Folate-Conjugated Cell Membrane Mimetic Polymer Micelles for Tumor-Cell-Targeted Delivery of Doxorubicin

被引:28
作者
Lu, Qjan [1 ]
Yi, Meijun [1 ]
Zhang, Mengchen [1 ]
Shi, Zhangyu [1 ]
Zhang, Shiping [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Natl Demonstrat Ctr Expt Chem Educ,Minist Educ, Xian 710127, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
DRUG-DELIVERY; COPOLYMER MICELLES; PRODRUG MICELLES; IN-VITRO; NANOPARTICLES; PHOSPHORYLCHOLINE; PHAGOCYTOSIS; NANOCARRIERS; CARRIERS; RELEASE;
D O I
10.1021/acs.langmuir.8b03693
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tumor-targeting nano-drug-delivery systems hold great potential to improve the therapeutic efficacy and alleviate the side effects of cancer treatments. Herein, folic acid (FA)-decorated amphiphilic copolymer of FA-P(MPC-co-MaPCL) (MPC: 2-methacryloxoethyl phosphorylcholine, MaPCL: poly(epsilon-caprolactone) macromonomer) is synthesized and its micelles are fabricated for doxorubicin (DOX) delivery. And non-FA-decorated P(MPC-co-MaPCL) micelles are used as the control. Dynamic light scattering and scanning electron microscopy measurements reveal that FA-P(MPC-co-MaPCL) and P(MPC-co-MaPCL) micelles are spherical with average diameters of 140 and 90 nm, respectively. The evaluation in vitro demonstrates that the blank micelles are nontoxic, while DOX-loaded FA-P(MPC-co-MaPCL) micelles show significant cytotoxicity to HeLa cells and slight cytotoxicity to L929 cells. Moreover, the cellular uptake of DOX-loaded FA-P(MPC-co-MaPCL) micelles in HeLa cells are 4.3 fold and 1.7-fold higher than that of DOX-loaded P(MPC-co-MaPCL) micelles and free DOX after 6 h of incubation, respectively. These results indicate the great potential of this system in anticancer target drug-delivery applications.
引用
收藏
页码:504 / 512
页数:9
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