BioMedicine Design, Pfizer Inc. Andover, MA 01810, USA.
Bioanalysis. 2020 Sep;12(18):1279-1293. doi: 10.4155/bio-2020-0091. Epub 2020 Sep 18.
Drug interference poses great analytical challenges for cell-based neutralizing antidrug antibodies (NAb) assay. The work aimed to improve assay drug tolerance through biotin-drug extraction with acid dissociation method optimization and developing new approach. The NAb extraction with biotin-drug extraction with acid dissociation approach has been optimized by reducing biotinylated drug leaching and improving NAb elution efficiency, resulting in drug tolerance of up to 160 μg/ml. To circumvent the low acid elution efficiency of NAb from drug, a novel drug depletion approach was developed, which combined acid dissociation and drug targeted crosslinked capture, achieved drug tolerance up to 400 μg/ml. At last, a strategy workflow for sample pretreatment approach selection and optimization was established for improving drug tolerance of NAb assay. We demonstrated that reduced biotinylated drug leaching and the high NAb elution efficiency was critical for improving assay drug tolerance. Drug depletion offers an alternative approach to overcome low NAb elution efficiency.
药物干扰对基于细胞的中和性抗药物抗体(NAb)分析检测构成了巨大挑战。本工作旨在通过优化酸解离法的生物素-药物提取和开发新方法来提高检测药物耐受性。通过减少生物素化药物浸出和提高 NAb 洗脱效率,优化了基于酸解离的 NAb 生物素提取方法,从而使药物耐受度高达 160μg/ml。为了避免药物对 NAb 的低酸洗脱效率,开发了一种新的药物耗尽方法,该方法结合了酸解离和药物靶向交联捕获,使药物耐受度高达 400μg/ml。最后,建立了用于改善 NAb 分析检测药物耐受性的样品预处理方法选择和优化策略工作流程。我们证明,减少生物素化药物浸出和提高 NAb 洗脱效率对于提高检测药物耐受性至关重要。药物耗尽提供了一种克服低 NAb 洗脱效率的替代方法。