寡核苷酸合成
寡核苷酸
模块化设计
药品
过程(计算)
组合化学
计算机科学
生化工程
药物发现
计算生物学
化学
工程类
药理学
医学
生物
DNA
生物化学
操作系统
作者
Dominik Altevogt,Isaiah Cedillo,Corrine Curtis,Louis J. Diorazio,J. Faber,Michael T. Jones,Alex Telford,Gillian Turner,Christian Wetter
标识
DOI:10.1021/acs.oprd.3c00303
摘要
High Resolution Image Download MS PowerPoint Slide Synthetic therapeutic oligonucleotide drug substances are commonly manufactured using the same basic unit operations, i.e., solid phase oligonucleotide synthesis, cleavage and deprotection, purification, and isolation. The platform nature of oligonucleotide drug substance manufacturing provides opportunities to optimize process development, streamline process validation, and expedite regulatory submissions. In this publication, we discuss a modular approach to platform strategies for synthetic oligonucleotide drug substances, the opportunities associated with the application of platform knowledge, and how such information could be presented in regulatory filings.
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