Direct formation of cationic polypeptide vesicle as potential carrier for drug and gene

被引:31
作者
Ding, Jianxun [1 ,2 ]
Xiao, Chunsheng [1 ,2 ]
Zhuang, Xiuli [1 ]
He, Chaoliang [1 ]
Chen, Xuesi [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomaterials; Carrier; Cationic polypeptide; Nanoparticles; Vesicle; DELIVERY;
D O I
10.1016/j.matlet.2011.12.092
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The pH-responsive polypeptide grafted with polycation was prepared through copper(I)-catalyzed "click chemistry". The amphiphilic polypeptide directly formed into cationic vesicle when it was dissolved in phosphate buffer solution (PBS). The hydrophilic DOX center dot HCl was loaded into the hollow core of vesicle. The in vitro release behavior of DOX center dot HCl from vesicle in PBS could be adjusted by the pH of release media. In vitro cell experiments demonstrated that the DOX center dot HCI loaded vesicle showed effective cellular proliferation inhibition. In addition, the preliminary gel retardation assay revealed that PLG-g-PAMA could efficiently bind to DNA, indicating its potential use as gene carrier. The more in-depth studies of PLG-g-PAMA vesicle for drug and gene co-delivery are in progress. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 20
页数:4
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