Enzyme-linked immuno-strip biosensor to detect Escherichia coli O157:H7

被引:48
作者
Park, Sojung [1 ]
Kim, Hajin [1 ]
Paek, Se-Hwan [2 ]
Hong, Jong Wook [3 ]
Kim, Young-Kee [1 ]
机构
[1] Hankyong Natl Univ, Dept Chem Engn, Kyonggi Do 456749, South Korea
[2] Korea Univ, Dept Biotechnol, Jochiwon 339700, Choongnam, South Korea
[3] Auburn Univ, Mat Res & Educ Ctr, Dept Engn Mech, Auburn, AL 36849 USA
关键词
biosensor; ELISA; Escherichia coli O157 : H7; scanning electron microscope;
D O I
10.1016/j.ultramic.2008.04.063
中图分类号
TH742 [显微镜];
学科分类号
摘要
A strip-based biosensor using the enzyme-linked immunosorbent assay technique was fabricated to detect Escherichia coli O157:H7. Two types of antibody specified to E. coli O15T:H7 were used to form sandwich-binding complexes. To fabricate an immuno-strip, capture antibody (monoclonal antibody) was immobilized onto signal generation pad and polyclonal antibody conjugated with horseradish peroxidase (HRP) was utilized as detection antibody. Four different functional membranes have been used to fabricate immuno-chromatographic assay strip. A sample application pad was a glass fiber membrane pre-treated with polyvinyl alcohol. A conjugate release pad was fabricated using a glass membrane. A signal generation pad was made on nitrocellulose membrane. Finally, a cellulose membrane was used as an absorption pad. Under optimal conditions of analysis, a color signal in proportion to the E. coli O157:H7 concentration was measured using a detector. The measurement range was 1.8 x 10(3)-1.8 x 10(8) CFU/mL. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1348 / 1351
页数:4
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