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基于主客体作用的新型磁性纳米粒子分子识别表面方法

A Novel Approach to Molecular Recognition Surface of Magnetic Nanoparticles Based on Host-Guest Effect.

出版信息

Nanoscale Res Lett. 2009 Apr 23;4(7):738-47. doi: 10.1007/s11671-009-9314-x.

Abstract

A novel route has been developed to prepared beta-cyclodextrin (beta-CD) functionalized magnetic nanoparticles (MNPs). The MNPs were first modified with monotosyl-poly(ethylene glycol) (PEG) silane and then tosyl units were displaced by amino-beta-CD through the nucleophilic substitution reaction. The monotosyl-PEG silane was synthesized by modifying a PEG diol to form the corresponding monotosyl-PEG, followed by a reaction with 3-isocyanatopropyltriethoxysilane (IPTS). The success of the synthesis of the monotosyl-PEG silane was confirmed with (1)H NMR and Fourier transform infrared (FTIR) spectroscopy. The analysis of FTIR spectroscopy and X-ray photoelectron spectroscopy (XPS) confirmed the immobilization of beta-CD onto MNPs. Transmission electron microscopy (TEM) indicated that the beta-CD functionalized MNPs were mostly present as individual nonclustered units in water. The number of beta-CD molecules immobilized on each MNP was about 240 according to the thermogravimetric analysis (TGA) results. The as-prepared beta-CD functionalized MNPs were used to detect dopamine with the assistance of a magnet.

摘要

一种新的路线已经被开发出来,用于制备β-环糊精(β-CD)功能化的磁性纳米颗粒(MNPs)。首先,MNPs 用单对甲苯磺酰基聚(乙二醇)(PEG)硅烷进行修饰,然后通过亲核取代反应将对甲苯磺酰基被氨基-β-CD 取代。单对甲苯磺酰基 PEG 硅烷是通过修饰 PEG 二醇形成相应的单对甲苯磺酰基 PEG,然后与 3-异氰酸丙基三乙氧基硅烷(IPTS)反应合成的。(1)H NMR 和傅里叶变换红外(FTIR)光谱证实了单对甲苯磺酰基 PEG 硅烷的合成成功。FTIR 光谱和 X 射线光电子能谱(XPS)的分析证实了β-CD 被固定在 MNPs 上。透射电子显微镜(TEM)表明,β-CD 功能化的 MNPs 在水中主要以单个非聚集单元存在。根据热重分析(TGA)结果,每个 MNPs 上固定的β-CD 分子数约为 240。所制备的β-CD 功能化的 MNPs 在磁铁的辅助下用于检测多巴胺。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b78f/3243436/452c910de8a6/1556-276X-4-738-i1.jpg

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