Emerging applications of polymersomes in delivery: From molecular dynamics to shrinkage of tumors

被引:326
作者
Discher, Dennis E. [1 ]
Ortiz, Vanessa
Srinivas, Goundla
Klein, Michael L.
Kim, Younghoon
Christian, David
Cai, Shenshen
Photos, Peter
Ahmed, Fariyal
机构
[1] Univ Penn, NanoBio Polymers Lab, Philadelphia, PA 19104 USA
[2] Univ Penn, Ctr Mol Modeling, Dept Chem, Philadelphia, PA 19104 USA
关键词
liposomes; amphiphile; block copolymers; nano-particles; controlled release; BLOCK-COPOLYMER VESICLES; DISSIPATIVE PARTICLE DYNAMICS; DIBLOCK COPOLYMERS; DRUG-DELIVERY; WORM MICELLES; IN-VIVO; POLY(ETHYLENE OXIDE)-BLOCK-POLYCAPROLACTONE; COMPUTER-SIMULATION; TRIGGERED RELEASE; GIANT AMPHIPHILES;
D O I
10.1016/j.progpolymsci.2007.05.011
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymersomes are self-assembled shells of amphiphilic block copolymers that are currently being developed by many groups for fundamental insights into the nature of self-assembled states as well as for a variety of applications. While recent reviews have highlighted distinctive properties-particularly stability-that are strongly influenced by both copolymer type and polymer molecular weight, here we first review some of the more recent developments in computational molecular dynamics (MD) schemes that lend insight into assembly. We then review polymersome loading, in vivo stealthiness, degradation-based disassembly for controlled release, and tumor shrinkage in vivo. Comparisons of polymersomes with viral capsids are shown to encompass and inspire many aspects of current and emerging designs. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:838 / 857
页数:20
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