A Sensitive and reliable quantification method for Bisphenol A based on modified competitive ELISA method

被引:91
作者
Kim, Andre
Li, Chun-Ri
Jin, Chun-Feng
Lee, Keun Woo
Lee, Sang-Hoon
Shon, Kwang-Jae
Park, Nam Gyu
Kim, Dong-Kyoo
Kang, Shin-Won
Shim, Yoon-Bo
Park, Jang-Su [1 ]
机构
[1] Pusan Natl Univ, Dept Chem, Pusan 609735, South Korea
[2] Pusan Natl Univ, Ctr Innovat Biophys Sensor Technol, Pusan 609735, South Korea
[3] Pukyong Natl Univ, Dept Bioengn & Biotechnol, Pusan 608737, South Korea
[4] Inje Univ, Dept Chem, Kimhae 621749, South Korea
[5] Inje Univ, Biohtlh Prod Res Ctr, Kimhae 621749, South Korea
[6] Korea Basic Sci Inst, Taejon 305333, South Korea
基金
新加坡国家研究基金会;
关键词
bisphenol A; BHPVA; BHPVA-BSA; BHPVA-HRP; competitive ELISA;
D O I
10.1016/j.chemosphere.2007.01.079
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Bisphenol A (BPA), generally known as bisphenols, has been identified as a potential estrogenic substance. BPA must be conjugated to carrier protein and BSA was commonly used. 4,4-Bis(4-hydroxyphenyl) valeric acid (BHPVA) has a bisphenolic structure and a long carbon chain with a reactive carboxyl group on the end. In this study, BHPVA-BSA was used to produce polyclonal antibody against bisphenolic structure, and a modified competitive ELISA method for quantification of BPA was developed. This system was based on BHPVA-BSA for polyclonal antibody production against bisphenolic structure, and BHPVA-HRP for determination of BPA substituting detection antibody in competitive reaction. Recovery was assessed at 10 different concentrations (2-1000 ng/ml) of BHPVA, and the recovery range was from 96.3% to 107.2%. The variation was from 6.2% to 9.8% for intra assay and from 10.1% to 12.6% for inter assay. The quadratic was used to establish the curve regression. The range was found to be between 2 and 1000 ng/ml. This modified competitive ELISA method has proven to be a very useful tool for quantification of BPA without the unexpected interaction of BSA and anti-BSA polyclonal antibody. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1204 / 1209
页数:6
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