Varut Renata Maria, Ciolofan Mircea Sorin, Veronica Maria Elena, Radivojević Kristina, Trasca Diana Maria, Popescu Cristina, Diaconu Oana, Singer Cristina Elena
Research Methodology Department, Faculty of Pharmacy, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Department of ENT, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Pharmaceutics. 2025 Jun 7;17(6):752. doi: 10.3390/pharmaceutics17060752.
: Cyclodextrins (CDs) have garnered increasing attention in pharmaceutical research due to their ability to enhance drug solubility, bioavailability, and therapeutic efficacy. Meanwhile, the gut microbiota, a key regulator of human health, has emerged as an important target in evaluating the safety and broader implications of pharmaceutical excipients. This review aims to synthesize current knowledge regarding the effects of CDs on the composition and function of the gut microbiota. : A literature search following PRISMA guidelines was conducted in PubMed, ScienceDirect, and Google Scholar to identify studies on cyclodextrins and their interactions with gut microbiota. : Cyclodextrins, particularly α-, β-, and γ-CDs, demonstrated the capacity to modulate gut microbiota composition, promoting the growth of beneficial bacteria such as and . Supplementation with CDs was also associated with an increased production of short-chain fatty acids (SCFAs), which are essential for maintaining intestinal homeostasis and metabolic health. Moreover, CDs exhibited potential in lowering lipid levels and improving postprandial glycemic control without enhancing insulin secretion. Although generally recognized as safe, the toxicological profile of CDs varies depending on their type, dosage, and route of administration. : Cyclodextrins hold considerable promise not only as pharmaceutical excipients but also as modulators of gut microbial communities, suggesting a dual therapeutic and prebiotic role. Future studies integrating metagenomic and metabolomic approaches are necessary to further elucidate the molecular mechanisms underlying CD-microbiota interactions and to optimize their application in enhancing drug delivery efficiency and promoting intestinal health.
环糊精(CDs)因其能够提高药物溶解度、生物利用度和治疗效果,在药物研究中受到越来越多的关注。与此同时,肠道微生物群作为人类健康的关键调节因子,已成为评估药物辅料安全性和更广泛影响的重要靶点。本综述旨在综合当前关于环糊精对肠道微生物群组成和功能影响的知识。:按照PRISMA指南在PubMed、ScienceDirect和谷歌学术上进行文献检索,以确定关于环糊精及其与肠道微生物群相互作用的研究。:环糊精,特别是α-、β-和γ-环糊精,显示出调节肠道微生物群组成的能力,促进有益细菌如[具体细菌名称缺失]和[具体细菌名称缺失]的生长。补充环糊精还与短链脂肪酸(SCFAs)产量增加有关,短链脂肪酸对于维持肠道稳态和代谢健康至关重要。此外,环糊精在不增加胰岛素分泌的情况下具有降低血脂水平和改善餐后血糖控制的潜力。尽管环糊精通常被认为是安全的,但其毒理学特征因类型、剂量和给药途径而异。:环糊精不仅作为药物辅料,而且作为肠道微生物群落的调节剂具有很大的前景,表明其具有双重治疗和益生元作用。未来有必要整合宏基因组学和代谢组学方法的研究,以进一步阐明环糊精与微生物群相互作用的分子机制,并优化它们在提高药物递送效率和促进肠道健康方面的应用。