甲基丙烯酸酯
乙二醇
聚合物
纳米颗粒
转铁蛋白
共聚物
共轭体系
高分子化学
体外
PEG比率
化学
组合化学
材料科学
生物物理学
化学工程
纳米技术
有机化学
生物化学
财务
经济
工程类
生物
作者
Adelene S. M. Wong,Ewa Czuba,Moore Z. Chen,Daniel Yuen,Kristofer I. Cupic,Shenglin Yang,Rebecca Y. Hodgetts,Laura I. Selby,Angus P. R. Johnston,Georgina K. Such
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2017-03-09
卷期号:6 (3): 315-320
被引量:13
标识
DOI:10.1021/acsmacrolett.7b00044
摘要
Targeting nanoparticles to specific cellular receptors has the potential to deliver therapeutic compounds to target sites while minimizing side effects. To this end, we have conjugated a targeting protein, holo-transferrin (holo-Tf), to pH-responsive polymers, poly(2-(diethylamino)ethyl methacrylate) (PDEAEMA) and poly(2-(diethylamino)ethyl methacrylate)-ran-poly(2-(diisopropylamino)ethyl methacrylate (PDEAEMA-r-PDPAEMA). These protein-polymer hybrid materials were observed to self-assemble when the pH is increased above the pKa of the polymer. We demonstrate that their response to pH could be tuned depending on the polymer constituent attached to holo-Tf. Importantly, the targeting behavior of these nanoparticles could be maximized by tuning the density of holo-Tf on the nanoparticle surface by the introduction of a (PDEAEMA-r-PDPAEMA)-b-poly(ethylene glycol) (PEG) copolymer.
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