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Oral drug delivery platforms for biomedical applications

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dc.contributor.authorOuyang, Jiang-
dc.contributor.authorZhang, Zhongyang-
dc.contributor.authorDeng, Bo-
dc.contributor.authorLiu, Jinggong-
dc.contributor.authorWang, Liqiang-
dc.contributor.authorLiu, Haijun-
dc.contributor.authorKoo, Seyoung-
dc.contributor.authorChen, Shuying-
dc.contributor.authorLi, Yongjiang-
dc.contributor.authorYaremenko, Alexey V.-
dc.contributor.authorHuang, Xiangang-
dc.contributor.authorChen, Wei-
dc.contributor.authorLee, Yuhan-
dc.contributor.authorTao, Wei-
dc.date.accessioned2024-05-02T05:30:22Z-
dc.date.available2024-05-02T05:30:22Z-
dc.date.issued2023-01-
dc.identifier.issn1369-7021-
dc.identifier.issn1873-4103-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/118942-
dc.description.abstractOral administration is perhaps the most commonly used and acceptable route for drug delivery to patients, mainly due to its non-invasiveness, simplicity, and versatility. Conventional delivery media such as tablets or capsule-based formulations, however, could result in low drug bioavailability and insufficient therapeutic efficiency, especially for delivering biologics (e.g., peptide, protein, antibody, nucleic acid). Therefore, with the advancement of material science and micro-/nano-fabrication techniques, various carriers have been developed to protect drugs and improve their absorption in the gastrointestinal (GI) tract. Herein, we first summarized various types of drug molecules being used for oral administration. Then we discussed the major physiological barriers (including various biochemical, mucosal diffusion, and cellular permeation barriers) that hinder drug transportation and absorption, as well as the main targeting regions in the GI tract. On this basis, we reviewed recently emerged oral drug delivery platforms and discussed their widely investigated biomedical applications. Finally, we present future perspectives for materials science-enabled oral drug delivery platforms, and potential challenges for clinical translation. © 2023 Elsevier Ltd-
dc.format.extent31-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleOral drug delivery platforms for biomedical applications-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.mattod.2023.01.002-
dc.identifier.scopusid2-s2.0-85147263806-
dc.identifier.wosid000957111900001-
dc.identifier.bibliographicCitationMaterials Today, v.62, pp 296 - 326-
dc.citation.titleMaterials Today-
dc.citation.volume62-
dc.citation.startPage296-
dc.citation.endPage326-
dc.type.docType정기 학술지(Review)-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusSOLID LIPID NANOPARTICLES-
dc.subject.keywordPlusPOLYMERIC NANOPARTICLES-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusGOLD NANOPARTICLES-
dc.subject.keywordPlusTHERAPEUTIC APPLICATIONS-
dc.subject.keywordPlusNANOCOMPOSITE HYDROGELS-
dc.subject.keywordPlusGASTROINTESTINAL MUCUS-
dc.subject.keywordPlusBIFIDOBACTERIUM-LONGUM-
dc.subject.keywordPlusSILICA NANOPARTICLES-
dc.subject.keywordPlusMETABOLIC SYNDROME-
dc.subject.keywordAuthorBiomedical applications-
dc.subject.keywordAuthorDelivery platforms-
dc.subject.keywordAuthorgastrointestinal (GI) tract-
dc.subject.keywordAuthorOral drug-
dc.subject.keywordAuthorPhysiological barriers-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1369702123000020-
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