Cited 14 time in
Site-selective oral delivery of therapeutic antibodies to the inflamed colon via a folic acid-grafted organic/inorganic hybrid nanocomposite system
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Sang Hoon | - |
| dc.contributor.author | Song, Jae Geun | - |
| dc.contributor.author | Han, Hyo-Kyung | - |
| dc.date.accessioned | 2023-04-27T08:40:51Z | - |
| dc.date.available | 2023-04-27T08:40:51Z | - |
| dc.date.issued | 2022-11 | - |
| dc.identifier.issn | 2211-3835 | - |
| dc.identifier.issn | 2211-3843 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/2259 | - |
| dc.description.abstract | This study aimed to develop a pH-responsive folic acid-grafted organic/inorganic hybrid nanocomposite system for site-selective oral delivery of therapeutic antibodies. A folic acid-grafted aminoclay (FA-AC) was prepared via an in situ sol‒gel method. Then, a drug-loaded nanocomplex was prepared via the electrostatic interaction of FA-AC with infliximab (IFX), a model antibody, and coated with Eudragit® S100 (EFA-AC-IFX). FA-AC exhibited favorable profiles as a drug carrier including low cytotoxicity, good target selectivity, and capability to form a nanocomplex with negatively charged macromolecules. A pH-responsive FA-AC-based nanocomplex containing IFX (EFA-AC-IFX) was also obtained in a narrow size distribution with high entrapment efficiency (>87%). The conformational stability of IFX entrapped in EFA-AC-IFX was well maintained in the presence of proteolytic enzymes. EFA-AC-IFX exhibited pH-dependent drug release, minimizing premature drug release in gastric conditions and the upper intestine. Accordingly, oral administration of EFA-AC-IFX to colitis-induced mice was effective in alleviating the progression of ulcerative colitis, while oral IFX solution had no efficacy. These results suggest that a pH-responsive FA-AC-based nanocomposite system can be a new platform for the site-selective oral delivery of therapeutic antibodies. © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences | - |
| dc.format.extent | 13 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Elsevier BV | - |
| dc.title | Site-selective oral delivery of therapeutic antibodies to the inflamed colon via a folic acid-grafted organic/inorganic hybrid nanocomposite system | - |
| dc.type | Article | - |
| dc.publisher.location | 네델란드 | - |
| dc.identifier.doi | 10.1016/j.apsb.2022.06.006 | - |
| dc.identifier.scopusid | 2-s2.0-85133253768 | - |
| dc.identifier.wosid | 000898383000006 | - |
| dc.identifier.bibliographicCitation | Acta Pharmaceutica Sinica B, v.12, no.11, pp 4249 - 4261 | - |
| dc.citation.title | Acta Pharmaceutica Sinica B | - |
| dc.citation.volume | 12 | - |
| dc.citation.number | 11 | - |
| dc.citation.startPage | 4249 | - |
| dc.citation.endPage | 4261 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.subject.keywordPlus | INFLAMMATORY-BOWEL-DISEASE | - |
| dc.subject.keywordPlus | NECROSIS FACTOR ANTIBODIES | - |
| dc.subject.keywordPlus | FOLATE RECEPTOR-BETA | - |
| dc.subject.keywordPlus | DRUG-DELIVERY | - |
| dc.subject.keywordPlus | NANOPARTICLES | - |
| dc.subject.keywordPlus | MACROPHAGES | - |
| dc.subject.keywordPlus | MAGNESIUM | - |
| dc.subject.keywordPlus | RELEASE | - |
| dc.subject.keywordAuthor | Aminoclay | - |
| dc.subject.keywordAuthor | Antibody | - |
| dc.subject.keywordAuthor | Colonic delivery | - |
| dc.subject.keywordAuthor | Folate receptor | - |
| dc.subject.keywordAuthor | Inflammation | - |
| dc.subject.keywordAuthor | Infliximab | - |
| dc.subject.keywordAuthor | Nanocomposite | - |
| dc.subject.keywordAuthor | TNF-α | - |
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