生物分析
多路复用
体内
药代动力学
免疫分析
化学
药理学
药物发现
色谱法
计算生物学
医学
生物信息学
生物
生物化学
免疫学
抗体
生物技术
作者
Nicole Woodbury,Eric Bald,Brian Geist,Tong‐Yuan Yang
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2019-12-01
卷期号:11 (24): 2251-2268
被引量:4
标识
DOI:10.4155/bio-2019-0147
摘要
Aim: Meso Scale Discovery U-PLEX® provides an opportunity to develop multiplexed pharmacokinetic (PK) immunoassays. Two case studies demonstrate the utility of multiplexed PK methods. Materials & methods: Development of PK ligand-binding assays quantify of nonclinical plasma concentrations of a biotherapeutic that has degraded due to in vivo biotransformation, and clinical serum concentrations from two biotherapeutics spiked into a single sample. Results: Data from multiplexed U-PLEX PK methods are comparable to results from single-readout streptavidin Meso Scale Discovery gold PK methods. Multiplex measurement of a nonclinical study showed acceptable performance for accuracy, precision and dilutional linearity while a clinical study additionally passed selectivity, specificity and stability. Conclusion: Regulated, validation-ready multiplex PK methods for both nonclinical and clinical studies allow opportunities for high-throughput bioanalysis.
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