代谢性疾病口服生物大分子治疗研究进展

IF 6.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2025-02-12 DOI:10.3390/pharmaceutics17020238
Qiuxia Jiao, Yuan Huang, Jinhan He, Yining Xu
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摘要

肥胖和糖尿病等代谢性疾病正在增加,生物大分子(如蛋白质、多肽、抗体和寡核苷酸)治疗在治疗中起着至关重要的作用。然而,这些药物传统上是注射的。对于慢性疾病(如代谢性疾病)患者,长期注射伴随着不方便和低依从性。口服给药是首选,但由于胃肠道障碍,生物大分子的递送具有挑战性。本文就目前治疗代谢性疾病的生物大分子药物作一介绍。本文还探讨了口服药物给药的胃肠道障碍和克服这些障碍的策略。然后,我们讨论了减轻代谢缺陷的策略,包括葡萄糖代谢、脂质代谢和能量代谢,口服生物大分子如胰岛素、胰高血糖素样肽-1受体激动剂、蛋白转化酶枯草素/ keexin 9型抑制剂、成纤维细胞生长因子21类似物和肽YY类似物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Advances in Oral Biomacromolecule Therapies for Metabolic Diseases.

Metabolic diseases like obesity and diabetes are on the rise, and therapies with biomacromolecules (such as proteins, peptides, antibodies, and oligonucleotides) play a crucial role in their treatment. However, these drugs are traditionally injected. For patients with chronic diseases (e.g., metabolic diseases), long-term injections are accompanied by inconvenience and low compliance. Oral administration is preferred, but the delivery of biomacromolecules is challenging due to gastrointestinal barriers. In this article, we introduce the available biomacromolecule drugs for the treatment of metabolic diseases. The gastrointestinal barriers to oral drug delivery and strategies to overcome these barriers are also explored. We then discuss strategies for alleviating metabolic defects, including glucose metabolism, lipid metabolism, and energy metabolism, with oral biomacromolecules such as insulin, glucagon-like peptide-1 receptor agonists, proprotein convertase subtilisin/kexin type 9 inhibitors, fibroblast growth factor 21 analogues, and peptide YY analogues.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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