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配体结合分析:使用单一供应商支持的平台的风险。

Ligand-binding assays: risk of using a platform supported by a single vendor.

作者信息

Yohrling Jennifer

机构信息

Clinical Pharmacology Sciences, Centocor Research & Development, Inc., 200 Great Valley Parkway, Malvern, PA 19355, USA.

出版信息

Bioanalysis. 2009 Jun;1(3):629-36. doi: 10.4155/bio.09.46.

Abstract

The use of biological reagents in ligand-binding assays (LBAs) presents inherent challenges when measuring the concentration of large molecules in complex matrices. As a result, there are relatively few platforms that provide the accuracy, precision and robustness needed to determine the concentration of macromolecular therapies and biomarkers, and demonstrate the presence or absence of an immune response. Some bioanalytical laboratories use only one LBA platform to reduce costs, increase efficiency and maintain optimal assay performance. However, the business and regulatory risks of using a single platform supported by only one vendor should be considered. This article summarizes the immunological methods used to support bioanalysis for large molecules that are supported by a single vendor, the benefits of being dedicated to a single platform for bioanalysis used for regulatory filings, the costs associated with restructuring if an immunoassay platform is discontinued and recommendations to mitigate risk when using LBAs in drug development. The experience with the recent discontinuation of the BioVeris™ electrochemiluminescent-based platform is discussed.

摘要

在复杂基质中测量大分子浓度时,在配体结合分析(LBA)中使用生物试剂存在一些固有挑战。因此,能够提供测定大分子疗法和生物标志物浓度所需的准确性、精密度和稳健性,并证明免疫反应存在与否的平台相对较少。一些生物分析实验室仅使用一个LBA平台,以降低成本、提高效率并保持最佳分析性能。然而,应考虑使用仅由一家供应商支持的单一平台所带来的商业和监管风险。本文总结了用于支持由单一供应商提供的大分子生物分析的免疫学方法、致力于用于监管申报的单一生物分析平台的益处、如果免疫分析平台停止使用所涉及的重组成本,以及在药物开发中使用LBA时降低风险的建议。文中还讨论了近期BioVeris™基于电化学发光的平台停用的相关经验。

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