Avcioglu Gamze, Yilmaz Gulsen, Yalcin Sahiner Safak, Kozaci L Didem, Bal Ceylan, Yilmaz Fatma Meric
Department of Medical Biochemistry, Karadeniz Ereğli State Hospital, Zonguldak, Turkey.
Department of Medical Biochemistry, Ankara Yıldırım Beyazıt University Faculty of Medicine, Ankara, Turkey.
Clin Biochem. 2021 Jul;93:112-118. doi: 10.1016/j.clinbiochem.2021.04.009. Epub 2021 Apr 18.
The aim of this study was to evaluate the analytical performance of the Kite Biotechnology Oral fluid (OF) screening test device, which is used for roadside screening of cannabis, opiates, amphetamines, methamphetamine, 3,4-methylenedioxymethamphetamine (MDMA), cocaine and benzodiazepines by comparing samples with matched plasma samples, analysed via liquid chromatography-tandem mass spectrometry (LC-MS/MS) for confirmation.
OF and plasma samples were obtained simultaneously from a total of 100 subjects. OF samples were analysed by OF screening test based on immunochromatography. The OF screening test cut-off values were 50 ng/mL for amphetamines (d-amphetamine) and methamphetamine/MDMA (d-methamphetamine), 30 ng/mL for cocaine (benzoylecgonine), 40 ng/mL for opiates (morphine), 20 ng/mL for benzodiazepines (nordazepam), and 25 ng/mL for cannabis (Δ-tetrahydrocannabinol). LC-MS/MS method validation was performed according to the CLSI C62-A recommendations with the following parameters: matrix effect, lower limit of quantification (LLOQ), linearity, intra-day and inter-day precision and accuracy.
The overall specificity, accuracy and negative predictive values (NPV) were acceptable and met the DRUID standard of >80%. The OF screening test device showed good sensitivity for cocaine, amphetamines and opiates, whereas it indicated poor sensitivity for methamphetamine/MDMA (66.7%) and failed to detect cannabis and benzodiazepines.
The present study is the first report to evaluate the Kite Biotechnology OF screening test device. The diagnostic performance of the OF screening test device was acceptable for opiates, cocaine and amphetamines, but it was insufficient for methamphetamine/MDMA, benzodiazepines and cannabis because of sensitivity issues.
本研究的目的是通过将样本与经液相色谱 - 串联质谱法(LC - MS/MS)分析以进行确证的匹配血浆样本进行比较,评估用于路边筛查大麻、阿片类药物、苯丙胺、甲基苯丙胺、3,4 - 亚甲基二氧基甲基苯丙胺(摇头丸)、可卡因和苯二氮䓬类药物的风筝生物技术口服液(OF)筛查测试装置的分析性能。
从总共100名受试者中同时获取OF和血浆样本。OF样本通过基于免疫色谱法的OF筛查测试进行分析。OF筛查测试的截断值为:苯丙胺(右旋苯丙胺)和甲基苯丙胺/摇头丸(右旋甲基苯丙胺)为50 ng/mL,可卡因为(苯甲酰爱康宁)30 ng/mL,阿片类药物(吗啡)为40 ng/mL,苯二氮䓬类药物(去甲西泮)为20 ng/mL,大麻为(Δ - 四氢大麻酚)25 ng/mL。根据CLSI C62 - A建议,采用以下参数进行LC - MS/MS方法验证:基质效应、定量下限(LLOQ)、线性、日内和日间精密度及准确度。
总体特异性、准确性和阴性预测值(NPV)可接受,符合>80%的DRUID标准。OF筛查测试装置对可卡因、苯丙胺和阿片类药物显示出良好的敏感性,而对甲基苯丙胺/摇头丸的敏感性较差(66.7%),并且未能检测到大麻和苯二氮䓬类药物。
本研究是评估风筝生物技术OF筛查测试装置的首份报告。OF筛查测试装置对阿片类药物、可卡因和苯丙胺的诊断性能可接受,但由于敏感性问题,对甲基苯丙胺/摇头丸、苯二氮䓬类药物和大麻而言,其性能不足。