材料科学
胶束
原子转移自由基聚合
纳米载体
磷酰胆碱
聚合物
聚乙二醇
甲基丙烯酸酯
木筏
PEG比率
聚合
表面改性
纳米技术
化学工程
纳米颗粒
有机化学
化学
复合材料
水溶液
生物化学
财务
工程类
经济
作者
Ning Chen,Sidi Li,Xueping Li,Lixia Long,Xubo Yuan,Xin Hou,Jin Zhao
标识
DOI:10.1007/s11706-021-0554-8
摘要
The synergistic effect of polyethylene glycol (PEG) and poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) can effectively reduce the protein absorption, which is beneficial to theranostics. However, PEG–PMPC-based polymers have rarely been used as nanocarriers in the theranostic field due to their limited modifiability and weak interaction with other materials. Herein, a plain method was proposed to endow them with the probable ability of loading small active agents, and the relationship between the structure and the ability of loading hydrophobic agents was explored, thus expanding their applications. Firstly, mPEG–PMPC or 4-arm-PEG–PMPC polymer was synthesized by atom transfer radical polymerization (ATRP) using mPEG-Br or 4-arm-PEG-Br as the macroinitiator. Then a strong hydrophobic segment, poly(butyl methacrylate) (PBMA), was introduced and the ability to load small hydrophobic agents was further explored. The results showed that linear mPEG–PMPC–PBMA could form micelles 50–80 nm in size and load the hydrophobic agent such as Nile red efficiently. In contrast, star-like 4-arm-PEG–PMPC–PBMA, a monomolecular micelle (10–20 nm), could hardly load any hydrophobic agent. This work highlights effective strategies for engineering PEG–PMPC-based polymers and may facilitate the further application in numerous fields.
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