Li Junbo, Liang Lijuan, Liang Ju, Wu Wenlan, Zhou Huiyun, Guo Jinwu
School of Chemical Engineering & Pharmaceutics, Henan University of Science & Technology, 263# Kaiyuan Road, Luoyang 471023, China.
School of Medicine, Henan University of Science & Technology, 263# Kaiyuan Road, Luoyang 471023, China.
Nanomaterials (Basel). 2017 Nov 13;7(11):387. doi: 10.3390/nano7110387.
A strategy for constructing polyion complex vesicles (PICsomes) with asymmetric structure is described. Poly(methylacrylic acid)--poly(-isopropylacrylamide) modified gold nanoparticles (PMAA--PNIPAm-@-Au NPs) were prepared and then assembled with poly(ethylene glycol)--poly[1-methyl-3-(2-methacryloyloxy propylimidazolium bromine)] (PEG--PMMPImB) via polyion complex of PMMA and PMMPImB. After removing the Au NPs template, asymmetric PICsomes composed of a PNIPAm inner-shell, PIC wall, and PEG outer-corona were obtained. These PICsomes have low protein absorption and thermally tunable permeability, provided by the PEG outer-corona and the PNIPAm inner-shell, respectively. Moreover, PICsome size can be tailored by using templates of predetermined sizes. This novel strategy for constructing asymmetric PICsomes with well-defined properties and controllable size is valuable for applications such as drug delivery, catalysis and monitoring of chemical reactions, and biomimetics.
本文描述了一种构建具有不对称结构的聚离子复合囊泡(PICsomes)的策略。制备了聚(甲基丙烯酸)-聚(N-异丙基丙烯酰胺)修饰的金纳米颗粒(PMAA-PNIPAm-@-Au NPs),然后通过聚甲基丙烯酸甲酯(PMMA)和聚[1-甲基-3-(2-甲基丙烯酰氧基丙基咪唑溴)](PMMPImB)的聚离子复合作用与聚(乙二醇)-聚[1-甲基-3-(2-甲基丙烯酰氧基丙基咪唑溴)](PEG-PMMPImB)组装。去除金纳米颗粒模板后,得到了由PNIPAm内壳、PIC壁和PEG外壳组成的不对称PICsomes。这些PICsomes分别具有低蛋白吸附性和由PEG外壳和PNIPAm内壳提供的热可调渗透性。此外,可以使用预定尺寸的模板来定制PICsomes的尺寸。这种构建具有明确性质和可控尺寸的不对称PICsomes的新策略对于药物递送、催化和化学反应监测以及仿生学等应用具有重要价值。