Abstract:This paper is a review with more than 100 references discussing the immunochemical methods reported in the literature for the most important man-made chemicals with suspected endocrine disrupting activity. Details regarding immunizing hapten design, antibody production, and the features (limit of detection, dynamic range, specificity) of the most important immunochemical methods developed (ELISA, FIIA, immunosorbents, immunosensors, etc.) are presented for important environmental pollutants such as bisphenol A… Show more
“…Therefore, the specificity of the antibody and of the ELISA was determined by the crossreactivity studies with 11 structural analogues of BPA including the degradation products: PP, 4-CP, diOH-BP, hexestrol, DES, BPF, BPS, 4,4′-thiodiphenol, BPA-butyrate, BPA-valerate, and 4-hydroxybenzoic acid ( Table 2). The cross-reactivity of the assays for all of the tested analogues was much lower than the published work [20][21][22]24], in particular, the cross-reactivity of 4-CP. The direct format displayed higher cross-reactivity than the indirect format.…”
Section: Assay Specificitycontrasting
confidence: 61%
“…The most sensitive assay was based on Ab∝BPA-V2#4 and BPA-acetate-BSA in an indirect format with an IC 50 of 0.78± 0.01 μg L −1 , and a LOD of 0.10±0.03 μg L −1 for BPA. The sensitivity was higher than most of the previous studies [20][21][22][23][24]. Additionally, all three selected assays were optimized to quantify BPA residues in three food and beverage sample types.…”
Section: Discussionmentioning
confidence: 99%
“…The degree of crossreactivity for each cross-reacting compound can be influenced by the assay format, assay conditions and competing hapten used, and relative concentrations of an antibody and a conjugate in an assay [20,25,31], and this was also evident from this study, e.g., 4-CP. Thus cross-reactivity of an immunoassay could be manipulated to some degree by assay format and assay conditions.…”
Section: Specificity Of the Direct Elisamentioning
confidence: 91%
“…The most frequently used methods for monitoring BPA are gas chromatography-mass spectrometry, liquid chromatography with tandem mass spectrometry, and high-performance liquid chromatography [15][16][17][18][19]. These techniques are highly sensitive and specific; however, most of them are cumbersome, expensive, and require extensive sample preparation and clean-up procedures prior to analysis [20]. Contrarily, enzyme-linked immunosorbent assays (ELISAs) offer many advantages that can complement instrumental analysis.…”
Enzyme-linked immunosorbent assays (ELISAs) are investigated in this work for the detection of bisphenol-A (BPA), a plastic monomer and a critical contaminant in food and environment. A series of polyclonal antibodies generated in vivo using BPA-butyrate-protein conjugate and BPA-valerate-protein conjugate were evaluated on direct and indirect competitive assay formats with five competing haptens (BPA-butyrate, BPA-valerate, BPA-crotonate, BPA-acetate, and BPA-2-valerate). Two indirect ELISAs and one direct ELISA exhibiting high sensitivity and specificity for BPA were developed. The 50 % inhibition of antibody binding (IC(50)) values were 0.78 ± 0.01-1.20 ± 0.26 μg L(-1), and the limits of detection as measured by the IC(20) values were 0.10 ± 0.03-0.20 ± 0.04 μg L(-1). The assays were highly specific to BPA, only displaying low cross-reactivity (3-8 % for the indirect assays and 26 % for the direct assay) for 4-cumylphenol (4-CP), at pH 7.2. The degree of cross-reaction of 4-CP was influenced by the antibody/hapten conjugate combination, assay conditions, and the assay format. The assays were optimized for the analysis of BPA in canned vegetables, bottled water and carbonated drinks. The limits of quantification for these three evaluated sample types, based on the spike and recovery data, were 0.5, 2.5, and 100 μg L(-1), respectively.
“…Therefore, the specificity of the antibody and of the ELISA was determined by the crossreactivity studies with 11 structural analogues of BPA including the degradation products: PP, 4-CP, diOH-BP, hexestrol, DES, BPF, BPS, 4,4′-thiodiphenol, BPA-butyrate, BPA-valerate, and 4-hydroxybenzoic acid ( Table 2). The cross-reactivity of the assays for all of the tested analogues was much lower than the published work [20][21][22]24], in particular, the cross-reactivity of 4-CP. The direct format displayed higher cross-reactivity than the indirect format.…”
Section: Assay Specificitycontrasting
confidence: 61%
“…The most sensitive assay was based on Ab∝BPA-V2#4 and BPA-acetate-BSA in an indirect format with an IC 50 of 0.78± 0.01 μg L −1 , and a LOD of 0.10±0.03 μg L −1 for BPA. The sensitivity was higher than most of the previous studies [20][21][22][23][24]. Additionally, all three selected assays were optimized to quantify BPA residues in three food and beverage sample types.…”
Section: Discussionmentioning
confidence: 99%
“…The degree of crossreactivity for each cross-reacting compound can be influenced by the assay format, assay conditions and competing hapten used, and relative concentrations of an antibody and a conjugate in an assay [20,25,31], and this was also evident from this study, e.g., 4-CP. Thus cross-reactivity of an immunoassay could be manipulated to some degree by assay format and assay conditions.…”
Section: Specificity Of the Direct Elisamentioning
confidence: 91%
“…The most frequently used methods for monitoring BPA are gas chromatography-mass spectrometry, liquid chromatography with tandem mass spectrometry, and high-performance liquid chromatography [15][16][17][18][19]. These techniques are highly sensitive and specific; however, most of them are cumbersome, expensive, and require extensive sample preparation and clean-up procedures prior to analysis [20]. Contrarily, enzyme-linked immunosorbent assays (ELISAs) offer many advantages that can complement instrumental analysis.…”
Enzyme-linked immunosorbent assays (ELISAs) are investigated in this work for the detection of bisphenol-A (BPA), a plastic monomer and a critical contaminant in food and environment. A series of polyclonal antibodies generated in vivo using BPA-butyrate-protein conjugate and BPA-valerate-protein conjugate were evaluated on direct and indirect competitive assay formats with five competing haptens (BPA-butyrate, BPA-valerate, BPA-crotonate, BPA-acetate, and BPA-2-valerate). Two indirect ELISAs and one direct ELISA exhibiting high sensitivity and specificity for BPA were developed. The 50 % inhibition of antibody binding (IC(50)) values were 0.78 ± 0.01-1.20 ± 0.26 μg L(-1), and the limits of detection as measured by the IC(20) values were 0.10 ± 0.03-0.20 ± 0.04 μg L(-1). The assays were highly specific to BPA, only displaying low cross-reactivity (3-8 % for the indirect assays and 26 % for the direct assay) for 4-cumylphenol (4-CP), at pH 7.2. The degree of cross-reaction of 4-CP was influenced by the antibody/hapten conjugate combination, assay conditions, and the assay format. The assays were optimized for the analysis of BPA in canned vegetables, bottled water and carbonated drinks. The limits of quantification for these three evaluated sample types, based on the spike and recovery data, were 0.5, 2.5, and 100 μg L(-1), respectively.
“…The traditional methods for analyzing 4-tert-OP in food samples are high-performance liquid chromatography (Zhou et al 2011) and gas chromatography or liquid chromatography coupled to mass spectrometry (GC-MS, LC-MS) (Estévez-Alberola and Marco 2004;Chen et al 2012;Rocha et al 2013). Despite the high sensitivity and accuracy of these methods, which are well-suited for such trace and multiresidue analyses, they are limited by high operating costs, the requirement of highly trained operators, and being relatively time consuming in terms of sample preparation.…”
The rational hapten design and development of an indirect enzyme-linked immunosorbent assay (ELISA) for the detection of 4-tert-octylphenol (4-tert-OP), an endocrinedisrupting compound belonging to alkylphenols (APs), is described. The polyclonal antibody highly specific to 4-tert-OP was raised against a hapten with a linker attached to the ortho-position of the phenol ring. Using 5-(2-hydroxy-5-nonylphenyl)-5-oxo-pentanoic acid (NP1) as a competing hapten, an indirect competitive assay exhibiting an IC 50 value of 100 μg L −1 and the limit of detection (LOD) of 10 μg L −1 was developed. The assay was highly specific to 4-tert-OP and only displayed a moderate cross-reactivity (29 %) with IGEPAL® CA-520. The immunodominance was suggested to be both the 4-tert-octyl chain and the phenol group. The assay was optimized for the analysis of 4-tert-OP in prawn and clam samples with the LOD of 20 μg L −1 and the % recovery of 80-120 %.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.