in the process.

  8. Effects of sterilization on poly(ethylene glycol) hydrogels.

    PubMed

    Kanjickal, Deenu; Lopina, Stephanie; Evancho-Chapman, M Michelle; Schmidt, Steven; Donovan, Duane

    2008-12-01

    The past few decades have witnessed a dramatic increase in the development of polymeric biomaterials. These biomaterials have to undergo a sterilization procedure before implantation. However, many sterilization procedures have been shown to profoundly affect polymer properties. Poly(ethylene glycol) hydrogels have gained increasing importance in the controlled delivery of therapeutics and in tissue engineering. We evaluated the effect of ethylene oxide (EtO), hydrogen peroxide (H(2)O(2)), and gamma sterilization of poly(ethylene glycol) hydrogels on properties relevant to controlled drug delivery and tissue engineering. We observed that the release of cyclosporine (CyA) (an immunosuppressive drug that is effective in combating tissue rejection following organ transplantation) was significantly affected by the type of sterilization. However, that was not the case with rhodamine B, a dye. Hence, the drug release characteristics were observed to be dependent not only on the sterilization procedure but also on the type of agent that needs to be delivered. In addition, differences in the swelling ratios for the sterilized and unsterilized hydrogels were statistically significant for 1:1 crosslinked hydrogels derived from the 8000 MW polymer. Significant differences were also observed for gamma sterilization for 1:1 crosslinked hydrogels derived from the 3350 MW polymer and also the 2:1 crosslinked hydrogels derived from the 8000 MW polymer. Atomic force microscopy (AFM) studies revealed that the roughness parameter for the unsterilized and EtO-sterilized PEG hydrogels remained similar. However, a statistically significant reduction of the roughness parameter was observed for the H(2)O(2) and gamma-sterilized samples. Electron spin resonance (ESR) studies on the unsterilized and the sterilized samples revealed the presence of the peroxy and the triphenyl methyl carbon radical in the samples. The gamma and the H(2)O(2)-sterilized samples were observed to have a much

  9. The pros and cons of polyethylene sterilization with gamma irradiation.

    PubMed

    Hopper, Robert H; Engh, C Anderson; Fowlkes, LaTonya B; Engh, Charles A

    2004-12-01

    This retrospective study evaluated the implant, patient and surgical factors associated with polyethylene wear for one type of porous-coated hemispheric total hip arthroplasty cup. Radiographic wear measurements among 567 Duraloc cups (512 patients) revealed that liners sterilized by gamma-irradiation wore 0.085 mm/year less than those that were sterilized by gas-plasma, a noncross-linking chemical surface treatment. The substantially decreased wear rate associated with gamma-irradiation was attributed to sterilization-induced polyethylene cross-linking. Shelf-aging adversely affected liners that were gamma irradiated in air. On average, highly crystalline Hylamer liners showed a 0.064 mm/year increase in wear rates for each year of shelf storage after terminal sterilization with gamma-irradiation in air. Among conventional Enduron liners, the effect of shelf aging after gamma-irradiation in air was more modest, increasing wear rates by 0.014 mm/year for each year of shelf storage. Because Hylamer's wear performance degraded at about five times the rate of Enduron's, the improved wear resistance associated with gamma-irradiation in air would be lost after 1.3 years of shelf aging for Hylamer compared with 6.1 years for Enduron. For every additional year of age at the time of surgery, the wear rate decreased by 0.003 mm/year. Increased body mass index, a preoperative diagnosis of inflammatory arthritis, and a ceramic femoral head also were associated with decreased wear rates. PMID:15577466

  10. Subunit Stabilization and Polyethylene Glycolation of Cocaine Esterase Improves In Vivo Residence Time

    SciTech Connect

    Narasimhan, Diwahar; Collins, Gregory T.; Nance, Mark R.; Nichols, Joseph; Edwald, Elin; Chan, Jimmy; Ko, Mei-Chuan; Woods, James H.; Tesmer, John J.G.; Sunahara, Roger K.

    2012-03-15

    No small-molecule therapeutic is available to treat cocaine addiction, but enzyme-based therapy to accelerate cocaine hydrolysis in serum has gained momentum. Bacterial cocaine esterase (CocE) is the fastest known native enzyme that hydrolyzes cocaine. However, its lability at 37 C has limited its therapeutic potential. Cross-linking subunits through disulfide bridging is commonly used to stabilize multimeric enzymes. Herein we use structural methods to guide the introduction of two cysteine residues within dimer interface of CocE to facilitate intermolecular disulfide bond formation. The disulfide-crosslinked enzyme displays improved thermostability, particularly when combined with previously described mutations that enhance stability (T172R-G173Q). The newly modified enzyme yielded an extremely stable form of CocE (CCRQ-CocE) that retained greater than 90% of its activity after 41 days at 37 C, representing an improvement of more than 4700-fold over the wild-type enzyme. CCRQ-CocE could also be modified by polyethylene glycol (PEG) polymers, which improved its in vivo residence time from 24 to 72 h, as measured by a cocaine lethality assay, by self-administration in rodents, and by measurement of inhibition of cocaine-induced cardiovascular effects in rhesus monkeys. PEG-CCRQ elicited negligible immune response in rodents. Subunit stabilization and PEGylation has thus produced a potential protein therapeutic with markedly higher stability both in vitro and in vivo.

  11. Injectable Dopamine-Modified Poly(ethylene glycol) Nanocomposite Hydrogel with Enhanced Adhesive Property and Bioactivity

    PubMed Central

    2015-01-01

    A synthetic mimic of mussel adhesive protein, dopamine-modified four-armed poly(ethylene glycol) (PEG-D4), was combined with a synthetic nanosilicate, Laponite (Na0.7+(Mg5.5Li0.3Si8)O20(OH)4)0.7–), to form an injectable naoncomposite tissue adhesive hydrogel. Incorporation of up to 2 wt % Laponite significantly reduced the cure time while enhancing the bulk mechanical and adhesive properties of the adhesive due to strong interfacial binding between dopamine and Laponite. The addition of Laponite did not alter the degradation rate and cytocompatibility of PEG-D4 adhesive. On the basis of subcutaneous implantation in rat, PEG-D4 nanocomposite hydrogels elicited minimal inflammatory response and exhibited an enhanced level of cellular infiltration as compared to Laponite-free samples. The addition of Laponite is potentially a simple and effective method for promoting bioactivity in a bioinert, synthetic PEG-based adhesive while simultaneously enhancing its mechanical and adhesive properties. PMID:25222290

  12. ExtraPEG: A Polyethylene Glycol-Based Method for Enrichment of Extracellular Vesicles

    PubMed Central

    Rider, Mark A.; Hurwitz, Stephanie N.; Meckes, David G.

    2016-01-01

    Initially thought to be a means for cells to eliminate waste, secreted extracellular vesicles, known as exosomes, are now understood to mediate numerous healthy and pathological processes. Though abundant in biological fluids, purifying exosomes has been challenging because their biophysical properties overlap with other secreted cell products. Easy-to-use commercial kits for harvesting exosomes are now widely used, but the relative low-purity and high-cost of the preparations restricts their utility. Here we describe a method for purifying exosomes and other extracellular vesicles by adapting methods for isolating viruses using polyethylene glycol. This technique, called ExtraPEG, enriches exosomes from large volumes of media rapidly and inexpensively using low-speed centrifugation, followed by a single small-volume ultracentrifugation purification step. Total protein and RNA harvested from vesicles is sufficient in quantity and quality for proteomics and sequencing analyses, demonstrating the utility of this method for biomarker discovery and diagnostics. Additionally, confocal microscopy studies suggest that the biological activity of vesicles is not impaired. The ExtraPEG method can be easily adapted to enrich for different vesicle populations, or as an efficient precursor to subsequent purification techniques, providing a means to harvest exosomes from many different biological fluids and for a wide variety of purposes. PMID:27068479

  13. Biomimetic hydration lubrication with various polyelectrolyte layers on cross-linked polyethylene orthopedic bearing materials.

    PubMed

    Kyomoto, Masayuki; Moro, Toru; Saiga, Kenichi; Hashimoto, Masami; Ito, Hideya; Kawaguchi, Hiroshi; Takatori, Yoshio; Ishihara, Kazuhiko

    2012-06-01

    Natural joints rely on fluid thin-film lubrication by the hydrated polyelectrolyte layer of cartilage. However, current artificial joints with polyethylene (PE) surfaces have considerably less efficient lubrication and thus much greater wear, leading to osteolysis and aseptic loosening. This is considered a common factor limiting prosthetic longevity in total hip arthroplasty (THA). However, such wear could be mitigated by surface modification to mimic the role of cartilage. Here we report the development of nanometer-scale hydrophilic layers with varying charge (nonionic, cationic, anionic, or zwitterionic) on cross-linked PE (CLPE) surfaces, which could fully mimic the hydrophilicity and lubricity of the natural joint surface. We present evidence to support two lubrication mechanisms: the primary mechanism is due to the high level of hydration in the grafted layer, where water molecules act as very efficient lubricants; and the secondary mechanism is repulsion of protein molecules and positively charged inorganic ions by the grafted polyelectrolyte layer. Thus, such nanometer-scaled hydrophilic polymers or polyelectrolyte layers on the CLPE surface of acetabular cup bearings could confer high durability to THA prosthetics. PMID:22465336

  14. Carbohydrate-mediated polyethylene glycol conjugation of TSH improves its pharmacological properties.

    PubMed

    Park, Anna; Honey, Denise M; Hou, Lihui; Bird, Julie J; Zarazinski, Christine; Searles, Michelle; Braithwaite, Christian; Kingsbury, Jonathan S; Kyazike, Josephine; Culm-Merdek, Kerry; Greene, Ben; Stefano, James E; Qiu, Huawei; McPherson, John M; Pan, Clark Q

    2013-03-01

    Thyrogen (thyrotropin alfa for injection), recombinant human TSH (rhTSH), has been successfully used to enhance diagnostic radioiodine scanning and thyroglobulin testing in the follow-up of patients with thyroid cancer and as an adjunctive treatment for radioiodine thyroid remnant ablation. However, the short half-life of rhTSH in the circulation requires a multidose regimen. We developed novel sialic acid-mediated and galactose-mediated conjugation chemistries for targeting polyethylene glycol (PEG) to the three N-linked glycosylation sites on the protein, to prolong plasma half-life by eliminating kidney filtration and potential carbohydrate-mediated clearance. Conjugates of different PEG sizes and copy numbers were screened for reaction yield, TSH receptor binding, and murine phamacokinetics/pharmacodynamics studies. The best performing of these products, a 40-kDa mono-PEGylated sialic acid-mediated conjugate, exhibited a 3.5-fold longer duration of action than rhTSH in rats, as a 5-fold lower affinity was more than compensated by a 23-fold extension of circulation half-life. Biochemical characterization confirmed conjugation through the sialic acids. Correlation of PEG distribution on the three N-linked glycosylation sites and the PEG effect on receptor binding supported the previously reported structure-function relationship of rhTSH glycosylation. This long-acting rhTSH has the potential to significantly improve patient convenience and provider flexibility while reducing potential side effects associated with a sudden elevation of serum TSH. PMID:23389953

  15. Subunit Stabilization and Polyethylene Glycolation of Cocaine Esterase Improves In Vivo Residence TimeS⃞

    PubMed Central

    Narasimhan, Diwahar; Collins, Gregory T.; Nance, Mark R.; Nichols, Joseph; Edwald, Elin; Chan, Jimmy; Ko, Mei-Chuan; Woods, James H.; Tesmer, John J. G.

    2011-01-01

    No small-molecule therapeutic is available to treat cocaine addiction, but enzyme-based therapy to accelerate cocaine hydrolysis in serum has gained momentum. Bacterial cocaine esterase (CocE) is the fastest known native enzyme that hydrolyzes cocaine. However, its lability at 37°C has limited its therapeutic potential. Cross-linking subunits through disulfide bridging is commonly used to stabilize multimeric enzymes. Herein we use structural methods to guide the introduction of two cysteine residues within dimer interface of CocE to facilitate intermolecular disulfide bond formation. The disulfide-crosslinked enzyme displays improved thermostability, particularly when combined with previously described mutations that enhance stability (T172R-G173Q). The newly modified enzyme yielded an extremely stable form of CocE (CCRQ-CocE) that retained greater than 90% of its activity after 41 days at 37°C, representing an improvement of more than 4700-fold over the wild-type enzyme. CCRQ-CocE could also be modified by polyethylene glycol (PEG) polymers, which improved its in vivo residence time from 24 to 72 h, as measured by a cocaine lethality assay, by self-administration in rodents, and by measurement of inhibition of cocaine-induced cardiovascular effects in rhesus monkeys. PEG-CCRQ elicited negligible immune response in rodents. Subunit stabilization and PEGylation has thus produced a potential protein therapeutic with markedly higher stability both in vitro and in vivo. PMID:21890748

  16. Poly(ethylene glycol)-containing hydrogel surfaces for antifouling applications in marine and freshwater environments.

    PubMed

    Ekblad, Tobias; Bergström, Gunnar; Ederth, Thomas; Conlan, Sheelagh L; Mutton, Robert; Clare, Anthony S; Wang, Su; Liu, Yunli; Zhao, Qi; D'Souza, Fraddry; Donnelly, Glen T; Willemsen, Peter R; Pettitt, Michala E; Callow, Maureen E; Callow, James A; Liedberg, Bo

    2008-10-01

    This work describes the fabrication, characterization, and biological evaluation of a thin protein-resistant poly(ethylene glycol) (PEG)-based hydrogel coating for antifouling applications. The coating was fabricated by free-radical polymerization on silanized glass and silicon and on polystyrene-covered silicon and gold. The physicochemical properties of the coating were characterized by infrared spectroscopy, ellipsometry, and contact angle measurements. In particular, the chemical stability of the coating in artificial seawater was evaluated over a six-month period. These measurements indicated that the degradation process was slow under the test conditions chosen, with the coating thickness and composition changing only marginally over the period. The settlement behavior of a broad and diverse group of marine and freshwater fouling organisms was evaluated. The tested organisms were barnacle larvae (Balanus amphitrite), algal zoospores (Ulva linza), diatoms (Navicula perminuta), and three bacteria species (Cobetia marina, Marinobacter hydrocarbonoclasticus, and Pseudomonas fluorescens). The biological results showed that the hydrogel coating exhibited excellent antifouling properties with respect to settlement and removal. PMID:18759475

  17. Prevention of peritendinous adhesions with electrospun polyethylene glycol/polycaprolactone nanofibrous membranes.

    PubMed

    Chen, Chih-Hao; Chen, Shih-Hsien; Shalumon, K T; Chen, Jyh-Ping

    2015-09-01

    Postoperative adhesion formation is the major complication that could occur after acute tendon surgery. The application of an anti-adhesive membrane at the post-surgical site is deemed as a potential way to solve this problem by preventing adhesive fibrotic tissue development. In this study, we fabricated electrospun composite poly(ethylene glycol) (PEG)/poly(caprolactone) (PCL) nanofibrous membrane (NFM) to prevent peritendinous adhesions, which could act as a barrier between the tendon and surrounding tissues, without interrupting mass transfer and normal tendon gliding. PCL/PEG NFMs of 0% PEG (PCL), 25% PEG (25PECL), 50% PEG (50PECL) and 75% PEG (75PECL) were prepared and characterized for physico-chemical properties. The PCL NFM shows the lowest protein permeability while 25PECL NFM exhibited the largest fiber diameter, smallest pore size and the largest ultimate stress and strain. The 75PECL NFM had the lowest water contact angle and the highest Young's modulus. In vitro cell adhesion and migration experiments with fibroblasts indicate that all NFMs could prevent cell penetration, with 75PECL NFM having the least cell attachment. In vivo application of 75PECL NFM on the repaired site of rabbit flexor tendon rupture model demonstrated improved efficacy compared with the PCL NFM and a commercial anti-adhesion barrier (Seprafilm™), from gross observation, histological analysis and functional assays. We concluded that 75PECL NFM could function as an effective anti-adhesion membrane after tendon surgery in a clinical setting. PMID:26115533

  18. Protective Effect of Intravenous High Molecular Weight Polyethylene Glycol on Fatty Liver Preservation

    PubMed Central

    Bejaoui, Mohamed; Pantazi, Eirini; Folch-Puy, Emma; Panisello, Arnau; Calvo, María; Pasut, Gianfranco; Rimola, Antoni; Navasa, Miquel; Adam, René; Roselló-Catafau, Joan

    2015-01-01

    Ischemia reperfusion injury (IRI) leads to significant tissue damage in liver surgery. Polyethylene glycols (PEGs) are water soluble nontoxic polymers that have proved their effectiveness against IRI. The objective of our study was to investigate the potential protective effects of intravenous administration of a high molecular weight PEG of 35 kDa (PEG 35) in steatotic livers subjected to cold ischemia reperfusion. In this study, we used isolated perfused rat liver model to assess the effects of PEG 35 intravenous administration after prolonged cold ischemia (24 h, 4°C) and after reperfusion (2 h, 37°C). Liver injury was measured by transaminases levels and mitochondrial damage was determined by confocal microscopy assessing mitochondrial polarization (after cold storage) and by measuring glutamate dehydrogenase activity (after reperfusion). Also, cell signaling pathways involved in the physiopathology of IRI were assessed by western blot technique. Our results show that intravenous administration of PEG 35 at 10 mg/kg ameliorated liver injury and protected the mitochondria. Moreover, PEG 35 administration induced a significant phosphorylation of prosurvival protein kinase B (Akt) and activation of cytoprotective factors e-NOS and AMPK. In conclusion, intravenous PEG 35 efficiently protects steatotic livers exposed to cold IRI. PMID:26543868

  19. Polyethylene glycol acrylate-grafted polysulphone membrane for artificial lungs: plasma modification and haemocompatibility improvement.

    PubMed

    Wang, Weiping; Huang, Xin; Yin, Haiyan; Fan, Wenling; Zhang, Tao; Li, Lei; Mao, Chun

    2015-12-01

    In this study, polyethylene glycol acrylate (PEGA) was introduced onto the surface of polysulphone (PSF) membrane to prepare PSF-PEGA membranes through low-temperature plasma technology for haemocompatibility improvement of artificial lungs. The effects of plasma power, PEGA solution concentration and dipcoating temperature on surface modification were systematically investigated. Results of Fourier transform infrared spectroscopy, x-ray photoelectron spectroscopy and PEGA grafting degree confirmed that PEGA was successfully grafted onto the PSF membranes. Contact angle values showed that the hydrophilicity of the PSF-PEGA membrane surface increased by 21.5%. The results of the protein adsorption, platelet adhesion and coagulation tests further showed the excellent haemocompatibility of the modified membrane. Gas exchange tests also revealed that at a porcine blood flow rate of 5 l min(-1), O2 and CO2 exchange rates through the PSF-PEGA membrane were 198.6 and 170.9 ml min(-1), respectively; approximately this is the gas exchange capacity of commercial respiratory assistance devices. PMID:26658212

  20. Subunit stabilization and polyethylene glycolation of cocaine esterase improves in vivo residence time.

    PubMed

    Narasimhan, Diwahar; Collins, Gregory T; Nance, Mark R; Nichols, Joseph; Edwald, Elin; Chan, Jimmy; Ko, Mei-Chuan; Woods, James H; Tesmer, John J G; Sunahara, Roger K

    2011-12-01

    No small-molecule therapeutic is available to treat cocaine addiction, but enzyme-based therapy to accelerate cocaine hydrolysis in serum has gained momentum. Bacterial cocaine esterase (CocE) is the fastest known native enzyme that hydrolyzes cocaine. However, its lability at 37°C has limited its therapeutic potential. Cross-linking subunits through disulfide bridging is commonly used to stabilize multimeric enzymes. Herein we use structural methods to guide the introduction of two cysteine residues within dimer interface of CocE to facilitate intermolecular disulfide bond formation. The disulfide-crosslinked enzyme displays improved thermostability, particularly when combined with previously described mutations that enhance stability (T172R-G173Q). The newly modified enzyme yielded an extremely stable form of CocE (CCRQ-CocE) that retained greater than 90% of its activity after 41 days at 37°C, representing an improvement of more than 4700-fold over the wild-type enzyme. CCRQ-CocE could also be modified by polyethylene glycol (PEG) polymers, which improved its in vivo residence time from 24 to 72 h, as measured by a cocaine lethality assay, by self-administration in rodents, and by measurement of inhibition of cocaine-induced cardiovascular effects in rhesus monkeys. PEG-CCRQ elicited negligible immune response in rodents. Subunit stabilization and PEGylation has thus produced a potential protein therapeutic with markedly higher stability both in vitro and in vivo. PMID:21890748

  1. Injectable dopamine-modified poly(ethylene glycol) nanocomposite hydrogel with enhanced adhesive property and bioactivity.

    PubMed

    Liu, Yuan; Meng, Hao; Konst, Shari; Sarmiento, Ryan; Rajachar, Rupak; Lee, Bruce P

    2014-10-01

    A synthetic mimic of mussel adhesive protein, dopamine-modified four-armed poly(ethylene glycol) (PEG-D4), was combined with a synthetic nanosilicate, Laponite (Na(0.7+)(Mg5.5Li0.3Si8)O20(OH)4)(0.7-)), to form an injectable naoncomposite tissue adhesive hydrogel. Incorporation of up to 2 wt % Laponite significantly reduced the cure time while enhancing the bulk mechanical and adhesive properties of the adhesive due to strong interfacial binding between dopamine and Laponite. The addition of Laponite did not alter the degradation rate and cytocompatibility of PEG-D4 adhesive. On the basis of subcutaneous implantation in rat, PEG-D4 nanocomposite hydrogels elicited minimal inflammatory response and exhibited an enhanced level of cellular infiltration as compared to Laponite-free samples. The addition of Laponite is potentially a simple and effective method for promoting bioactivity in a bioinert, synthetic PEG-based adhesive while simultaneously enhancing its mechanical and adhesive properties. PMID:25222290

  2. Polyethylene glycol-containing polyurethane hydrogel coatings for improving the biocompatibility of neural electrodes.

    PubMed

    Rao, Li; Zhou, Haihan; Li, Tao; Li, Chengyan; Duan, Yanwen Y

    2012-07-01

    The instability of the interface between chronically implanted neuroprosthetic devices and neural tissue is a major obstacle to the long-term use of such devices in clinical practice. In this study, we investigate the feasibility of polyethylene glycol (PEG)-containing polyurethane (PU) hydrogel as coatings for polydimethylsiloxane (PDMS)-based neural electrodes in order to achieve a stable neural interface. The influence of PU hydrogel coatings on electrode electrochemical behaviour was investigated. Importantly, the biocompatibility of PU hydrogel coatings was evaluated in vitro and in vivo. Changes in the electrochemical impedance of microelectrodes with PU coatings were negligible. The amount of protein adsorption on the PDMS substrate was reduced by 93% after coating. Rat pheochromocytoma (PC12) cells exhibited more and longer neurites on PU films than on PDMS substrates. Furthermore, PDMS implants with (n=10) and without (n=8) PU coatings were implanted into the cortex of rats and the tissue response to the implants was evaluated 6 weeks post-implantation. GFAP staining for astrocytes and NeuN staining for neurons revealed that PU coatings attenuated glial scarring and reduced the neuronal cell loss around the implants. All of these findings suggest that PU hydrogel coating is feasible and favourable for neural electrode applications. PMID:22406507

  3. Biodegradable DNA-enabled poly(ethylene glycol) hydrogels prepared by copper-free click chemistry.

    PubMed

    Barker, Karolyn; Rastogi, Shiva K; Dominguez, Jose; Cantu, Travis; Brittain, William; Irvin, Jennifer; Betancourt, Tania

    2016-01-01

    Significant research has focused on investigating the potential of hydrogels in various applications and, in particular, in medicine. Specifically, hydrogels that are biodegradable lend promise to many therapeutic and biosensing applications. Endonucleases are critical for mechanisms of DNA repair. However, they are also known to be overexpressed in cancer and to be present in wounds with bacterial contamination. In this work, we set out to demonstrate the preparation of DNA-enabled hydrogels that could be degraded by nucleases. Specifically, hydrogels were prepared through the reaction of dibenzocyclooctyne-functionalized multi-arm poly(ethylene glycol) with azide-functionalized single-stranded DNA in aqueous solutions via copper-free click chemistry. Through the use of this method, biodegradable hydrogels were formed at room temperature in buffered saline solutions that mimic physiological conditions, avoiding possible harmful effects associated with other polymerization techniques that can be detrimental to cells or other bioactive molecules. The degradation of these DNA-cross-linked hydrogels upon exposure to the model endonucleases Benzonase(®) and DNase I was studied. In addition, the ability of the hydrogels to act as depots for encapsulation and nuclease-controlled release of a model protein was demonstrated. This model has the potential to be tailored and expanded upon for use in a variety of applications where mild hydrogel preparation techniques and controlled material degradation are necessary including in drug delivery and wound healing systems. PMID:26541212

  4. Surface embrittlement of polyethylene pipe grade resin. Final report, 1 Sep 1979 - 31 Oct 1980

    SciTech Connect

    Broutman, L.J.

    1981-11-01

    Techniques were developed to simulate the effect of a brittle surface on the mechanical behavior of polyethylene. Polyethylene films were exposed to ultraviolet radiation so as to degrade them. These films were than heat fused to polyethylene substrates. It was demonstrated that specimens having bonded films on their surface were embrittled. In addition to attempting to simulate naturally embrittled surfaces by bonding of brittle films to the polyethylene substrate, specimens of polyethylene were subjected to U.V. radiation to determine the effect of surface embrittlement. Severe embrittlement was demonstrated by measuring tensile ultimate strain to failure which was much more sensitive to embrittlement than conventional impact strength. Additional experiments were conducted utilizing sharp razor notches of various depths in surface of polyethylene to evaluate their effect on tensile strain to failure. Experiments were conducted as a function of strain rate which has been demonstrated to have a strong influence on thenotch length required to cause embrittlement. It is shown that the notch length required to cause embrittlement is greater than the film thickness required to cause embrittlement. It has also been shown that U.V. exposure of the polyethylene surface increases the degree of crystallinity and hence establishes a residual stress state in the exposed polymer which has been measured by curvature techniques.

  5. Influence of Pelvic Tilt on Polyethylene Wear after Total Hip Arthroplasty

    PubMed Central

    Tezuka, Taro; Inaba, Yutaka; Kobayashi, Naomi; Ike, Hiroyuki; Kubota, So; Kawamura, Masaki; Saito, Tomoyuki

    2015-01-01

    We aimed to evaluate the effects of pelvic tilt on polyethylene wear after total hip arthroplasty (THA). A total of 105 joints treated with primary THA were included; conventional polyethylene (CPE) liners were used in 43 hips and highly cross-linked polyethylene (HXLPE) liners were used in the remaining 62 hips. The pelvis was tilted 6° posteriorly in the standing position as compared to the supine position, which resulted in significant increases of 1.7° and 2.8° in cup inclination in the CPE and HXLPE groups, respectively. Moreover, the change in pelvic tilt resulted in significant increases of 3.6° and 4.9° in cup anteversion in the CPE and HXLPE groups, respectively. For the CPE group, multiple regression analysis showed a significant association between the angle of pelvic tilt (PTA) and cup inclination and the polyethylene wear ratio. The adjusted R2 of the regression model was larger for measures obtained in the standing position as compared to the supine position. For the HXLPE group, there was no significant relationship between radiographic parameters and polyethylene wear. Close observation of polyethylene wear is recommended for patients with severe posterior pelvic tilt who have undergone THA with conventional polyethylene. PMID:26258136

  6. Pyrolysis-gas chromatography-isotope ratio mass spectrometry of polyethylene.

    PubMed

    González-Pérez, J A; Jiménez-Morillo, N T; de la Rosa, J M; Almendros, G; González-Vila, F J

    2015-04-01

    Polyethylene is probably the most used plastic material in daily life and its accurate analysis is of importance. In this communication the chemical structure of polyethylenes is studied in detail using conventional analytical pyrolysis (Py-GC/MS), bulk stable isotopic analysis (IRMS) and pyrolysis compound specific stable isotopic analysis (Py-CSIA) to measure stable isotope proportions (δ(13)C, δ(15)N and δD) of polyethylene pyrolysis compounds. Polyethylene pyrolysis yields triplet peaks of n-alkanes, α-alkenes and α,ω-alkanedienes. No differences were found for bulk δ(13)C among different polyethylene types. However, conspicuous differences in δD were evident. It was possible to assign structure δ(13)C and δD values to specific polyethylene pyrolysis products in the range 12-18 carbon chain length. Conspicuous differences were found for the pyrolysis products with unsaturated moieties showing significant higher δD values than saturated chains (alkanes) that were deuterium depleted. In addition, a full isotopic fingerprinting (δ(13)C, δ(15)N and δD) for a dye (o-chloroaniline) contained in a polyethylene is reported. To the best of our knowledge this is the first application Py-CSIA to the study of a synthetic polymer. This hyphenated analytical technique is a promising tool to study synthetic materials, providing not only a fingerprinting, but also allowing the traceability of the polymerization process and the origin of the materials. PMID:25725959

  7. Preparation of polyethylene sacks for collection of precipitation samples for chemical analysis

    USGS Publications Warehouse

    Schroder, L.J.; Bricker, A.W.

    1985-01-01

    Polyethylene sacks are used to collect precipitation samples. Washing polyethylene with acetone, hexane, methanol, or nitric acid can change the adsorptive characteristics of the polyethylene. In this study, simulated precipitation at pH 4.5 was in contact with the polyethylene sacks for 21 days; subsamples were removed for chemical analysis at 7, 14, and 21 days after intitial contact. Sacks washed with acetone adsorbed iron and lithium; sacks washed with hexane adsorbed barium, iron , and lithium; sacks washed with methanol adsorbed calcium and iron; and sacks washed with 0.30 N nitric acid adsorbed iron. Leaching the plastic sacks with 0.15 N nitric acid did not result in 100-percent recovery of any of the adsorbed metals. Washing polyethylene sacks with dilute nitric acid caused the pH of the simulated precipitation to be decreased by 0.2 pH unit after 1 week of contact with the polyethylene. The specific conductance increased by 10 microsiemens per centimeter. Contamination of precipitation samples by lead was determined to be about 0.1 microgram per liter from contact with precleaned polyethylene sacks. No measurable contamination of precipitation samples by zinc occurred. (USGS)

  8. Degradation of polyethylene by Trichoderma harzianum--SEM, FTIR, and NMR analyses.

    PubMed

    Sowmya, H V; Ramalingappa; Krishnappa, M; Thippeswamy, B

    2014-10-01

    Trichoderma harzianum was isolated from local dumpsites of Shivamogga District for use in the biodegradation of polyethylene. Soil sample of that dumpsite was used for isolation of T. harzianum. Degradation was carried out using autoclaved, UV-treated, and surface-sterilized polyethylene. Degradation was monitored by observing weight loss and changes in physical structure by scanning electron microscopy, Fourier transform infrared spectroscopy, and nuclear magnetic resonance spectroscopy. T. harzianum was able to degrade treated polyethylene (40%) more efficiently than autoclaved (23%) and surface-sterilized polyethylene (13%). Enzymes responsible for polyethylene degradation were screened from T. harzianum and were identified as laccase and manganese peroxidase. These enzymes were produced in large amount, and their activity was calculated using spectrophotometric method and crude extraction of enzymes was carried out. Molecular weight of laccase was determined as 88 kDa and that of manganese peroxidase was 55 kDa. The capacity of crude enzymes to degrade polyethylene was also determined. By observing these results, we can conclude that this organism may act as solution for the problem caused by polyethylene in nature. PMID:25052326

  9. Effect of ultraviolet radiation in the photo-oxidation of High Density Polyethylene and Biodegradable Polyethylene films

    NASA Astrophysics Data System (ADS)

    Martínez-Romo, A.; González Mota, R.; Bernal, J. J. Soto; Frausto Reyes, C.; Rosales Candelas, I.

    2015-01-01

    One of the most widely used plastics in the world is the High density polyethylene (HDPE), it is a stable material due to its carbon-carbon bonds, causing their slow degradation; which is why we are looking for alternative ways to accelerate the degradation process of this polymer. An alternative is the addition of oxidized groups in its molecular structure, which results in the development of polymers susceptible to biodegradation (PE-BIO). In this paper, HDPE and PE-BIO films were exposed to UV-B radiation (320-280 nm) at different exposure times, 0-60 days. The effects of UV radiation in samples of HDPE and PE-BIO were characterized using infrared spectroscopy with attenuated total reflectance (ATR). The results show that the exposed materials undergo changes in their molecular structure, due to the infrared bands formed which corresponds to the photo-oxidation of HDPE and PE films when submitted to UV-B radiation.

  10. Electrochemical measurements of diffusion coefficients of redox-labeled poly(ethylene glycol) dissolved in poly(ethylene glycol) melts

    SciTech Connect

    Haas, O.; Velazquez, C.S.; Porat, Z.; Murray, R.W.

    1995-10-12

    Ferrocene labeled monomethoxy-poly(ethylene glycol)s (MPEG) with molecular weights of 1900 and 750 were used as redox probe solutes in poly(ethylene glycol) melt solvents of molecular weight 750, 2000, and 20000. Cyclic voltammetry and chronoamperometry at microdisk electrodes were employed to measure the diffusion coefficients of the redox probes, which were independent of the probe concentration and varied between 10{sup -7} and 10{sup -10} cm{sup 2}/s. Diffusional activation barrier results also suggest that the ferrocene label does not significantly influence the diffusivity of the probe molecule in the host solvent. Activation barrier, viscosity, and ionic conductivity results show that the LiClO{sub 4} electrolyte does not influence the diffusion barrier or viscosity as long as the ether O/Li{sup +} ratio is >=250 (ca. 0.1 M) which is still a sufficient electrolyte concentration to allow quantitative electrochemical diffusion measurements. 21 refs., 7 figs., 2 tabs.

  11. Graphite/Ultra-High Modulus Polyethylene Hybrid Fiber Composites with Epoxy and Polyethylene Matrices for Cosmic Radiation Shielding

    NASA Technical Reports Server (NTRS)

    2003-01-01

    One of the most significant technical challenges in long-duration space missions is that of protecting the crew from harmful radiation. Protection against such radiation on a manned Mars mission will be of vital importance both during transit and while on the surface of the planet. The development of multifunctional materials that serve as integral structural members of the space vehicle and provide the necessary radiation shielding for the crew would be both mission enabling and cost effective. Additionally, combining shielding and structure could reduce total vehicle mass. Hybrid laminated composite materials having both ultramodulus polyethylene (PE) and graphite fibers in epoxy and PE matrices could meet such mission requirements. PE fibers have excellent physical properties, including the highest specific strength of any known fiber. Moreover, the high hydrogen (H) content of polyethylene makes the material an excellent shielding material for cosmic radiation. When such materials are incorporated into an epoxy or PE matrix a very effective shielding material is expected. Boron (B) may be added to the matrix resin or used as a coating to further increase the shielding effectiveness due to B s ability to slow thermal neutrons. These materials may also serve as micrometeorites shields due to PE s high impact energy absorption properties. It should be noted that such materials can be fabricated by existing equipment and methods. It is the objective of this work therefore to: (a) perform preliminary analysis of the radiation transport within these materials; (b) fabricate panels for mechanical property testing before and after radiation exposure. Preliminary determination on the effectiveness of the combinations of material components on both shielding and structural efficiency will be made.

  12. Hot embossed polyethylene through-hole chips for bead-based microfluidic devices

    PubMed Central

    Chou, Jie; Du, Nan; Ou, Tina; Floriano, Pierre N.; Christodoulides, Nicolaos; McDevitt, John T.

    2013-01-01

    Over the past decade, there has been a growth of interest in the translation of microfluidic systems into real-world clinical practice, especially for use in point-of-care or near patient settings. While initial fabrication advances in microfluidics involved mainly the etching of silicon and glass, the economics of scaling of these materials is not amendable for point-of-care usage where single-test applications forces cost considerations to be kept low and throughput high. As such, a materials base more consistent with point-of-care needs is required. In this manuscript, the fabrication of a hot embossed, through-hole low-density polyethylene ensembles derived from an anisotropically etched silicon wafer is discussed. This semi-opaque polymer that can be easily sterilized and recycled provides low background noise for fluorescence measurements and yields more affordable cost than other thermoplastics commonly used for microfluidic applications such as cyclic olefin copolymer (COC). To fabrication through-hole microchips from this alternative material for microfluidics, a fabrication technique that uses a high-temperature, high-pressure resistant mold is described. This aluminum-based epoxy mold, serving as the positive master mold for embossing, is casted over etched arrays of pyramidal pits in a silicon wafer. Methods of surface treatment of the wafer prior to casting and PDMS casting of the epoxy are discussed to preserve the silicon wafer for future use. Changes in the thickness of polyethylene are observed for varying embossing temperatures. The methodology described herein can quickly fabricate 20 disposable, single use chips in less than 30 minutes with the ability to scale up 4x by using multiple molds simultaneously. When coupled as a platform supporting porous bead sensors, as in the recently developed Programmable Bio-Nano-Chip, this bead chip system can achieve limits of detection, for the cardiac biomarker C-reactive protein, of 0.3 ng/mL, thereby

  13. Hot embossed polyethylene through-hole chips for bead-based microfluidic devices.

    PubMed

    Chou, Jie; Du, Nan; Ou, Tina; Floriano, Pierre N; Christodoulides, Nicolaos; McDevitt, John T

    2013-04-15

    Over the past decade, there has been a growth of interest in the translation of microfluidic systems into real-world clinical practice, especially for use in point-of-care or near patient settings. While initial fabrication advances in microfluidics involved mainly the etching of silicon and glass, the economics of scaling of these materials is not amendable for point-of-care usage where single-test applications force cost considerations to be kept low and throughput high. As such, materials base more consistent with point-of-care needs is required. In this manuscript, the fabrication of a hot embossed, through-hole low-density polyethylene ensembles derived from an anisotropically etched silicon wafer is discussed. This semi-opaque polymer that can be easily sterilized and recycled provides low background noise for fluorescence measurements and yields more affordable cost than other thermoplastics commonly used for microfluidic applications such as cyclic olefin copolymer (COC). To fabrication through-hole microchips from this alternative material for microfluidics, a fabrication technique that uses a high-temperature, high-pressure resistant mold is described. This aluminum-based epoxy mold, serving as the positive master mold for embossing, is casted over etched arrays of pyramidal pits in a silicon wafer. Methods of surface treatment of the wafer prior to casting and PDMS casting of the epoxy are discussed to preserve the silicon wafer for future use. Changes in the thickness of polyethylene are observed for varying embossing temperatures. The methodology described herein can quickly fabricate 20 disposable, single use chips in less than 30 min with the ability to scale up 4 times by using multiple molds simultaneously. When coupled as a platform supporting porous bead sensors, as in the recently developed Programmable Bio-Nano-Chip, this bead chip system can achieve limits of detection, for the cardiac biomarker C-reactive protein, of 0.3 ng/mL, thereby

  14. Fracture of a polyethylene tibial post in a Scorpio posterior-stabilized knee prosthesis.

    PubMed

    Lim, Hong Chul; Bae, Ji Hoon; Hwang, Jin Ho; Kim, Seung Joo; Yoon, Ji Yeol

    2009-06-01

    We report the case of a polyethylene tibial post fracture in a 72-year-old woman 14 months after a Scorpio posterior-stabilized (PS) total knee arthroplasty. The polyethylene wear was found around the fracture site of the post, especially over the anterior aspect of the post base. The failure mechanism of the post fracture in the present case was anterior impingement with excessive wear over the base of the anterior aspect of the tibial post, which became a stress-riser of post and cam articulation. This is the first report of a polyethylene tibial post fracture of a Scorpio PS prosthesis. PMID:19885065

  15. Effect of Short Chain Poly(ethylene glycol)s on the Hydration Structure and Dynamics around Human Serum Albumin.

    PubMed

    Samanta, Nirnay; Luong, Trung Quan; Das Mahanta, Debasish; Mitra, Rajib Kumar; Havenith, Martina

    2016-01-26

    We report the changes in the hydration dynamics around a globular protein, human serum albumin (HSA), in the presence of two short chain crowding agents, namely poly(ethylene glycol)s (PEG 200 and 400). The change in the network water structure is investigated using FTIR spectroscopy in the far-infrared (FIR) frequency range. Site specific changes are obtained by time-resolved fluorescence spectroscopic technique using the intrinsic fluorophore tryptophan (Trp214) of HSA. The collective hydration dynamics of HSA in the presence of PEG molecules are obtained using terahertz (THz) time domain spectroscopy (TTDS) and high intensity p-Ge THz measurements. Our study affirms a considerable perturbation of HSA hydration beyond a critical concentration of PEG. PMID:26720549

  16. Wear simulation of a polyethylene-on-metal cervical total disc replacement under different concentrations of bovine serum lubricant.

    PubMed

    Hyde, P J; Fisher, J; Hall, R M

    2016-05-01

    Metal-on-polyethylene total disc replacements have been an alternative to spinal fusion in the lumbar spine under certain indications for more than a decade. Recently, cervical total disc replacement has also become an alternative to cervical fusion. Knowledge acquired from years of in vitro simulator studies on other joint replacements has highlighted the risks associated with premature wear due to unforeseen adverse clinical conditions and the effect of particulate debris on surrounding natural tissues. Having no evidence of the type and composition of the lubricating fluid that will result after spinal arthroplasty, a study on the effects of lubricant serum concentration was undertaken. The wear rate was shown to be inversely proportional to protein content of the serum over a range of 50%-3% bovine serum to water concentration. PMID:27160565

  17. Solution and film properties of sodium caseinate/glycerol and sodium caseinate/polyethylene glycol edible coating systems.

    PubMed

    Siew, D C; Heilmann, C; Easteal, A J; Cooney, R P

    1999-08-01

    The aim of this study is to determine the effects of plasticizer hydrogen bonding capability and chain length on the molecular structure of sodium caseinate (NaCAS), in NaCAS/glycerol and NaCAS/polyethylene glycol 400 (PEG) systems. Both solution and film phases were investigated. Glycerol and PEG reduced the viscosity of aqueous NaCAS, with the latter having a greater effect. This was explained in terms of protein/plasticizer aggregate size and changes to the conformation of the caseinate chain. In the film phase, glycerol caused more pronounced changes to the film tensile strength compared with PEG. However, the effect of glycerol on film water vapor permeability was smaller. These observations are attributed to the differences in plasticizer size and hydrogen bonding strength that controls the protein-plasticizer and protein-protein interactions in the films. Glass transition calculations from the tensile strength data indicate that the distribution of bonding interactions is more homogeneous in NaCAS/PEG films than in NaCAS/glycerol films. PMID:10552668

  18. Multiplex Immunoassay Platforms Based on Shape-Coded Poly(ethylene glycol) Hydrogel Microparticles Incorporating Acrylic Acid

    PubMed Central

    Park, Saemi; Lee, Hyun Jong; Koh, Won-Gun

    2012-01-01

    A suspension protein microarray was developed using shape-coded poly(ethylene glycol) (PEG) hydrogel microparticles for potential applications in multiplex and high-throughput immunoassays. A simple photopatterning process produced various shapes of hydrogel micropatterns that were weakly bound to poly(dimethylsiloxane) (PDMS)-coated substrates. These micropatterns were easily detached from substrates during the washing process and were collected as non-spherical microparticles. Acrylic acids were incorporated into hydrogels, which could covalently immobilize proteins onto their surfaces due to the presence of carboxyl groups. The amount of immobilized protein increased with the amount of acrylic acid due to more available carboxyl groups. Saturation was reached at 25% v/v of acrylic acid. Immunoassays with IgG and IgM immobilized onto hydrogel microparticles were successfully performed with a linear concentration range from 0 to 500 ng/mL of anti-IgG and anti-IgM, respectively. Finally, a mixture of two different shapes of hydrogel microparticles immobilizing IgG (circle) and IgM (square) was prepared and it was demonstrated that simultaneous detection of two different target proteins was possible without cross-talk using same fluorescence indicator because each immunoassay was easily identified by the shapes of hydrogel microparticles. PMID:22969408

  19. Polyethylene glycol versus dual sugar assay for gastrointestinal permeability analysis: is it time to choose?

    PubMed Central

    van Wijck, Kim; Bessems, Babs AFM; van Eijk, Hans MH; Buurman, Wim A; Dejong, Cornelis HC; Lenaerts, Kaatje

    2012-01-01

    Background Increased intestinal permeability is an important measure of disease activity and prognosis. Currently, many permeability tests are available and no consensus has been reached as to which test is most suitable. The aim of this study was to compare urinary probe excretion and accuracy of a polyethylene glycol (PEG) assay and dual sugar assay in a double-blinded crossover study to evaluate probe excretion and the accuracy of both tests. Methods Gastrointestinal permeability was measured in nine volunteers using PEG 400, PEG 1500, and PEG 3350 or lactulose-rhamnose. On 4 separate days, permeability was analyzed after oral intake of placebo or indomethacin, a drug known to increase intestinal permeability. Plasma intestinal fatty acid binding protein and calprotectin levels were determined to verify compromised intestinal integrity after indomethacin consumption. Urinary samples were collected at baseline, hourly up to 5 hours after probe intake, and between 5 and 24 hours. Urinary excretion of PEG and sugars was determined using high-pressure liquid chromatography-evaporative light scattering detection and liquid chromatography-mass spectrometry, respectively. Results Intake of indomethacin increased plasma intestinal fatty acid-binding protein and calprotectin levels, reflecting loss of intestinal integrity and inflammation. In this state of indomethacin-induced gastrointestinal compromise, urinary excretion of the three PEG probes and lactulose increased compared with placebo. Urinary PEG 400 excretion, the PEG 3350/PEG 400 ratio, and the lactulose/rhamnose ratio could accurately detect indomethacin-induced increases in gastrointestinal permeability, especially within 2 hours of probe intake. Conclusion Hourly urinary excretion and diagnostic accuracy of PEG and sugar probes show high concordance for detection of indomethacin-induced increases in gastrointestinal permeability. This comparative study improves our knowledge of permeability analysis in man

  20. Osteogenic potential of poly(ethylene glycol)-poly(dimethylsiloxane) hybrid hydrogels.

    PubMed

    Munoz-Pinto, Dany J; Jimenez-Vergara, Andrea Carolina; Hou, Yaping; Hayenga, Heather N; Rivas, Alejandra; Grunlan, Melissa; Hahn, Mariah S

    2012-08-01

    Growth factors have been shown to be potent mediators of osteogenesis. However, their use in tissue-engineered scaffolds not only can be costly but also can induce undesired responses in surrounding tissues. Thus, the ability to specifically induce osteogenic differentiation in the absence of exogenous growth factors through manipulation of scaffold material properties would be desirable for bone regeneration. Previous research indicates that addition of inorganic or hydrophobic components to organic, hydrophilic scaffolds can enhance multipotent stem cell (MSC) osteogenesis. However, the combined impact of scaffold inorganic content and hydrophobicity on MSC behavior has not been systematically explored, particularly in three-dimensional (3D) culture systems. The aim of the present study was therefore to examine the effects of simultaneous increases in scaffold hydrophobicity and inorganic content on MSC osteogenic fate decisions in a 3D culture environment toward the development of intrinsically osteoinductive scaffolds. Mouse 10T½ MSCs were encapsulated in a series of novel scaffolds composed of varying levels of hydrophobic, inorganic poly(dimethylsiloxane) (PDMS) and hydrophilic, organic poly(ethylene glycol) (PEG). After 21 days of culture, increased levels of osteoblast markers, runx2 and osteocalcin, were observed in scaffolds with increased PDMS content. Bone extracellular matrix (ECM) molecules, collagen I and calcium phosphate, were also elevated in formulations with higher PDMS:PEG ratios. Importantly, this osteogenic response appeared to be specific in that markers for chondrocytic, smooth muscle cell, and adipocytic lineages were not similarly affected by variations in scaffold PDMS content. As anticipated, the increase in scaffold hydrophobicity accompanying increasing PDMS levels was associated with elevated scaffold serum protein adsorption. Thus, scaffold inorganic content combined with alterations in adsorbed serum proteins may underlie the

  1. Osteogenic Potential of Poly(Ethylene Glycol)–Poly(Dimethylsiloxane) Hybrid Hydrogels

    PubMed Central

    Munoz-Pinto, Dany J.; Jimenez-Vergara, Andrea Carolina; Hou, Yaping; Hayenga, Heather N.; Rivas, Alejandra; Grunlan, Melissa

    2012-01-01

    Growth factors have been shown to be potent mediators of osteogenesis. However, their use in tissue-engineered scaffolds not only can be costly but also can induce undesired responses in surrounding tissues. Thus, the ability to specifically induce osteogenic differentiation in the absence of exogenous growth factors through manipulation of scaffold material properties would be desirable for bone regeneration. Previous research indicates that addition of inorganic or hydrophobic components to organic, hydrophilic scaffolds can enhance multipotent stem cell (MSC) osteogenesis. However, the combined impact of scaffold inorganic content and hydrophobicity on MSC behavior has not been systematically explored, particularly in three-dimensional (3D) culture systems. The aim of the present study was therefore to examine the effects of simultaneous increases in scaffold hydrophobicity and inorganic content on MSC osteogenic fate decisions in a 3D culture environment toward the development of intrinsically osteoinductive scaffolds. Mouse 10T½ MSCs were encapsulated in a series of novel scaffolds composed of varying levels of hydrophobic, inorganic poly(dimethylsiloxane) (PDMS) and hydrophilic, organic poly(ethylene glycol) (PEG). After 21 days of culture, increased levels of osteoblast markers, runx2 and osteocalcin, were observed in scaffolds with increased PDMS content. Bone extracellular matrix (ECM) molecules, collagen I and calcium phosphate, were also elevated in formulations with higher PDMS:PEG ratios. Importantly, this osteogenic response appeared to be specific in that markers for chondrocytic, smooth muscle cell, and adipocytic lineages were not similarly affected by variations in scaffold PDMS content. As anticipated, the increase in scaffold hydrophobicity accompanying increasing PDMS levels was associated with elevated scaffold serum protein adsorption. Thus, scaffold inorganic content combined with alterations in adsorbed serum proteins may underlie the

  2. Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) elastomer via photo-initiated graft polymerization of poly(ethylene glycol)

    NASA Astrophysics Data System (ADS)

    Li, Xiaomeng; Luan, Shifang; Yang, Huawei; Shi, Hengchong; Zhao, Jie; Jin, Jing; Yin, Jinghua; Stagnaro, Paola

    2012-01-01

    Poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) copolymer biomedical elastomer was covalently grafted with poly(ethylene glycol) methyl ether methacrylate (PEGMA) via a photo-initiated graft polymerization technique. The surface graft polymerization of SEBS with PEGMA was verified by ATR-FTIR and XPS. Effect of graft polymerization parameters, i.e., monomer concentration, UV irradiation time and initiator concentration on the grafting density was investigated. Comparing with the virgin SEBS film, the PEGMA-modified SEBS film presented an enhanced wettability and a larger surface energy. Besides, the surface grafting of PEGMA imparted excellent anti-platelet adhesion and anti-protein adsorption to the SEBS surface.

  3. Identification of phosphoproteins in Arabidopsis thaliana leaves using polyethylene glycol fractionation, immobilized metal-ion affinity chromatography, two-dimensional gel electrophoresis and mass spectrometry.

    PubMed

    Aryal, Uma K; Krochko, Joan E; Ross, Andrew R S

    2012-01-01

    Reversible protein phosphorylation is a key regulatory mechanism in cells. Identification and characterization of phosphoproteins requires specialized enrichment methods, due to the relatively low abundance of these proteins, and is further complicated in plants by the high abundance of Rubisco in green tissues. We present a novel method for plant phosphoproteome analysis that depletes Rubisco using polyethylene glycol fractionation and utilizes immobilized metal-ion affinity chromatography to enrich phosphoproteins. Subsequent protein separation by one- and two-dimensional gel electrophoresis is further improved by extracting the PEG-fractionated protein samples with SDS/phenol and methanol/chloroform to remove interfering compounds. Using this approach, we identified 132 phosphorylated proteins in a partial Arabidopsis leaf extract. These proteins are involved in a range of biological processes, including CO(2) fixation, protein assembly and folding, stress response, redox regulation, and cellular metabolism. Both large and small subunits of Rubisco were phosphorylated at multiple sites, and depletion of Rubisco enhanced detection of less abundant phosphoproteins, including those associated with state transitions between photosystems I and II. The discovery of a phosphorylated form of AtGRP7, a self-regulating RNA-binding protein that affects floral transition, as well as several previously uncharacterized ribosomal proteins confirm the utility of this approach for phosphoproteome analysis and its potential to increase our understanding of growth and development in plants. PMID:22092075

  4. The lexicon of polyethylene wear in artificial joints.

    PubMed

    McKellop, Harry A

    2007-12-01

    The analysis of wear on polyethylene components that have been retrieved after use in patients has provided invaluable understanding of how wear occurs in vivo, and how it may be minimized through improved materials and implant design. The great number of such studies that have been published over the past three decades has lead to an extensive vocabulary to describe the tribology of prosthetic joints. However, these also have led to some confusion, due to the occasional misuse of terms from classical tribology, along with the use of multiple terms to describe the same wear phenomenon, and vice versa. The author has proposed that our understanding of wear in artificial joints may be enhanced by recognizing that there are four general subject areas: Modes, Mechanisms, Damage and Debris. Wear Mode 1 occurs when the two bearing surfaces are articulating against each other in the manner intended by the implant designer. Mode 2 occurs when a bearing surface articulates against a non-bearing surface. Mode 3 occurs when third-body abrasive particles have become entrapped between the two bearing surfaces, and Mode 4 occurs when two non-bearing surfaces are wearing against each other. The least wear occurs in Mode 1, whereas severe wear typically occurs in Modes 2, 3 and 4. The classical wear mechanisms that apply to prosthetic joints include adhesion, abrasion and fatigue. These can occur in varying amounts in either of the four wear modes. As used in the literature for the past three decades, wear "damage" can best be defined as the change surface texture or morphology that is caused by the action of the wear mechanisms. Although a wide variety of terms have been used, an overview of the literature indicates that about eight terms have been sufficient to describe the types of damage that occur on retrieved polyethylene components, i.e., burnishing, abrasion, scratches, plastic deformation, cracks, pits, delamination, and embedded third bodies. The author suggests that, as

  5. Optimization of Protein Extraction for Lichen Thalli

    PubMed Central

    Kondratiuk, Anna S.; Savchuk, Oleksiy M.

    2015-01-01

    Lichen-forming fungal proteins have been seldom searched due to many difficulties in their extraction. Phenols, quinones, proteases, and other components released during cell disruption have been known to be the greatest challenges related to protein extraction from lichens. To overcome these problems and maintain good electrophoretic resolution and high protein concentration, an extraction buffer containing polyvinylpolypyrrolidone, ascorbic acid, Triton X-100, polyethylene glycol, proteinase, and oxidase inhibitors in sodium phosphate buffer was developed. This extraction buffer showed high efficiency for all lichen species tested in the study. PMID:26190923

  6. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... Order, Finding, or Suspended Investigation; Opportunity to Request an Administrative Review, 75 FR 38074... Countervailing Duty Administrative Reviews and Deferral of Initiation of Administrative Review, 75 FR 53274... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  7. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... Duty Order, Finding, or Suspended Investigation; Opportunity to Request an Administrative Review, 75 FR... Countervailing Duty Administrative Reviews and Deferral of Initiation of Administrative Review, 75 FR 53274... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  8. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions.

    PubMed

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-06-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment. PMID:27386559

  9. The effect of different particle sizes of polyethylene on the absorption of myrrh in mixtures

    NASA Astrophysics Data System (ADS)

    Xu, Lei; Li, Bin; Zuo, Jian; Zhang, Cunlin

    2015-08-01

    Terahertz radiation lies between far-infrared and microwave in electromagnetic spectrum with frequency from 0.1 to 10 THz. Absorption spectra of different mass ratio of the myrrh and polyethylene can be gained by Fourier transform infrared spectrometer in this paper. It is found that absorption spectra show a slight red-shift with the decrease of the mass ratio of myrrh and polyethylene. On the other hand, different particle sizes of polyethylene (PE) mixed with myrrh absorption spectra were measured. Due to the different sizes of polyethylene particles, there are some differences in the vibration peak intensity, peak position and peak numbers in the absorption spectra. The experimental results show that the scattering effect leads to this phenomenon.

  10. Hemoglobin precipitation by polyethylene glycols leads to underestimation of membrane pore sizes.

    PubMed

    Quijano, Jairo C; Lemeshko, Victor V

    2008-12-01

    The size of pores formed in the plasma membrane by various substances is frequently determined using polyethylene glycols as osmotic protectants. In this work, we have found that the size of pores formed by saponin in the red blood cell membrane determined by hemolysis versus molecular weight of polyethylene glycol was different to that estimated by light dispersion of cell suspensions. After complete swelling of cells induced by saponin in semiisotonic salt media containing 150 mOsm PEG-4000 or PEG-3000, a significant increase in the light absorbance at 640 nm was developed resulting from the formation of hemoglobin precipitates. Easily sedimenting aggregates were also formed when the supernatant of lysed cells was added to the equiosmotic solutions of polyethylene glycols with molecular weight higher than 1000. We suggest that the real size of large pores could be underestimated due to the phenomenon of hemoglobin precipitation by polyethylene glycols. PMID:18692020

  11. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions

    PubMed Central

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-01-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment. PMID:27386559

  12. Kinetics and microscopic processes of long term fracture in polyethylene piping materials

    NASA Astrophysics Data System (ADS)

    Brown, N.; Lu, X.

    1992-07-01

    The report contains 9 completed works as follows: The Dependence of Slow Crack Growth in a Polyethylene Copolymer on Testing Temperature and Morphology; A Test of Slow Crack Growth Failure of PE Under Constant Load; Effect of Annealing on Slow Crack Growth in an Ethylene-Hexene Copolymer; The Fundamental Material Parameters that Govern Slow Crack Growth in Linear Polyethylene; Slow Crack Growth in Blends of HDPE and UHMWPE; The Mechanism of Fatigue Failure in a Polyethylene Copolymer; PENT Quality Control Test for PE Gas Pipes and Resins; International Round Robin Study of a Fatigue Test Approach to the Ranking of Polyethylene Pipe Material; and Proposed ASTM Specification for ASTM F17.40 Test Methods Committee.

  13. Improving mechanical properties of polyethylene orthopaedic implants by high frequency cold plasma surface activation

    NASA Astrophysics Data System (ADS)

    Tudoran, Cristian D.; Vlad, Iulia E.; Dadarlat, Dorin N.; Anghel, Sorin D.

    2013-11-01

    Although a tremendous progress has been made in developing new methods and materials for manufacturing orthopaedic implants, the new technology still faces various problems. Polyethylene implants are relatively easy to manufacture and at lower cost compared to metallic or ceramic implants, but they present a fundamental problem: during usage and in time, due to their manufacturing technology, the material suffers from pitting and delamination which leads to crack propagation and finally to sudden fracture. Our studies and tests performed on polyethylene showed that, using cold plasma surface activation during the manufacturing process of the orthopaedic implants made from polyethylene can significantly increase their mechanical properties. The breaking tests revealed an increase of the tensile strength in the laminated polyethylene samples by a factor of 4 after plasma activation. "Aging" tests have been also performed to investigate how the cold plasma treated samples maintain their properties in time, after the surface activation process.

  14. Detection of cracks in polyethylene components of retrieved knee joint prostheses.

    PubMed

    Koizumi, M; Tomita, N; Tamai, S; Oonishi, H; Ikada, Y

    1998-01-01

    Subsurface cracks that had formed in polyethylene artificial knee components were observed nondestructively with a new method, scanning acoustic tomography (SAT). Standardization of the SAT observation was done by in-vitro rolling fatigue testing on an unimplanted ultra high molecular weight polyethylene (UHMWPE) knee component. Retrieved knee components were of two types; KOM (Kyocera, Kyoto, Japan) sterilized with ethylene oxide gas, and MG (Zimmer, IN, USA) sterilized with gamma-irradiation. The SAT images revealed cracks in all the retrieved components, and these existed mainly 0. 3-1.0 mm from the surface. Comparison of crack formation in each portion of the contact area of the polyethylene components showed that the middle portion of the MG type had the highest concentration of cracks. When the distribution of compressive stress on the polyethylene components was assessed by mechanical testing, the strongest compressive stress was seen in the middle portion of MG type components. PMID:9811985

  15. Effectiveness of Vitamin-E-Doped Polyethylene in Joint Replacement: A Literature Review

    PubMed Central

    Gigante, Antonio; Bottegoni, Carlo; Ragone, Vincenza; Banci, Lorenzo

    2015-01-01

    Since polyethylene is one of the most frequently used biomaterials, such as in bearing components in joint arthroplasty, strong efforts have been made to improve the design and material properties over the last decades. Antioxidants, such as vitamin-E, seem to be a promising alternative to further increase durability and reduce polyethylene wear and degradation in the long-term. Nevertheless, even if several promising in vitro results are available, there is yet no clinical evidence that vitamin-E polyethylenes show these advantages in vivo. The aim of this paper was to provide a comprehensive overview on the current knowledge regarding the biological and mechanical proprieties of this biomaterial, underlying the in vitro and in vivo evidence for effectiveness of vitamin-E-doped polyethylene in joint arthroplasty. PMID:26371052

  16. Melt index of low-density polyethylene and its effect on rotational molding

    NASA Astrophysics Data System (ADS)

    Yuldashev, A. Kh.; Negmatov, S. S.; Abed-Negmatova, N. S.; Abdurakhmanov, A. G.; Bozorov, Sh. A.; Eminov, Sh. Sh.; Aripova, A.; Khodjikariev, D. M.

    2012-07-01

    The melt index of low density polyethylene is directly correlated to the "in service" strength. This correlation together with other chemical properties allowed us to select the best material for rotational molding process.

  17. Use of prompt gamma emissions from polyethylene to estimate neutron ambient dose equivalent

    NASA Astrophysics Data System (ADS)

    Priyada, P.; Sarkar, P. K.

    2015-06-01

    The possibility of using measured prompt gamma emissions from polyethylene to estimate neutron ambient dose equivalent is explored theoretically. Monte Carlo simulations have been carried out using the FLUKA code to calculate the response of a high density polyethylene cylinder to emit prompt gammas from interaction of neutrons with the nuclei of hydrogen and carbon present in polyethylene. The neutron energy dependent responses of hydrogen and carbon nuclei are combined appropriately to match the energy dependent neutron fluence to ambient dose equivalent conversion coefficients. The proposed method is tested initially with simulated spectra and then validated using experimental measurements with an Am-Be neutron source. Experimental measurements and theoretical simulations have established the feasibility of estimating neutron ambient dose equivalent using measured neutron induced prompt gammas emitted from polyethylene with an overestimation of neutron dose at very low energies.

  18. Polyethylene/Potassium Titanate Separators For Ni/H2 Cells

    NASA Technical Reports Server (NTRS)

    Scott, William E.

    1995-01-01

    Experimental separators fabricated on paper-making machine. Two-layer, paperlike composite of polyethylene fibers and potassium titanate pigment shows promise for replacing asbestos as separator material in nickel/hydrogen electrochemical cells.

  19. Effectiveness of Vitamin-E-Doped Polyethylene in Joint Replacement: A Literature Review.

    PubMed

    Gigante, Antonio; Bottegoni, Carlo; Ragone, Vincenza; Banci, Lorenzo

    2015-01-01

    Since polyethylene is one of the most frequently used biomaterials, such as in bearing components in joint arthroplasty, strong efforts have been made to improve the design and material properties over the last decades. Antioxidants, such as vitamin-E, seem to be a promising alternative to further increase durability and reduce polyethylene wear and degradation in the long-term. Nevertheless, even if several promising in vitro results are available, there is yet no clinical evidence that vitamin-E polyethylenes show these advantages in vivo. The aim of this paper was to provide a comprehensive overview on the current knowledge regarding the biological and mechanical proprieties of this biomaterial, underlying the in vitro and in vivo evidence for effectiveness of vitamin-E-doped polyethylene in joint arthroplasty. PMID:26371052

  20. Enhanced Cutinase-Catalyzed Hydrolysis of Polyethylene Terephthalate by Covalent Fusion to Hydrophobins

    PubMed Central

    Ribitsch, Doris; Herrero Acero, Enrique; Przylucka, Agnieszka; Zitzenbacher, Sabine; Marold, Annemarie; Gamerith, Caroline; Tscheließnig, Rupert; Jungbauer, Alois; Rennhofer, Harald; Lichtenegger, Helga; Amenitsch, Heinz; Bonazza, Klaus; Kubicek, Christian P.; Guebitz, Georg M.

    2015-01-01

    Cutinases have shown potential for hydrolysis of the recalcitrant synthetic polymer polyethylene terephthalate (PET). We have shown previously that the rate of this hydrolysis can be enhanced by the addition of hydrophobins, small fungal proteins that can alter the physicochemical properties of surfaces. Here we have investigated whether the PET-hydrolyzing activity of a bacterial cutinase from Thermobifida cellulosilytica (Thc_Cut1) would be further enhanced by fusion to one of three Trichoderma hydrophobins, i.e., the class II hydrophobins HFB4 and HFB7 and the pseudo-class I hydrophobin HFB9b. The fusion enzymes exhibited decreased kcat values on soluble substrates (p-nitrophenyl acetate and p-nitrophenyl butyrate) and strongly decreased the hydrophilicity of glass but caused only small changes in the hydrophobicity of PET. When the enzyme was fused to HFB4 or HFB7, the hydrolysis of PET was enhanced >16-fold over the level with the free enzyme, while a mixture of the enzyme and the hydrophobins led only to a 4-fold increase at most. Fusion with the non-class II hydrophobin HFB9b did not increase the rate of hydrolysis over that of the enzyme-hydrophobin mixture, but HFB9b performed best when PET was preincubated with the hydrophobins before enzyme treatment. The pattern of hydrolysis by the fusion enzymes differed from that of Thc_Cut1 as the concentration of the product mono(2-hydroxyethyl) terephthalate relative to that of the main product, terephthalic acid, increased. Small-angle X-ray scattering (SAXS) analysis revealed an increased scattering contrast of the fusion proteins over that of the free proteins, suggesting a change in conformation or enhanced protein aggregation. Our data show that the level of hydrolysis of PET by cutinase can be significantly increased by fusion to hydrophobins. The data further suggest that this likely involves binding of the hydrophobins to the cutinase and changes in the conformation of its active center. PMID:25795674

  1. Extremely High Thermal Conductivity of Aligned Carbon Nanotube-Polyethylene Composites

    PubMed Central

    Liao, Quanwen; Liu, Zhichun; Liu, Wei; Deng, Chengcheng; Yang, Nuo

    2015-01-01

    The ultra-low thermal conductivity of bulk polymers may be enhanced by combining them with high thermal conductivity materials such as carbon nanotubes. Different from random doping, we find that the aligned carbon nanotube-polyethylene composites has a high thermal conductivity by non-equilibrium molecular dynamics simulations. The analyses indicate that the aligned composite not only take advantage of the high thermal conduction of carbon nanotubes, but enhance thermal conduction of polyethylene chains. PMID:26552843

  2. Spontaneous dislocation of the polyethylene component following knee revision arthroplasty: case report☆

    PubMed Central

    Migon, Eduardo Zaniol; de Freitas, Geraldo Luiz Schuck; Rodrigues, Marcos Wainberg; de Oliveira, Gustavo Kaempf; de Almeida, Luis Gustavo Morato Pinto; Schwartsmann, Carlos Roberto

    2014-01-01

    Dislocation of the polyethylene component in knee arthroplasty is a rare complication. The main triggering factor is failure of the locking mechanism, which may result from technical errors of insertion, trauma or even implant failure. Here, a case of dislocation of the polyethylene component from the tibial base, nine years after revision arthroplasty, is reported. It is believed that this is the first such case reported in the Brazilian literature. PMID:26229887

  3. Development of an extremely wear-resistant ultra high molecular weight polyethylene for total hip replacements.

    PubMed

    McKellop, H; Shen, F W; Lu, B; Campbell, P; Salovey, R

    1999-03-01

    Osteolysis induced by ultra high molecular weight polyethylene wear debris is one of the primary factors limiting the lifespan of total hip replacements. Crosslinking polyethylene is known to improve its wear resistance in certain industrial applications, and crosslinked polyethylene acetabular cups have shown improved wear resistance in two clinical studies. In the present study, crosslinked polyethylene cups were produced by two methods. Chemically crosslinked cups were produced by mixing a peroxide with ultra high molecular weight polyethylene powder and then molding the cups directly to shape. Radiation-crosslinked cups were produced by exposing conventional extruded ultra high molecular weight polyethylene bar stock to gamma radiation at various doses from 3.3 to 100 Mrad (1 Mrad = 10 kGy), remelting the bars to extinguish residual free radicals (i.e., to minimize long-term oxidation), and then machining the cups by conventional techniques. In hip-joint simulator tests lasting as long as 5 million cycles, both types of cross-linked cups exhibited dramatically improved resistance to wear. Artificial aging of the cups by heating for 30 days in air at 80 degrees C induced oxidation of the chemically crosslinked cups. However, a chemically crosslinked cup that was aged 2.7 years at room temperature had very little oxidation. Thus, whether substantial oxidation of chemically crosslinked polyethylene would occur at body temperature remains unclear. The radiation-crosslinked remelted cups exhibited excellent resistance to oxidation. Because crosslinking can reduce the ultimate tensile strength, fatigue strength, and elongation to failure of ultra high molecular weight polyethylene, the optimal crosslinking dose provides a balance between these physical properties and the wear resistance of the implant and might substantially reduce the incidence of wear-induced osteolysis with total hip replacements. PMID:10221831

  4. An analysis of hylamer and polyethylene bearings from retrieved acetabular components.

    PubMed

    Collier, J P; Bargmann, L S; Currier, B H; Mayor, M B; Currier, J H; Bargmann, B C

    1998-08-01

    Hylamer and conventional polyethylene acetabular liners of the same design, revised for a variety of reasons, were examined and compared to assess the performance of Hylamer as a bearing material. Clinical damage modes, linear wear rates, oxidation levels, and mechanical properties were measured. In both series, many liners were retrieved for dislocation. Wear/osteolysis was the most common reason for retrieval in the Hylamer series, while none of the conventional polyethylene liners were retrieved for this reason. Nearly all liners exhibited abrasion, burnishing, scratching, and creep. The Hylamer liners had more cracking, delamination, and pitting. The Hylamer liners had an average linear wear rate of 0.32 mm/year, while the conventional polyethylene liners had an average wear rate of 0.20 mm/year. Due to sample size, no statistical difference in wear rate was noted between the two groups. In general, both the Hylamer and conventional polyethylene showed oxidation peaks subsurface, resulting from their exposure to gamma radiation in air. Liners with elevated oxidation had decreased ultimate tensile strength, elongation, and toughness. For given oxidation levels, the corresponding mechanical properties of Hylamer appeared lower than those of conventional polyethylene. The ultimate tensile strength values ranged from 14 to 33 MPa for Hylamer and 19 to 32 MPa for conventional polyethylene. Elongation ranges were 19% to 350% (Hylamer) and 80% to 375% (conventional). The Hylamer retrievals in this study gave initial indications of performance; Hylamer appeared to behave similarly, but not superiorly, to conventional polyethylene, in the early functional period with respect to clinical wear and clinical performance. Both Hylamer and conventional polyethylene liners were degraded by gamma sterilization in air, with Hylamer liners demonstrating greater property changes. PMID:9731668

  5. Spontaneous Insertion, Helix Formation, and Hydration of Polyethylene Oxide in Carbon Nanotubes.

    PubMed

    Dahal, Udaya R; Dormidontova, Elena E

    2016-07-01

    Hydration strongly affects macromolecular conformation in solution and under nanoconfinement as encountered in nature and nanomaterials. Using atomistic molecular dynamics simulations we demonstrate that polyethylene oxide spontaneously enters single wall carbon nanotubes (CNTs) from aqueous solutions and forms rodlike, helix, and wrapped chain conformations depending on the CNT diameter. We show that water organization and the stability of the polyethylene oxide hydration shell under confinement is responsible for the helix formation, which can have significant implications for nanomaterial design. PMID:27447525

  6. Spontaneous Insertion, Helix Formation, and Hydration of Polyethylene Oxide in Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Dahal, Udaya R.; Dormidontova, Elena E.

    2016-07-01

    Hydration strongly affects macromolecular conformation in solution and under nanoconfinement as encountered in nature and nanomaterials. Using atomistic molecular dynamics simulations we demonstrate that polyethylene oxide spontaneously enters single wall carbon nanotubes (CNTs) from aqueous solutions and forms rodlike, helix, and wrapped chain conformations depending on the CNT diameter. We show that water organization and the stability of the polyethylene oxide hydration shell under confinement is responsible for the helix formation, which can have significant implications for nanomaterial design.

  7. Extremely High Thermal Conductivity of Aligned Carbon Nanotube-Polyethylene Composites

    NASA Astrophysics Data System (ADS)

    Liao, Quanwen; Liu, Zhichun; Liu, Wei; Deng, Chengcheng; Yang, Nuo

    2015-11-01

    The ultra-low thermal conductivity of bulk polymers may be enhanced by combining them with high thermal conductivity materials such as carbon nanotubes. Different from random doping, we find that the aligned carbon nanotube-polyethylene composites has a high thermal conductivity by non-equilibrium molecular dynamics simulations. The analyses indicate that the aligned composite not only take advantage of the high thermal conduction of carbon nanotubes, but enhance thermal conduction of polyethylene chains.

  8. Single-stage small satellite launcher with combustible tank of polyethylene

    NASA Astrophysics Data System (ADS)

    Yemets, Vitaly; Sanin, Fedir; Dzhur, Yevgen; Masliany, Mykola; Kostritsyn, Oleg; Minteev, Grygory

    2009-01-01

    A solid propellant version of the single-stage launch vehicle with polyethylene case that consumed as fuel is considered as means for launching small satellites. Emphasis is on experimental investigating gasification of a polyethylene structure element by a chamber of special design. Photographs and the reference to electronic annex containing an experimental video record are included in the paper. Main previous experiments are also briefly reviewed. Conclusions concern improvements of the gasification chamber design and a speculation about next experiments.

  9. Stability of β-carotene in polyethylene oxide electrospun nanofibers

    NASA Astrophysics Data System (ADS)

    Peinado, I.; Mason, M.; Romano, A.; Biasioli, F.; Scampicchio, M.

    2016-05-01

    β-carotene (βc) was successfully incorporated into electrospun nanofibers of poly-(ethylene oxide) (PEO) with the aim of prolonging its shelf life and thermal stability. The physical and thermal properties of the βc-PEO-nanofibers were determined by scanning electron microscopy (SEM), color analysis, and differential scanning calorimetry (DSC). The nanofibers of PEO and βc-PEO exhibited average fiber diameters of 320 ± 46 and 230 ± 21 nm, with colorimetric coordinates L* = 95.7 ± 2.4 and 89.4 ± 4.6 and b* = -0.5 ± 0.1 and 6.2 ± 3.0 respectively. Thermogravimetric analysis coupled with Proton Transfer-Mass Spectroscopy (TGA/PTR-ms) demonstrated that coated βc inside PEO nanofibers increased thermal stability when compared to standard βc in powder form. In addition, β-carotene in the membranes showed higher stability during storage when compared with β-carotene in solution with a decrease in concentration of 57 ± 4% and 70 ± 2% respectively, thus should extend the shelf life of this compound. Also, TGA coupled with PTR-MS resulted in a promising technique to online-monitoring thermal degradation.

  10. An Investigation of Surface Velocimetry of Shocked Polyethylene Using Hetv

    NASA Astrophysics Data System (ADS)

    Routley, N. R.; Price, E.; Keightley, P. T.; Millett, J. C. F.; Bourne, N. K.; Brown, E. N.; Gray, G. T.

    2007-12-01

    The velocity history of a shocked free surface has traditionally been measured using established techniques such as VISAR or Fabry-Perot. In recent years a third type of velocimetry has been developed by LLNL which uses Heterodyne techniques, Photon Doppler Velocimetry (PDV). This technique generates a Doppler beat frequency between light incident on the surface and light internally reflected within the system. Unlike the other two techniques PDV does not use an interferometer, instead it relies upon having the ability to directly record the high beat frequency. The setting up and fielding of PDV is therefore much simpler. A low power (Class 1 laser) system using this principal, locally known as Heterodyne Velocimetry (HetV) has been developed and assembled. A series of experiments has been carried out to investigate the Hugoniot of polyethylene using HetV and embedded stress gauges. The results obtained with HetV have been directly compared with the embedded gauge data from the same experiment.

  11. Synthesis and properties of oligodeoxyribonucleotide-polyethylene glycol conjugates.

    PubMed Central

    Jäschke, A; Fürste, J P; Nordhoff, E; Hillenkamp, F; Cech, D; Erdmann, V A

    1994-01-01

    Pools of oligonucleotide conjugates consisting of 10-400 different molecular species were synthesized. The conjugates contained a varying number of ethylene glycol units attached to 3'-terminal, 5'-terminal and internal positions of the oligonucleotides. Conjugate synthesis was performed by phosphoramidite solid phase chemistry using suitably protected polyethylene glycol phosphoramidites and PEG-derivatized solid supports containing polydisperse PEGs of various molecular weight ranges. The pools were analyzed and fractionated by chromatographic and electrophoretic techniques, and the composition of isolated conjugates was revealed by matrix-assisted laser desorption/ionization mass spectrometry. The number and attachment sites of coupled ethylene glycol units greatly influence the hydrophobicity of the conjugates, as well as their electrophoretic mobilities. Conjugation had little effect on the hybridization behavior of oligonucleotide conjugates with unmodified complementary oligonucleotide strands. Melting temperatures were between 67 and 73 degrees C, depending on the size and number of coupled PEG chains, compared to 68 degrees C for the unmodified duplex. Conjugates with PEG coupled to both 3'- and 5'-terminal positions showed a more than 10-fold increase in exonuclease stability. PMID:7984434

  12. Safety Evaluation of Polyethylene Glycol (PEG) Compounds for Cosmetic Use

    PubMed Central

    Shin, Chan Young; Kim, Kyu-Bong

    2015-01-01

    Polyethylene glycols (PEGs) are products of condensed ethylene oxide and water that can have various derivatives and functions. Since many PEG types are hydrophilic, they are favorably used as penetration enhancers, especially in topical dermatological preparations. PEGs, together with their typically nonionic derivatives, are broadly utilized in cosmetic products as surfactants, emulsifiers, cleansing agents, humectants, and skin conditioners. The compounds studied in this review include PEG/PPG-17/6 copolymer, PEG-20 glyceryl triisostearate, PEG-40 hydrogenated castor oil, and PEG-60 hydrogenated castor oil. Overall, much of the data available in this review are on PEGylated oils (PEG-40 and PEG-60 hydrogenated castor oils), which were recommended as safe for use in cosmetics up to 100% concentration. Currently, PEG-20 glyceryl triisostearate and PEGylated oils are considered safe for cosmetic use according to the results of relevant studies. Additionally, PEG/PPG-17/6 copolymer should be further studied to ensure its safety as a cosmetic ingredient. PMID:26191379

  13. Incipient and Progressive Damage in Polyethylene Under Extreme Tensile Conditions

    SciTech Connect

    Furmanski, Jevan; Brown, Eric; Trujillo, Carl P.; Martinez, Daniel Tito; Gray, George T. III

    2012-06-07

    The Dynamic-Tensile-Extrusion (Dyn-Ten-Ext) test was developed at LANL by Gray and coworkers to probe the tensile response of materials at large strains (>1) and high strain-rates (>1000/s) by firing projectiles through a conical die at 300-700 m/s. This technique has recently been applied to various polymers, such as the fluoropolymers PTFE (Teflon) and the chemically similar PCTFE, which respectively exhibited catastrophic fragmentation and distributed dynamic necking. This work details investigations of the Dyn-Ten-Ext response of high density polyethylene, both to failure and sub-critical conditions. At large extrusion ratios ({approx}7.4) and high velocities, such as those previously employed, HDPE catastrophically fragmented in a craze-like manner in the extruded jet. At more modest extrusion ratios and high velocities the specimen extruded a stable jet that ruptured cleanly, and at lower velocities was recovered intact after sustaining substantial internal damage. Thermomechanical finite element simulations showed that the damage corresponded to a locus of shear stress in the presence of hydrostatic tension. X-ray computed tomography corroborated the prediction of a shear damage mechanism by finding the region of partially damaged material to consist of macroscopic shear-mode cracks nearly aligned with the extrusion axis, originating from the location of damage inception.

  14. Cyclic steady state stress-strain behavior of UHMW polyethylene.

    PubMed

    Krzypow, D J; Rimnac, C M

    2000-10-01

    To increase the long-term performance of total joint replacements, finite element analyses of ultra high molecular weight polyethylene (UHMWPE) components have been conducted to predict the effect of load on the stress and strain distributions occurring on and within these components. Early models incorporated the monotonic behavior of UHMWPE without considering the unloading and cyclic loading behavior. However, UHMWPE components undergo cyclic loading during use and at least two wear damage modes (pitting and delamination) are thought to be associated with the fatigue fracture properties of UHMWPE. The objective of this study was to examine the fully reversed uniaxial tension/compression cyclic steady state stress-strain behavior of UHMWPE as a first step towards developing a cyclic constitutive relationship for UHMWPE. The hypothesis that cycling results in a permanent change in the stress-strain relationship, that is, that the cyclic steady state represents a new cyclically stabilized state, was examined. It was found that, like other ductile polymers, UHMWPE substantially cyclically softens under fully reversed uniaxial straining. More cyclic softening occurred in tension than in compression. Furthermore, cyclic steady state was attained, but not cyclic stability. It is suggested that it may be more appropriate to base a material constitutive relationship for UHMWPE for finite element analyses of components upon a cyclically modified stress-strain relationship. PMID:10966018

  15. Fluoroalkylated polyethylene glycol as potential surfactant for perfluorocarbon emulsion.

    PubMed

    Peng, C A; Hsu, Y C

    2001-11-01

    So far, perfluorocarbon (PFC) emulsions have been manufactured based mainly on two surfactants, Pluronic F-68 and egg yolk phospholipids (EYP) for clinical use. However, they have been documented to induce inflammatory or allergic responses when PFC emulsions were injected into human bloodstream. The cause of these side effects is associated with the phagocytosis of emulsified PFC microparticles by cells such as macrophages. In order to lessen the side effects, it is logic to develop surfactants, which are more phagocytosis-resistant and biocompatible. In this study, a perfluoroalkylated polyethylene glycol (R(F)-PEG) surfactant was synthesized by reacting perfluorooctanoyl chloride (C7F15COCl) with PEG of molecular weigh 8000. Both R(F)-PEG 8000 and EYP were used to make PFC emulsions separately by an ultrasonic homogenizer. Individual PFC emulsions were then incubated with mouse macrophage J774A.1 cells to examine the degree of phagocytosis. From microscopic observation of cell morphology, our results showed that the process of phagocytosis was retarded to a large extend using the R(F)-PEG surfactant. We also harnessed 19F-NMR to quantitatively detect the amount of PFC emulsions phagocytosed by J774A.1 cells. 19F-NMR result was consistent with the qualitative microscopic observation aforementioned. PMID:11795633

  16. High sensitivity of positron annihilation to thermal oxidation of polyethylene

    NASA Astrophysics Data System (ADS)

    Ito, Kenji; Kobayashi, Yoshinori; Nanasawa, Atsushi

    2003-01-01

    We demonstrate the high sensitivity of positron annihilation to compositional changes related to the thermal degradation of polyethylene (PE). Positron annihilation γ-ray and lifetime measurements were conducted for PE films with and without antioxidant (1000-ppm Ciba® IRGANOX® 1076), subjected to heat treatment at 100 °C for different periods, to a maximum of 30 days. For the film without antioxidant, the positron Doppler parameter (S) and ortho-positronium formation probability (Io-Ps) appreciably decreased with increased heat treatment times, whereas they barely changed for the film with antioxidant. This, together with the Fourier transform infrared measurements, demonstrated that the variations of S and Io-Ps are caused by the thermal oxidation of PE. The S parameter was found to be sensitive to the early stage of degradation, where the carbonyl concentration is inferred to be lower than 100 ppm. The high sensitivity results from the large positron mobility in PE and from the high positron affinity of oxygen-containing polar groups. This work provides the basis for an application of positron annihilation to sensitive detection of the initial degradation of PE and other nonpolar polymers.

  17. Chain Ends and the Ultimate Tensile Strength of Polyethylene Fibers

    NASA Astrophysics Data System (ADS)

    O'Connor, Thomas C.; Robbins, Mark O.

    Determining the tensile yield mechanisms of oriented polymer fibers remains a challenging problem in polymer mechanics. By maximizing the alignment and crystallinity of polyethylene (PE) fibers, tensile strengths σ ~ 6 - 7 GPa have been achieved. While impressive, first-principal calculations predict carbon backbone bonds would allow strengths four times higher (σ ~ 20 GPa) before breaking. The reduction in strength is caused by crystal defects like chain ends, which allow fibers to yield by chain slip in addition to bond breaking. We use large scale molecular dynamics (MD) simulations to determine the tensile yield mechanism of orthorhombic PE crystals with finite chains spanning 102 -104 carbons in length. The yield stress σy saturates for long chains at ~ 6 . 3 GPa, agreeing well with experiments. Chains do not break but always yield by slip, after nucleation of 1D dislocations at chain ends. Dislocations are accurately described by a Frenkel-Kontorova model, parametrized by the mechanical properties of an ideal crystal. We compute a dislocation core size ξ = 25 . 24 Å and determine the high and low strain rate limits of σy. Our results suggest characterizing such 1D dislocations is an efficient method for predicting fiber strength. This research was performed within the Center for Materials in Extreme Dynamic Environments (CMEDE) under the Hopkins Extreme Materials Institute at Johns Hopkins University. Financial support was provided by Grant W911NF-12-2-0022.

  18. Cell adhesion and proliferation on polyethylene grafted with Au nanoparticles

    NASA Astrophysics Data System (ADS)

    Kasálková, N. Slepičková; Slepička, P.; Kolská, Z.; Sajdl, P.; Bačáková, L.; Rimpelová, S.; Švorčík, V.

    2012-02-01

    Plasma treatment and subsequent Au nano-particles grafting of polyethylene (PE) lead to changes in surface morphology, roughness and wettability, significantly increasing the attractiveness of the material for cells. The PE samples were exposed to argon plasma. Plasma modified PE was chemically grafted by immersion to biphenyldithiol and consequently into solution of Au nano-particles. Changes in chemical structure of the modified PE were studied using X-ray Photoelectron Spectroscopy (XPS) and electrokinetic analysis ( ζ-potential). The surface wettability of the modified PE samples was examined by measurement of the contact angle by standard goniometry. The surface morphology of the plasma modified PE and that grafted with Au nano-particles was studied by Atomic Force Microscopy (AFM). The modified PE samples were seeded with rat vascular smooth muscle cells (VSMCs) and their adhesion and proliferation were studied. Chemically bounded biphenyldithiol increases the number of the incorporated gold nano-particles and changes sample surface properties. The presence of the biphenyldithiol and the gold nano-particles on the PE surface influences dramatically adhesion and proliferation of VSMCs.

  19. Optical clearing of skin tissue ex vivo with polyethylene glycol

    NASA Astrophysics Data System (ADS)

    Tuchina, D. K.; Genin, V. D.; Bashkatov, A. N.; Genina, E. A.; Tuchin, V. V.

    2016-01-01

    Alterations of the optical and structural (weight, thickness, and square) parameters of skin caused by polyethylene glycol (PEG) with molecular weights of 300 and 400 Da were studied experimentally. The objects of the study were ex vivo skin samples of albino laboratory rats. Collimated transmittance of the skin was measured in the wavelength range 500-900 nm. As a result of exposure to the agents, an increase in the collimated transmittance and a decrease in weight, thickness, and square of skin samples were observed. Analysis of the kinetics of parameters alterations allowed us to measure the diffusion coefficient of the agents in the skin as (1.83 ± 2.22) × 10-6 and (1.70 ± 1.47) × 10-6 cm2/s for PEG-300 and PEG-400, respectively, and the rate of alterations of the structural parameters. The results obtained in this study can be used for the improvement of existing and development of new methods of noninvasive diagnostics and therapy of subcutaneous diseases.

  20. Mechanisms of lithium transport in amorphous polyethylene oxide.

    PubMed

    Duan, Yuhua; Halley, J W; Curtiss, Larry; Redfern, Paul

    2005-02-01

    We report calculations using a previously reported model of lithium perchlorate in polyethylene oxide in order to understand the mechanism of lithium transport in these systems. Using an algorithm suggested by Voter, we find results for the diffusion rate which are quite close to experimental values. By analysis of the individual events in which large lithium motions occur during short times, we find that no single type of rearrangement of the lithium environment characterizes these events. We estimate the free energies of the lithium ion as a function of position during these events by calculation of potentials of mean force and thus derive an approximate map of the free energy as a function of lithium position during these events. The results are consistent with a Marcus-like picture in which the system slowly climbs a free energy barrier dominated by rearrangement of the polymer around the lithium ions, after which the lithium moves very quickly to a new position. Reducing the torsion forces in the model causes the diffusion rates to increase. PMID:15740341