Self-assembled star-shaped chlorin-core poly(c-caprolactone)-poly(ethylene glycol) diblock copolymer micelles for dual chemo-photodynamic therapies

被引:154
作者
Peng, Cheng-Liang [1 ,2 ]
Shieh, Ming-Jium [1 ,2 ,3 ]
Tsai, Ming-Hsien [1 ,2 ]
Chang, Cheng-Chung [4 ]
Lai, Ping-Shan [4 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Biomed Engn, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Engn, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 100, Taiwan
[4] Natl Chung Hsing Univ, Dept Chem, Taichung 402, Taiwan
关键词
star-shaped copolymer; micelle; photodynamic therapy; paclitaxel; cancer therapy;
D O I
10.1016/j.biomaterials.2008.05.018
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Amphiphilic 4-armed star-shaped chlorin-core diblock copolymers based on methoxy poly(ethylene glycol) (mPEG) and poly(E-caprolactone) (PCL) were synthesized and characterized in this study. The synthesized photosensitizer-centered amphiphilic star block copolymer that forms assembled micelle-like structures can be used in a photodynamic therapy (PDT)-functionalized drug delivery system. Moreover, the hydrophobic chemotherapeutic agent, paclitaxel, can be trapped in the hydrophobic inner core of micelles. In our results, the star-polymer-formed micelle exhibited efficient singlet oxygen generation, whereas the hydrophobic photosensitizer failed due to aggregation in aqueous solution. The chlorin-core micelle without paclitaxel loading exhibited obvious phototoxicity in MCF-7 breast cancer cells with 7 J/cm(2) or 14 J/cm(2) light irradiation at a chlorin concentration of 125 mu g/ml. After paclitaxel loading, the size of micelle increased from 71.4 nm to 103.2 nm. Surprisingly, these micelles were found to improve the cytotoxicity of paclitaxel significantly in MCF-7 cells after irradiation through a synergistic effect evaluated by median effect analysis. This functionalized micellar delivery system is a potential dual carrier for the synergistic combination of photodynamic therapy and chemotherapy for the treatment of cancer. Crown Copyright (c) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3599 / 3608
页数:10
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