Amgen Inc., 1201 Amgen Court West, Seattle, WA 98119-3105, USA.
J Immunol Methods. 2013 Jul 31;393(1-2):70-3. doi: 10.1016/j.jim.2013.03.011. Epub 2013 Apr 6.
Bioanalytical support of discovery programs for human monoclonal antibody therapies involves quantitation by immunoassay. Historically, preclinical samples have been analyzed by the traditional Enzyme-Linked Immuno-Sorbent Assay (ELISA). We investigated transferring our generic ELISA for quantitating human IgG constructs in preclinical serum samples to an automated microfluidics immunoassay platform based on nanoscale streptavidin bead columns. Transfer of our immunoassay to the automated platform resulted in not only the anticipated reduction in analysts' time required for manual manipulation (ELISA) but also a substantial increase in the dynamic range of the immunoassay. The generic nature and wide dynamic range of this automated microcolumn immunoassay permit bioanalytical support of novel therapeutic candidates without the need to develop new, specific assay reagents and minimize the chances that sample reassays will be required due to out of range concentration results. Improved process efficiencies and enhanced workflow during the analysis of preclinical PK samples that enable high throughput assessment of a human monoclonal antibody lead in early discovery programs.
生物分析支持人类单克隆抗体治疗的发现计划,涉及免疫测定的定量分析。从历史上看,临床前样本是通过传统的酶联免疫吸附测定(ELISA)进行分析的。我们研究了将我们通用的 ELISA 从临床前血清样本中定量测定人 IgG 构建体转移到基于纳米级链霉亲和素珠柱的自动化微流控免疫分析平台。将我们的免疫测定转移到自动化平台不仅预期减少了分析人员进行手动操作(ELISA)所需的时间,而且还大大增加了免疫测定的动态范围。这种自动化微柱免疫分析的通用性和宽动态范围允许对新型治疗候选物进行生物分析支持,而无需开发新的、特定的检测试剂,并最大限度地减少由于浓度结果超出范围而需要重新检测样品的可能性。改进的工艺效率和增强的工作流程,使我们能够在早期发现计划中高通量评估人类单克隆抗体先导药物,从而在临床前 PK 样本分析中得到了改善。