Natural liposomes and synthetic polymeric structures for biomedical applications

被引:42
|
作者
Mueller, Laura K. [1 ]
Landfester, Katharina [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
Liposome; Polymersome; Drug delivery; Amphiphilic copolymer; AMPHIPHILIC BLOCK-COPOLYMERS; LIPID-LIKE MATERIALS; RNA INTERFERENCE; DRUG-DELIVERY; PROLONGED CIRCULATION; IN-VITRO; BIODEGRADABLE POLYMERSOMES; ENCAPSULATED HEMOGLOBIN; POLY(ETHYLENE GLYCOL); SERUM STABILITY;
D O I
10.1016/j.bbrc.2015.08.088
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last decades, the development and design of drug delivery systems have attracted great attention. Especially siRNA carriers have been of special interest since discovered as suitable tool for gene silencing. Self-assembled structures consisting of amphiphilic molecules are the most investigated carriers with regards to siRNA delivery. Liposomes as drug vehicles already found their way into clinical use, as they are highly biocompatible and their colloidal stability and circulation time in blood can be significantly enhanced by PEGylation. Fully synthetic polymersomes inspired by these natural structures provide enhanced stability and offer a wide range of modification-possibilities. Therefore, their design as carrier vehicles has become of great interest. This mini-review highlights the possibilities of using polymeric vesicles for potential drug delivery and gives a brief overview of their potential regarding fine-tuning towards targeted delivery or triggered drug release. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:411 / 418
页数:8
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