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首页> 外文期刊>Journal of Analytical Toxicology >Improved screen and confirmation test of 7-aminoflunitrazepam in urine specimens for monitoring flunitrazepam (Rohypnol) exposure.
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Improved screen and confirmation test of 7-aminoflunitrazepam in urine specimens for monitoring flunitrazepam (Rohypnol) exposure.

机译:改进尿液标本中7-氨基氟硝西epa的筛查和确认测试,以监测氟尼西epa(Rohypnol)暴露。

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摘要

Confirmed and alleged misuses of flunitrazepam (FM2, Rohypnol) have brought about serious interest in the development of an analytical methodology that can be effectively used for preliminary screen and confirmatory test of FM2 (or its metabolites) in urine specimens under high-volume settings. Reported methods do not serve this need well for the following reasons: (1) common benzodiazepine (BZ) immunoassays (IAs) have broad cross-reactivities toward widely prescribed BZs (and their metabolites) and are therefore likely to generate an unacceptable number of false positives and (2) because FM2 is typically used at low doses (1-4 mg), IAs with low cross-reactivities toward FM2 (and its metabolites) are likely to generate false-negative results. In this current study, a familiar and effective two-step IA/gas chromatography-mass spectrometry (GC-MS) approach is successfully developed and applied to clinical specimens. Cross-reacting characteristics of the following BZ IAs toward various BZs (and their metabolites) are evaluated focusing on their effectiveness in serving as the preliminary test reagent in a two-step testing protocol: TDx, Beckman, CEDIA, Roche Cobas Integra, Emit II Plus, and Cozart ELISA. Although other IAs show broad cross-reactivities toward various BZs and their metabolites, diazepam is the only non-FM2 derived compound that exhibits noticeable cross-reactivity toward Cozart ELISA reagent. Cross-reactivity data and data derived from studies conducted on a limited number of clinical specimens demonstrate that, when used to monitor FM2 exposure in a large population group (including those exposed to other BZs), Cozart ELISA has the potential of being as effective as (or better than) those currently used in various workplace drug-testing programs for monitoring respectively targeted drugs. Data derived from this study further suggest that 50 ng/mL apparent 7-aminoflunitrazepam (Cozart ELISA) and 30 ng/mL free 7-aminoflunitrazepam (GC-MS) are potentially effective preliminary test and confirmation test cut-offs. To maximize efficiency, it is further suggested that urine specimens are first diluted by a factor of 5 for the preliminary test in which a 10-ng/mL 7-aminoflunitrazepam standard is used as the assay's cut-off standard.
机译:已确认和据称滥用氟尼西epa(FM2,Rohypnol)引起了对分析方法开发的极大兴趣,该分析方法可有效用于大体积设置下尿液样本中FM2(或其代谢物)的初步筛选和确证测试。报告的方法由于以下原因不能很好地满足这种需求:(1)普通的苯二氮卓(BZ)免疫测定法(IAs)对广泛处方的BZs(及其代谢产物)具有广泛的交叉反应性,因此很可能产生不可接受的错误数量阳性和(2),因为FM2通常以低剂量(1-4毫克)使用,对FM2(及其代谢物)交叉反应性低的IAs可能会产生假阴性结果。在本研究中,成功​​开发了一种熟悉且有效的两步IA /气相色谱-质谱(GC-MS)方法,并将其应用于临床标本。评估以下BZ IA对各种BZ(及其代谢物)的交叉反应特性,重点在于它们在两步测试规程中作为初步测试试剂的有效性:TDx,Beckman,CEDIA,Roche Cobas Integra,Emit II加号和Cozart ELISA。尽管其他IAs对各种BZ及其代谢物表现出广泛的交叉反应性,但地西epa是唯一一种非FM2衍生的化合物,对Cozart ELISA试剂表现出明显的交叉反应性。交叉反应性数据和对有限数量的临床标本进行的研究得出的数据表明,当用于监测大量人群(包括暴露于其他BZ的人群)中FM2暴露时,Cozart ELISA的有效性与(或优于)目前在各种工作场所药物测试计划中用于监视目标药物的药物。来自这项研究的数据进一步表明,50 ng / mL表观7-氨基氟硝西epa(Cozart ELISA)和30 ng / mL游离7-氨基氟硝西epa(GC-MS)是潜在的有效的初步测试和确认测试的标准。为了最大程度地提高效率,进一步建议将尿液样本稀释5倍以进行初步测试,在该测试中,将10 ng / mL的7-氨基氟硝西standard标准品用作测定的标准品。

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