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聚合物囊泡载体:从自组装到小干扰RNA及蛋白质疗法

Polymersome carriers: from self-assembly to siRNA and protein therapeutics.

作者信息

Christian David A, Cai Shenshen, Bowen Diana M, Kim Younghoon, Pajerowski J David, Discher Dennis E

机构信息

Biophysical Engineering and NanoBio-Polymers Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Eur J Pharm Biopharm. 2009 Mar;71(3):463-74. doi: 10.1016/j.ejpb.2008.09.025. Epub 2008 Oct 17.

Abstract

Polymersomes are polymer-based vesicular shells that form upon hydration of amphiphilic block copolymers. These high molecular weight amphiphiles impart physicochemical properties that allow polymersomes to stably encapsulate or integrate a broad range of active molecules. This robustness together with recently described mechanisms for controlled breakdown of degradable polymersomes as well as escape from endolysosomes suggests that polymersomes might be usefully viewed as having structure/property/function relationships somewhere between lipid vesicles and viral capsids. Here we summarize the assembly and development of controlled release polymersomes to encapsulate therapeutics ranging from small molecule anti-cancer drugs to siRNA and therapeutic proteins.

摘要

聚合物囊泡是基于聚合物的囊泡壳,由两亲性嵌段共聚物水合形成。这些高分子量两亲物赋予其物理化学性质,使聚合物囊泡能够稳定地包裹或整合多种活性分子。这种稳定性以及最近描述的可降解聚合物囊泡的可控分解机制和从内溶酶体逃逸的机制表明,聚合物囊泡在结构/性质/功能关系方面可能介于脂质囊泡和病毒衣壳之间,具有一定的参考价值。在这里,我们总结了控释聚合物囊泡的组装和发展,以包裹从小分子抗癌药物到siRNA和治疗性蛋白质等各种治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b05f/2702089/1c1996643f57/nihms102711f1.jpg

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