Detection of illegal growth promoters in biological samples using receptor binding assays

被引:38
作者
Scippo, ML
Van de Weerdt, C
Willemsen, P
François, JM
Rentier-Delrue, F
Muller, M
Martial, JA
Maghuin-Rogister, G
机构
[1] Univ Liege, Lab Anal Denrees Alimentaires Origine Anim, B-4000 Liege, Belgium
[2] Univ Liege, Lab Biol Mol & Genie Genet, B-4000 Liege, Belgium
关键词
radio-receptor assay; steroid hormone receptor; veterinary drug residue; anabolics;
D O I
10.1016/S0003-2670(02)00770-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the European Union (EU), the use of growth-promoting substances in meat production is banned. The control of growth promoters, especially steroid hormones, is presently based on expensive and time-consuming chromatographic methods of analysis or, sometimes, for screening purposes, on radio- or enzyme-immunoassays, all of which are often too specific to allow effective multi-analyte control. In order to develop rapid and inexpensive multi-analyte detection tests, we proposed the use of hormonal receptors as detection tools. The system described here (radio-receptor assays) is based on a direct bindin g assay of steroid hormones to their respective receptors. Human receptors to estrogens (hERalpha), androgens (hAR), progestagens (hPR) and glucocorticoids (hGR) have been produced by genetic engineering in bacteria or in eucaryotic cells. Binding analyses revealed that the obtained receptor proteins retained a high affinity for their corresponding native ligand. In addition, competition studies continued that each of the four receptors displays a specificity profile for a series of analogs in agreement with the literature. Finally, the stability of these recombinant receptors is sufficient to allow their use in test kits. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:135 / 141
页数:7
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