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新型温度敏感聚合物包覆磁性纳米粒子的制备与表征

Formulation and characterization of novel temperature sensitive polymer-coated magnetic nanoparticles.

作者信息

Rahimi Maham, Meletis Efstathios I, You Shaoxin, Nguyen Kytai

机构信息

Biomedical Engineering Programs, University of Texas Southwestern Medical Center at Dallas and University of Texas at Arlington, Arlington, TX 76019, USA.

出版信息

J Nanosci Nanotechnol. 2010 Sep;10(9):6072-81. doi: 10.1166/jnn.2010.2596.

DOI:10.1166/jnn.2010.2596
PMID:21133151
Abstract

The objective of this research was to develop novel polymer coated magnetic nanoparticles for controlled drug delivery applications. To form these novel nanoparticles, silane-coated magnetic nanoparticles (MNPs) were used as a template for a free radial polymerization of three monomers, N-isopropylacrylamide, acrylamide, and allylamine (NIPA-AAm-AH), on the surface of MNPs. Transmission electron microscope results indicated that the size of the NIPA-AAm-AH coated MNPs was approximately 100 nm. To investigate the chemical composition and chemical state of our nanoparticles, FTIR and XPS were used. Results from chemical analysis illustrated the presence of the constituent functional groups of the NIPA-AAm-AH coated MNPs. In addition, the magnetic properties of different layers on the MNPs, analyzed by SQUID, indicated a decrease in saturation magnetization after each layer of coating. The nanoparticles were successfully conjugated to fluorescent PEG to prolong their circulating half life. Furthermore, bovine serum albumin (BSA) was used in order to investigate the protein release profile of the nanoparticles as a function of the temperature. The protein release profile indicated that the NIPA-AAm-AH coated MNPs have a significantly higher percent release at 41 degrees C compared to those of 4 degrees C and 37 degrees C, which demonstrates their temperature sensitivity. In the future, the release profile of therapeutic drugs from nanoparticles at various temperatures and pHs as well as targeted capability of the synthesized nanoparticles for possible applications in controlled and targeted delivery will be investigated.

摘要

本研究的目的是开发用于可控药物递送应用的新型聚合物包覆磁性纳米颗粒。为了制备这些新型纳米颗粒,以硅烷包覆的磁性纳米颗粒(MNPs)为模板,在MNPs表面进行三种单体N-异丙基丙烯酰胺、丙烯酰胺和烯丙胺(NIPA-AAm-AH)的自由基聚合反应。透射电子显微镜结果表明,NIPA-AAm-AH包覆的MNPs尺寸约为100 nm。为了研究纳米颗粒的化学成分和化学状态,使用了傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)。化学分析结果表明存在NIPA-AAm-AH包覆的MNPs的组成官能团。此外,通过超导量子干涉仪(SQUID)分析MNPs不同层的磁性,结果表明每包覆一层后饱和磁化强度降低。纳米颗粒成功地与荧光聚乙二醇(PEG)偶联,以延长其循环半衰期。此外,使用牛血清白蛋白(BSA)来研究纳米颗粒的蛋白质释放曲线与温度的关系。蛋白质释放曲线表明,与4℃和37℃相比,NIPA-AAm-AH包覆的MNPs在41℃时的释放百分比显著更高,这证明了它们的温度敏感性。未来,将研究纳米颗粒在不同温度和pH值下治疗药物的释放曲线,以及合成纳米颗粒在可控和靶向递送中可能应用的靶向能力。

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