马来酰亚胺
结合
化学
表面改性
恶唑啉
高分子化学
药物输送
组合化学
聚合物
生物结合
水溶液
硫醇
化学改性
聚合物囊泡
自愈水凝胶
壳聚糖
高分子
有机化学
共聚物
两亲性
生物化学
催化作用
数学分析
数学
物理化学
作者
Jonas F. Nawroth,Jonathan R. McDaniel,Ashutosh Chilkoti,Rainer Jordan,Robert Luxenhofer
标识
DOI:10.1002/mabi.201500376
摘要
The design of drug delivery systems capable of efficiently delivering poorly soluble drugs to target sites still remains a major challenge. Such materials require several different functionalities; typically, these materials should be biodegradable and nontoxic, nonimmunogenic, responsive to their environment, and soluble in aqueous solution while retaining the ability to solubilize hydrophobic drugs. Here, a polypeptide‐polymer hybrid of elastin‐like polypeptides (ELPs) and poly(2‐oxazoline)s (POx) is reported. This paper describes the chemical synthesis, physical characteristics, and drug loading potential of these novel hybrid macromolecules. A novel method is introduced for terminal functionalization of POx with protected maleimide moieties. Following recovery of the maleimide group via a retro Diels–Alder reaction, the consecutive Michael addition of thiol‐functionalized ELPs yields the desired protein‐polymer conjugate. These conjugates form nanoparticles in aqueous solution capable of solubilizing the anti‐cancer drug paclitaxel with up to 8 wt% loading. image
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