共聚物
单体
药物输送
溶解度
聚合物
聚乙烯吡咯烷酮
反应性(心理学)
高分子化学
化学
材料科学
化学工程
组合化学
纳米技术
有机化学
医学
替代医学
病理
工程类
作者
Jonas Engström,Lars Lindgren,Bertil Helgée
标识
DOI:10.1002/macp.200500479
摘要
Abstract Summary: Polyvinylpyrrolidone (PVP) is a synthetic, non‐toxic, water‐soluble polymer commonly used in a wide range of applications including several pharmaceutical applications. One example of an important application is the controlled release and delivery of therapeutic agents into sites of inflammation or tumours. However, PVP lacks reactive groups, which limits the possibility of adding new functions to the polymer in order to modify its physical and chemical properties. Furthermore, large differences in radical reactivity between 1‐vinylpyrrolidin‐2‐one (NVP) and most other monomers lead to compositional drift during copolymerization. This complicates the introduction of reactive groups into the polymer using this method. Monomers that are derivatives of NVP itself are expected to show smaller differences in radical reactivity and therefore provide a way of preparing PVP with adjustable properties. Here we present the synthesis of five NVP‐based monomers and their use in the preparation of functional PVP with adjustable properties in terms of solubility, loading of functional groups, and molar mass. The results show the possibility of tailoring PVP for different biomedical applications e.g. drug delivery systems. Copolymers from 1‐vinylpyrrolidin‐2‐one. magnified image Copolymers from 1‐vinylpyrrolidin‐2‐one.
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