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从酶联免疫吸附测定法(ELISA)转换至Gyrolab™平台:一种新型通用试剂无需更换关键试剂。

Platform switching from ELISA to Gyrolab™: a novel generic reagent omits the need to change critical reagents.

作者信息

Jordan Gregor, Moheysen-Zadeh Miriam, Heinrich Julia, Staack Roland F

机构信息

Roche Pharma Research & Early Development (pRED), Pharmaceutical Sciences, Global DMPK & Bioanalytical R&D, Roche Innovation Center Munich, Germany.

出版信息

Bioanalysis. 2016 Apr;8(8):807-14. doi: 10.4155/bio-2015-0011. Epub 2016 Mar 15.

Abstract

During development of biotherapeutics, availability of specific assay reagents is usually limited. The possibility to switch from one ligand binding assay technology to another, while using the same reagents, would be desirable. Here, we report on an Alexa647(®)-labeled monoclonal antibody against digoxigenin (mAb-Alexa647(®)) that enables the detection of digoxigenylated analyte-specific ELISA reagents by Gyrolab(™). In an analysis of non-monoclonal antibody (mAb) and mAb drugs, this approach maintained the dynamic range, accuracy and precision of the standard Gyrolab™ approach using analyte-specific Alexa647(®)-labeled Ab. In a rat PK study, results of our approach, standard Gyrolab™ and ELISA were comparable, with difference values within the incurred sample reanalysis acceptance criteria. Therefore, mAb-Alexa647(®) enables an easy switch between ELISA and Gyrolab™, providing an effective way to benefit from both platforms.

摘要

在生物治疗药物的研发过程中,特定检测试剂的可用性通常有限。若能在使用相同试剂的情况下,从一种配体结合检测技术转换至另一种技术,将是非常理想的。在此,我们报告一种抗地高辛配基的Alexa647(®)标记单克隆抗体(mAb-Alexa647(®)),它能够通过Gyrolab(™)检测地高辛配基化的分析物特异性ELISA试剂。在对非单克隆抗体(mAb)和mAb药物的分析中,该方法保持了使用分析物特异性Alexa647(®)标记抗体的标准Gyrolab™方法的动态范围、准确性和精密度。在一项大鼠药代动力学研究中,我们的方法、标准Gyrolab™方法和ELISA的结果具有可比性,差异值在再分析已测样品的接受标准范围内。因此,mAb-Alexa647(®)能够在ELISA和Gyrolab™之间轻松转换,提供了一种从两个平台都能获益的有效方法。

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