协同链行走聚合和原子转移激素聚合,以高效合成树突纳米粒子,用于生物结合
Guanghui Chen1, Devan Huynh, Philip L Felgner
1Department of Chemistry, 516 Rowland Hall, University of California, Irvine, 92697-2025, USA.
Journal of the American Chemical Society
|March 30, 2006
概括
研究人员开发了一种新方法来制造用于生物结合的聚合物纳米粒子. 这种高效的合成允许控制纳米颗粒大小和高药物或蛋白质负载,显示出各种应用的潜力.
科学领域:
- 聚合物化学 聚合物化学
- 纳米技术 纳米技术
- 生物结合的生物结合
背景情况:
- 开发高效的合成精确定义纳米颗粒的方法对于生物结合应用至关重要.
- 聚合物纳米粒子为药物输送和诊断提供可调节的特性.
研究的目的:
- 为高效合成聚合物纳米颗粒开发一个双重聚合方法.
- 创建适合生物结合的纳米粒子,具有受控的分子量和大小.
主要方法:
- 采用了结合链路行走聚合 (CWP) 和原子转移基聚合 (ATRP) 的双重聚合策略.
- 利用-α-二胺催化剂为CWP合成具有多个启动位点的树突聚合物.
- 使用合成的聚合物作为宏观启动器进行Cu (I) 中介的ATRP.
- 纳入的N-acryloyloxysuccinamide (NAS) 单体用于NHS激活.
主要成果:
- 成功合成了具有受控分子量和尺寸的水溶性核心外聚合物纳米粒子.
- 通过添加NAS单体,获得了NHS激活的聚合物纳米粒子.
- 与小染料分子和卵蛋白蛋白成功结合.
- 获得的纳米粒子与高染料或蛋白质每颗粒比率结合.
结论:
- 开发的双重聚合法为合成功能性聚合物纳米粒子提供了一条有效的途径.
- 这些纳米粒子表现出良好的生物相容性和生物分子的高负载能力.
- 合成的纳米颗粒对各种生物结合应用具有重大潜力.
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