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The Immobilization of Gossypol Derivative on<i>N</i>-Polyvinylpyrrolidone Increases its Water Solubility and Modifies Membrane-Active Properties

Максим ЙоновDepartment of General Biophysics, University of Lodz, Lodz, PolandN. GordiyenkoNational Eye Institute, National Institutes of Health, Bethesda, MarylandEwa OlchowikDepartment of Biophysics, University of Bialystok, Swierkowa 20C, 159-50 Bialystok, PolandN. I. BaramInstitute of Bioorganic Chemistry, Academy of Sciences, Tashkent, UzbekistanKhairulla ZijaevInstitute of Bioorganic Chemistry, Academy of Sciences, Tashkent, UzbekistanB. A. SalakhutdinovInstitute of Bioorganic Chemistry, Academy of Sciences, Tashkent, UzbekistanMaria BryszewskaDepartment of General Biophysics, University of Lodz, Lodz, PolandMaria ZamaraevaDepartment of Biophysics, University of Bialystok, Swierkowa 20C, 159-50 Bialystok, Poland
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Аннотация

The conjugate of the gossypol derivative megosin (1) with N-polyvinylpyrrolidone named rometin (2) was synthesized. The effects of 1 and 2 on the structure and permeability of human erythrocytes and rat liver mitochondria were compared. Compound 1 induced dose-dependent erythrocyte hemolysis and increased mitochondrial permeability, with concomitant changes in membrane structure as determined by ESR and fluorescence anisotropy methods. Immobilization of 1 on N-polyvinylpyrrolidone (compound 2) increased its water solubility and reduced the intensity of its effects on erythrocyte membrane integrity and mitochondrial permeability, which correlated with a decrease in the membranes structural changes induced by the compound. Although the same concentrations of free and N-polyvinylpyrrolidone bound 1 were used, far less (14)C-labeled 1 was incorporated into the membranes from complex than free 1. The increase in water solubility and the reduction of membrane-active properties of 1 after immobilization on N-polyvinylpyrrolidone could explain our previous observation of the decreased toxicity of 1.

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