[Mechanism of the interaction of the individual components of levorin and nystatin preparations with lipid membranes].

Kh M Kasumov, A A Samedova, Iu D Shenin
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引用次数: 0

Abstract

Mechanism of interaction between separate levorin and nystatin component and lipid membranes was studied. It was shown that components A0, A1, A2 and A3 of levorin and components A1, A2, A3 and B1 of nystatin had a markedly pronounced membranotropic activity. Ion channel assembly and membrane conductivity were irreversibly controlled by concentration and membrane potential. Changes in selectivity of biomolecular lipid membranes depended on the structure of the antibiotics. The action of the levorin and nystatin components was based on increasing membrane conductivity by the mechanism of ion channel formation with parameters altering in relation to the antibiotic structure. Recommendations for directed synthesis of the antibiotic derivatives with high therapeutic efficacy are presented.

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[左旋素和制霉菌素制剂中单个成分与脂质膜相互作用的机制]。
研究了左旋素和制霉菌素组分与脂膜相互作用的机理。结果表明,左旋素的组分A0、A1、A2和A3以及制霉菌素的组分A1、A2、A3和B1具有显著的趋膜活性。离子通道组装和膜电导率受浓度和膜电位的不可逆控制。生物分子脂膜的选择性变化取决于抗生素的结构。左旋素和制霉菌素成分的作用是通过离子通道形成机制增加膜电导率,其参数随抗生素结构的变化而变化。提出了有针对性地合成具有高疗效的抗生素衍生物的建议。
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[Monoclonal antibodies to the yellow fever virus]. [Interferon and bacterial infections]. [Isolation, structure and biological action of yeast mannans]. [Effect of protoplast formation on the antibiotic activity of the Streptomyces fradiae 165 strain--a producer of tylosin]. [Preclinical toxicological study of the new antibiotic eremomycin. Its acute toxicity for laboratory animals].
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