An overview of oral bioavailability enhancement through self-emulsifying drug delivery systems.

Expert opinion on drug delivery Pub Date : 2025-05-01 Epub Date: 2025-03-19 DOI:10.1080/17425247.2025.2479759
Flavia Laffleur, Gioconda Millotti, Jennifer Lagast
{"title":"An overview of oral bioavailability enhancement through self-emulsifying drug delivery systems.","authors":"Flavia Laffleur, Gioconda Millotti, Jennifer Lagast","doi":"10.1080/17425247.2025.2479759","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The pharmaceutical technologists face a lot of challenges and limitations when designing novel drug delivery systems such as low oral bioavailability of many drugs, primarily due to poor solubility, slow dissolution rates, limited permeability through gastrointestinal mucosa, and rapid degradation within the body.</p><p><strong>Areas covered: </strong>The biopharmaceutical classification (BCS) classification represents a map in drug delivery research. Numerous active ingredients are characterized by low bioavailability due to poor water solubility, especially active ingredients of BCS class II and IV. Self-emulsifying drug delivery systems (SEDDS) could act as game changer in order to overcome the challenges and limitations of poor bioavailability. In this review, timelines representing the launch of self-emulsifying drug delivery systems, their introduction to the pharmaceutical platform and their benefits will be discussed in detail.</p><p><strong>Expert opinion: </strong>The development of multifunctional systems capable of combining controlled release, targeted delivery, and diagnostic capabilities is a promising avenue. As the technology matures, self-microemulsifying drug delivery systems and self-nanoemulsifying drug delivery systems are likely to become a standard approach for delivering BCS class II and IV drugs, transforming the pharmaceutical landscape.</p>","PeriodicalId":94004,"journal":{"name":"Expert opinion on drug delivery","volume":" ","pages":"659-671"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert opinion on drug delivery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17425247.2025.2479759","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The pharmaceutical technologists face a lot of challenges and limitations when designing novel drug delivery systems such as low oral bioavailability of many drugs, primarily due to poor solubility, slow dissolution rates, limited permeability through gastrointestinal mucosa, and rapid degradation within the body.

Areas covered: The biopharmaceutical classification (BCS) classification represents a map in drug delivery research. Numerous active ingredients are characterized by low bioavailability due to poor water solubility, especially active ingredients of BCS class II and IV. Self-emulsifying drug delivery systems (SEDDS) could act as game changer in order to overcome the challenges and limitations of poor bioavailability. In this review, timelines representing the launch of self-emulsifying drug delivery systems, their introduction to the pharmaceutical platform and their benefits will be discussed in detail.

Expert opinion: The development of multifunctional systems capable of combining controlled release, targeted delivery, and diagnostic capabilities is a promising avenue. As the technology matures, self-microemulsifying drug delivery systems and self-nanoemulsifying drug delivery systems are likely to become a standard approach for delivering BCS class II and IV drugs, transforming the pharmaceutical landscape.

通过自乳化给药系统提高口服生物利用度的综述。
导读:制药技术人员在设计新型给药系统时面临着许多挑战和限制,例如许多药物的口服生物利用度低,主要是由于溶解度差,溶解速度慢,通过胃肠道粘膜的渗透性有限,以及在体内的快速降解。涵盖领域:生物制药分类(BCS)分类代表了药物传递研究的地图。由于水溶性差,许多活性成分具有低生物利用度的特点,特别是BCS II类和IV类活性成分。自乳化给药系统(SEDDS)可以作为游戏规则的改变者,以克服生物利用度差的挑战和局限性。在这篇综述中,将详细讨论自乳化给药系统的推出时间,它们在制药平台上的介绍及其益处。专家意见:能够结合控制释放、靶向给药和诊断功能的多功能系统的开发是一个有前途的途径。随着技术的成熟,自微乳化给药系统和自纳米乳化给药系统可能成为递送BCS II类和IV类药物的标准方法,从而改变制药行业的格局。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信