Centro de Investigação em Ciências da Saúde (CICS-UBI), Universidade da Beira Interior, Covilhã, Portugal; Laboratório de Fármaco-Toxicologia - UBIMedical, Universidade da Beira Interior, Covilhã, Portugal.
Section of Legal Medicine, Università Politecnica delle Marche, Ancona, Italy.
J Pharm Biomed Anal. 2019 Jun 5;170:63-67. doi: 10.1016/j.jpba.2019.02.039. Epub 2019 Mar 16.
A fast and sensitive ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) method was developed and validated for the measurement of the most common drugs of abuse and some new psychoactive substances in oral fluid. The target compounds were 6-monoacetylmorphine, morphine, codeine, cocaine, benzoylecgonine, amphetamine, methamphetamine, 3,4-methylenedioxymethamphetamine, Δ-9-tetrahydrocannabinol, cannabidiol, mephedrone, ketamine and synthetic cannabinoid 5F-AKB48 (5F-APINACA). Oral fluid (OF) samples were 1/3 diluted with water and separated by reversed phase chromatography with gradient elution of 0.1% formic acid in water and 0.1% formic acid in acetonitrile and detected with tandem mass spectrometry operated in positive multiple reaction monitoring mode. The method was linear for all analytes under investigation from limit of quantification (LOQ, range: 0.5-5 ng/ml) to 250 ng/mL OF. Recovery of analytes under investigation and matrix effect were always higher than 90% (recovery range: 90.6-105.5% and matrix effect range 90.6-101.3%) whereas intra-assay and inter-assay precision and accuracy were always better than 15%. The developed method was successfully applied to ten OF specimens obtained from a proficiency test program and previously analyzed by gas-chromatography mass spectrometry. Analytes concentration between the two methods presented an excellent agreement (r = 0.952) with overlapping values demonstrating method feasibility for high throughput laboratories needing indisputable results for clinical and/or forensic purposes.
建立并验证了一种快速灵敏的超高效液相色谱串联质谱(UHPLC-MS/MS)法,用于检测唾液中常见的滥用药物和一些新精神活性物质。目标化合物包括 6-单乙酰吗啡、吗啡、可待因、可卡因、苯甲酰古柯碱、苯丙胺、甲基苯丙胺、3,4-亚甲二氧基甲基苯丙胺、Δ-9-四氢大麻酚、大麻二酚、美沙酮和合成大麻素 5F-AKB48(5F-APINACA)。唾液(OF)样品用 1/3 水稀释,采用反相色谱法,以 0.1%甲酸水和 0.1%甲酸乙腈进行梯度洗脱,串联质谱采用正离子多反应监测模式检测。该方法对所有研究分析物均呈线性,从定量下限(LOQ,范围:0.5-5ng/ml)到 250ng/ml OF。研究分析物的回收率和基质效应始终高于 90%(回收率范围:90.6-105.5%和基质效应范围 90.6-101.3%),而日内和日间精密度和准确度始终优于 15%。该方法成功应用于从能力验证计划中获得的十个 OF 标本,并与之前通过气相色谱质谱法分析的结果进行了比较。两种方法分析物浓度之间具有极好的一致性(r=0.952),重叠值表明该方法适用于需要用于临床和/或法医目的的无可争议结果的高通量实验室。