Light-Responsive Polyion Complex Micelles with Switchable Surface Charge for Efficient Protein Delivery

被引:39
|
作者
Jin, Qiao [1 ]
Cai, Tongjiang [1 ]
Wang, Yin [1 ]
Wang, Haibo [1 ]
Ji, Jian [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, Minist Educ, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
来源
ACS MACRO LETTERS | 2014年 / 3卷 / 07期
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
POLYMERIC MICELLES; DRUG-DELIVERY; NANOPARTICLES; PH; NANOGELS; RELEASE; CELLS; TUMOR; POLY(CARBOXYBETAINE); COPOLYMERS;
D O I
10.1021/mz500290s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this letter, light-responsive protein-encapsulated polyion complex (PIC) micelles were prepared by self-assembly of cationic block copolymer poly(N,N-dimethyl-N-(2-(methacryloyloxy)ethyl)-N-((2-nitrobenzyl)oxy)-2-oxoe-thanaminium bromide)-block-poly(carboxybetaine methacrylate) (PDMNBMA-b-PCBMA) and negatively charged bovine serum albumin (BSA). The PIC micelles were well characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). From the zeta potential measurement, the increase of the zeta potential of PIC micelles from similar to 10 to similar to 20 mV was observed when the solution pH decreased from 7.4 to 6.5, which could enhance the intracellular protein delivery efficiency. Moreover, the positively charged PDMNBMA blocks can be transformed to zwitterionic carboxybetaine units under UV irradiation, which could result in the disassembly of the PIC micelles. The release of BSA can therefore be drastically accelerated in the presence of UV irradiation. Meanwhile, the circular dichroism (CD) spectroscopy confirmed that the secondary structure of BSA was unaffected during the UV irradiation process.
引用
收藏
页码:679 / 683
页数:5
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