State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, 38 Science Park Road, Changping District, Beijing, China.
Anhui Medical University, No.81 Meishan Road, Hefei, China.
ChemMedChem. 2022 May 18;17(10):e202100758. doi: 10.1002/cmdc.202100758. Epub 2022 Mar 15.
Bovine milk is rich in extracellular vesicles (mEVs) which have been suggested as a possible drug delivery vehicle with oral bioavailability. As the digestive fluids contain many lipid- and protein-degrading enzymes, we explored whether mEVs given sublingually could be taken up systemically. mEVs were isolated using three different protocols, which were 120 nm in diameter and carried bovine CD81. Fluorescently stained mEVs given by sublingual route were detected in the circulation, whereas mEVs given by gavage were detected at 2-Log lower concentrations. As proof of the concept, we loaded mEVs with the antidiabetic drug Liraglutide (LRT-EV), which reduced blood glucose levels when given by the sublingual route but showed no efficacy via gavage. This study suggests that mEV may be an efficient delivery vehicle for drugs that are not orally bioavailable, and LRT-loaded EVs have the potential as the next-generation drug delivery platform for the treatment of chronic diseases, including diabetes.
牛奶中富含细胞外囊泡(mEVs),这些囊泡被认为是具有口服生物利用度的潜在药物递送载体。由于消化液中含有许多脂质和蛋白质降解酶,我们探讨了舌下给予 mEVs 是否可以被系统吸收。使用三种不同的方案分离 mEVs,其直径为 120nm 并携带牛 CD81。通过舌下途径给予荧光染色的 mEVs 在循环中被检测到,而通过灌胃给予的 mEVs 则以低 2 个对数的浓度被检测到。作为概念验证,我们将 mEV 装载上抗糖尿病药物利拉鲁肽(LRT-EV),通过舌下途径给予时可降低血糖水平,但通过灌胃途径给予时则没有效果。本研究表明,mEV 可能是一种有效的非口服生物利用度药物递送载体,而负载 LRT 的 EV 有可能成为治疗糖尿病等慢性病的下一代药物递送平台。