Milk-derived exosomes as a promising vehicle for oral delivery of hydrophilic biomacromolecule drugs

被引:23
|
作者
Li, Yuting
Xing, Liyun
Wang, Lingling
Liu, Xi
Wu, Licheng
Ni, Mingjie
Zhou, Zhou
Li, Lian
Liu, Xiuxiu [1 ]
Huang, Yuan [1 ]
机构
[1] Sichuan Univ, Key Lab Drug Targeting & Drug Delivery Syst, Sichuan Engn Lab Plant Sourced Drug, Educ Minist & Sichuan Prov, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Milk-derived exosomes; Loading efficiency; Drug lipophilicity; Molecular weight; Drug release; Oral delivery;
D O I
10.1016/j.ajps.2023.100797
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exosomes, as promising vehicles, have been widely used in the research of oral drug delivery, but the generally low drug loading efficiency of exosomes seriously limits its application and transformation. In this study, we systematically investigated the effects of drug loading methods and physicochemical properties (lipophilicity and molecular weight) on drug loading efficiency of milk-derived exosomes to explore the most appropriate loading conditions. Our finding revealed that the drug loading efficiency of exosomes was closely related to the drug loading method, drug lipophilicity, drug molecular weight and exosome/drug proportions. Of note, we demonstrated the universality that hydrophilic biomacromolecule drugs were the most appropriate loading drugs for milk-derived exosomes, which was attributed to the efficient loading capacity and sustained release behavior. Furthermore, milk-derived exosomes could significantly improve the transepithelial transport and oral bioavailability of model hydrophilic biomacromolecule drugs (octreotide, exendin-4 and salmon calcitonin). Collectively, our results suggested that the encapsulation of hydrophilic biomacromolecule drugs might be the most promising direction for milk exosomes as oral drug delivery vehicles.(c) 2023 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
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页数:13
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