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Inflamed Tissue-Targeting Polyphenol-Condensed Antioxidant Nanoparticles with Therapeutic Potential

Title
Inflamed Tissue-Targeting Polyphenol-Condensed Antioxidant Nanoparticles with Therapeutic Potential
Authors
Jang, Dohyub; Choi, Honghwan; Lee, Juhyang; Chun, Yousun; Heo, Yoon-Ho; Lee, Luke P.; Ahn, Dong June; Shin, Ik-Soo; Kim, Dong Ha; Seo, Young Hun; Kim, Sehoon
Ewha Authors
김동하
SCOPUS Author ID
김동하scopus
Issue Date
2025
Journal Title
ADVANCED HEALTHCARE MATERIALS
ISSN
2192-2640JCR Link

2192-2659JCR Link
Citation
ADVANCED HEALTHCARE MATERIALS vol. 14, no. 11
Keywords
anti-inflammatory effect; nanotherapeutic; polyphenol; reactive oxygen species (ROS) scavenging; systemic inflammation
Publisher
WILEY
Indexed
SCOPUS WOS scopus
Document Type
Article
Abstract
Inflammation is essential for pathogen eradication and tissue repair; However, chronic inflammation can bring on multi-organ dysfunction due to an overproduction of reactive oxygen species (ROS). Among various anti-inflammatory agents, polyphenol-based nanotherapeutics offer potential advantages, including enhanced stability, targeted delivery, multiple therapeutic functions, and personalized therapy tailored to the severity. Despite these advantages, the development of biocompatible nanomedicines capable of selective accumulation in inflamed tissues and efficient inhibition of ROS-induced inflammatory signaling pathways remains a considerable challenge. In this study, a novel anti-inflammatory nanotherapeutic is engineered through the temperature-dependent condensation of polyphenolic catechin facilitated by hydrothermal reactions. The resulting catechin-condensed nanotherapeutic (CCN150), synthesized at a relatively low temperature, retains physicochemical and functional properties akin to its precursor, catechin, but with a marked enhancement in water solubility. CCN150 protects cells from oxidative stress by eliminating intracellular ROS and augmenting antioxidant enzymes. In vivo studies reveal that intravenously administered CCN150 predominantly accumulates in inflamed tissues, with minimal distribution to healthy regions. Furthermore, CCN150 effectively reduces systemic inflammation in mouse models by disrupting the cycles of ROS instigated by a pro-inflammatory oxidative milieu. Exhibiting negligible toxicity, CCN150 holds substantial promise for extensive therapeutic applications in the treatment of various ROS-mediated inflammatory diseases.
DOI
10.1002/adhm.202500495
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자연과학대학 > 화학·나노과학전공 > Journal papers
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