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利用工作场所药物检测计划中的尿液,评估丁丙诺啡 LUCIO 免疫分析法与 GC-MS 的检测效果。

Evaluation of buprenorphine LUCIO immunoassay versus GC-MS using urines from a workplace drug testing program.

机构信息

Faculty of Pharmaceutical Science of Ribeirão Preto, São Paulo University, Cafè Avenue, Ribeirão Preto 14040-903, São Paulo, Brazil.

出版信息

J Anal Toxicol. 2013 Apr;37(3):175-8. doi: 10.1093/jat/bkt006. Epub 2013 Feb 13.

Abstract

The buprenorphine (BUP) LUCIO Nal Von Minden screening assay was evaluated. Urine samples from subjects enrolled in a workplace drug testing program were screened according to the manufacturer's instruction using a Roche COBAS Integra 800 analyser. For gas chromatography-mass spectrometry (GC-MS) confirmatory analysis, samples were submitted to enzymatic hydrolysis with β-glucuronidase and mixed-mode solid-phase extraction. Imprecision (coefficient of variation) for 3.0, 7.0, and 13.0 ng/mL calibrators varied within 2.8-8.7 intra-day (n = 20) and 7.7-8.6 inter-day (n = 19). Inaccuracy (bias) was between -5.6-30.5 intra-day and -13.2-4.2 inter-day. At the 5 ng/mL cut-off, the immunoassay showed 100% sensitivity and 88% specificity, with an overall agreement of 94% between immunoassay and GC-MS. Raising the cut-off to 10 ng/mL provided an identical overall agreement between immunoassay and GC-MS (94%), despite the decrease in sensitivity (90%) and the increase in specificity (100%). According to these results, the BUP LUCIO Nal Von Minden screening assay provides adequate sensitivity and specificity for BUP screening in urine samples using a cut-off concentration of 5 ng/mL.

摘要

对丁丙诺啡(BUP)LUCIO Nal Von Minden 筛查检测试剂盒进行了评估。根据制造商的说明,使用罗氏 COBAS Integra 800 分析仪对参加工作场所药物测试计划的受试者的尿液样本进行了筛查。对于气相色谱-质谱(GC-MS)确证分析,将样品提交给β-葡萄糖醛酸酶和混合模式固相萃取进行酶解。3.0、7.0 和 13.0 ng/mL 校准品的精密度(变异系数)在 20 个日内和 19 个日际内的变化范围为 2.8-8.7%和 7.7-8.6%。准确度(偏差)在 20 个日内为-5.6-30.5%,在 19 个日际内为-13.2-4.2%。在 5ng/mL 截止值下,免疫测定的灵敏度为 100%,特异性为 88%,免疫测定和 GC-MS 之间的总符合率为 94%。将截止值提高到 10ng/mL 时,免疫测定和 GC-MS 之间的总符合率仍为 94%(尽管灵敏度下降(90%),特异性提高(100%))。根据这些结果,BUP LUCIO Nal Von Minden 筛查检测试剂盒在使用 5ng/mL 截止值时,对尿液样本中的 BUP 筛查具有足够的灵敏度和特异性。

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