Micelles from Amphiphilic Block Copolyphosphates for Drug Delivery

被引:31
|
作者
Zhai, Xiang [1 ]
Huang, Wei [1 ]
Liu, Jinyao [1 ]
Pang, Yan [1 ]
Zhu, Xinyuan [1 ]
Zhou, Yongfeng [1 ]
Yan, Deyue [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
amphiphilic; block copolyphosphates; drug delivery systems; drug release; micelles; SELF-ASSEMBLED MICELLES; TRIBLOCK COPOLYMERS; POLYMERIC MICELLES; CANCER-THERAPY; POLYPHOSPHOESTER; RELEASE; DESIGN; TRANSPORT; KINETICS; TISSUE;
D O I
10.1002/mabi.201100163
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amphiphilic block copolyphosphates (PEP-b-PIPPs) are synthesized by two-step ROP of cyclic phosphate monomers with different pedant groups. They can spontaneously self-assemble into approximately spherical micelles ranging in size between 89 and 198nm in water. A typical hydrophobic anti-cancer drug DOX is encapsulated into the micelles. The release rate of DOX slows down with increasing hydrophobic block length of PIPP. DOX-loaded micelles are investigated for the proliferation inhibition of Hela cells and the DOX dose required for 50% cellular growth inhibition is found to be 0.8 mu gmL(-1). It is demonstrated that PEP-b-PIPP micelles can be used as a safe and promising drug delivery system.
引用
收藏
页码:1603 / 1610
页数:8
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