Pozo Oscar J, Van Eenoo Peter, Van Thuyne Wim, Deventer Koen, Delbeke Frans T
DoCoLab, UGent, Department of Clinical Chemistry, Microbiology and Immunology, Technologiepark 30, Zwijnaarde, Belgium.
J Chromatogr A. 2008 Mar 7;1183(1-2):108-18. doi: 10.1016/j.chroma.2008.01.045. Epub 2008 Jan 26.
A method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the direct quantification of glucuronides of testosterone (TG), epitestosterone (EPG), androsterone (AG) and etiocholanolone (ETG) has been developed. The method allowed for the direct determination of these analytes avoiding hydrolysis and derivatization, which are usual steps in commonly used methods based on gas chromatography-mass spectrometry (GC-MS). The electrospray ionization and the product ion spectra of the glucuronides have been studied in order to obtain the most specific transitions. The use of the selected transitions is necessary for the determination of the analytes at low ng/ml concentration levels. Two different approaches have been tested for sample preparation: direct injection after filtration and acidic liquid-liquid extraction (LLE) with ethyl acetate. Both approaches have been validated obtaining satisfactory values for accuracy and precision with limits of detection lower than 1 ng/ml for TG and EPG. Ion suppression was more pronounced after LLE probably due to the concentration of interferences from acidic urine. The applicability of the method has been checked by the analysis of 40 urine samples. The results were compared with those obtained with the common GC-MS method. Results have shown a good correlation between both methods with correlation coefficients higher than 0.97. A slope close to 1 was obtained for all analytes except for AG possibly due to losses during the extraction process prior to GC-MS.
已开发出一种基于液相色谱 - 串联质谱法(LC-MS/MS)直接定量睾酮葡萄糖醛酸苷(TG)、表睾酮葡萄糖醛酸苷(EPG)、雄酮葡萄糖醛酸苷(AG)和本胆烷醇酮葡萄糖醛酸苷(ETG)的方法。该方法可直接测定这些分析物,避免了水解和衍生化步骤,而水解和衍生化是基于气相色谱 - 质谱法(GC-MS)的常用方法中的常规步骤。为了获得最具特异性的跃迁,对葡萄糖醛酸苷的电喷雾电离和产物离子谱进行了研究。使用选定的跃迁对于在低纳克/毫升浓度水平下测定分析物是必要的。已对两种不同的样品制备方法进行了测试:过滤后直接进样和用乙酸乙酯进行酸性液 - 液萃取(LLE)。两种方法均已得到验证,准确度和精密度值令人满意,TG和EPG的检测限低于1纳克/毫升。LLE后离子抑制更为明显,这可能是由于酸性尿液中的干扰物浓缩所致。通过分析40份尿液样本检验了该方法的适用性。将结果与用常用GC-MS方法获得的结果进行了比较。结果表明两种方法之间具有良好的相关性,相关系数高于0.97。除AG外,所有分析物的斜率均接近1,这可能是由于在GC-MS之前的萃取过程中有损失。