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Automated in tube solid-phase microextraction coupled with liquid chromatography/electrospray ionization mass spectrometry for the determination of beta-blockers and metabolites in urine and serum samples

机译:全自动管固相微萃取结合液相色谱/电喷雾电离质谱法测定尿液和血清样品中的β-受体阻滞剂和代谢物

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The technique of automated in-tube solid-phase microextraction (SPME) coupled with liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) was evaluated for the determination of beta-blockers in urine and serum samples. In-tube SPME is an extraction technique for organic compounds in aqueous samples, in which analytes are extracted from the sample directly into an open tubular capillary by repeated draw/eject cycles of sample solution. LC/MS analyses of beta-blockers were initially performed by liquid injection onto a LC column. Nine beta-blockers tested in this study gave very simple ESI mass spectra, and strong signals corresponding to [M + H](+) were observed for all beta-blockers. The beta-blockers were separated with a Hypersil BDS C-18 column using acetonitrile/methanol/water/acetic acid (15:15:70:1) as a mobile phase. To optimize the extraction of beta-blockers, several in-tube SPME parameters were examined. The optimum extraction conditions were 15 draw/eject cycles of 30 mu L of sample in 100 mM Tris-HCl (pH 8.5) at a now rate of 100 mu L/min using an Omegawax 250 capillary (Supelco, Bellefonte, PA). The beta-blockers extracted by the capillary were easily desorbed by mobile-phase now, and carryover of beta-blockers was not observed. Using in-tube SPME/LC/ESI-MS with selected ion monitoring, the calibration curves of beta-blockers were linear in the range from 2 to 100 ng/mL with correlation coefficients above 0.9982 (n = 18) and detection limits (S/N = 3) of 0.1-1.2 ng/mL, This method was successfully applied to the analysis of biological samples without interference peaks. The recoveries of beta-blockers spiked into human urine and serum samples were above 84 and 71%, respectively. A serum sample from a patient administrated propranolol was analyzed using this method and both propranolol and its metabolites were detected. [References: 41]
机译:评估了自动管内固相微萃取(SPME)技术与液相色谱/电喷雾电离质谱(LC / ESI-MS)的结合,以确定尿液和血清样品中的β受体阻滞剂。管内SPME是一种用于含水样品中有机化合物的提取技术,其中,通过重复进行样品溶液的抽取/喷射循环,将分析物从样品中直接提取到敞开的管状毛细管中。首先通过液体注入LC色谱柱对β-阻滞剂进行LC / MS分析。在这项研究中测试的九种β-受体阻滞剂给出了非常简单的ESI质谱,并且所有β-受体阻滞剂均观察到了与[M + H](+)相对应的强信号。使用Hypersil BDS C-18色谱柱,使用乙腈/甲醇/水/乙酸(15:15:70:1)作为流动相分离β-受体阻滞剂。为了优化β受体阻滞剂的提取,检查了几种管内SPME参数。最佳提取条件是使用Omegawax 250毛细管(Supelco,Bellefonte,PA)在100 mL Tris-HCl(pH 8.5)中以30μL的样品以15μL/ min的速率进行15个抽/注循环,现在的速率为100μL / min。现在,毛细管提取的β-受体阻滞剂很容易被流动相解吸,没有观察到β-受体阻滞剂的残留。使用管内SPME / LC / ESI-MS进行选定的离子监测,β受体阻滞剂的校准曲线在2至100 ng / mL范围内呈线性,相关系数高于0.9982(n = 18),检出限(S / N = 3)为0.1-1.2 ng / mL,该方法已成功应用于没有干扰峰的生物样品的分析。掺入人尿和血清样品中的β受体阻滞剂的回收率分别高于84%和71%。使用这种方法分析了患者服用普萘洛尔的血清样品,并检测了普萘洛尔及其代谢产物。 [参考:41]

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