{"title":"Development and Validation GC/MS Method for Methamphetamine Analysis in Urine by Miniaturization QuEChERS","authors":"Soraya Aulia, R. Primaharinastiti, D. Purwanto","doi":"10.26554/sti.2023.8.3.451-460","DOIUrl":null,"url":null,"abstract":"This paper explains the development of a quick and easy gas chromatography (GC) approach to identify methamphetamine in urine. This research used gas chromatography with mass spectroscopy and a capillary column TG-5SILMS (5% phenyl methyl siloxane, 30 m x 0.32 x 25 m). The carrier gas flow rate was set at 1.0 mL/minute, the temperature inlet and detector had been set at 300°C, and the oven temperature was programmed to initiate at 50°C and held for 1.5 minutes before being raised to 300°C at a rate 40°C/minute and held for 3 minutes. Sample pre-treatment by modification of the QuEChERS method includes using a relatively large amount of inorganic salt, extraction volume and extraction cycle. The optimal conditions for processing a 400 uL urine sample were 160 mg magnesium sulphate, 40 mg sodium chloride, and 400 uL acetonitrile for organic solvent. According to the validation test, the detection limit for methamphetamine was 0.36 ug/mL; the quantitation limit was 1.09 ug/mL, and the calibration curve followed the regression line. y=1.0489x-3.7914, coefficient (r) was 0.9973. The recovery of the analyte spiked into urine at 5, 7 and 9 ug/mL on average was 100.5±2.33% for intraday dan 93.3±7.21% for interday. The precision was excellent, with an average coefficient of variation of 2.31%. The procedure was applied to four urine samples from drug users and the first abuser (25.51 ug/mL), the second abuser (15.05 ug/mL), the third abuser (17.72 ug/mL) and the last abuser (3.08 ug/mL) were all satisfactorily quantitated.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science and Technology Indonesia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26554/sti.2023.8.3.451-460","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
This paper explains the development of a quick and easy gas chromatography (GC) approach to identify methamphetamine in urine. This research used gas chromatography with mass spectroscopy and a capillary column TG-5SILMS (5% phenyl methyl siloxane, 30 m x 0.32 x 25 m). The carrier gas flow rate was set at 1.0 mL/minute, the temperature inlet and detector had been set at 300°C, and the oven temperature was programmed to initiate at 50°C and held for 1.5 minutes before being raised to 300°C at a rate 40°C/minute and held for 3 minutes. Sample pre-treatment by modification of the QuEChERS method includes using a relatively large amount of inorganic salt, extraction volume and extraction cycle. The optimal conditions for processing a 400 uL urine sample were 160 mg magnesium sulphate, 40 mg sodium chloride, and 400 uL acetonitrile for organic solvent. According to the validation test, the detection limit for methamphetamine was 0.36 ug/mL; the quantitation limit was 1.09 ug/mL, and the calibration curve followed the regression line. y=1.0489x-3.7914, coefficient (r) was 0.9973. The recovery of the analyte spiked into urine at 5, 7 and 9 ug/mL on average was 100.5±2.33% for intraday dan 93.3±7.21% for interday. The precision was excellent, with an average coefficient of variation of 2.31%. The procedure was applied to four urine samples from drug users and the first abuser (25.51 ug/mL), the second abuser (15.05 ug/mL), the third abuser (17.72 ug/mL) and the last abuser (3.08 ug/mL) were all satisfactorily quantitated.
本文介绍了一种快速简便的气相色谱法(GC)检测尿液中甲基苯丙胺的方法。本研究使用了气相色谱质谱和毛细管柱TG-5SILMS(5%苯基甲基硅氧烷,30m x 0.32 x 25m)。载气流速设定为1.0 mL/分钟,温度入口和检测器设定为300°C,烘箱温度设定为在50°C启动并保持1.5分钟,然后以40°C/分钟的速度升至300°C并保持3分钟。通过改进QuEChERS方法对样品进行预处理,包括使用相对大量的无机盐、提取体积和提取周期。处理400微升尿样的最佳条件是160毫克硫酸镁、40毫克氯化钠和400微升乙腈作为有机溶剂。根据验证试验,甲基苯丙胺的检测限为0.36微克/毫升;定量限为1.09ug/mL,校准曲线遵循回归线。y=1.0489x-3.7914,系数(r)为0.9973。以5、7和9微克/毫升的浓度掺入尿液的分析物的平均回收率为100.5±2.33%,日间为93.3±7.21%。该程序应用于吸毒者的四份尿液样本,第一次吸毒者(25.51微克/毫升)、第二次吸毒者、第三次吸毒者和最后一次吸毒者的尿液样本均能令人满意地定量。