Generation of anti-trenbolone monoclonal antibody and establishment of an indirect competitive enzyme-linked immunosorbent assay for detection of trenbolone in animal tissues, feed and urine |
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Authors: | Zhang Yuanyang He Fangyang Wan Yuping Meng Meng Xu Jing Yi Jian Wang Yabin Feng Caiwei Wang Shanliang Xi Rimo |
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Affiliation: | a The School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong 250100, PR China b College of Pharmacy, Nankai University, 94 Weijin Road, Tianjin 300071, PR China c Beijing Wanger Biotechnology Co., Ltd., Beijing 102206, PR China |
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Abstract: | Trenbolone (TRE) is a steroid used by veterinarians on livestock to increase appetite and body weight. The use of TRE has been restricted because of its harmful side effect for consumers. To effectively control TRE residue in food and food product, a rapid and convenient immunoassay was developed by preparing an anti-TRE monoclonal antibody. The immunogen and coating antigen were prepared by coupling TRE hapten with carrier proteins via 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (EDC) method. The optimized method gave an average IC50 value of 0.323 ng mL−1 towards TRE and an average detection limit (LOD) of 0.06 ng mL−1, which is much lower than the maximum residue levels (2.0 ng g−1) accepted by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). The specificity of the antibody was evaluated by measuring cross-reactivity of six structurally related compounds, including 19-nortestosterone (9.7%), testosterone (0.13%), methyltestosterone (<0.01%), methandrostenolone (<0.01%), (+)-dehydroisoandrosterone (<0.001%) and β-estradiol (<0.001%). The recovery rates of the test in detection of TRE-fortified animal tissue, urine and animal feed samples were in the range of 81.3-89.4%, while the intra- and inter-assay coefficients of variation were less than 12.0%. |
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Keywords: | BSA, bovine serum albumin cFA, complete Freund's adjuvant DMF, N,N-dimethyl formamide EDC, 1-ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride ELISA, enzyme linked immunosorbent assay IC50, concentration at 50% inhibition iFA, incomplete Freund's adjuvant HRP, horseradish peroxidase KLH, keyhole limpet hemocyanin LOD, limit of detection MRL, maximum residue level NHS, N-hydroxysuccinimide PBS, phosphate buffered saline PBST, phosphate-buffered saline containing 0.05% Tween 20 TMB, 3,3&prime ,5,5&prime -tetramethylbenzidine TRE, trenbolone |
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