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dc.contributor.authorLih, Eugene-
dc.contributor.authorPark, Wooram-
dc.contributor.authorPark, Ki Wan-
dc.contributor.authorChun, So Young-
dc.contributor.authorKim, Hyuncheol-
dc.contributor.authorJoung, Yoon Ki-
dc.contributor.authorKwon, Tae Gyun-
dc.contributor.authorHubbell, Jeffrey A.-
dc.contributor.authorHan, Dong Keun-
dc.date.accessioned2024-01-19T20:31:41Z-
dc.date.available2024-01-19T20:31:41Z-
dc.date.created2021-09-02-
dc.date.issued2019-03-27-
dc.identifier.issn2374-7943-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120193-
dc.description.abstractKidney diseases are a worldwide public health issue. Renal tissue regeneration using functional scaffolds with biomaterials has attracted a great deal of attention due to limited donor organ availability. Here, we developed a bioinspired scaffold that can efficiently induce renal tissue regeneration. The bioinspired scaffold was designed with poly(lactide-co-glycolide) (PLGA), magnesium hydroxide (Mg(OH)(2)), and decellularized renal extracellular matrix (ECM). The Mg(OH)(2) inhibited materials-induced inflammatory reactions by neutralizing the acidic microenvironment formed by degradation products of PLGA, and the acellular ECM helped restore the biological function of kidney tissues. When the PLGA/ECM/Mg(OH)(2) scaffold was implanted in a partially nephrectomized mouse model, it led to the regeneration of renal glomerular tissue with a low inflammatory response. Finally, the PLGA/ECM/Mg(OH)(2) scaffold was able to restore renal function more effectively than the control groups. These results suggest that the bioinspired scaffold can be used as an advanced scaffold platform for renal disease treatment.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectPUBLIC-HEALTH PROBLEM-
dc.subjectKIDNEY-DISEASE-
dc.subjectGROWTH-FACTOR-
dc.subjectIN-VIVO-
dc.subjectPLGA-
dc.subjectDEGRADATION-
dc.subjectMICROSPHERES-
dc.subjectFABRICATION-
dc.subjectCOMPLEMENT-
dc.subjectPROTEINS-
dc.titleA Bioinspired Scaffold with Anti-Inflammatory Magnesium Hydroxide and Decellularized Extracellular Matrix for Renal Tissue Regeneration-
dc.typeArticle-
dc.identifier.doi10.1021/acscentsci.8b00812-
dc.description.journalClass1-
dc.identifier.bibliographicCitationACS CENTRAL SCIENCE, v.5, no.3, pp.458 - 467-
dc.citation.titleACS CENTRAL SCIENCE-
dc.citation.volume5-
dc.citation.number3-
dc.citation.startPage458-
dc.citation.endPage467-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000462498900012-
dc.identifier.scopusid2-s2.0-85060724097-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusPUBLIC-HEALTH PROBLEM-
dc.subject.keywordPlusKIDNEY-DISEASE-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusPLGA-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusMICROSPHERES-
dc.subject.keywordPlusFABRICATION-
dc.subject.keywordPlusCOMPLEMENT-
dc.subject.keywordPlusPROTEINS-
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KIST Article > 2019
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