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离子液体作为治疗性蛋白质制剂的稳定剂:胰岛素和单克隆抗体综述

Ionic liquids as stabilisers of therapeutic protein formulations: a review of insulin and monoclonal antibodies.

作者信息

Tien Samuel, Kayser Veysel

机构信息

Sydney School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006 Australia.

出版信息

Biophys Rev. 2024 Dec 26;17(1):89-101. doi: 10.1007/s12551-024-01261-y. eCollection 2025 Feb.

DOI:10.1007/s12551-024-01261-y
PMID:40060006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11885717/
Abstract

Therapeutic proteins such as insulin and monoclonal antibodies (mAbs) have become an essential part of the modern healthcare system and play a crucial role in the treatment of various diseases including cancer and autoimmune disorders. However, their long-term stability is a significant concern, affecting efficacy, shelf-life, and safety. Ionic liquids (ILs) have emerged as promising additives to enhance protein stability and address the aforementioned issues. Indeed, recent studies indicate that biocompatible ILs, particularly choline-based ILs, have significant potential to improve stability while preserving proteins' functionality. For instance, choline valinate has been shown to increase the melting temperature of insulin by almost 13 °C (Judy and Kishore Biochimie 207:20-32, 2023), while choline dihydrogen phosphate has increased the melting temperature of trastuzumab by over 21 °C (Reslan et al. Chem Commun 54:10622-10625, 2018). However, it is worth noting that the use of some ILs introduces a complex trade-off: while they can increase thermal stability, they may also promote protein unfolding, thereby reducing conformational stability. Moreover, selecting the most suitable IL and its optimal concentration is challenging, as different protein formulations may exhibit varying effects. This review provides a comprehensive overview of the existing literature on ILs as stabilisers for insulin and mAbs, documenting specific IL-protein combinations and conditions to identify potential future stabilising agents for biologics in general.

摘要

胰岛素和单克隆抗体(mAbs)等治疗性蛋白质已成为现代医疗体系的重要组成部分,在包括癌症和自身免疫性疾病在内的各种疾病治疗中发挥着关键作用。然而,它们的长期稳定性是一个重大问题,会影响疗效、保质期和安全性。离子液体(ILs)已成为有前景的添加剂,可增强蛋白质稳定性并解决上述问题。事实上,最近的研究表明,生物相容性离子液体,特别是胆碱基离子液体,在保持蛋白质功能的同时,具有显著的提高稳定性的潜力。例如,已证明缬氨酸胆碱可使胰岛素的熔点提高近13℃(朱迪和基肖尔,《生物化学》207:20 - 32,2023),而磷酸二氢胆碱可使曲妥珠单抗的熔点提高超过21℃(雷斯兰等人,《化学通讯》54:10622 - 10625,2018)。然而,值得注意的是,使用某些离子液体存在复杂的权衡:虽然它们可以提高热稳定性,但也可能促进蛋白质展开,从而降低构象稳定性。此外,选择最合适的离子液体及其最佳浓度具有挑战性,因为不同的蛋白质制剂可能表现出不同的效果。本综述全面概述了关于离子液体作为胰岛素和单克隆抗体稳定剂的现有文献,记录了特定的离子液体 - 蛋白质组合和条件,以确定未来一般生物制品潜在的稳定剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/11885717/792cba2ba0c4/12551_2024_1261_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/11885717/bebd6957452c/12551_2024_1261_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/11885717/792cba2ba0c4/12551_2024_1261_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/11885717/bebd6957452c/12551_2024_1261_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/11885717/792cba2ba0c4/12551_2024_1261_Fig2_HTML.jpg

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