期刊
INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷 348, 期 1-2, 页码 95-106出版社
ELSEVIER
DOI: 10.1016/j.ijpharm.2007.07.026
关键词
injectable hydrogel; block copolymer; PEGylation; camptothecin (CPT); sustained release
The paper employs the spontaneous physical gelling property of a biodegradable polymer in water to prepare an injectable sustained release carrier for a PEGylated drug. A series of thermogelling PLGA-PEG-PLGA triblock copolymers were synthesized. The PEGylated camptothecin (CPT) was also prepared and employed as the model of a PEGylated drug, and the solubility of this hydrophobic drug was significantly enhanced to over 150 mg/mL. The model drug was completely entrapped into the polymeric hydrogel, and the sustained release lasted for I month. The mechanism of the sustained release was diffusion-controlled at the first stage and then was the combination of diffusion and degradation at the late stage. In vivo anti-tumor tests in mice further confirmed the efficacy of the model PEGylated drug released from the hydrogel. This work also revealed the specificity of the PEGylated drug in such a kind of carrier systems by decreasing the critical gelling temperature and increasing the viscosity of the sol. Due to the very convenient drug formulation and highly tunable release rate, an injectable carrier platform for PEGylated drugs is thus set up. (c) 2007 Elsevier B.V All rights reserved.
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