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首页> 外文期刊>Journal of Analytical Toxicology >Comparison of EMIT II, CEDIA, and DPC RIA assays for the detection of lysergic acid diethylamide in forensic urine samples.
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Comparison of EMIT II, CEDIA, and DPC RIA assays for the detection of lysergic acid diethylamide in forensic urine samples.

机译:EMIT II,CEDIA和DPC RIA分析在法医尿液样品中麦角酸二乙酰胺检测中的比较。

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摘要

In an effort to determine a practical, efficient, and economical alternative for the use of a radioimmunoassay (RIA) for the detection of lysergic acid diethylamide (LSD) in human urine, the performance of two photometric immunoassays (Dade Behring EMIT II and Microgenics CEDIA) and the Diagnostics Products Corp. (DPC) RIA were compared. Precision, accuracy, and linearity of the 3 assays were determined by testing 60 replicates (10 for RIA) at 5 different concentrations below and above the 500-pg/mL LSD cut-off. The CEDIA and RIA exhibited better accuracy and precision than the EMIT II immunoassay. In contrast, the EMIT II and CEDIA demonstrated superior linearity r2 = 0.9809 and 0.9540, respectively, as compared with the RIA (r2 = 0.9062). The specificity of the three assays was assessed using compounds that have structural and chemical properties similar to LSD, common over-the-counter products, prescription drugs and some of their metabolites, and other drugs of abuse. Of the 144 compounds studied, the EMIT II cross-reacted with twice as many compounds as did the CEDIA and RIA. Specificity was also assessed in 221 forensic human urine specimens that previously screened positive for LSD by the EMIT II assay. Of these, only 11 tested positive by CEDIA, and 3 were positive by RIA. This indicated a comparable specificity performance between CEDIA and RIA. This also was consistent with a previously reported high false-positive rate of EMIT II (low specificity). Each of the immunoassays correctly identified LSD in 23 out of 24 human urine specimens that had previously been found to contain LSD by gas chromatography-mass spectrometry at a cut-off concentration of 200 pg/mL. The CEDIA exhibited superior precision, accuracy, and decreased cross-reactivity to compounds other than LSD as compared with the EMIT II assay and does not necessitate the handling of radioactive materials.
机译:为了确定一种实用,有效和经济的替代方法,以使用放射免疫测定法(RIA)检测人尿中的麦角酸二乙酰胺(LSD),两种光度免疫测定法(Dade Behring EMIT II和Microgenics CEDIA)的性能)和Diagnostics Products Corp.(DPC)的RIA进行了比较。通过在500pg / mL LSD临界值以下和以上的5种不同浓度下测试60个重复样品(RIA为10个样品)来确定3种测定的精密度,准确性和线性。与EMIT II免疫测定法相比,CEDIA和RIA表现出更好的准确性和精密度。相比之下,与RIA(r2 = 0.9062)相比,EMIT II和CEDIA分别显示出优异的线性度r2 = 0.9809和0.9540。使用具有与LSD相似的结构和化学特性的化合物,常见的非处方产品,处方药及其某些代谢产物以及其他滥用药物,评估了这三种测定的特异性。在研究的144种化合物中,EMIT II与CEDIA和RIA的化合物发生了两倍的交叉反应。还对先前通过EMIT II分析筛查LSD阳性的221个法医人类尿液样本进行了特异性评估。其中,只有11个通过CEDIA测试呈阳性,而3个通过RIA呈阳性。这表明CEDIA和RIA之间具有相当的特异性表现。这也与先前报道的EMIT II假阳性率高(特异性低)相符。每种免疫测定法都正确鉴定了24种人类尿液样本中的23种LSD,这些样本先前已通过气相色谱-质谱法以200 pg / mL的截断浓度被发现含有LSD。与EMIT II分析法相比,CEDIA具有更高的精密度,准确性和与LSD以外的化合物的交叉反应性降低,并且无需处理放射性物质。

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