Author/Authors :
Zhang، نويسنده , , Yuanyang and He، نويسنده , , Fangyang and Wan، نويسنده , , Yuping and Meng، نويسنده , , Meng and Xu، نويسنده , , Jing and Yi، نويسنده , , Jian and Wang، نويسنده , , Yabin and Feng، نويسنده , , Caiwei and Wang، نويسنده , , Shanliang and Xi، نويسنده , , Rimo Xi، نويسنده ,
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%.
Keywords :
Trenbolone , Drug Residue , ELISA , monoclonal antibody