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Interaction of triblock co-polymer micelles with phospholipid-bilayer: a spectroscopic investigation using a potential chloride channel blocker

机译:三嵌段共聚物胶束与磷脂双层的相互作用:使用潜在的氯离子通道阻滞剂的光谱研究

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摘要

Interaction of a potential chloride channel blocker, 9-methyl anthroate (9-MA), has been studied with zwitterionic L-alpha-phosphatidylcholine (egg-PC) lipid vesicles, which ascertains the utility of the drug as an efficient molecular reporter for probing the microheterogeneous environment of lipid-bilayers. The effect of a non-ionic triblock co-polymer P123 on the stability of these drug-bound lipid-bilayers has also been investigated by means of steady state and time-resolved spectroscopic techniques exploiting the fluorescence properties of the drug. Experimental results reveal that the addition of P123 to the drug-bound lipid results in a preferential complexation of the drug with the Pluronic leaving the lipid vesicles aside, which has been attributed to a substantially stronger binding interaction of the drug with P123 than that with egg-PC. The result is of potential interest from a medical perspective owing to the context of excess drug desorption from bio-membranes.
机译:已经研究了潜在的氯离子通道阻滞剂9-甲基邻苯二甲酸酯(9-MA)与两性离子L-α-磷脂酰胆碱(egg-PC)脂质囊泡的相互作用,这确定了该药物作为探测分子的有效分子工具的效用脂质双层的微异质环境。还已经通过利用药物的荧光性质的稳态和时间分辨光谱技术研究了非离子三嵌段共聚物P123对这些药物结合的脂质双分子层的稳定性的影响。实验结果表明,在与药物结合的脂质中添加P123会导致药物与Pluronic优先复合,而将脂质囊泡置于一旁,这归因于该药物与P123的结合相互作用远强于与蛋的结合相互作用-PC。由于过量的药物从生物膜中解吸,这种结果从医学角度可能引起人们的兴趣。

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