Amphiphilic Unimolecular Nanoparticles Based on a Hyperbranched Polyacrylate Core and a PNIPAm Shell: Synthesis via ATRP and Properties

被引:14
|
作者
Cai, Yong [1 ,2 ]
Liu, Yu-Yang [1 ,2 ]
机构
[1] Northwestern Polytech Univ, Key Lab Space Appl Phys & Chem, Minist Educ, Dept Appl Chem, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ, Key Lab Macromol Sci & Technol Shaanxi Prov, Dept Appl Chem, Xian 710072, Peoples R China
关键词
amphiphilic nanoparticles; encapsulation and release; hyperbranched polyacrylates; temperature sensitivity; CONDENSING VINYL POLYMERIZATION; TRANSFER RADICAL POLYMERIZATION; N-ISOPROPYLACRYLAMIDE; CLICK CHEMISTRY; STAR POLYMERS; RELEASE; FLUORESCENCE; TEMPERATURE; SOLUBILITY; COPOLYMERS;
D O I
10.1002/macp.201200598
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel amphiphilic unimolecular nanoparticle, multi-HPBPEA-g-PNIPAm, for encapsulation and release of hydrophobic guest molecules, is developed. The polymer shows coreshell architecture and is synthesized from inimer 2-((2-bromopropionyl)oxy)ethyl acrylate (BPEA) by atom transfer radical polymerization (ATRP) in three steps. The hydrophobic core (multi-HPBPEA) is composed of hyperbranched poly(2-((2-bromopropionyl)oxy)ethyl acrylate) (HPBPEA), which is synthesized by self-condensing vinyl polymerization (SCVP) of BPEA. Multi-HPBPEA-g-PNIPAm is obtained by multi-HPBPEA core initiating ATRP of N-isopropylacrylamide (NIPAm). The encapsulation behavior of the core of multi-HPBPEA-g-PNIPAm in an aqueous solution is investigated by fluorescent spectra. It is found that multi-HPBPEA-g-PNIPAm can efficiently encapsulate and release a hydrophobic drug like nifedipine.
引用
收藏
页码:882 / 891
页数:10
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