Intestinal therapeutic agent delivery microrobot with magnetic targeting and pH-triggered degradation abilities

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dc.contributor.authorH Lee-
dc.contributor.authorN E Mun-
dc.contributor.authorD Yoon-
dc.contributor.authorY J Choi-
dc.contributor.authorJam-Eon Park-
dc.contributor.authorD J Kim-
dc.contributor.authorS W Yoo-
dc.contributor.authorSeung Hwan Park-
dc.contributor.authorS Park-
dc.date.accessioned2025-07-29T16:32:58Z-
dc.date.available2025-07-29T16:32:58Z-
dc.date.issued2026-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/39071-
dc.description.abstractOral drug delivery remains a clinically preferred route for colorectal cancer therapy due to its noninvasive nature and patient compliance. However, conventional formulations suffer from premature degradation in the gastric environment and poor site-specific targeting in the intestine, significantly reducing therapeutic efficacy. Here, we introduce an intestinal therapeutic agent delivery microrobot (ITAM) composed of a therapeutic agent (TA) encapsulated core, a magnetic nanoparticle (MNP) layer for precise magnetic guidance, and a protective layer to minimize the loss of functional materials. This layered structure enables gastric-resilient transit, magnetic localization to colorectal lesions, and colonic pH-triggered release of TAs. In vivo studies demonstrate that ITAM achieves superior lesion-specific targeting and therapeutic efficacy enhancement compared to conventional oral delivery. Furthermore, ITAM serves as a versatile platform for delivering various therapeutic substances, including drugs, cells, and beneficial microorganisms, broadening its potential applications in intestinal disease treatment and gut health modulation.-
dc.publisherElsevier-
dc.titleIntestinal therapeutic agent delivery microrobot with magnetic targeting and pH-triggered degradation abilities-
dc.title.alternativeIntestinal therapeutic agent delivery microrobot with magnetic targeting and pH-triggered degradation abilities-
dc.typeArticle-
dc.citation.titleBiomaterials-
dc.citation.number0-
dc.citation.endPage123561-
dc.citation.startPage123561-
dc.citation.volume325-
dc.contributor.affiliatedAuthorJam-Eon Park-
dc.contributor.affiliatedAuthorSeung Hwan Park-
dc.contributor.alternativeName이효령-
dc.contributor.alternativeName문나은-
dc.contributor.alternativeName윤덕희-
dc.contributor.alternativeName최윤정-
dc.contributor.alternativeName박잠언-
dc.contributor.alternativeName김동재-
dc.contributor.alternativeName유수웅-
dc.contributor.alternativeName박승환-
dc.contributor.alternativeName박석호-
dc.identifier.bibliographicCitationBiomaterials, vol. 325, pp. 123561-123561-
dc.identifier.doi10.1016/j.biomaterials.2025.123561-
dc.subject.keywordMicrorobot-
dc.subject.keywordColorectal cancer-
dc.subject.keywordMagnetic targeting-
dc.subject.keywordpH-triggering degradation-
dc.subject.keywordTherapeutic agent delivery-
dc.subject.localColorectal cancer-
dc.subject.localcolorectal cancer-
dc.subject.localColorectal Cancer-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Biological Resource Center > 1. Journal Articles
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