生物分析
生物制药
模式
化学
寡核苷酸
色谱法
计算生物学
生物化学
生物
生物技术
DNA
社会科学
社会学
作者
Srikanth Kotapati,Madhura Deshpande,Aarti Jashnani,Dharam Thakkar,Hong-Wu Xu,Gavin Dollinger
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2021-05-17
卷期号:13 (11): 931-954
被引量:19
标识
DOI:10.4155/bio-2021-0009
摘要
Ligand-binding assay (LBA) and LC–MS have been the preferred bioanalytical techniques for the quantitation and biotransformation assessment of various therapeutic modalities. This review provides an overview of the applications of LBA, LC–MS/MS and LC–HRMS for the bioanalysis of complex protein therapeutics including antibody–drug conjugates, fusion proteins and PEGylated proteins as well as oligonucleotide therapeutics. The strengths and limitations of LBA and LC–MS, along with some guidelines on the choice of appropriate bioanalytical technique(s) for the bioanalysis of these therapeutic modalities are presented. With the discovery of novel and more complex therapeutic modalities, there is an increased need for the biopharmaceutical industry to develop a comprehensive bioanalytical strategy integrating both LBA and LC–MS.
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