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Oral gene delivery platform based on glycol chitosan-PEG-lactoferrin conjugate
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jang, Seonmi | - |
| dc.contributor.author | Priscilla, Lia | - |
| dc.contributor.author | Lee, Chang Woo | - |
| dc.contributor.author | Lee, Seung Ah | - |
| dc.contributor.author | Lee, Minhyung | - |
| dc.contributor.author | Lee, Dong Yun | - |
| dc.date.accessioned | 2026-01-23T02:30:25Z | - |
| dc.date.available | 2026-01-23T02:30:25Z | - |
| dc.date.issued | 2026-01 | - |
| dc.identifier.issn | 0168-3659 | - |
| dc.identifier.issn | 1873-4995 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210449 | - |
| dc.description.abstract | Oral 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.extent | 15 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | ELSEVIER | - |
| dc.title | Oral gene delivery platform based on glycol chitosan-PEG-lactoferrin conjugate | - |
| dc.type | Article | - |
| dc.publisher.location | 네델란드 | - |
| dc.identifier.doi | 10.1016/j.jconrel.2025.114463 | - |
| dc.identifier.scopusid | 2-s2.0-105023158565 | - |
| dc.identifier.wosid | 001632626100003 | - |
| dc.identifier.bibliographicCitation | Journal of Controlled Release, v.389, pp 1 - 15 | - |
| dc.citation.title | Journal of Controlled Release | - |
| dc.citation.volume | 389 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 15 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.subject.keywordPlus | INSULIN SENSITIVITY | - |
| dc.subject.keywordPlus | FGF21 | - |
| dc.subject.keywordPlus | NANOPARTICLES | - |
| dc.subject.keywordPlus | EXPRESSION | - |
| dc.subject.keywordPlus | DNA | - |
| dc.subject.keywordPlus | MODULATION | - |
| dc.subject.keywordPlus | ACTIVATION | - |
| dc.subject.keywordPlus | MECHANISMS | - |
| dc.subject.keywordPlus | RESISTANCE | - |
| dc.subject.keywordPlus | STABILITY | - |
| dc.subject.keywordAuthor | Gene therapy | - |
| dc.subject.keywordAuthor | Oral delivery | - |
| dc.subject.keywordAuthor | Glycol chitosan-maleimide-polyethylene glycol-N-hydroxysuccinimide ester-lactoferrin | - |
| dc.subject.keywordAuthor | (GPL) | - |
| dc.subject.keywordAuthor | Fibroblast growth factor 21 (FGF21) | - |
| dc.subject.keywordAuthor | Type 2 diabetes mellitus (T2D) | - |
| dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0168365925010776?via%3Dihub | - |
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