Meatherall R
Department of Biochemistry, St. Boniface General Hospital, Winnipeg, MB, Canada.
J Anal Toxicol. 1995 Sep;19(5):316-22. doi: 10.1093/jat/19.5.316.
Amphetamine and methamphetamine are extracted from 200 microL of urine into an organic solvent containing propylchloroformate. The amines immediately react to form propylcarbamate derivatives. The aqueous phase is removed, and a portion of the organic phase is analyzed by gas chromatography-mass spectrometry. Either the deuterated analogues or N-propylamphetamine internal standards give acceptable results. For day-to-day precision, coefficients of variation in the range of 6-10% are found. The method is linear to 10,000 ng/mL. Limits of quantitation and detection are 50 and 5 ng/mL, respectively, when using N-propylamphetamine as the internal standard. Extracts are stable at room temperature for at least 60 days. There is no interference from other amphetamine drugs.
将200微升尿液中的苯丙胺和甲基苯丙胺萃取到含有氯甲酸丙酯的有机溶剂中。胺类物质立即反应形成丙基氨基甲酸酯衍生物。去除水相,取一部分有机相通过气相色谱-质谱联用仪进行分析。氘代类似物或N-丙基苯丙胺内标均可给出可接受的结果。对于日常精密度,变异系数在6%-10%范围内。该方法在10,000纳克/毫升范围内呈线性。以N-丙基苯丙胺作为内标时,定量限和检测限分别为50和5纳克/毫升。提取物在室温下至少60天稳定。无其他苯丙胺类药物干扰。