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Qualitative Confirmation of 9 Synthetic Cannabinoids and 20 Metabolites in Human Urine Using LC-MS/MS and Library Search

机译:使用LC-MS / MS和库检索对人尿液中9种合成大麻素和20种代谢物的定性确认

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Introduction: Synthetic cannabinoids are an emerging illicit drug class. The variety of available substances is large and ever-changing, making it difficult for laboratories to remain current. We present a qualitative LC--MS/MS method identifying urinary metabolites of JWH-018, JWH-073, JWH-081, JWH-122, JWH-200, JWH-210, JWH-250, RCS-4, and AM2201 and the parent compounds JWH-018, JWH-073, JWH-081, JWH-122, JWH-210, JWH-250, RCS-4, AM2201, and MAM2201. Methods: After enzymatic hydrolysis, urinary proteins were precipitated with acetonitrile. Chromatography utilized a 10 min gradient on a Kinetex XB-C18 column with 0.1% formic acid in water and acetonitrile. Scheduled multiple reaction monitoring "survey scans" were followed by information-dependent acquisition-enhanced product ion scan experiments on an ABSciex 5500 QTRAP mass spectrometer. Analytes were identified by software-assisted library searching against reference spectra. Results: The method was fully validated, including proof of selectivity (no exogenous or endogenous interferences were observed), assessment of matrix effects (95-122%) and recovery (53-95%), determination of limits of detection (0.5-10 ng/ mL), carry-over studies (thresholds between 100 and 1000 ng/mL), and determination of autosampler stability (samples were stable for at least 3 days). Hydrolysis efficiency was thoroughly investigated for a wide range of glucuronides and for the reference standard, JWH-018 5-hydroxypentyl glucuronide.
机译:简介:合成大麻素是新兴的非法药物类别。可用物质的种类繁多,并且在不断变化,这使得实验室很难保持最新状态。我们提出了定性的LC-MS / MS方法,确定了JWH-018,JWH-073,JWH-081,JWH-122,JWH-200,JWH-210,JWH-250,RCS-4和AM2201的尿液代谢产物母体化合物JWH-018,JWH-073,JWH-081,JWH-122,JWH-210,JWH-250,RCS-4,AM2201和MAM2201。方法:酶水解后,尿蛋白用乙腈沉淀。色谱法在Kinetex XB-C18色谱柱上使用10分钟的梯度,其中含有0.1%的甲酸和水和乙腈溶液。在ABSciex 5500 QTRAP质谱仪上进行预定的多反应监测“调查扫描”,然后进行依赖信息的获取增强型产物离子扫描实验。通过软件辅助库对参考光谱进行搜索来鉴定分析物。结果:该方法得到了充分验证,包括选择性证明(未观察到外源或内源性干扰),评估基质效应(95-122%)和回收率(53-95%),确定检测限(0.5-10) ng / mL),残留物研究(阈值在100和1000 ng / mL之间)和自动进样器稳定性的测定(样品稳定至少3天)。广泛研究了各种葡糖醛酸内酯和参考标准品JWH-018 5-羟基戊基葡糖醛酸内酯的水解效率。

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