Drug release from pH-responsive thermogelling pentablock copolymers

被引:58
作者
Determan, Michael D.
Cox, James P.
Mallapragada, Surya K.
机构
[1] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50011 USA
[2] Ames Lab, Ames, IA 50011 USA
关键词
thermoresponsive; pH-dependent; copolymer; protein release; in situ gelation;
D O I
10.1002/jbm.a.30991
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A novel pH-dependent injectable sustained delivery system was developed by utilizing a cationic pentablock copolymer that exhibits a thermoreversible sol-gel transition. Aqueous solutions of the pentablock copolymer, consisting of poly(2-diethylaminoethyl-methyl methacrylate)poly(ethylene oxide) -poly(propylene oxide)-poly (ethylene oxide)-poly(2-diethylaminoethyl-methyl methacrylate) (PDEAEM(25)-PEO100-PPO65-PEO100-PDEAEM(25)) exhibit temperature and pH dependent micellization due to the lower critical solution temperature of the PPO blocks and the polyelectrolyte character of the PDEAEM blocks, respectively. Aqueous solutions of the copolymers above 12 wt % are free flowing liquids at room temperature and form elastic physical hydrogels reversibly above 37 degrees C. Hydrophobic probe absorbance studies indicate that pentablock copolymer micelles increase the solubility of sparingly soluble drugs. Solutions of the pentablock copolymer that form gels at body temperature exhibit sustained zero-order release in in vitro experiments. The release rates of model drugs and proteins were significantly influenced by the pH of the release media, thereby making these polymers ideal candidates for modulated drug delivery. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:326 / 333
页数:8
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