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用于生物制剂口服递送的合成与生物源材料:从实验室到临床应用

Synthetic and Biogenic Materials for Oral Delivery of Biologics: From Bench to Bedside.

作者信息

Ding Suwan, Alexander Elena, Liang Huiyi, Kulchar Rachel J, Singh Rahul, Herzog Roland W, Daniell Henry, Leong Kam W

机构信息

Department of Biomedical Engineering, Columbia University, 500 West 120th Street, New York, New York 10027, United States.

Department of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, 240 South 40th Street, Philadelphia, Pennsylvania 19104, United States.

出版信息

Chem Rev. 2025 Apr 23;125(8):4009-4068. doi: 10.1021/acs.chemrev.4c00482. Epub 2025 Apr 1.

Abstract

The development of nucleic acid and protein drugs for oral delivery has lagged behind their production for conventional nonoral routes. Over the past decade, the evolution of DNA- and RNA-based technologies combined with the innovation of state-of-the-art delivery vehicles for nucleic acids has brought rapid advancements to the biopharmaceutical field. Nucleic acid therapies have the potential to achieve long-lasting effects, or even cures, by inhibiting or editing genes, which is not possible with conventional small-molecule drugs. However, challenges and limitations must be addressed before these therapies can provide cures for chronic conditions and rare diseases, rather than only offering temporary relief. Nucleic acids and proteins face premature degradation in the acidic, enzyme-rich stomach environment and are rapidly cleared by the liver. To overcome these challenges, various delivery vehicles have been developed to transport therapeutic compounds to the intestines, where the active compounds are released and gut microbiota and mucosal immune system also play an important role. This review provides a comprehensive overview of the promises and pitfalls associated with the oral route of administration of biologics, current delivery systems, applications of orally delivered therapeutics, and the challenges and considerations for translation of nucleic acid and protein therapeutics into clinical practice.

摘要

用于口服给药的核酸和蛋白质药物的研发落后于其用于传统非口服途径的生产。在过去十年中,基于DNA和RNA的技术的发展,以及用于核酸的先进递送载体的创新,给生物制药领域带来了快速进展。核酸疗法有潜力通过抑制或编辑基因实现长效效果甚至治愈疾病,这是传统小分子药物无法做到的。然而,在这些疗法能够治愈慢性病和罕见病而非仅提供暂时缓解之前,必须应对挑战和限制。核酸和蛋白质在酸性、富含酶的胃部环境中会过早降解,并且会被肝脏迅速清除。为克服这些挑战,已开发出各种递送载体将治疗性化合物输送到肠道,在肠道中活性化合物会释放出来,并且肠道微生物群和黏膜免疫系统也发挥着重要作用。本综述全面概述了与生物制剂口服给药相关的前景与问题、当前的递送系统、口服疗法的应用,以及将核酸和蛋白质疗法转化为临床实践所面临的挑战和考量。

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