Khovratovich, N. N.; Novikova, T. M.; Khmel'Nitskii, A. I.; Cherenkevich, S. N.; Loban, V. A.
We investigate IR spectra of the solid phase of products obtained at different stages in the process of ozonizing aqueous solutions of pyrocatechin. We found that melanin structures are formed in the process of pyrocatechin ozonization. The existence of intra- and intermolecular interactions in the melanin preparations formed, leading to the formation of molecular associates, is shown. Thorough treatment of preparations with ozone leads to destruction of polymer systems and formation of water-soluble products of acid type.
Matorin, D N; Plekhanov, S E; Bratkovskaia, L B; Iakovleva, O V; Alekseev, A A
The effect of phenols, present in drains of the tsellyulozo-paper industry, on photosynthesis of the microalgae Scenedesmus quadricauda has been studied. The analysis of induction curves of the slowed-down fluorescence and light curves of non-photochemical quenching of chlorophyll fluorescence of microalgae Scenedesmus quadricauda is carried out. It was observed that energization of photosynthetic membranes was inhibited at low concentration of phenol and pyrocatechin (0.1 mM). At higher concentrations phenol and pyrocatechin inhibited electron transport in FSII and increased a share of QB not restoring centers. As a result of it the rate of P700 pigment regeneration slowed down. The results obtained indicate that parameters of induction curves of the fast and slowed-down fluorescence can be used for detecting phenol and pyrocatechin in the environment at early stages of toxic effects.
Husztik, E; Lázár, G; Szabó, E
Peliosis hepatis has been induced immunologically with anti-rat glomerular basal membrane rabbit serum in rats pre-sensitized with a rare earth metal complex, neodymium pyrocatechin disulphonate (NPD). This is the first experimental evidence that peliosis hepatis may develop as a result of an immunological process. It is noteworthy that in this experimental form of peliosis hepatis and in that observed earlier in rats treated with basic polyglutamic acid derivatives, severe defibrination was detected and, as in most human cases, not only the liver but other organs were also involved in the peliotic lesions. Since the rare earth metal compounds, among them the pyrocatechin disulphonate complex of neodymium, depress the reticulo-endothelial activity, a role of the reticulo-endothelial system in the pathogenesis of this experimental form of peliosis hepatis is suggested.
Yu, Xinxin; Lin, Ting; Lv, Huafei; Pan, Sujuan; Wu, Shijun; Zeng, Di; Jiang, Yufeng; Wang, Yuhua; Yang, Hongqin; Huang, Yide; Peng, Yiru
Metal phthalocyanines (MPcs) have been found to be a promising photosensitizers for photodynamic therapy (PDT) of cancers and non-cancer diseases. Nevertheless, phthalocyanines are substantially limited in clinical applications owing to their poor solubility, aggregation and insufficient selectivity for cancer cells. Catechol is an important pharmaceutical intermediate, playing important in vivo biological activity in medicine. Using catechol (pyrocatechin) as axial ligands, utilizing of the pharmaceutical effect of catechins, could improve the bioavailability, and achieve synergistic therapeutic effect in PDT. To address these issues, a novel catechol axially substituted tetra-α-(pentyloxy) titanium(IV) (TiPc(OC5H11)4-Catechol) was synthesized. The structure of TiPc(OC5H11)4-Catechol was characterized by elemental analysis, IR, 1HNMR and MS methods. The photophysical properties of TiPc(OC5H11)4 and TiPc(OC5H11)4-Catechol have been studied by UV/Vis and steady-state fluorescence spectra. After being axially substituted with catechin groups, no obviously intensity and position of maximum wavelength in Q-band of TiPc(OC5H11)4 and TiPc(OC5H11)4-Catechol were observed. The fluorescence intensity of TiPc(OC5H11)4 was stronger than that of TiPc(OC5H11)4-Catechol, but the fluorescence lifetime of TiPc(OC5H11)4-Catechol was longer than that of TiPc(OC5H11)4. TiPc(OC5H11)4-Catechol may be considered as a promising photosensitizer for PDT.
Humic acids (HA) play an important role in processes of heavy metals migration, controlling their geochemical streams in environment. Accumulative and detoxification abilities of HA to heavy metals are realized by means of formation of steady complexes salycylate and pyrocatechin types. Modern researches show that HA of the Arctic and Subarctic areas are poorly enriched by aromatic frames, so and metalbinding centres. The work purpose is to study interaction mechanisms of Hg (II) ions with HA and to define tread possibilities of a tundra soils humic acids. It is established that binding ability of Hg (II) ions depends on concentration of an element, on quantity of functional groups in peripheral and nuclear parts of HA molecule as well as on a solution pH. coomplexation proceeds at pH 2.5-3.5 efficiently. On the basis of kinetic models it is shown that HA interaction with Hg (II) ions, at microconcentration of a pollutant (0.025-5.0 mkmol/dm3), has a zero order of reaction. Rate of a reaction does not depend on initial components concentration and is defined by process of Hg (II) ions diffusion to organic ligands. High correlation of a HA sorption capacity to Hg (II) ions is observed: with the nitrogen content and maintenance of amino groups (according to a 13C-NMR, element composition) and negative correlation - with degree of HA aromaticity. It testifies to primary binding of Hg (II) ions by amino-acid fragments of a HA molecule peripheral part. When concentration of Hg (II) ions increases, binding proceeds on carboxylic and phenolic groups of a molecule nuclear part. Higher order of kinetic models reaction and FTIR spectroscopy data testify to it. Comparison of FTIR spectra of HA preparations and mercury humates, shows that Hg (II) ions binding in humate complexes is carried out mainly by -COOH. Reduction of a spectral line intensity not ionized -COOH at 1700-1720 sm-1 and intensity increases of dissymetric valency vibration at 1610-1650 sm-1 diagnose increase