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Orally Deliverable Iron-Ceria Nanotablets for Treatment of Inflammatory Bowel Disease

Authors
Baik, SeungminKim,HyunminLee,YunjungKang, TaegyuShin, KwangsooSong,ChangyeongPark, Ok KyuKang, ByeonggeunLee, NohyunKim, DokyoonChoi, Seung Hong.Kim, Seung HanSoh,MinHyeon, TaeghwanKim,Chi Kyung
Issue Date
Sep-2024
Publisher
John Wiley and Sons Inc
Keywords
anti-inflammations; enteric delivery; inflammatory bowel diseases; iron-ceria nanoparticles; nanomedicines
Citation
Advanced Healthcare Materials, v.14, no.8, pp 1 - 13
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
Advanced Healthcare Materials
Volume
14
Number
8
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/120512
DOI
10.1002/adhm.202401994
ISSN
2192-2640
2192-2659
Abstract
Ceria-based nanoparticles are versatile in treating various inflammatory diseases, but their feasibility in clinical translation is undermined by safety concerns and a limited delivery system. Meanwhile, the idiopathic nature of inflammatory bowel disease (IBD) calls for a wider variety of therapeutics via moderation of the intestinal immune system. In this regard, the synthesis and oral formulation of iron-ceria nanoparticles (CF NPs) with enhanced nanozymic activity and lower toxicity risk than conventional ceria-based nanoparticles are reported. CF NPs are clustered in calcium phosphate (CaP) and coated with a pH-responsive polymer to provide the enteric formulation of iron-ceria nanotablets (CFNT). CFNT exhibits a marked alleviative efficacy in the dextran sodium sulfate (DSS)-induced enterocolitis model in vivo by modulating the pro-inflammatory behavior of innate immune cells including macrophages and neutrophils, promoting anti-inflammatory cytokine profiles, and downregulating key transcription factors of inflammatory pathways. © 2024 Wiley-VCH GmbH.
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ERICA 첨단융합대학 (ERICA 바이오나노공학전공)
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