Preparation and characterization of water-soluble pH-sensitive nanocarriers for drug delivery

被引:76
作者
Dufresne, MH
Le Garrec, D
Sant, V
Leroux, JC
Ranger, M
机构
[1] Univ Montreal, Fac Pharm, Canada Res Chair Drug Delivery, Montreal, PQ H3C 3J7, Canada
[2] Labopharm Inc, Technol Innovat, Laval, PQ H7L 5A2, Canada
关键词
block copolymers; pH-controlled release; polymeric micelles; anticancer agents; poorly soluble drugs;
D O I
10.1016/j.ijpharm.2003.07.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
pH-sensitive drug delivery systems can be engineered to release their contents or change their physicochemical properties in response to variations in the acidity of the surroundings. The present work describes the preparation and characterization of novel polymeric micelles (PM) composed of amphiphilic pH-responsive poly(N-isopropylacrylamide) (PNIPAM) or poly(alkyl(meth)acrylate) derivatives. On one hand, acidification of the PNIPAM copolymers induces a coil-to-globule transition that can be exploited to destabilize the intracellular vesicle membranes. In this work, PNIPAM-based PM were loaded with either doxorubicin or aluminium chloride phthalocyanine and their cytotoxicity was assessed in murine tumoral models. On the other hand, poly(alkyl(meth)acrylate) copolymers can be designed to interact with either hydrophobic drugs or polyions and release their cargo upon an increase in pH. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 90
页数:10
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