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Updated: May 5, 2026

Purification of High Yield Extracellular Vesicle Preparations Away from Virus
Published on: September 12, 2019
Optimized Tangential Flow Filtration for Efficient Isolation of Highly Pure and Bioactive sEVs
Lei Luo1,2, Yuhang Du1, Xin Niu1
1Institute of Microsurgery on Extremities, Department of Orthopedic Surgery, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai Jiao Tong University, 600 Yishan Road, Shanghai 200233, China.
None:
Small extracellular vesicles (sEVs) have demonstrated significant therapeutic potential. However, the lack of efficient and scalable methods for sEV separation remains a critical barrier to their large-scale production as therapeutic agents. Tangential flow filtration (TFF) has emerged as a promising technique for large-scale sEV separation, but the absence of comprehensive and systematic studies makes it challenging to determine optimal TFF parameters for sEV isolation. In this study, we investigated the effects of key TFF parameters, including shear stress, molecular weight cutoff (MWCO), transmembrane pressure (TMP), and washing-filtration cycles, on sEVs separation and impurity removal. We evaluated particle concentration, size distribution, morphology, chemical properties, fluorescence, and protein content to assess the impact of these parameters. The results revealed that excessive shear stress (>9.05 Pa) during TFF led to protein aggregation and sEV damage. Using a filter membrane with an MWCO of 750 kDa and maintaining TMP between 3 and 5 psi prevented sEV leakage and achieved moderately high filtration efficiency. Based on these findings, optimal TFF parameters were identified. sEVs isolated using optimized TFF conditions (TFF-sEVs) were then compared with sEVs isolated via ultracentrifugation (UC-sEVs). TFF-sEVs exhibited comparable physical properties and purity to UC-sEVs but demonstrated superior proliferation-promoting activity and a 3-fold higher recovery rate. Quantitative proteomic analysis revealed that TFF-sEVs were enriched with extracellular vesicle membrane proteins and corona proteins, contributing to their enhanced bioactivity. In summary, optimizing TFF parameters enables efficient purification of sEVs, balancing purity, recovery, and bioactivity, paving the way for scalable production of sEVs and accelerating the clinical translation of sEV-based therapeutics.
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