Nakamura S, Sian T H, Daishima S
Yokogawa Analytical Systems Inc., Musashino-shi, Tokyo, Japan.
J Chromatogr A. 2001 Jun 15;919(2):275-82. doi: 10.1016/s0021-9673(01)00851-2.
A method for the determination of estrogens (17alpha-estradiol, 17beta-estradiol, estrone, ethynyl estradiol, and estriol) as pentafluorobenzyl-trimethylsilyl (PFB-TMS) derivatives by gas chromatography-mass spectrometry (GC-MS) with negative-ion chemical-ionization (NICI) is described. The NICI of all the derivatives produced an intense [M-PFB]- ion as the base peak. The reagent gas (methane) flow-rate and the ion source temperature were determined to be 2.0 ml/min and 240 degrees C, respectively, for the optimized NICI-selected ion monitoring (SIM) conditions. The sensitivities of the PFB-TMS derivatives in the NICI mode were 8.0-130 times higher than those of the PFB-TMS derivatives in electron ionization (EI) mode, and 12-25 times higher than those of all the TMS derivatives in the EI mode. This method was applied to the analysis of estrogens in river water using a solid-phase extraction as the sample preparation. The recoveries of the target chemicals from a river-water sample spiked with standards at 2 ng/l level were 85.8-126.5% (RSD, 6.2-13.0%). The methodical detection limits ranged from 0.10 to 0.28 ng/l.
描述了一种通过气相色谱-质谱联用(GC-MS)结合负离子化学电离(NICI)测定雌激素(17α-雌二醇、17β-雌二醇、雌酮、乙炔雌二醇和雌三醇)作为五氟苄基-三甲基硅烷基(PFB-TMS)衍生物的方法。所有衍生物的NICI产生一个强烈的[M-PFB]-离子作为基峰。对于优化的NICI选择离子监测(SIM)条件,确定试剂气(甲烷)流速和离子源温度分别为2.0 ml/min和240℃。NICI模式下PFB-TMS衍生物的灵敏度比电子电离(EI)模式下的PFB-TMS衍生物高8.0-130倍,比EI模式下所有TMS衍生物高12-25倍。该方法应用于河水雌激素分析,采用固相萃取作为样品制备方法。在2 ng/l水平加标标准品的河水样品中,目标化合物的回收率为85.8-126.5%(相对标准偏差,6.2-13.0%)。方法检出限为0.10至0.28 ng/l。