共轭体系
共聚物
胶束
乙二醇
药物输送
两亲性
化学
结合
毒品携带者
荧光
组合化学
高分子化学
材料科学
水溶液
有机化学
聚合物
物理
数学分析
量子力学
数学
作者
Feng Qiu,Dali Wang,Qi Zhu,Lijuan Zhu,Gangsheng Tong,Yunfeng Lu,Deyue Yan,Xinyuan Zhu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2014-03-07
卷期号:15 (4): 1355-1364
被引量:83
摘要
Chemotherapy is one of the major systemic treatments for cancer, in which the drug release kinetics is a key factor for drug delivery. In the present work, a versatile fluorescence-based real-time monitoring system for intracellular drug release has been developed. First, two kinds of star-conjugated copolymers with different connections (e.g., pH-responsive acylhydrazone and stable ether) between a hyperbranched conjugated polymer (HCP) core and many linear poly(ethylene glycol) (PEG) arms were synthesized. Owing to the amphiphilic three-dimensional architecture, the star-conjugated copolymers could self-assemble into multimicelle aggregates from unimolecular micelles with excellent emission performance in the aqueous medium. When doxorubicin (DOX) as a model drug was encapsulated into copolymer micelles, the emission of star-conjugated copolymer and DOX was quenched. In vitro biological studies revealed that fluorescent intensities of both star-conjugated copolymer and DOX were activated when the drug was released from copolymeric micelles, resulting in the enhanced cellular proliferation inhibition against cancer cells. Importantly, pH-responsive feature of the star-conjugated copolymer with acylhydrazone linkage exhibited accelerated DOX release at a mildly acidic environment, because of the fast breakage of acylhydrazone in endosome or lysosome of tumor cells. Such fluorescent star-conjugated copolymers may open up new perspectives to real-time study of drug release kinetics of polymeric drug delivery systems for cancer therapy.
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