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Simultaneous Screening and Quantification of 29 Drugs of Abuse in Oral Fluid by Solid-Phase Extraction and Ultraperformance LC-MS/MS

机译:固相萃取和超高性能LC-MS / MS同时筛查和定量29种口服液中的滥用药物

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The European DRUID (Driving under the Influence of Drugs, Alcohol And Medicines) project calls for analysis of oral fluid (OF) samples, collected randomly and anonymously at the roadside from drivers in Denmark throughout 2008-2009. To analyze these samples we developed an ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for detection of 29 drugs and illicit compounds in OF. The drugs detected were opioids, amphetamines, cocaine, benzodiazepines, and Δ-9-tetrahydrocannabinol. Solid-phase extraction was performed with a Gilson ASPEC XL4 system equipped with Bond Elut Certify sample cartridges. OF samples (200 mg) diluted with 5mL of ammonium acetate/methanol (vol/vol 90: 10) buffer were applied to the columns and eluted with 3mL of acetonitrile with aqueous ammonium hydroxide. Target drugs were quantified by use of a Waters ACQUITY UPLC system coupled to a Waters Quattro Premier XE triple quadrupole (positive electrospray ionization mode, multiple reaction monitoring mode). Extraction recoveries were 36%-114% for all analytes, including Δ-9-tetrahydrocannabinol and benzoylecgonine. The lower limit of quantification was 0.5 µg/kg for all analytes. Total imprecision (CV) was 5.9%-19.4%.With the use of deuterated internal standards for most compounds, the performance of the method was not influenced by matrix effects. A preliminary account of OF samples collected at the roadside showed the presence of amphetamine, cocaine, codeine, Δ-9-tetrahydrocannabinol, tramadol, and zopiclone. The UPLC-MS/MS method makes it possible to detect all 29 analytes in 1 chromatographic run (15 min), including Δ-9-tetrahydrocannabinol and benzoylecgonine, which previously have been difficult to incorporate into multicomponent methods.
机译:欧洲DRUID(受毒品,酒精和药品影响驾驶)项目要求分析整个2008-2009年间在丹麦路边随机和匿名收集的口服液(OF)样品。为了分析这些样品,我们开发了一种超高效液相色谱-串联质谱(UPLC-MS / MS)方法,用于检测OF中的29种药物和非法化合物。检测到的药物是阿片类药物,安非他命,可卡因,苯并二氮杂卓和Δ-9-四氢大麻酚。固相萃取是用装有Bond Elut Certify样品盒的Gilson ASPEC XL4系统进行的。将用5mL乙酸铵/甲醇(体积/体积90:10)缓冲液稀释的OF样品(200 mg)加到色谱柱上,并用3mL乙腈和氢氧化铵水溶液洗脱。通过使用结合了Waters Quattro Premier XE三重四极杆的Waters ACQUITY UPLC系统(正电喷雾电离模式,多反应监测模式)对目标药物进行定量。所有分析物(包括Δ-9-四氢大麻酚和苯甲酰芽子碱)的提取回收率为36%-114%。所有分析物的定量下限为0.5 µg / kg。总不精确度(CV)为5.9%-19.4%。对于大多数化合物,使用氘代内标,该方法的性能不受基质效应的影响。在路边收集的OF样品的初步记录显示,存在苯丙胺,可卡因,可待因,Δ-9-四氢大麻酚,曲马多和佐匹克隆。 UPLC-MS / MS方法可在1次色谱运行中(15分钟)检测所有29种分析物,包括Δ-9-四氢大麻酚和苯甲酰芽子碱,以前难以将其纳入多组分方法。

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    《Clinical Chemistry》 |2009年第11期|p.2004-2018|共15页
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    Nora Badawi,1 Kirsten Wiese Simonsen,1 Anni Steentoft,1 Inger Marie Bernhoft,2 and Kristian Linnet1*1 Section of Forensic Chemistry, Department of Forensic Medicine, Faculty of Health Sciences, University of Copenhagen, 2 Department of Transport, Technical University of Denmark, Kgs. Lyngby, Denmark.* Address correspondence to this author at: Section of Forensic Chemistry, Department of Forensic Medicine, Faculty of Health Sciences, University of Copenhagen, Frederik V's vej 11, 3. DK-2100, Denmark. Fax +45-3532-6085, e-mail kristian.linnet@forensic.ku.dk.Received December 11, 2008, accepted July 30, 2009.Previously published online at DOI: 10.1373/clinchem.2008.122341,;

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