Graphene oxide-cellulose composite cryogels for extracellular vesicle isolation

buir.contributor.authorYılmaz, Eylül Gülşen
buir.contributor.authorAkceoğlu, Garbis Atam
buir.contributor.authorİnci, Fatih
buir.contributor.orcidYılmaz, Eylül Gülşen|0000-0002-5295-344X
buir.contributor.orcidAkceoğlu, Garbis Atam|0000-0002-8274-4569
buir.contributor.orcidİnci, Fatih|0000-0002-9918-5038
dc.citation.epage116029-11
dc.citation.spage116029-1
dc.citation.volumeNumber219
dc.contributor.authorSaylan, Yeşeren
dc.contributor.authorAltıntaş, Özge
dc.contributor.authorYılmaz, Eylul Gülşen
dc.contributor.authorAkceoğlu, Garbis Atam
dc.contributor.authorİnci, Fatih
dc.contributor.authorYılmaz, Fatma
dc.contributor.authorDenizli, Adil
dc.date.accessioned2026-04-15T11:10:01Z
dc.date.available2026-04-15T11:10:01Z
dc.date.issued2025-11-02
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)
dc.description.abstractHerein, we present an innovative approach for the selective and high-efficiency isolation of extracellular vesicles (EVs) derived from microfluidic chips that replicate the tumor microenvironment. This is achieved through the development of graphene oxide-cellulose-based composite cryogels imprinted with EVs. In the experiments, MCF-7 cells were cultured under flow conditions within microfluidic chips, simulating the dynamic tumor microenvironment. The isolated EVs were comprehensively characterized in terms of biological, morphological, and quantitative attributes using scanning electron microscopy and nanoparticle tracking analysis. Subsequently, the EVs were imprinted onto graphene oxide-cellulose-based composite cryogels, yielding a novel polymeric material designed for highly selective EV isolation. The physicochemical properties of the composite cryogels were thoroughly analyzed using multiple characterization techniques, and their kinetic performance was evaluated under varying parameters (pH, concentration, temperature, ionic strength, flow rate and selectivity). The maximum adsorption capacity was calculated to be 231 particles/g in a pH 5.0 buffer solution at room temperature. Non-composite and non-imprinted composite cryogels were also prepared for comparison experiments. Finally, the efficacy and validation of the platform were confirmed via high-performance liquid chromatography (HPLC) analysis, demonstrating its potential as a powerful tool for EV isolation in cancer research.
dc.embargo.release2027-11-02
dc.identifier.doi10.1016/j.microc.2025.116029
dc.identifier.eissn1095-9149
dc.identifier.issn0026-265X
dc.identifier.urihttps://hdl.handle.net/11693/119036
dc.language.isoEnglish
dc.publisherElsevier Inc.
dc.relation.isversionofhttps://dx.doi.org/10.1016/j.microc.2025.116029
dc.rightsCC BY 4.0 DEED (Attribution 4.0 International)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.source.titleMicrochemical Journal
dc.subjectExtracellular vesicle
dc.subjectGraphene oxide-cellulose
dc.subjectCryogel
dc.subjectMolecular imprinting
dc.titleGraphene oxide-cellulose composite cryogels for extracellular vesicle isolation
dc.typeArticle

Files

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
Graphene_oxide-cellulose_composite_cryogels_for_extracellular_vesicle_isolation.pdf
Size:
4.63 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.1 KB
Format:
Item-specific license agreed upon to submission
Description: