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Site-selective oral delivery of therapeutic antibodies to the inflamed colon via a folic acid-grafted organic/inorganic hybrid nanocomposite system

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dc.contributor.authorLee, Sang Hoon-
dc.contributor.authorSong, Jae Geun-
dc.contributor.authorHan, Hyo-Kyung-
dc.date.accessioned2023-04-27T08:40:51Z-
dc.date.available2023-04-27T08:40:51Z-
dc.date.issued2022-11-
dc.identifier.issn2211-3835-
dc.identifier.issn2211-3843-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/2259-
dc.description.abstractThis 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.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleSite-selective oral delivery of therapeutic antibodies to the inflamed colon via a folic acid-grafted organic/inorganic hybrid nanocomposite system-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.apsb.2022.06.006-
dc.identifier.scopusid2-s2.0-85133253768-
dc.identifier.wosid000898383000006-
dc.identifier.bibliographicCitationActa Pharmaceutica Sinica B, v.12, no.11, pp 4249 - 4261-
dc.citation.titleActa Pharmaceutica Sinica B-
dc.citation.volume12-
dc.citation.number11-
dc.citation.startPage4249-
dc.citation.endPage4261-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusNECROSIS FACTOR ANTIBODIES-
dc.subject.keywordPlusFOLATE RECEPTOR-BETA-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusMAGNESIUM-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordAuthorAminoclay-
dc.subject.keywordAuthorAntibody-
dc.subject.keywordAuthorColonic delivery-
dc.subject.keywordAuthorFolate receptor-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorInfliximab-
dc.subject.keywordAuthorNanocomposite-
dc.subject.keywordAuthorTNF-α-
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