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Membrane interactions of ionic liquids: Possible determinants for biological activity and toxicity

机译:离子液体的膜相互作用:生物活性和毒性的可能决定因素

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Ionic liquids (ILs) are a class of diverse organic salts with relatively low melting points (below 100 °C) which have attracted considerable interest as a promising green substitute for organic solvents. The broad solvation properties of ILs and their high solubility in water, however, present health risks, in particular since it was shown that many ILs exhibit cytotoxic properties. In this context, interactions of ILs with the cellular membrane are believed to constitute a primary culprit for toxicity. We present a comprehensive biophysical and microscopy study of membrane interactions of a series of ILs having different side-chain compositions and lengths, and cationic head-group structures and orientations. The experimental data reveal that the ILs studied exhibit distinct mechanisms of membrane binding, insertion, and disruption which could be correlated with their biological activities. The results indicate, in particular, that both the side chain composition and particularly the head-groups of ILs constitute determinants for membrane activity and consequent cell toxicity. This work suggests that tuning membrane interactions of ILs should be an important factor for designing future compounds with benign environmental impact.
机译:离子液体(ILs)是一类具有相对较低的熔点(低于100°C)的有机盐,作为有机溶剂的有前途的绿色替代品已引起了广泛的关注。然而,IL的广泛的溶剂化性质及其在水中的高溶解度存在健康风险,特别是因为已表明许多IL显示出细胞毒性性质。在这种情况下,IL与细胞膜的相互作用被认为是毒性的主要元凶。我们提出了一系列具有不同侧链组成和长度,以及阳离子头基结构和方向的IL的膜相互作用的全面的生物物理和显微镜研究。实验数据表明,所研究的IL表现出独特的膜结合,插入和破坏机制,这可能与其生物学活性有关。结果特别表明,IL的侧链组成,特别是IL的头基组成膜活性和随后的细胞毒性的决定因素。这项工作表明,调节IL的膜相互作用应该是设计对未来环境有益的化合物的重要因素。

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