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基于表面增强拉曼散射的大肠杆菌计数高灵敏度检测平台。

A highly sensitive detection platform based on surface-enhanced Raman scattering for Escherichia coli enumeration.

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Gazi University, 06330 Ankara, Turkey.

出版信息

Anal Bioanal Chem. 2010 Jun;397(4):1595-604. doi: 10.1007/s00216-010-3676-x. Epub 2010 Apr 18.

DOI:10.1007/s00216-010-3676-x
PMID:20401720
Abstract

A very sensitive and highly specific heterogeneous immunoassay system, based on surface-enhanced Raman scattering (SERS) and gold nanoparticles, was developed for the detection of bacteria and other pathogens. Two different types of gold nanoparticles (citrate-stabilized gold nanosphere and hexadecyltrimethylammonium bromide (CTAB)-stabilized gold nanorod particles) were examined and this immunoassay was applied for the detection of Escherichia coli. Raman labels were constructed by using these spherical and rod-shaped gold nanoparticles which were first coated with 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) and subsequently with a molecular recognizer. The working curve was obtained by plotting the intensity of the SERS signal of the symmetric NO(2) stretching of DTNB at 1,333 cm(-1) versus the concentration of the E. coli. The analytical performance of gold particles was evaluated via a sandwich immunoassay, and linear calibration graphs were obtained in the E. coli concentration range of 10(1)-10(5) cfu/mL with a 60-s accumulation time. The sensitivity of the Raman label fabricated with gold nanorods was more than three times higher than spherical gold nanoparticles. The selectivity of the developed sensor was examined with Enterobacter aerogenes and Enterobacter dissolvens, which did not produce any significant response. The usefulness of the developed immunoassay to detect E. coli in real water samples was also demonstrated.

摘要

建立了一种基于表面增强拉曼散射(SERS)和金纳米粒子的高灵敏度和高特异性的均相免疫分析体系,用于检测细菌和其他病原体。研究了两种不同类型的金纳米粒子(柠檬酸稳定的金纳米球和十六烷基三甲基溴化铵(CTAB)稳定的金纳米棒颗粒),并将该免疫分析应用于大肠杆菌的检测。通过使用这些球形和棒状金纳米粒子构建了拉曼标记物,这些金纳米粒子首先用 5,5'-二硫代双(2-硝基苯甲酸)(DTNB)进行涂层,然后用分子识别剂进行涂层。通过绘制 DTNB 的对称 NO(2)伸缩的 SERS 信号强度与大肠杆菌浓度的关系来获得工作曲线。通过夹心免疫测定评估了金颗粒的分析性能,并在 60 秒的积累时间内获得了大肠杆菌浓度范围为 10(1)-10(5) cfu/mL 的线性校准曲线。用金纳米棒制成的拉曼标记物的灵敏度比球形金纳米粒子高三倍以上。用产酸克雷伯菌和阴沟肠杆菌对所开发传感器的选择性进行了检测,这两种菌均未产生任何显著响应。还证明了所开发的免疫分析在实际水样中检测大肠杆菌的有用性。

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