电穿孔
Zeta电位
细胞外小泡
生物物理学
材料科学
分散性
小泡
脉搏(音乐)
细胞外
粒子(生态学)
脂质体
药物输送
分析化学(期刊)
化学
粒径
悬挂(拓扑)
纳米技术
胞外囊泡
微流控
不可逆电穿孔
拉伤
作者
Mohini Singh,G. Mazaheri-Tehrani,Ignacio Martín-Fabiani,Owen G. Davies
出处
期刊:Drug Delivery
[Taylor & Francis]
日期:2025-09-22
卷期号:32 (1): 2562224-2562224
被引量:8
标识
DOI:10.1080/10717544.2025.2562224
摘要
Extracellular vesicles (EVs) are promising drug delivery systems (DDSs). Electroporation is widely applied in the loading of therapeutic payloads but has not been optimized for EV loading. Understanding the potential effects of electroporation on EV profile and integrity is important if they are to be applied therapeutically. In the present study, EVs were isolated and subjected to electroporation at different voltages (500-1000 mV), pulse numbers (1-3), and pulse widths (10-30 ms). Particle concentration, size distribution, polydispersity index (PDI), zeta potential (ZP), and protein concentration were analyzed and western blotting was performed to evaluate possible variations in EV surface markers. Suspension in electroporation buffer (EB) significantly reduced EV concentration, increased particle size, and reduced the ZP. Native EV profile could not be recovered following washing. Electroporation parameters (EPs) applied had variable effects on in EV profile, with reductions in surface protein concentration and a more neutral ZP observed. In conclusion, we identified that the electroporation protocol had a considerable impact on basic EV properties, which could impact their application as DDS. Further optimization of EBs and protocols is required to retain native EV profile following loading.
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