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细胞外囊泡作为新型口服递药载体在炎症性疾病治疗中的应用的新兴趋势。

Emerging Trends in the Application of Extracellular Vesicles as Novel Oral Delivery Vehicles for Therapeutics in Inflammatory Diseases.

机构信息

Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.

Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Aug 21;19:8573-8601. doi: 10.2147/IJN.S475532. eCollection 2024.

Abstract

Inflammation involves complex immune responses where cytokines such as TNF-α, IL-1, and IL-6 promote vasodilation and increased vascular permeability to facilitate immune cell migration to inflammation sites. Persistent inflammation is linked to diseases like cancer, arthritis, and neurodegenerative disorders. Although oral anti-inflammatory drugs are favored for their non-invasiveness and cost-effectiveness, their efficacy is often compromised due to gastrointestinal degradation and limited bioavailability. Recent advancements highlight the potential of extracellular vesicles (EVs) as nanocarriers that enhance drug delivery by encapsulating therapeutic agents, ensuring targeted release and reduced toxicity. These EVs, derived from dietary sources and cell cultures, exhibit excellent biocompatibility and stability, presenting a novel approach in anti-inflammatory therapies. This review discusses the classification and advantages of orally administered EVs (O-EVs), their mechanism of action, and their emerging role in treating inflammatory conditions, positioning them as promising vectors in the development of innovative anti-inflammatory drug delivery systems.

摘要

炎症涉及复杂的免疫反应,其中细胞因子如 TNF-α、IL-1 和 IL-6 促进血管扩张和血管通透性增加,以促进免疫细胞迁移到炎症部位。持续性炎症与癌症、关节炎和神经退行性疾病等疾病有关。虽然口服抗炎药因其非侵入性和成本效益而受到青睐,但由于胃肠道降解和有限的生物利用度,其疗效往往受到影响。最近的进展强调了细胞外囊泡 (EVs) 作为纳米载体的潜力,通过封装治疗剂来增强药物递送,确保靶向释放和降低毒性。这些 EVs 源自饮食来源和细胞培养物,具有极好的生物相容性和稳定性,为抗炎治疗提供了一种新方法。本文综述了口服给药的 EVs (O-EVs) 的分类和优势、它们的作用机制以及它们在治疗炎症性疾病中的新兴作用,将它们定位为开发创新抗炎药物递送系统的有前途的载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/695d/11345024/070113af7f11/IJN-19-8573-g0001.jpg

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