Meunier-Solère Véronique, Maume Daniel, André François, Le Bizec Bruno
Laboratoire d'Etude des Résidus et Contaminants dans les Aliments (LABERCA) Ecole Nationale Vétérinaire de Nantes, BP 50707, 44307 Nantes Cedex 3, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Feb 25;816(1-2):281-8. doi: 10.1016/j.jchromb.2004.11.047.
Mixtures such as N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA), ammonium iodide and dithioerythreitol (DTE) or MSTFA, trimethyliodosilane and DTE were used for derivatisation of anabolic steroids extracted from 2 g kidney fat and present at ng kg(-1) level. They are leading to unexpected products. Their identity and mechanism of formation have been discussed. A new silylation mixture was developed to overcome these pitfalls: N,O-bis-trimethylsilyl-acetamide was used in combination of 2.5% of MSTFA/I(2) (1000:10 (v/w)). A single product consisting in ether-TMS and/or enol-TMS derivative was observed for all tested steroids with a stability demonstrated for at least 48 h. Quantitative application was proved even at the low ng kg(-1) level in a complex biological matrices, i.e. kidney fat.