Enhancement of Cellular Uptake and Antitumor Efficiencies of Micelles with Phosphorylcholine

被引:48
|
作者
Tu, Song [1 ,2 ]
Chen, Yuan-Wei [1 ,2 ]
Qiu, Yong-Bin [1 ,2 ]
Zhu, Kun [1 ,2 ]
Luo, Xiang-Lin [1 ,2 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, State Key Lab Polymer Mat & Engn, Chengdu 610065, Peoples R China
关键词
cytotoxicity; drug delivery systems; internalization; phosphorylcholine; self-assembly; TRANSFER RADICAL POLYMERIZATION; BLOCK-COPOLYMERS; DRUG-DELIVERY; 2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE; INTRACELLULAR DELIVERY; PHOSPHOLIPID POLYMERS; CELLS; NANOPARTICLES; THERAPY; CANCER;
D O I
10.1002/mabi.201100111
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
Internalization of drug delivery micelles into cancer cells is a crucial step for antitumor therapeutics. Novel amphiphilic star-shaped copolymers with zwitterionic phosphorylcholine (PC) block, 6-arm star poly(epsilon-caprolactone)-b-poly(2-methacryloyloxyethyl phosphorylcholine) (6sPCL-b-PMPC), have been developed for encapsulation of poorly water-soluble drugs and enhancement of their cellular uptake. The star-shaped copolymers were synthesized by a combination of ring-opening polymerization (ROP) and atom transfer radical polymerization (ATRP). The copolymers self-assembled to form spherical micelles with low critical micelle concentration (CMC). The sizes of the micelles range from 80 to 170nm and increase 30 approximate to 80% after paclitaxel (PTX) loading. Labeled with fluorescein isothiocyanate (FITC), the micelles were confirmed by fluorescence microscopy to have been internalized efficiently by tumor cells. Direct visualization of the micelles within tumor cells by transmission electron microscopy (TEM) confirmed that the 6sPCL-b-PMPC micelles were more efficiently uptaken by tumor cells compared to PCL-b-PEG micelles. When incorporated with PTX, the 6sPCL-b-PMPC micelles show much higher cytotoxicity against Hela cells than PCL-b-PEG micelles, in response to the higher efficiency of cellular uptake.
引用
收藏
页码:1416 / 1425
页数:10
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