Xiao X, McCalley D
Faculty of Applied Sciences, University of the West of England, Bristol, UK.
Rapid Commun Mass Spectrom. 2000;14(21):1991-2001. doi: 10.1002/1097-0231(20001115)14:21<1991::AID-RCM125>3.0.CO;2-H.
A sensitive procedure for the determination of estrogens in urine has been developed, using enzymatic hydrolysis and ether extraction followed by capillary gas chromatography with negative chemical ionisation mass spectrometry (GC/NCI-MS) of the pentafluorobenzoyl derivatives. These derivatives were superior for GC/NCI-MS to trifluoroacetyl, heptafluorobutyl, pentadecafluorooctanoyl and perfluorotolyl derivatives, giving characteristic negative molecular ions as the base peak for each of the naturally occurring estrogens estrone, estradiol and estriol, and for the synthetic estrogen ethynylestradiol used in contraceptive pills. The method was also suitable for determination of some metabolites of estrone and estradiol. The specificity and sensitivity of the GC/NCI-MS method simplifies sample preparation. Recovery of spiked samples was in the range 84-101% for the natural estrogens based on additions to increase the concentration by 5 and 1 microg L(-1). The repeatability of the method was 1-8% for all estrogens.
已开发出一种灵敏的尿液中雌激素测定方法,该方法采用酶水解和乙醚萃取,然后对五氟苯甲酰衍生物进行毛细管气相色谱-负化学电离质谱联用(GC/NCI-MS)分析。这些衍生物在GC/NCI-MS分析中比三氟乙酰、七氟丁基、十五氟辛酰和全氟甲苯基衍生物更具优势,能为天然存在的雌激素雌酮、雌二醇和雌三醇以及避孕药中使用的合成雌激素乙炔雌二醇提供特征性的负分子离子作为基峰。该方法也适用于雌酮和雌二醇某些代谢物的测定。GC/NCI-MS方法的特异性和灵敏度简化了样品制备过程。基于添加量使浓度增加5和1 μg L⁻¹,加标样品中天然雌激素的回收率在84%至101%之间。该方法对所有雌激素的重复性为1%至8%。