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无标记多孔硅免疫传感器在盲法临床研究中对阿片类药物的广泛检测及与商业分析化学技术的结果比较。

Label-free porous silicon immunosensor for broad detection of opiates in a blind clinical study and results comparison to commercial analytical chemistry techniques.

机构信息

Department of Biomedical Engineering, University of Rochester, Rochester, New York, USA.

出版信息

Anal Chem. 2010 Dec 1;82(23):9711-8. doi: 10.1021/ac101804s. Epub 2010 Nov 9.

Abstract

In this work, we evaluate for the first time the performance of a label-free porous silicon (PSi) immunosensor assay in a blind clinical study designed to screen authentic patient urine specimens for a broad range of opiates. The PSi opiate immunosensor achieved 96% concordance with liquid chromatography-mass spectrometry/tandem mass spectrometry (LC-MS/MS) results on samples that underwent standard opiate testing (n = 50). In addition, successful detection of a commonly abused opiate, oxycodone, resulted in 100% qualitative agreement between the PSi opiate sensor and LC-MS/MS. In contrast, a commercial broad opiate immunoassay technique (CEDIA) achieved 65% qualitative concordance with LC-MS/MS. Evaluation of important performance attributes including precision, accuracy, and recovery was completed on blank urine specimens spiked with test analytes. Variability of morphine detection as a model opiate target was <9% both within-run and between-day at and above the cutoff limit of 300 ng mL(-1). This study validates the analytical screening capability of label-free PSi opiate immunosensors in authentic patient samples and is the first semiquantitative demonstration of the technology's successful clinical use. These results motivate future development of label-free PSi technology to reduce complexity and cost of diagnostic testing particularly in a point-of-care setting.

摘要

在这项工作中,我们首次评估了无标记多孔硅(PSi)免疫传感器分析在一项旨在筛选广泛阿片类药物的真实患者尿液标本的盲法临床研究中的性能。PSi 阿片类免疫传感器在接受标准阿片类药物检测的(n=50)样品上与液相色谱-串联质谱/质谱(LC-MS/MS)结果达到 96%的一致性。此外,对一种常用的阿片类药物,羟考酮的成功检测导致 PSi 阿片类传感器和 LC-MS/MS 之间达到 100%的定性一致。相比之下,商业广泛阿片类免疫分析技术(CEDIA)与 LC-MS/MS 的定性一致性达到 65%。在空白尿液标本中用测试分析物进行加标,对包括精密度、准确度和回收率在内的重要性能属性进行了评估。在 300ng mL(-1)以上的截止值处,吗啡检测作为模型阿片类目标的变异性在运行内和日间均<9%。本研究验证了无标记 PSi 阿片类免疫传感器在真实患者样本中的分析筛选能力,是该技术在临床应用中首次成功的半定量证明。这些结果推动了无标记 PSi 技术的进一步发展,以降低诊断测试的复杂性和成本,特别是在即时护理环境中。

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