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新型电化学发光(ECL)及生物传感器技术的应用。

Applications for the new electrochemiluminescent (ECL) and biosensor technologies.

作者信息

Swanson S J, Jacobs S J, Mytych D, Shah C, Indelicato S R, Bordens R W

机构信息

Schering-Plough Research Institute, Kenilworth, NJ 07033, USA.

出版信息

Dev Biol Stand. 1999;97:135-47.

Abstract

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.

摘要

在先灵葆雅公司,生物传感器和电化学发光(ECL)检测正取代酶联免疫吸附测定(ELISA),成为监测细胞因子水平以及在细胞因子治疗期间检测抗细胞因子抗体反应的首选免疫测定方法。这些新检测方法提高了灵敏度,并且与生物学检测有更好的相关性。正在采用使用BIACORE 2000(瑞典乌普萨拉的BIACORE公司)的生物传感器检测来支持临床前和临床试验,以检测能够结合IL-10和IL-4的抗体。使用生物传感器检测的显著优势在于,实时且无标记检测可提高通量,并直接检测结合相互作用,从而能够检测ELISA无法检测到的低亲和力抗体。我们已采用使用ORIGEN分析仪(美国马里兰州盖瑟斯堡的IGEN公司)的ECL检测来取代现有的ELISA,用于定量血清IL-10和血清干扰素α水平,该检测更灵敏,且受基质效应的影响较小。本文描述了这些检测方法验证过程中获得的数据。

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