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首页> 外文期刊>Analytical and bioanalytical chemistry >Development and validation of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) procedure for screening of urine specimens for 100 analytes relevant in drug-facilitated crime (DFC)
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Development and validation of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) procedure for screening of urine specimens for 100 analytes relevant in drug-facilitated crime (DFC)

机译:液相色谱-串联质谱(LC-MS / MS)程序的开发和验证,该程序用于筛查尿液样本中与毒品促成犯罪(DFC)相关的100种分析物

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In recent years, drug-facilitated crime (DFC) has become an increasing problem. A minimum list of 80 analytes to be monitored in such cases has been proposed by the Society of Forensic Toxicologists (SOFT) including the recommended minimum performance limits (RMPL). In the present study, two liquid chromatography-tandem mass spectrometry-based screening procedures, one in positive (method I) and one in negative (method II) electrospray ionization mode were developed and validated. Gradient elution was performed on a ZORBAX Eclipse XDB-C18 column after protein precipitation of the urine samples. Detection was carried out in the scheduled multiple reaction monitoring (MRM) mode monitoring two transitions per compound. A total of 100 analytes (91 basic in method I and nine acidic in method II) could be identified using the described procedure. No interferences were observed in 30 tested blank urine samples. The RMPLs were achieved for all analytes and ranged from 1 ng/mL for fentanyl to 10 μg/mL for γ-hydroxybutyrate (GHB). Matrix effects (ME) were evaluated using the same 30 urine samples and ranged from ?90 % for tetrazepam to >6,000 % for the 11-nor-9-carboxy-tetrahydrocannabinol (THC-COOH). The relative standard deviations of MEwere below 25%for the vast majority of analytes. Results for urine specimens from nine authentic DFC cases were always negative with exception of drugs prescribed to the victims. Reanalysis with the developed procedure of 24 urine samples, with a positive screening result during routine clinical toxicology analysis, confirmed the routine findings. In an excretion study after a single oral doxylamine dose (30 mg), the parent drug and its nor metabolite could be detected in urine specimens from a young female volunteer for 10 days. The developed procedure allows a selective and sensitive screening of urine samples for almost all recommended analytes relevant in DFC cases.
机译:近年来,毒品犯罪(DFC)已成为一个日益严重的问题。法医毒理学家学会(SOFT)提出了在这种情况下要监测的80种分析物的最低清单,其中包括建议的最低性能限值(RMPL)。在本研究中,开发并验证了两种基于液相色谱-串联质谱的筛查程序,一种为正(方法I),另一种为负(方法II)电喷雾电离模式。尿液样品中的蛋白质沉淀后,在ZORBAX Eclipse XDB-C18色谱柱上进行梯度洗脱。检测是在计划的多反应监测(MRM)模式下进行的,每个化合物监测两个过渡。使用所描述的程序可以鉴定出总共100种分析物(方法I中为91种碱性,方法II中为9种酸性)。在30个测试的空白尿液样本中未观察到干扰。所有分析物均达到了RMPL,范围从芬太尼1 ng / mL到γ-羟基丁酸酯(GHB)的10μg/ mL不等。使用相同的30个尿液样品评估基质效应(ME),其范围从四氮p的90%到11-nor-9-羧基-四氢大麻酚(THC-COOH)的> 6,000%。对于绝大多数分析物,ME的相对标准偏差低于25%。 9例DFC确诊病例的尿液标本结果始终为阴性,但开给受害者的药物除外。用已开发的程序对24个尿液样本进行重新分析,并在常规临床毒理学分析期间筛查结果为阳性,证实了常规发现。在单次口服多西拉敏(30毫克)后的排泄研究中,可以从一名年轻的女性志愿者的尿液样本中检测母体药物及其非代谢产物达10天。开发的程序可以对DFC病例中几乎所有推荐的分析物进行尿液样本的选择性和灵敏筛选。

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