Department of Biomedical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan 44919, Korea.
Lab Chip. 2024 Mar 26;24(7):2069-2079. doi: 10.1039/d3lc00830d.
The current challenge in using extracellular vesicles (EVs) as drug delivery vehicles is to precisely control their membrane permeability, specifically in the ability to switch between permeable and impermeable states without compromising their integrity and functionality. Here, we introduce a rapid, efficient, and gentle loading method for EVs based on tonicity control (TC) using a lab-on-a-disc platform. In this technique, a hypotonic solution was used for temporarily permeabilizing a membrane ("on" state), allowing the influx of molecules into EVs. The subsequent isotonic washing led to an impermeable membrane ("off" state). This loading cycle enables the loading of different cargos into EVs, such as doxorubicin hydrochloride (Dox), ssDNA, and miRNA. The TC approach was shown to be more effective than traditional methods such as sonication or extrusion, with loading yields that were 4.3-fold and 7.2-fold greater, respectively. Finally, the intracellular assessments of miRNA-497-loaded EVs and doxorubicin-loaded EVs confirmed the superior performance of TC-prepared formulations and demonstrated the impact of encapsulation heterogeneity on the therapeutic outcome, signifying potential opportunities for developing novel exosome-based therapeutic systems for clinical applications.
目前,将细胞外囊泡(EVs)用作药物递送载体的挑战在于精确控制其膜通透性,特别是在不损害其完整性和功能的情况下,能够在可渗透和不可渗透状态之间进行切换。在这里,我们介绍了一种基于碟式实验室平台的渗透压控制(TC)的快速、高效和温和的 EVs 加载方法。在该技术中,使用低渗溶液暂时使膜渗透化(“开”状态),允许分子流入 EVs。随后的等渗洗涤导致不可渗透的膜(“关”状态)。这种加载循环能够将不同的货物(如盐酸多柔比星(Dox)、ssDNA 和 miRNA)加载到 EVs 中。TC 方法比超声处理或挤出等传统方法更有效,其加载产率分别高出 4.3 倍和 7.2 倍。最后,miRNA-497 加载的 EVs 和多柔比星加载的 EVs 的细胞内评估证实了 TC 制备配方的卓越性能,并证明了封装异质性对治疗结果的影响,这为开发用于临床应用的新型基于外泌体的治疗系统提供了潜在机会。