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Oral gene delivery platform based on glycol chitosan-PEG-lactoferrin conjugate

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dc.contributor.authorJang, Seonmi-
dc.contributor.authorPriscilla, Lia-
dc.contributor.authorLee, Chang Woo-
dc.contributor.authorLee, Seung Ah-
dc.contributor.authorLee, Minhyung-
dc.contributor.authorLee, Dong Yun-
dc.date.accessioned2026-01-23T02:30:25Z-
dc.date.available2026-01-23T02:30:25Z-
dc.date.issued2026-01-
dc.identifier.issn0168-3659-
dc.identifier.issn1873-4995-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210449-
dc.description.abstractOral gene delivery offers an alternative to parenteral administration for managing chronic metabolic disorders such as type 2 diabetes mellitus (T2D). However, its development has been limited by enzymatic degradation within the gastrointestinal tract and inefficient intestinal absorption. To overcome these obstacles, we developed a non-viral oral gene delivery system based on a glycol chitosan-maleimide-polyethylene glycol-N-hydroxysuccinimide ester-lactoferrin (GPL) platform. We then applied this platform to deliver fibroblast growth factor 21 (FGF21), a key regulator of glucose and lipid metabolism, through lactoferrin receptor–mediated transcytosis. Oral administration of the GPL/FGF21 polyplex achieved circulating FGF21 levels comparable to intraperitoneal injection. This resulted in a ∼ 37 % reduction in fasting glucose and a ∼ 47 % improvement in insulin sensitivity in high-fat diet (HFD)-induced T2D mice, accompanied by systemic FGF21 protein expression. Collectively, this GPL-based oral gene delivery system represents a promising gene therapeutic strategy with broad applicability for metabolic diseases.-
dc.format.extent15-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleOral gene delivery platform based on glycol chitosan-PEG-lactoferrin conjugate-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.jconrel.2025.114463-
dc.identifier.scopusid2-s2.0-105023158565-
dc.identifier.wosid001632626100003-
dc.identifier.bibliographicCitationJournal of Controlled Release, v.389, pp 1 - 15-
dc.citation.titleJournal of Controlled Release-
dc.citation.volume389-
dc.citation.startPage1-
dc.citation.endPage15-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusINSULIN SENSITIVITY-
dc.subject.keywordPlusFGF21-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordAuthorGene therapy-
dc.subject.keywordAuthorOral delivery-
dc.subject.keywordAuthorGlycol chitosan-maleimide-polyethylene glycol-N-hydroxysuccinimide ester-lactoferrin-
dc.subject.keywordAuthor(GPL)-
dc.subject.keywordAuthorFibroblast growth factor 21 (FGF21)-
dc.subject.keywordAuthorType 2 diabetes mellitus (T2D)-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0168365925010776?via%3Dihub-
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