Combination of quadrupole isotope dilution mass spectrometry with simultaneous derivatization and spray assisted droplet formation-liquid phase microextraction for the determination of methamphetamine in human urine and serum samples by gas chromatography mass spectrometry

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Journal of pharmacological and toxicological methods Pub Date : 2023-01-01 DOI:10.1016/j.vascn.2022.107207
Sude Oflu , Sezin Erarpat , Buse Tuğba Zaman , Ömer Tahir Günkara , Sezgin Bakırdere , Fatma Turak
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引用次数: 5

Abstract

In this study, an analytical method with high accuracy and precision was developed for the determination of methamphetamine in human urine and serum samples by gas chromatography–mass spectrometry (GC–MS). A simultaneous derivatization and spray assisted droplet formation-liquid phase microextraction (SADF-LPME) method was proposed to derivatize and preconcentrate target analyte. Quadruple isotope dilution (ID4) was used to provide high accuracy and precision for methamphetamine determination in the samples. After the optimization studies for the derivatization and microextraction parameters, limit of detection (LOD) and limit of quantitation (LOQ) for the developed SADF-LPME method were found to be 48.0 and 159.9 μg/kg, respectively. Recovery studies were implemented to verify the applicability and accuracy of the developed method for human urine and serum samples. The SADF-LPME method gave low percent recovery results (30.5–61.0%) for the spiked urine and serum samples showing that it failed to minimize or eliminate matrix effects for the analyte. Hence, methamphetamine acetamide-d3 was synthesized and purified in our research laboratory to be used as methamphetamine isotopic analogue in the ID4 method. When the SADF-LPME method was combined with ID4, the percent recovery values for urine and serum samples were calculated as 99.7–100.0% and 99.4–100.2%, respectively. These results demonstrated the applicability and accuracy of the proposed method for urine and serum samples.

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四极杆同位素稀释质谱-同时衍生化-喷雾辅助液滴形成-液相微萃取联合气相色谱质谱法测定人尿和血清样品中的甲基苯丙胺
本研究建立了一种准确度和精密度高的气相色谱-质谱联用(GC-MS)测定人尿液和血清样品中甲基苯丙胺的方法。提出了一种同时衍生化和喷雾辅助液滴形成-液相微萃取(SADF-LPME)方法对目标分析物进行衍生化和预浓缩。采用四倍同位素稀释法(ID4)测定样品中甲基苯丙胺的准确度和精密度较高。经衍生化和微萃取参数优化研究,SADF-LPME方法的检出限和定量限分别为48.0和159.9 μg/kg。进行了回收率研究,以验证所开发的方法对人类尿液和血清样本的适用性和准确性。SADF-LPME方法对加标尿液和血清样品的回收率较低(30.5-61.0%),表明该方法不能最大限度地减少或消除基质对分析物的影响。因此,我们的研究实验室合成并纯化了甲基苯丙胺乙酰酰胺-d3,用于ID4法中作为甲基苯丙胺同位素类似物。当SADF-LPME法与ID4联合使用时,尿液和血清样品的回收率分别为99.7 ~ 100.0%和99.4 ~ 100.2%。这些结果证明了该方法对尿液和血清样本的适用性和准确性。
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来源期刊
Journal of pharmacological and toxicological methods
Journal of pharmacological and toxicological methods PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
3.60
自引率
10.50%
发文量
56
审稿时长
26 days
期刊介绍: Journal of Pharmacological and Toxicological Methods publishes original articles on current methods of investigation used in pharmacology and toxicology. Pharmacology and toxicology are defined in the broadest sense, referring to actions of drugs and chemicals on all living systems. With its international editorial board and noted contributors, Journal of Pharmacological and Toxicological Methods is the leading journal devoted exclusively to experimental procedures used by pharmacologists and toxicologists.
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