Chemiluminescent Detect of E. coli O157:H7 Using Immunological Method Based on Magnetic Nanoparticles

被引:68
作者
Li, Zhiyang [1 ,2 ]
He, Lei [3 ]
He, Nongyue [1 ]
Shi, Zhiyang [4 ]
Wang, Hua [4 ]
Li, Song [1 ]
Liu, Hongna [1 ]
Li, Xiaolong [1 ]
Dai, Yabin [5 ]
Wang, Zhifei [6 ]
机构
[1] Southeast Univ, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[2] Yangtze Univ, Coll Life Sci, Jinzhou 434025, Peoples R China
[3] Southeast Univ, Sch Publ Hlth, Nanjing 210009, Peoples R China
[4] Jiangsu Prov Ctr Dis Control & Prevent, Nanjing 210009, Peoples R China
[5] Chinese Acad Agr Sci, Poultry Inst, Yangzhou 225003, Peoples R China
[6] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211198, Peoples R China
基金
中国博士后科学基金;
关键词
Magnetic Nanoparticles; Immunoassay; Alkaline Phosphatase; Chemiluminescence; Escherichia coli O157:H7; LINKED IMMUNOMAGNETIC CHEMILUMINESCENCE; DRUG-DELIVERY; O157-H7; IMMUNOASSAY; ANTIBODIES; PROTEINS; CELLS; FOOD;
D O I
10.1166/jnn.2010.1811
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The system of chemiluminescent magnetic enzyme-linked immunoassay was developed. E coli O157:H7 was sandwiched between rabbits anti-E coli O15:H7 polyclonal antibody-coated magnetic nanoparticles (immunomagnetic nanoparticles or IMNPs) and mouse anti-E. coli O15: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.
引用
收藏
页码:696 / 701
页数:6
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