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金以及磁性氧化物/金核壳纳米颗粒作为生物功能纳米探针。

Gold and magnetic oxide/gold core/shell nanoparticles as bio-functional nanoprobes.

作者信息

Lim I-Im S, Njoki Peter N, Park Hye-Young, Wang Xin, Wang Lingyan, Mott Derrick, Zhong Chuan-Jian

机构信息

Department of Chemistry, State University of New York at Binghamton, Binghamton, NY 13902, USA.

出版信息

Nanotechnology. 2008 Jul 30;19(30):305102. doi: 10.1088/0957-4484/19/30/305102. Epub 2008 Jun 16.

Abstract

The ability to create bio-functional nanoprobes for the detection of biological reactivity is important for developing bioassay and diagnostic methods. This paper describes the findings of an investigation of the surface functionalization of gold (Au) and magnetic nanoparticles coated with gold shells (M/Au) by proteins and spectroscopic labels for the creation of nanoprobes for use in surface enhanced Raman scattering (SERS) assays. Highly monodispersed Au nanoparticles and M/Au nanoparticles with two types of magnetic nanoparticle cores (Fe(2)O(3) and MnZn ferrite) were studied as model systems for the bio-functionalization and Raman labeling. Comparison of the SERS intensities obtained with different particle sizes (30-100 nm) and samples in solution versus on solid substrates have revealed important information about the manipulation of the SERS signals. In contrast to the salt-induced uncontrollable and irreversible aggregation of nanoparticles, the ability to use a centrifugation method to control the formation of stable small clustering sizes of nanoparticles was shown to enhance SERS intensities for samples in solution as compared with samples on solid substrates. A simple method for labeling protein-capped Au nanoparticles with Raman-active molecules was also described. The functionalized Au and M/Au nanoparticles are shown to exhibit the desired functional properties for the detection of SERS signals in the magnetically separated reaction products. These results are discussed in terms of the interparticle distance dependence of 'hot-spot' SERS sites and the delineation of the parameters for controlling the core-shell reactivity of the magnetic functional nanocomposite materials in bio-separation and spectroscopic probing.

摘要

创建用于检测生物反应性的生物功能纳米探针的能力对于开发生物测定和诊断方法至关重要。本文描述了一项关于用蛋白质和光谱标记对金(Au)和包覆金壳的磁性纳米颗粒(M/Au)进行表面功能化的研究结果,以创建用于表面增强拉曼散射(SERS)测定的纳米探针。研究了具有两种类型磁性纳米颗粒核(Fe(2)O(3)和MnZn铁氧体)的高度单分散金纳米颗粒和M/Au纳米颗粒,作为生物功能化和拉曼标记的模型系统。比较不同粒径(30 - 100 nm)的颗粒以及溶液和固体基质上的样品所获得的SERS强度,揭示了有关SERS信号操纵的重要信息。与盐诱导的纳米颗粒不可控且不可逆的聚集相反,使用离心方法控制纳米颗粒形成稳定的小聚集体尺寸的能力显示出,与固体基质上的样品相比,溶液中的样品SERS强度有所增强。还描述了一种用拉曼活性分子标记蛋白质包覆的金纳米颗粒的简单方法。功能化的金和M/Au纳米颗粒显示出在磁分离反应产物中检测SERS信号所需的功能特性。根据“热点”SERS位点的颗粒间距离依赖性以及在生物分离和光谱探测中控制磁性功能纳米复合材料核壳反应性的参数的描述,对这些结果进行了讨论。

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