电穿孔引起细胞外囊泡轮廓的改变。

IF 8.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2025-12-01 Epub Date: 2025-09-22 DOI:10.1080/10717544.2025.2562224
M Singh, G Mazaheri-Tehrani, I Martin-Fabiani, O G Davies
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引用次数: 0

摘要

细胞外囊泡(EVs)是一种很有前途的药物传递系统。电穿孔广泛应用于治疗有效载荷的负载,但尚未对EV负载进行优化。如果要将电穿孔应用于治疗,了解电穿孔对EV轮廓和完整性的潜在影响是很重要的。在本研究中,分离ev并在不同电压(500-1000 mV)、脉冲数(1-3)和脉冲宽度(10-30 ms)下进行电穿孔。分析颗粒浓度、大小分布、多分散性指数(PDI)、ζ电位(ZP)和蛋白浓度,并采用免疫印迹法评价EV表面标记物可能发生的变化。电穿孔缓冲液(EB)中的悬浮液显著降低EV浓度,增大粒径,降低ZP。本机EV配置文件在洗涤后无法恢复。应用电穿孔参数(EPs)对EV剖面有不同的影响,表面蛋白浓度降低,ZP更中性。总之,我们发现电穿孔协议对EV的基本性质有相当大的影响,这可能会影响它们作为DDS的应用。需要进一步优化EBs和协议,以便在加载后保留本地EV配置文件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroporation induced changes in extracellular vesicle profile.

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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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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