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高度聚乙二醇化的空间稳定胶束在水介质中的结构和动力学。

Structure and dynamics of highly PEG-ylated sterically stabilized micelles in aqueous media.

机构信息

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607, United States.

出版信息

J Am Chem Soc. 2011 Aug 31;133(34):13481-8. doi: 10.1021/ja204043b. Epub 2011 Aug 9.

Abstract

Molecular assemblies of highly PEG-ylated phospholipids are important in many biomedical applications. We have studied sterically stabilized micelles (SSMs) of self-assembled DSPE–PEG2000 in pure water and isotonic HEPES-buffered saline solution. The observed SSM sizes of 2–15 nm largely depend on the solvent and the lipid concentration used. The critical micelle concentration of DSPE–PEG2000 is 10 times higher in water than in buffer, and the viscosity of the dispersion dramatically increases with the lipid concentration. To explain the experimentally observed results, we performed atomistic molecular dynamics simulations of solvated SSMs. Our modeling revealed that the observed assemblies have very different aggregation numbers (N(agg) ≈ 90 in saline solution and N(agg) < 8 in water) because of very different screening of their charged PO4(–) groups. We also demonstrate that the micelle cores can inflate and their coronas can fluctuate strongly, thus allowing storage and delivery of molecules with different chemistries.

摘要

高度聚乙二醇化磷脂的分子组装在许多生物医学应用中非常重要。我们研究了自组装的 DSPE-PEG2000 在纯水中和等渗 HEPES 缓冲盐溶液中的刚性稳定胶束 (SSM)。观察到的 2-15nm 的 SSM 尺寸在很大程度上取决于所用的溶剂和脂质浓度。DSPE-PEG2000 在水中的临界胶束浓度比在缓冲液中高 10 倍,并且随着脂质浓度的增加,分散体的粘度急剧增加。为了解释实验观察到的结果,我们对溶剂化的 SSM 进行了原子分子动力学模拟。我们的模型表明,由于其带电 PO4(-) 基团的屏蔽作用非常不同,观察到的组装体具有非常不同的聚集数 (N(agg)在盐溶液中约为 90,在水中 N(agg) < 8)。我们还证明了胶束核心可以膨胀,其冠层可以强烈波动,从而允许储存和输送具有不同化学性质的分子。

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