毛细管电泳
寡核苷酸
生物分析
分离法
计算生物学
核酸
生化工程
药物开发
化学
药物发现
纳米技术
设计质量
计算机科学
组合化学
鉴定(生物学)
表征(材料科学)
分辨率(逻辑)
药品
适体
脱氧核酶
色谱分离
作者
Tímea Dérerová,Zuzana Kadlecová,Květa Kalíková
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2025-09-17
卷期号:17 (18): 1165-1180
被引量:1
标识
DOI:10.1080/17576180.2025.2565141
摘要
Therapeutic oligonucleotides are an emerging class of drugs designed for gene expression modulation. The increasing number of clinical trials and currently expanding market is facilitating further integration and accessibility of these therapeutics. A crucial step in drug development involves reliable analytical tools for characterization and quality control. For clinical applications, oligonucleotides must be separated and purified to ensure regulatory compliance. However, their analysis represents a complex bioanalytical challenge, grounded in their complex impurity profiles. Chemical stability and binding affinity of oligonucleotide-based therapeutics are enhanced during synthesis by extensive modifications, inducing formation of various synthesis failures or truncated sequences. Furthermore, meeting current guidelines or addressing manufacturing scale-up strategies remains challenging as each oligonucleotide typically necessitates a custom analytical protocol. Here, we provide an overview of the most recent advances in separation methods, including various chromatography methods and capillary electrophoresis for nucleic acid-based therapeutics.
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