There are no files associated with this item.
Cited time in
Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.citation.number | 5 | - |
| dc.citation.startPage | 051504 | - |
| dc.citation.title | BIOMICROFLUIDICS | - |
| dc.citation.volume | 18 | - |
| dc.contributor.author | Kim, Junyoung | - |
| dc.contributor.author | Ro, Jooyoung | - |
| dc.contributor.author | Cho, Yoon-Kyoung | - |
| dc.date.accessioned | 2024-10-14T10:05:07Z | - |
| dc.date.available | 2024-10-14T10:05:07Z | - |
| dc.date.created | 2024-10-08 | - |
| dc.date.issued | 2024-09 | - |
| dc.description.abstract | The vascular network plays an essential role in the maintenance of all organs in the body via the regulated delivery of oxygen and nutrients, as well as tissue communication via the transfer of various biological signaling molecules. It also serves as a route for drug administration and affects pharmacokinetics. Due to this importance, engineers have sought to create physiologically relevant and reproducible vascular systems in tissue, considering cell-cell and extracellular matrix interaction with structural and physical conditions in the microenvironment. Extracellular vesicles (EVs) have recently emerged as important carriers for transferring proteins and genetic material between cells and organs, as well as for drug delivery. Vascularized platforms can be an ideal system for studying interactions between blood vessels and EVs, which are crucial for understanding EV-mediated substance transfer in various biological situations. This review summarizes recent advances in vascularized platforms, standard and microfluidic-based techniques for EV isolation and characterization, and studies of EVs in vascularized platforms. It provides insights into EV-related (patho)physiological regulations and facilitates the development of EV-based therapeutics. | - |
| dc.identifier.bibliographicCitation | BIOMICROFLUIDICS, v.18, no.5, pp.051504 | - |
| dc.identifier.doi | 10.1063/5.0220840 | - |
| dc.identifier.issn | 1932-1058 | - |
| dc.identifier.scopusid | 2-s2.0-85205732459 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/84051 | - |
| dc.identifier.wosid | 001318791100002 | - |
| dc.language | 영어 | - |
| dc.publisher | AIP Publishing | - |
| dc.title | Vascularized platforms for investigating cell communication via extracellular vesicles | - |
| dc.type | Article | - |
| dc.description.isOpenAccess | FALSE | - |
| dc.relation.journalWebOfScienceCategory | Biochemical Research Methods; Biophysics; Nanoscience & Nanotechnology; Physics, Fluids & Plasmas | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology; Biophysics; Science & Technology - Other Topics; Physics | - |
| dc.type.docType | Review | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.subject.keywordPlus | MINIMAL EXPERIMENTAL REQUIREMENTS | - |
| dc.subject.keywordPlus | BLOOD-BRAIN-BARRIER | - |
| dc.subject.keywordPlus | ENDOTHELIAL-CELLS | - |
| dc.subject.keywordPlus | TUMOR MICROENVIRONMENT | - |
| dc.subject.keywordPlus | CLINICAL-APPLICATIONS | - |
| dc.subject.keywordPlus | MICROFLUIDIC DEVICE | - |
| dc.subject.keywordPlus | PERMEABILITY | - |
| dc.subject.keywordPlus | IMMUNE-RESPONSE | - |
| dc.subject.keywordPlus | CANCER-DERIVED EXOSOMES | - |
| dc.subject.keywordPlus | ON-A-CHIP | - |
Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.
Tel : 052-217-1403 / Email : scholarworks@unist.ac.kr
Copyright (c) 2023 by UNIST LIBRARY. All rights reserved.
ScholarWorks@UNIST was established as an OAK Project for the National Library of Korea.