Cited 37 time in
Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(R)S100
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Sang Hoon | - |
| dc.contributor.author | Back, Seung-Yun | - |
| dc.contributor.author | Song, Jae Geun | - |
| dc.contributor.author | Han, Hyo-Kyung | - |
| dc.date.accessioned | 2023-04-27T22:40:43Z | - |
| dc.date.available | 2023-04-27T22:40:43Z | - |
| dc.date.issued | 2020-07-25 | - |
| dc.identifier.issn | 1477-3155 | - |
| dc.identifier.issn | 1477-3155 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/6409 | - |
| dc.description.abstract | This study aimed to develop a ternary nanocomposite system of organoclay, glycol-chitosan, and Eudragit(R)S100 as an effective colon targeted drug delivery carrier to enhance the oral absorption of insulin. A nanocomplex of insulin and aminoclay was prepared via spontaneous co-assembly, which was then coated with glycol-chitosan and Eudragit S(R)100 (EGAC-Ins). The double coated nanocomplex, EGAC-Ins demonstrated a high entrapment efficiency of greater than 90% and a pH-dependent drug release. The conformational stability of insulin entrapped in EGAC-Ins was effectively maintained in the presence of proteolytic enzymes. When compared to a free insulin solution, EGAC-Ins enhanced drug permeability by approximately sevenfold in Caco-2 cells and enhanced colonic drug absorption in rats. Accordingly, oral EGAC-Ins significantly reduced blood glucose levels in diabetic rats while the hypoglycemic effect of an oral insulin solution was negligible. In conclusion, EGAC-Ins should be a promising colonic delivery system for improving the oral absorption of insulin. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | BMC | - |
| dc.title | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(R)S100 | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1186/s12951-020-00662-x | - |
| dc.identifier.scopusid | 2-s2.0-85088625704 | - |
| dc.identifier.wosid | 000555953600001 | - |
| dc.identifier.bibliographicCitation | JOURNAL OF NANOBIOTECHNOLOGY, v.18, no.1 | - |
| dc.citation.title | JOURNAL OF NANOBIOTECHNOLOGY | - |
| dc.citation.volume | 18 | - |
| dc.citation.number | 1 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.subject.keywordPlus | GLYCOL CHITOSAN | - |
| dc.subject.keywordPlus | DRUG-DELIVERY | - |
| dc.subject.keywordPlus | POLYMERIC NANOPARTICLES | - |
| dc.subject.keywordPlus | CELLULAR UPTAKE | - |
| dc.subject.keywordPlus | PROTEIN | - |
| dc.subject.keywordPlus | BIOAVAILABILITY | - |
| dc.subject.keywordPlus | ABSORPTION | - |
| dc.subject.keywordPlus | AMINOCLAY | - |
| dc.subject.keywordPlus | PEPTIDES | - |
| dc.subject.keywordAuthor | Insulin | - |
| dc.subject.keywordAuthor | Oral delivery system | - |
| dc.subject.keywordAuthor | Colon targeting | - |
| dc.subject.keywordAuthor | Nano-carrier | - |
| dc.subject.keywordAuthor | Aminoclay | - |
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