...
首页> 外文期刊>Forensic science international >Performance characteristics of the Cozart((R)) RapiScan Oral Fluid Drug Testing System for opiates in comparison to ELISA and GC/MS following controlled codeine administration.
【24h】

Performance characteristics of the Cozart((R)) RapiScan Oral Fluid Drug Testing System for opiates in comparison to ELISA and GC/MS following controlled codeine administration.

机译:与受控可待因给药后的ELISA和GC / MS相比,用于鸦片制剂的Cozart(R)RapiScan口服液药物测试系统的性能特征。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Oral fluid is an interesting alternative matrix for drug testing in many environments, including law enforcement, workplace drug testing, and drug treatment facilities. Performance characteristics of the FDA-cleared, qualitative, Cozart((R)) RapiScan Opiate Oral Fluid Drug Testing System (Opiate Cozart((R)) RapiScan System or Opiate CRS) were compared to the semi-quantitative Cozart((R)) Microplate EIA Opiate Oral Fluid Kit (Opiate ELISA) and to gas chromatography/mass spectrometry (GC/MS). The following oral fluid opiate cutoffs were evaluated: the GC/MS limit of quantification (LOQ) of 2.5mg/l; 15microg/l currently used for oral fluid testing in the United Kingdom (UK); 30microg/l (Opiate CRS cutoff); and 40microg/l, the proposed Substance Abuse and Mental Health Services Administration (SAMHSA) cutoff. Subjects provided informed consent to participate in this IRB-approved research and resided on the closed research ward throughout the study. Three oral codeine doses of 60mg/70kg were administered over a 7-day period. After a 3-week break, subjects received three doses of 120mg/70kg within 7 days. Oral fluid specimens ( [Formula: see text] ) were analyzed for codeine (COD), norcodeine (NCOD), morphine (MOR) and normorphine (NMOR) by GC/MS with an LOQ of 2.5microg/l for all analytes. MOR and NMOR were not detected in any sample; 26.5% of the specimens were positive for COD and 13.7% for NCOD. Opiate CRS uses a preset, qualitative cutoff of 10microg/l; this is equivalent to 30microg/l in undiluted oral fluid as the oral fluid collection process involves a 1:3 dilution with buffer. Sensitivity, specificity, and efficiency of Opiate CRS compared to Opiate ELISA were 98.6, 98.1, and 98.2% at a 30microg/l cutoff and 99.0, 96.2, and 96.6% at a 40microg/l cutoff. Compared to the much lower GC/MS LOQ of 2.5microg/l, sensitivity, specificity and efficiency were 66.8, 99.3 and 90.7%. Increasing the GC/MS cutoff to the current UK level yielded performance characteristics of 81.5% (sensitivity), 99.3% (specificity), and 95.4% (efficiency). Using a GC/MS cutoff identical to the preset Opiate CRS cutoff yielded sensitivity, specificity, and efficiency of 88.5, 99.2, and 97.5%, respectively. At the proposed SAMSHA confirmation cutoff of 40microg/l, sensitivity increased with little change in specificity and efficiency (91.3% sensitivity, 98.9% specificity, and 97.5% efficiency). Oral fluid is a suitable matrix for detecting drugs of abuse. Opiate CRS, with a 30microg/l cutoff, is sufficiently sensitive, specific and efficient for oral fluid opiate analysis, performing similarly to Opiate ELISA at the same cutoff, and having performance characteristics >91% when compared to GC/MS at the proposed SAMHSA cutoff.
机译:口服液是在许多环境中进行药物测试的有趣替代基质,包括执法,工作场所药物测试和药物治疗设施。将FDA批准的定性Cozart(R)RapiScan阿片酸盐口服液药物测试系统(Opiate Cozart(R)RapiScan系统或Opiate CRS)的性能特征与半定量Cozart(R)进行比较微孔板EIA阿片类口服液套件(阿片类ELISA)和气相色谱/质谱(GC / MS)。评估了以下口服液鸦片的临界值:GC / MS的定量限(LOQ)为2.5mg / l;英国(UK)当前用于口腔液体测试的15microg / l; 30microg / l(阿片酸盐CRS截止值);和40microg / l(建议的物质滥用和精神卫生服务管理局(SAMHSA)临界值)。受试者提供了知情同意书,以参加该IRB批准的研究,并在整个研究期间居住在封闭的研究病房中。在7天内服用了三剂60mg / 70kg口服可待因。休息3周后,受试者在7天内接受了三剂120mg / 70kg的剂量。通过GC / MS分析了口腔液标本([分子式:正文])中的可待因(COD),去甲可待因(NCOD),吗啡(MOR)和去甲吗啡(NMOR),所有分析物的LOQ为2.5microg / l。在任何样品中均未检测到MOR和NMOR;标本中有26.5%的COD阳性,而NCOD的13.7%。阿片类CRS使用10microg / l的预设定性截止值;这相当于未稀释口腔液中的30microg / l,因为口腔液收集过程涉及用缓冲液按1:3稀释。与阿片类ELISA相比,阿片类CRS的敏感性,特异性和效率在30微克/升临界值下分别为98.6%,98.1和98.2%,在40微克/升临界值下分别为99.0、96.2和96.6%。与低得多的GC / MS LOQ(2.5微克/升)相比,灵敏度,特异性和效率分别为66.8、99.3和90.7%。将GC / MS截止值提高到当前的英国水平会产生81.5%(灵敏度),99.3%(特异性)和95.4%(效率)的性能特征。使用与预设的阿片酸盐CRS截止值相同的GC / MS截止值可分别获得88.5、99.2和97.5%的灵敏度,特异性和效率。在建议的SAMSHA确认截止值为40microg / l时,灵敏度增加,而特异性和效率几乎没有变化(灵敏度分别为91.3%,98.9%和97.5%)。口服液是检测滥用药物的合适基质。具有30microg / l临界值的Opiate CRS对于口服鸦片剂分析具有足够的敏感性,特异性和效率,在相同的临界值下与Opiate ELISA相似,并且在拟议的SAMHSA中与GC / MS相比具有> 91%的性能特征隔断。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号