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dc.contributor.authorSeo, Bo-Bae-
dc.contributor.authorYoungjoong Kwon-
dc.contributor.authorJun Kim-
dc.contributor.authorKi Hyun Hong-
dc.contributor.authorKim, S.-E.-
dc.contributor.authorSong, H.-R.-
dc.contributor.authorKim, Young Min-
dc.contributor.authorSong, Soo Chang-
dc.date.accessioned2024-01-19T13:02:47Z-
dc.date.available2024-01-19T13:02:47Z-
dc.date.created2021-10-21-
dc.date.issued2022-01-
dc.identifier.issn2452-199X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/115917-
dc.description.abstractTreatment of osteoarthritis (OA) by administration of corticosteroids is a commonly used method in clinics using anti-inflammatory medicine. Oral administration or intra-articular injection of corticosteroids can reduce the pain and progress of cartilage degeneration, but they are usually insufficient to show local and long-term anti-inflammatory effects because of their fast clearance in the body. In this study, we suggest an injectable anti-OA drug depot system for sustained drug release that provides long-term effective therapeutic advantages. Amphiphilic poly(organophosphazene), which has temperature-dependent nanoparticle forming and sol-gel transition behaviors when dissolved in aqueous solution, was synthesized for triamcinolone acetonide (TCA) delivery. Because hydrophobic parts of the polymer can interact with hydrophobic parts of the TCA, the TCA was encapsulated into the self-assembled polymeric nanoparticles. The TCA-encapsulated polymeric nanoparticles (TePNs) were well dispersed in an aqueous solution below room temperature so that they can be easily injected as a sol state into an intra-articular region. However, the TePNs solution transforms immediately to a viscose 3D hydrogel like a synovial fluid in the intra-articular region via the conducted body temperature. An in vitro TCA release study showed sustained TCA release for six weeks. One-time injection of the TePN hydrogel system in an early stage of OA-induced rat model showed a great inhibition effect against further OA progression. The OA-induced knees completely recovered as a healthy cartilage without any abnormal symptoms. ? 2021 The Authors-
dc.languageEnglish-
dc.publisherElsevier-
dc.titleInjectable polymeric nanoparticle hydrogel system for long-term anti-inflammatory effect to treat osteoarthritis-
dc.typeArticle-
dc.identifier.doi10.1016/j.bioactmat.2021.05.028-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBioactive Materials, v.7, pp.14 - 25-
dc.citation.titleBioactive Materials-
dc.citation.volume7-
dc.citation.startPage14-
dc.citation.endPage25-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000709370300004-
dc.identifier.scopusid2-s2.0-85112585426-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPluspolymerization-
dc.subject.keywordPlusRNA isolation-
dc.subject.keywordPluscorticosteroid-
dc.subject.keywordPlusdichlorophosphazene-
dc.subject.keywordPlusHexachlorocyclotriphosphazene-
dc.subject.keywordPlushyaluronic acid-
dc.subject.keywordPlushydrogel-
dc.subject.keywordPlushydroxyproline-
dc.subject.keywordPlusinorganic compound-
dc.subject.keywordPluslevofloxacin-
dc.subject.keywordPlusmacrogol-
dc.subject.keywordPlusmolecular scaffold-
dc.subject.keywordPlusstromelysin-
dc.subject.keywordPlustriamcinolone-
dc.subject.keywordPlustriamcinolone acetonide-
dc.subject.keywordPlustumor necrosis factor-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusanimal experiment-
dc.subject.keywordPlusanimal tissue-
dc.subject.keywordPlusantiinflammatory activity-
dc.subject.keywordPlusArticle-
dc.subject.keywordPlusbiocompatibility-
dc.subject.keywordPlusbiodegradability-
dc.subject.keywordPlusbiodegradation-
dc.subject.keywordPlusbody temperature-
dc.subject.keywordPluscartilage degeneration-
dc.subject.keywordPluscell viability-
dc.subject.keywordPluschondrocyte-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPluscytokine release-
dc.subject.keywordPluscytotoxicity-
dc.subject.keywordPlusdispersity-
dc.subject.keywordPlusdrug stability-
dc.subject.keywordPlusencapsulation-
dc.subject.keywordPlusflow kinetics-
dc.subject.keywordPlusgene expression-
dc.subject.keywordPlusgenetic transcription-
dc.subject.keywordPlusinflammation-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmouse-
dc.subject.keywordPlusmutagenicity-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusosteoarthritis-
dc.subject.keywordPluspolymerase chain reaction-
dc.subject.keywordAuthorOsteoarthritis-
dc.subject.keywordAuthorPolymer nanoparticle-
dc.subject.keywordAuthorSustained release-
dc.subject.keywordAuthorThermosensitive hydrogel-
dc.subject.keywordAuthorTriamcinolone acetonide-
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