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Meso-macroporous hydrogel for direct litre-scale isolation of extracellular vesicles

Authors
Kim, JunbeomKang, MinjinHan, GeonheeHyung, SujinKim, MinaJang, MinjeongLee, Han KyulSeo, YunheeGil, Ki CheolKim, ChangheonSong, SojinJeong, SeonghyeokKim, SeongchanKim, Min SooShim, Ji SungKang, Sung GuLee, Young ChanChung, SeokCho, Il-JooShim, Tae SoupSong, Kwang HoonMin, JouhaSeong, HyejeongLee, KyungeunLee, JeeyunLee, CheoljuKim, Hong NamLee, HyojinKim, Sun HwaKang, Ji YoonBong, Ki WanChoi, Nakwon
Issue Date
Nov-2025
Publisher
Nature Publishing Group
Citation
Nature Nanotechnology, v.20, no.11, pp 1678 - 1687
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Nature Nanotechnology
Volume
20
Number
11
Start Page
1678
End Page
1687
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/80743
DOI
10.1038/s41565-025-02011-1
ISSN
1748-3387
1748-3395
Abstract
Extracellular vesicles are cell-originated lipid bilayer membrane vesicles that play vital roles in cell-to-cell communications. While extracellular vesicles hold substantial biomedical potential, conventional methodologies for isolating extracellular vesicles require elaborate preprocessing and, therefore, remain labour intensive and limited by throughput. To overcome these challenges, we present a facile fabrication route for generating a meso-macroporous hydrogel matrix with pores of similar to 400 nm for customizable extracellular vesicle isolation. By combining surface charge-selective capture of extracellular vesicles within the hydrogel matrix and their recovery by high ionic strength, we report direct extracellular vesicle isolation with a throughput range from microlitre to litre scales, without preprocessing, for various biofluids, including whole blood, plasma, ascites, saliva, urine, bovine milk and cell culture media. Furthermore, we demonstrate that the meso-macroporous hydrogel also serves as a solid-phase matrix for preserving extracellular vesicles for on-demand downstream analyses, making it applicable for therapeutics, cosmeceuticals and disease diagnostics.
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