新型电化学发光(ECL)和生物传感器技术的应用。

S J Swanson, S J Jacobs, D Mytych, C Shah, S R Indelicato, R W Bordens
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引用次数: 0

摘要

生物传感器和电化学发光(ECL)检测正在取代先灵葆雅的酶联免疫吸附测定(elisa),成为在细胞因子治疗期间监测细胞因子水平和检测抗细胞因子抗体反应的首选免疫检测方法。这些新的检测方法提供了更高的灵敏度和与生物检测方法更好的相关性。使用BIACORE 2000 (BIACORE, Uppsala, Sweden)的生物传感器检测被用于支持能够结合IL-10和IL-4的抗体的临床前和临床试验。当使用生物传感器检测时,显著的优点是实时和无标签检测允许增加吞吐量和直接检测结合相互作用,从而可以检测ELISA无法检测到的低亲和力抗体。我们已经实施了使用ORIGEN分析仪(IGEN, Gaithersburg, MD)的ECL测定,以取代现有的用于定量血清IL-10和血清干扰素α水平的elisa,其灵敏度更高,受基质效应的影响更小。本文描述了这些试验验证过程中获得的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Applications for the new electrochemiluminescent (ECL) and biosensor technologies.

Biosensor and electrochemiluminescent (ECL) assays are replacing enzyme-linked immunosorbent assays (ELISAs) at Schering-Plough as immunoassays of choice to monitor cytokine levels and detect anti-cytokine antibody responses during cytokine therapy. These new assays provide increased sensitivity and a better correlation with biological assays. Biosensor assays using the BIACORE 2000 (BIACORE, Uppsala, Sweden) are being adopted to support preclinical and clinical trials for the detection of antibodies capable of binding to IL-10 and IL-4. Significant advantages when using a biosensor assay are that real-time and label-free detection permit increased throughput and direct detection of binding interactions which enables detection of low affinity antibodies that are not detected by ELISA. The ECL assays using the ORIGEN Analyser (IGEN, Gaithersburg, MD) that we have implemented to replace existing ELISAs for quantification of serum IL-10 and serum interferon alfa levels are more sensitive and less subject to matrix effects. Data obtained during the validation of these assays are described.

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