Journal
JOURNAL OF CONTROLLED RELEASE
Volume 142, Issue 1, Pages 40-46Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jconrel.2009.09.023
Keywords
Degradation; Polymersome; Micelle; pH-sensitive; Drug delivery; Anticancer drugs
Funding
- National Natural Science Foundation of China (NSFC) [50703028, 50973078, 20874070, 20974073]
- Jiangsu Higher Education Institutions of China [08KJB150016]
- Soochow University
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pH-Sensitive degradable polymersomes and micelles were prepared based on diblock copolymer of poly (ethylene glycol) (PEG) and an acid-labile polycarbonate, poly(2,4,6-trimethoxybenzylidenepentaerythritol carbonate) (PTMBPEC). Polymersomes of PEG( 1.9k)-PTMBPEC(6k) revealed average sizes of 100-200 nm. The acetals of polymersomes, similar to those of PEG(5k)-PTMBPEC(5.8k) micelles, though stable at pH 7.4 were prone to fast hydrolysis at mildly acidic pH of 4.0 and 5.0, with half lives of 0.5 and 3 d, respectively. The acetal hydrolysis resulted in significant size increase of polymersomes, to over 1000 nm in 24 h at pH 4.0. Drug encapsulation studies revealed that polymersomes were able to simultaneously load paclitaxel (PTX, hydrophobic) and doxorubicin hydrochloride (DOX center dot HCl, hydrophilic), whereas micelles loaded PTX only. Notably, polymersomes showed lower drug loading efficiencies for M than micelles (30.0-37.7% versus 61.4-65.2%). The in vitro release studies demonstrated that release of PTX and DOX center dot HCl from polymersomes was highly pH-dependent, i-e. significantly faster drug release at mildly acidic pH of 4.0 and 5.0 compared to physiological pH. Furthermore, much higher release rates were observed for M release from the polymersomes compared to that from the micelles under otherwise the same conditions. These pH-sensitive nano-sized degradable polymersomes hold great promise for combination therapy for cancers. (C) 2009 Elsevier B.V. All rights reserved.
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