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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >A thin-film interferometry-based label-free immunoassay for the detection of daratumumab interference in serum protein electrophoresis
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A thin-film interferometry-based label-free immunoassay for the detection of daratumumab interference in serum protein electrophoresis

机译:基于薄膜干涉测定的无标记免疫测定,用于检测血清蛋白电泳的达拉穆克干扰

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Background: Daratumumab (DARA) is a fully human anti-CD38 IgG1-kappa monoclonal antibody drug used in the treatment of multiple myeloma (MM). While serum protein electrophoresis (SPEP) is an important assay for diagnosis and monitoring of patients with MM, DARA can appear in the gamma-region as a single band and interfere with the interpretation of SPEP results. An approach to detect the interference is measuring the quantity of DARA in serum samples and assessing its impact on SPEP results. Immunoassays based on label-free technologies, i.e. label-free immunoassays (LFIA's), can achieve real-time immunometric measurement without attaching a reporter molecule (enzyme, fluorophore, etc.) to the immunocomplex. The recorded time course of the immunocomplex formation allows for quantitation on initial binding rate, which facilitates rapid measurement within a few minutes. Based on the thin-film interferometry (TFI) technology, a rapid LFIA was established for the quantitation of DARA in serum samples.
机译:背景:达拉姆姆(Dara)是一种用于治疗多发性骨髓瘤(MM)的全人抗CD38 IgG1-Kappa单克隆抗体药物。虽然血清蛋白电泳(SPEP)是用于诊断和监测MM患者的重要测定,但DARA可以作为单个频段出现在γ-区域中,并干扰SPEP结果的解释。检测干扰的方法是测量血清样品中Dara的数量,并评估其对SPEP结果的影响。基于无标签技术的免疫测定,即无标签免疫测定(LFIA),可以达到实时免疫测量,而无需将记者分子(酶,荧光团等)附着到免疫激活。免疫复合物形成的记录时间过程允许定量初始结合速率,这有利于在几分钟内快速测量。基于薄膜干涉测量(TFI)技术,建立了一种快速的LFIa,用于定量血清样品中的达拉。

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