DC Field | Value | Language |
---|---|---|
dc.contributor.author | E S Lee | - |
dc.contributor.author | Hyewon Ko | - |
dc.contributor.author | C H Kim | - |
dc.contributor.author | H C Kim | - |
dc.contributor.author | S K Choi | - |
dc.contributor.author | S W Jeong | - |
dc.contributor.author | S G Lee | - |
dc.contributor.author | S J Lee | - |
dc.contributor.author | H K Na | - |
dc.contributor.author | J H Park | - |
dc.contributor.author | J M Shin | - |
dc.date.accessioned | 2023-08-29T16:32:42Z | - |
dc.date.available | 2023-08-29T16:32:42Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1226-1226 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/32572 | - |
dc.description.abstract | Background: Exosomes are extracellular vesicles secreted by eukaryotic cells and have been extensively studied for their surface markers and internal cargo with unique functions. A deeper understanding of exosomes has allowed their application in various research areas, particularly in diagnostics and therapy. Main body: Exosomes have great potential as biomarkers and delivery vehicles for encapsulating therapeutic cargo. However, the limitations of bare exosomes, such as rapid phagocytic clearance and non-specific biodistribution after injection, pose significant challenges to their application as drug delivery systems. This review focuses on exosome-based drug delivery for treating rheumatoid arthritis, emphasizing pre/post-engineering approaches to overcome these challenges. Conclusion: This review will serve as an essential resource for future studies to develop novel exosome-based therapeutic approaches for rheumatoid arthritis. Overall, the review highlights the potential of exosomes as a promising therapeutic approach for rheumatoid arthritis treatment. | - |
dc.publisher | Springer-BMC | - |
dc.title | Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment | - |
dc.title.alternative | Disease-microenvironment modulation by bare- or engineered-exosome for rheumatoid arthritis treatment | - |
dc.type | Article | - |
dc.citation.title | Biomaterials Research | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 81 | - |
dc.citation.startPage | 81 | - |
dc.citation.volume | 27 | - |
dc.contributor.affiliatedAuthor | Hyewon Ko | - |
dc.contributor.alternativeName | 이은숙 | - |
dc.contributor.alternativeName | 고혜원 | - |
dc.contributor.alternativeName | 김찬호 | - |
dc.contributor.alternativeName | 김현철 | - |
dc.contributor.alternativeName | 최성균 | - |
dc.contributor.alternativeName | 정상원 | - |
dc.contributor.alternativeName | 이세건 | - |
dc.contributor.alternativeName | 이성준 | - |
dc.contributor.alternativeName | 나희경 | - |
dc.contributor.alternativeName | 박재형 | - |
dc.contributor.alternativeName | 신정민 | - |
dc.identifier.bibliographicCitation | Biomaterials Research, vol. 27, pp. 81-81 | - |
dc.identifier.doi | 10.1186/s40824-023-00418-2 | - |
dc.subject.keyword | Exosome | - |
dc.subject.keyword | Rheumatoid arthritis | - |
dc.subject.keyword | Disease microenvironment | - |
dc.subject.keyword | Engineered exosome | - |
dc.subject.local | Exosome | - |
dc.subject.local | exosome | - |
dc.subject.local | Rheumatoid Arthritis | - |
dc.subject.local | Rheumatoid arthritis | - |
dc.subject.local | rheumatoid arthritis | - |
dc.subject.local | rheumatoid arthritis (RA) | - |
dc.description.journalClass | Y | - |
There are no files associated with this item.
Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.