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Synthesis of an esterase‐sensitive degradable polyester as facile drug carrier for cancer therapy
Authors:Zhuxian Zhou  William J Murdoch  Youqing Shen
Institution:1. Department of Chemical and Biological Engineering, Center for Bionanoengineering and State Key Laboratory for Chemical Engineering, Zhejiang University, Hangzhou, China;2. Department of Chemical and Petroleum Engineering, University of Wyoming, Laramie, Wyoming;3. Department of Animal Science, University of Wyoming, Laramie, Wyoming
Abstract:Polyethylene glycol (PEG) is widely used as a carrier to improve the pharmaceutical properties of drugs with low molecular weight. However, PEG has few functional groups (usually two) for drug conjugation and the resulting low drug content (1–2%) has hampered its clinical applications. For this study, we synthesized biodegradable poly(ethylene glycol‐co‐anhydride). This polyester‐based polymer possesses multiple carboxylic acid groups that can be used as facile drug carriers. Two anticancer drugs, camptothecin (CPT) and doxorubicin (DOX) were loaded into the carrier and their releasing properties and in vitro anticancer activities were studied. The polymer–drug conjugates exhibited esterase‐promoted degradation and drug release. Their cytotoxicity against the human ovarian cancer cell line SKOV‐3 was comparable to unconjugated drugs. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 507–515
Keywords:cancer drug delivery  drug conjugate  biodegradable polymer  polyester  polycondensation  esterase‐sensitive  camptothecin  doxorubicin
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