Validation of Amphetamine and Methamphetamine Measurement Method by Gas Chromatography-Mass Spectrometry

Dewi Yudiana, Adi Hartono, Herix Sonata MS3
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Abstract

Drug abuse is still very common in Indonesia, including in West Sumatra, which will result in psychological changes in users. A reliable method is needed to be able to detect the presence of narcotics and their metabolites in human specimens. The purpose of the study was to validate the mass spectrophotometric gas chromatography method for the measurement of amphetamine and metamphetamine. The benefits of research to ensure that the analytical method is accurate, specific, reproducible and resistant to the range of analytes to be analysed. The research method is by measuring the sample with GCMS (gas chromatography mass spectrometry) and then conducting a linearity test, detection limit test, accuracy test and precision test. The matrix used is urine specimen, spike is done with amphetamine and methamphetamine standards. From the results of the validation of amphetamine and methamphetamine measurement methods obtained MDL (method detection limit) 3.10 µg/L, LoD (limit of detection) 2.962 µg/L and LoQ (limit of detection) 2.962 µg/L. of Quantification) 9.873 µg/L. In the measurement of methamphetamine MDL 7.072 µg/L, LoD 6.757 µg/L and LoQ 22.253 µg/L. Accuracy of amphetamine and methamphetamine measurement methods 101.9% and 95.2% and reproducibility of amphetamine and methamphetamine measurements 3.83% and 6.743%. Measuring range and linearity of measurement of amphetamine and methamphetamine 25.0 µg/L - 200 µg/L with r = 0.9972 and 0.9992. Based on these data, the amphetamine and methamphetamine measurement method with gas chromatography-mass spectrometry is sensitive to measure amphetamine and methamphetamine in urine and fulfils the required criteria.
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气相色谱-质谱联用测定安非他明和甲基苯丙胺方法的验证
药物滥用在印度尼西亚,包括在西苏门答腊,仍然非常普遍,这将导致使用者的心理变化。需要一种可靠的方法来检测人体标本中麻醉品及其代谢物的存在。本研究的目的是验证质谱气相色谱法测定安非他明和甲基苯丙胺的含量。研究的好处是确保分析方法是准确的,特异性的,可重复性的和对要分析的分析物范围的抗性。研究方法是采用气相色谱质谱法对样品进行测定,然后进行线性检验、检出限检验、准确度检验和精密度检验。所用基质为尿液标本,钉钉采用安非他明和甲基苯丙胺标准。从安非他明和甲基苯丙胺测定方法的验证结果得到MDL(方法检出限)3.10µg/L, LoD(检出限)2.962µg/L和LoQ(检出限)2.962µg/L。9.873µg/L。测定甲基苯丙胺MDL为7.072µg/L, LoD为6.757µg/L, LoQ为22.253µg/L。安非他明和甲基苯丙胺测定方法的准确度分别为101.9%和95.2%,安非他明和甲基苯丙胺测定方法的重现性分别为3.83%和6.743%。安非他明和甲基苯丙胺的测量范围为25.0µg/L ~ 200µg/L,线性度为r = 0.9972和0.9992。结果表明,气相色谱-质谱联用测定尿中苯丙胺和甲基苯丙胺灵敏度高,符合检测标准。
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