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脂质体药物递送系统的合理设计:脂质膜、脂质体及其聚乙二醇化的实验与计算联合研究综述

Rational design of liposomal drug delivery systems, a review: Combined experimental and computational studies of lipid membranes, liposomes and their PEGylation.

作者信息

Bunker Alex, Magarkar Aniket, Viitala Tapani

机构信息

Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.

Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland; Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.

出版信息

Biochim Biophys Acta. 2016 Oct;1858(10):2334-2352. doi: 10.1016/j.bbamem.2016.02.025. Epub 2016 Feb 23.

DOI:10.1016/j.bbamem.2016.02.025
PMID:26915693
Abstract

Combined experimental and computational studies of lipid membranes and liposomes, with the aim to attain mechanistic understanding, result in a synergy that makes possible the rational design of liposomal drug delivery system (LDS) based therapies. The LDS is the leading form of nanoscale drug delivery platform, an avenue in drug research, known as "nanomedicine", that holds the promise to transcend the current paradigm of drug development that has led to diminishing returns. Unfortunately this field of research has, so far, been far more successful in generating publications than new drug therapies. This partly results from the trial and error based methodologies used. We discuss experimental techniques capable of obtaining mechanistic insight into LDS structure and behavior. Insight obtained purely experimentally is, however, limited; computational modeling using molecular dynamics simulation can provide insight not otherwise available. We review computational research, that makes use of the multiscale modeling paradigm, simulating the phospholipid membrane with all atom resolution and the entire liposome with coarse grained models. We discuss in greater detail the computational modeling of liposome PEGylation. Overall, we wish to convey the power that lies in the combined use of experimental and computational methodologies; we hope to provide a roadmap for the rational design of LDS based therapies. Computational modeling is able to provide mechanistic insight that explains the context of experimental results and can also take the lead and inspire new directions for experimental research into LDS development. This article is part of a Special Issue entitled: Biosimulations edited by Ilpo Vattulainen and Tomasz Róg.

摘要

为了实现机理理解,对脂质膜和脂质体进行了实验与计算相结合的研究,这种协同作用使得基于脂质体药物递送系统(LDS)的疗法的合理设计成为可能。LDS是纳米级药物递送平台的主要形式,是药物研究领域中被称为“纳米医学”的一条途径,有望超越目前导致收益递减的药物开发模式。不幸的是,到目前为止,这个研究领域在发表论文方面比开发新的药物疗法更为成功。这部分是由于所采用的基于试错的方法。我们讨论了能够深入了解LDS结构和行为的实验技术。然而,单纯通过实验获得的见解是有限的;使用分子动力学模拟的计算建模可以提供其他方式无法获得的见解。我们回顾了利用多尺度建模范式的计算研究,用全原子分辨率模拟磷脂膜,用粗粒度模型模拟整个脂质体。我们更详细地讨论了脂质体聚乙二醇化的计算建模。总体而言,我们希望传达实验和计算方法联合使用所具有的力量;我们希望为基于LDS的疗法的合理设计提供一个路线图。计算建模能够提供机理见解,解释实验结果的背景,还能引领并激发LDS开发实验研究的新方向。本文是由伊尔波·瓦图莱宁(Ilpo Vattulainen)和托马什·罗格(Tomasz Róg)编辑的名为《生物模拟》的特刊的一部分。

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