Development of automated in-tube SPME/LC/MS method for drug analysis†

Hiroyuki Kataoka, Heather L. Lord, Shigeo Yamamoto, Shizuo Narimatsu, Janusz Pawliszyn
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引用次数: 52

Abstract

The technique of automated in-tube solid-phase microextraction (SPME) coupled with liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) was developed for the determination of stimulants and β-blockers in biological 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 column by repeated draw/eject cycles of sample solution. LC/MS analyses of stimulants and β-blockers were initially performed by liquid injection onto a LC column. Five stimulants and nine β-blockers tested in this study gave very simple ESI mass spectra, and strong signals corresponding to [M+H]+ were observed for all drugs. The stimulants were separated with a Supelcosil LC-CN column using acetonitrile/50 mM ammonium acetate (15:85) as a mobile phase. The β-blockers were separated with a Hypersil BDS C18 column using acetonitrile/methanol/water/acetic acid (15:15:70:1) as a mobile phase. In order to optimize the extraction of these drugs, several in-tube SPME parameters were examined. The optimum extraction conditions were 15 draw/eject cycles of 30–35 μL of sample in 50–100 mM Tris-HCl (pH 8.5) at a flow rate of 100 μL/min using Omegawax 250 capillary column (Supelco, Bellefonte, PA). The drugs extracted on the capillary column were easily desorbed by mobile phase flow, and carryover of drugs was not observed. Using in-tube SPME/LC/ESI-MS with selected ion monitoring, the calibration curves of drugs were linear in the range of 2–100 ng/mL with correlation coefficients above 0.9982 (n=18), and detection limits (S/N=3) of 0.1–1.2 ng/mL. This technique was successfully applied to the analysis of biological samples, such as urine and serum, without interference peaks. The recoveries of drugs spiked into human urine and serum samples were above 81 and 71%, respectively. © 2000 John Wiley & Sons, Inc. J Micro Sep 12: 493–500, 2000

全自动管内SPME/LC/MS药物分析方法的建立
建立了自动管内固相微萃取(SPME) -液相色谱/电喷雾电离质谱(LC/ESI-MS)联用技术测定生物样品中兴奋剂和β-阻滞剂的含量。管内SPME是一种提取水相样品中有机化合物的技术,通过对样品溶液进行反复的抽/出循环,将分析物从样品中直接提取到开管毛细管柱中。兴奋剂和β受体阻滞剂的LC/MS分析最初通过液相注射到LC柱上进行。本研究检测的5种兴奋剂和9种β受体阻滞剂的ESI质谱非常简单,所有药物均有强的[M+H]+对应信号。以乙腈/50 mM乙酸铵(15:85)为流动相,采用superelcosil LC-CN柱对兴奋剂进行分离。β阻断剂采用Hypersil BDS C18色谱柱分离,流动相为乙腈/甲醇/水/乙酸(15:15:70:1)。为了优化这些药物的提取工艺,考察了几种管内SPME参数。采用Omegawax 250毛细管柱(Supelco, Bellefonte, PA),在50-100 mM Tris-HCl (pH 8.5)溶液中,以100 μL/min流速萃取30-35 μL样品,萃取周期为15次。毛细管柱上提取的药物易被流动相流解吸,无药物携带现象。采用选择性离子监测的管内SPME/LC/ESI-MS,在2 ~ 100 ng/mL范围内呈线性关系,相关系数大于0.9982 (n=18),检出限(S/ n= 3)为0.1 ~ 1.2 ng/mL。该技术已成功应用于生物样品的分析,如尿液和血清,无干扰峰。人尿和血清中加标药物的加标回收率分别大于81%和71%。©2000 John Wiley &儿子,Inc. J Micro . Sep 12: 493 - 500,2000
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