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基于磁性纳米颗粒的免疫学法对大肠杆菌O157:H7的化学发光检测

Chemiluminescent detect of E. coli O157:H7 using immunological method based on magnetic nanoparticles.

作者信息

Li Zhiyang, He Lei, He Nongyue, Shi Zhiyang, Wang Hua, Li Song, Liu Hongna, Li Xiaolong, Dai Yabin, Wang Zhifei

机构信息

State Key Laboratory of Bioelectronics, Southeast University, Nanjing 210096, China.

出版信息

J Nanosci Nanotechnol. 2010 Feb;10(2):696-701. doi: 10.1166/jnn.2010.1811.

Abstract

The system of chemiluminescent magnetic enzyme-linked immunoassay was developed. E. coli O157:H7 was sandwiched between rabbits anti-E. coli O157:H7 polyclonal antibody-coated magnetic nanoparticles (immunomagnetic nanoparticles or IMNPs) and mouse anti-E. coli O157:H7 monoclonal antibody. Commercial alkaline phosphatase conjugated horse anti-mouse immunoglobulin (ALP-Ab) was used to bind with the monoclonal antibody, finally the chemiluminescent signals were detected by adding 3-(2'-spiroadamantane)-4-methoxy-4-(3"-phosphoryloxy)phenyl-1,2-dioxetane (AMPPD) which was the substrate reagent of ALP. Different solvents of AMPPD were compared to get an optimal chemiluminescent signal. The effects of sodium borohydride and glycine on blocking the aldehyde groups of IMNPs were compared either, and the specificity and sensitivity of this system for detecting E. coli O157:H7 were researched. The results indicated that Tris buffer was the best solvent of AMPPD, sodium borohydride was better than glycine in blocking IMNPs, and this method was of good specificity when using E. coli Top 10F' and Vibrio cholera as negative controls. The detection limit was 10(3) cells mL(-1) when the antigen solution was 1 mL, and the procedure duration was about 3 h.

摘要

开发了化学发光磁酶联免疫分析系统。大肠杆菌O157:H7夹在兔抗大肠杆菌O157:H7多克隆抗体包被的磁性纳米颗粒(免疫磁性纳米颗粒或IMNPs)和鼠抗大肠杆菌O157:H7单克隆抗体之间。使用商业碱性磷酸酶偶联的马抗小鼠免疫球蛋白(ALP-Ab)与单克隆抗体结合,最后通过加入3-(2'-螺金刚烷)-4-甲氧基-4-(3''-磷酰氧基)苯基-1,2-二氧杂环丁烷(AMPPD)来检测化学发光信号,AMPPD是ALP的底物试剂。比较了AMPPD的不同溶剂以获得最佳化学发光信号。还比较了硼氢化钠和甘氨酸对封闭IMNPs醛基的效果,并研究了该系统检测大肠杆菌O157:H7的特异性和灵敏度。结果表明,Tris缓冲液是AMPPD的最佳溶剂,硼氢化钠在封闭IMNPs方面优于甘氨酸,以大肠杆菌Top 10F'和霍乱弧菌作为阴性对照时该方法具有良好的特异性。当抗原溶液为1 mL时,检测限为10(3)个细胞mL(-1),整个过程持续约3小时。

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