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化学偶联技术制备抗体药物偶联物的工艺开发概述。

An overview of process development for antibody-drug conjugates produced by chemical conjugation technology.

作者信息

Matsuda Yutaka, Mendelsohn Brian A

机构信息

Research Institute for Bioscience Products & Fine Chemicals, Ajinomoto Co Inc., 1-1 Suzuki-cho, Kawasaki-ku, Kawasaki 210-8681, Japan.

Process Development & Tech Transfer, Ajinomoto Bio-Pharma Services, 11040 Roselle Street, San Diego, CA 92121, United States.

出版信息

Expert Opin Biol Ther. 2021 Jul;21(7):963-975. doi: 10.1080/14712598.2021.1846714. Epub 2020 Dec 1.

Abstract

: We discuss chemical conjugation strategies for antibody-drug conjugates (ADCs) from an industrial perspective and compare three promising chemical conjugation technologies to produce site-specific ADCs.: Currently, nine ADCs are commercially approved and all are produced by chemical conjugation technology. However, seven of these ADCs contain a relatively broad drug distribution, potentially limiting their therapeutic indices. In 2019, the first site-specific ADC was launched on the market by Daiichi-Sankyo. This achievement, and an analysis of clinical trials over the last decade, indicates that current industrial interest in the ADC field is shifting toward site-specific conjugation technologies. From an industrial point of view, we aim to provide guidance regarding established conjugation methodologies that have already been applied to scale-up stages. With an emphasis on highly productive, scalable, and synthetic process robustness, conjugation methodologies for ADC production is discussed herein.: All three chemical conjugation technologies described in this review have various advantages and disadvantages, therefore drug developers can utilize these depending on their biological and/or protein targets. The future landscape of the ADC field is also discussed.

摘要

我们从工业角度讨论抗体药物偶联物(ADC)的化学偶联策略,并比较三种有前景的化学偶联技术以生产位点特异性ADC。目前,有九种ADC已获商业批准,且均通过化学偶联技术生产。然而,其中七种ADC的药物分布相对较广,这可能会限制它们的治疗指数。2019年,第一类位点特异性ADC由第一三共公司推向市场。这一成果以及对过去十年临床试验的分析表明,目前ADC领域的行业兴趣正转向位点特异性偶联技术。从工业角度出发,我们旨在为已应用于扩大规模阶段的既定偶联方法提供指导。本文重点讨论了具有高生产率、可扩展性和合成过程稳健性的ADC生产偶联方法。本综述中描述的所有三种化学偶联技术都有各自的优缺点,因此药物研发人员可根据其生物学和/或蛋白质靶点加以利用。文中还讨论了ADC领域的未来前景。

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