Comparative evaluation of ultracentrifugation and PEG-based precipitation of mesenchymal stem cell‑derived extracellular vesicles: equivalent functionality with enhanced practicality.

IF 3.4 Q2 PHARMACOLOGY & PHARMACY
Therapeutic delivery Pub Date : 2026-07-01 Epub Date: 2026-08-12 DOI:10.1080/20415990.2026.2715875
Aishwarya Sivakumar, Vijayalakshmi Kumaravel, Senthamizh Gopal, Raghu Babu Pothireddy
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引用次数: 0

Abstract

Aim: The isolation efficiency of extracellular vesicles (EVs) is essential to ensure their purity and biological properties. Ultracentrifugation is a traditional method which utilizes high centrifugal forces to separate EVs based on their density. The polyethylene glycol (PEG)-based precipitation method is a scalable and cost-efficient alternative to ultracentrifugation. In this study, two popular techniques used for the isolation of EVs from umbilical cord tissue-derived mesenchymal stem cells (UCT-MSCs): ultracentrifugation and polyethylene glycol PEG-based precipitation methods are examined.

Materials and methods: The UCT-MSCs were cultured in a xeno-free environment using human platelet lysate (hPL) to avoid the risk of xenogenic contamination. The MSCs and EVs were characterized to confirm their physical and functional properties. Cytotoxicity was analyzed in both normal and cancer cells, and the cell migration assay was conducted on cancer cells treated with the EVs to examine the biocompatibility and migratory effects.

Results and conclusions: The similarity in physical, molecular, and functional characterization of UC-EVs and PEG-EVs suggests that PEG-based precipitation maintained the integrity and biological properties of EVs. Overall, the PEG-based precipitation method for EVs isolation is safe and efficient, making them suitable for regeneration and cancer research.

间充质干细胞来源的细胞外囊泡的超离心和聚乙二醇沉淀的比较评价:同等功能和增强的实用性。
目的:细胞外囊泡(EVs)的分离效率是保证其纯度和生物学特性的关键。超离心是一种传统的方法,它利用高离心力根据ev的密度分离ev。聚乙二醇(PEG)为基础的沉淀方法是一种可扩展和经济高效的超离心替代方案。在本研究中,研究了从脐带组织来源的间充质干细胞(UCT-MSCs)中分离ev的两种常用技术:超离心和聚乙二醇聚乙二醇沉淀法。材料和方法:使用人血小板裂解液(hPL)在无xeno环境中培养UCT-MSCs,以避免异种污染的风险。对MSCs和ev进行了表征,以确定其物理和功能特性。对正常细胞和癌细胞进行细胞毒性分析,并对经ev处理的癌细胞进行细胞迁移实验,考察其生物相容性和迁移效果。结果与结论:uc - ev和peg - ev在物理、分子和功能表征上的相似性表明,peg沉淀保持了ev的完整性和生物学特性。综上所述,聚乙二醇沉淀法分离电动汽车安全高效,适用于再生和癌症研究。
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来源期刊
Therapeutic delivery
Therapeutic delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.50
自引率
0.00%
发文量
25
期刊介绍: Delivering therapeutics in a way that is right for the patient - safe, painless, reliable, targeted, efficient and cost effective - is the fundamental aim of scientists working in this area. Correspondingly, this evolving field has already yielded a diversity of delivery methods, including injectors, controlled release formulations, drug eluting implants and transdermal patches. Rapid technological advances and the desire to improve the efficacy and safety profile of existing medications by specific targeting to the site of action, combined with the drive to improve patient compliance, continue to fuel rapid research progress. Furthermore, the emergence of cell-based therapeutics and biopharmaceuticals such as proteins, peptides and nucleotides presents scientists with new and exciting challenges for the application of therapeutic delivery science and technology. Successful delivery strategies increasingly rely upon collaboration across a diversity of fields, including biology, chemistry, pharmacology, nanotechnology, physiology, materials science and engineering. Therapeutic Delivery recognizes the importance of this diverse research platform and encourages the publication of articles that reflect the highly interdisciplinary nature of the field. In a highly competitive industry, Therapeutic Delivery provides the busy researcher with a forum for the rapid publication of original research and critical reviews of all the latest relevant and significant developments, and focuses on how the technological, pharmacological, clinical and physiological aspects come together to successfully deliver modern therapeutics to patients. The journal delivers this essential information in concise, at-a-glance article formats that are readily accessible to the full spectrum of therapeutic delivery researchers.
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