Fabrication of Poly(ethylene glycol) Capsules via Emulsion Templating Method for Targeted Drug Delivery

被引:5
|
作者
Yang, Shuang [1 ]
Ding, Feng [1 ]
Gao, Zhiliang [1 ]
Guo, Jianman [1 ]
Cui, Jiwei [1 ]
Zhang, Peiyu [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
emulsion; poly(ethylene glycol); polymer capsules; targeting drug delivery; POLYMER CAPSULES; NANOPARTICLES; PEGYLATION; NANOPLATFORM; PARTICLES; MICELLES; ANTIBODY; SIZE;
D O I
10.3390/polym12051124
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
To reduce nonspecific interactions and circumvent biological barriers, low-fouling material of poly(ethylene glycol) (PEG) is most used for the modification of drug nanocarriers. Herein, we report the fabrication of PEG capsules via the free-radical polymerization of linear PEG or 8-arm-PEG using an emulsion templating method for targeted drug delivery. Doxorubicin (DOX) could be loaded in capsules via electrostatic interactions. The obtained capsules composed of 8-arm-PEG result in a lower cell association (2.2%) compared to those composed of linear PEG (7.3%) and, therefore, demonstrate the stealth property. The functionalization of cyclic peptides containing Arg-Gly-Asp (cRGD) on PEG capsules induce high cell targeting to U87 MG cells. A cell cytotoxicity assay demonstrates the biocompatibility of PEG capsules and high drug delivery efficacy of the targeted capsules. The reported capsules with the stealth and targeting property provide a potential platform for improved drug delivery.
引用
收藏
页数:12
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