Department of Pharmacology and Toxicology, National Veterinary Research Institute, Pulawy, Poland.
Anal Bioanal Chem. 2012 Jul;403(10):2965-72. doi: 10.1007/s00216-012-5859-0. Epub 2012 Mar 6.
The liquid chromatography-tandem mass spectrometry method (LC-MS/MS) was developed and validated to detect androgenic steroids: trenbolone, nortestosterone, boldenone, methylboldenone, testosterone, methyltestosterone, 17β-1-testosterone and their metabolites in bovine urine. Sample preparation before LC-MS/MS analysis involved an enzymatic hydrolysis with glucuronidase AS-HP, isolation of free hormones from urine on C(18) SPE column and purification of the extract using liquid-liquid extraction with n-pentane and SPE NH(2) column. For the chromatographic separation of steroids, the Poroshell 120-EC C18 column (150 × 2.1 mm, 2.7 μm) was used. Mass spectrometric measurement was achieved using the API 4000 triple quadrupole (QqQ) instrument with a TurboIon-Spray source operating in positive electrospray ionization mode. The procedure was validated according to the Decision 2002/657/EC. Recovery ranged from 76.5% to 118.9% for all examined compounds. The repeatability was below 20% and reproducibility did not exceed the 25%. The linearity was good for all analytes in the whole range of tested concentrations, as proved by the correlation coefficients greater than 0.99. The decision limit (CCα) ranged from 0.10 to 0.17 μg L(-1) for all analytes, whereas the detection capability (CCβ) ranged from 0.17 to 0.29 μg L(-1). The application of an innovative Poroshell column allowed for very good chromatographic separation of steroids with a much shorter time of analysis.
建立并验证了液相色谱-串联质谱法(LC-MS/MS),用于检测牛尿中的雄激素类固醇:群勃龙、去甲睾酮、宝丹酮、美雄酮、睾酮、甲基睾酮、17β-1-睾酮及其代谢物。LC-MS/MS 分析前的样品制备包括用β-葡萄糖醛酸苷酶 AS-HP 进行酶水解,用 C(18)SPE 柱从尿液中分离游离激素,并用正戊烷和 SPE NH(2)柱进行液-液萃取净化。为了对类固醇进行色谱分离,使用了 Poroshell 120-EC C18 柱(150×2.1mm,2.7μm)。采用 API 4000 三重四极杆(QqQ)仪器,以正电喷雾电离模式的 TurboIon-Spray 源进行质谱测量。该程序是根据 2002/657/EC 号决定进行验证的。所有检测化合物的回收率在 76.5%至 118.9%之间。重复性低于 20%,再现性不超过 25%。所有分析物在整个测试浓度范围内的线性均良好,这可以通过相关系数大于 0.99 来证明。所有分析物的决策限(CCα)在 0.10 至 0.17μg/L 之间,检测限(CCβ)在 0.17 至 0.29μg/L 之间。采用创新的 Poroshell 柱可实现类固醇的极好色谱分离,分析时间大大缩短。