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pH‐ and β‐cyclodextrin‐responsive micelles based on polyaspartamide derivatives as drug carrier
Authors:Huan Yu  Jian Sun  Yunti Zhang  Guangyan Zhang  Yanfeng Chu  Renxi Zhuo  Xulin Jiang
Affiliation:1. Key Laboratory of Biomedical Polymers of Ministry of Education, Department of Chemistry, Wuhan University, Wuhan 430072, People's Republic of China;2. Hubei Provincial Key Laboratory of Green Materials for Light Industry, Department of Light Industry, Hubei University of Technology, Wuhan 430068, People's Republic of China
Abstract:A novel kind of graft polymer poly(aspartic acid)‐ethanediamine‐g‐adamantane/methyloxy polyethylene glycol (Pasp‐EDA‐g‐Ad/mPEG) was designed and synthesized for drug delivery in this study. The chemical structure of the prepared polymer was confirmed by proton NMR. The obtained polymer can self‐assemble into micelles which were stable under a physiological environment and displayed pH‐ and β‐cyclodextrin (β‐CD)‐responsive behaviors because of the acid‐labile benzoic imine linkage and hydrophobic adamantine groups in the side chains of the polymer. The doxorubicin (Dox)‐loaded micelles showed a slow release under physiological conditions and a rapid release after exposure to weakly acidic or β‐CD environment. The in vitro cytotoxicity results suggested that the polymer was good at biocompatibility and could remain Dox biologically active. Hence, the Pasp‐EDA‐g‐Ad/mPEG micelles may be applied as promising controlled drug delivery system for hydrophobic antitumor drugs. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1387–1395
Keywords:conjugated polymers  cyclodextrin‐responsive  drug delivery system  micelles  nanoparticles  pH‐responsive  polyaspartamide  polymeric micelles  stimuli‐sensitive polymers
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