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Biomimetic anti-inflammatory and osteogenic nanoparticles self-assembled with mineral ions and tannic acid for tissue engineeringopen access

Authors
Byun, HayeonJang, Gyu NamHong, Min-HoYeo, JiwonShin, HyunjungKim, Won JongShin, Heungsoo
Issue Date
Oct-2022
Publisher
SPRINGER
Keywords
Multi-functional biomaterial; Supramolecular self-assembly; Metal phenolic network; Tannic acid; Mineral nanoparticle; Anti-inflammation; Tissue engineering
Citation
NANO CONVERGENCE, v.9, no.1, pp.1 - 12
Indexed
SCIE
SCOPUS
KCI
Journal Title
NANO CONVERGENCE
Volume
9
Number
1
Start Page
1
End Page
12
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185798
DOI
10.1186/s40580-022-00338-2
ISSN
2196-5404
Abstract
Bone healing involves complex processes including inflammation, induction, and remodeling. In this context, anti-inflammatory and osteoconductive multi-functional nanoparticles have attracted considerable attention for application in improved bone tissue regeneration. In particular, nanoparticles that promote suppression of inflammatory response after injury and direction of desirable tissue regeneration events are of immense interest to researchers. We herein report a one-step method to prepare multi-functional nanoparticles using tannic acid (TA) and simulated body fluid (SBF) containing multiple mineral ions. Mineral-tannic acid nanoparticles (mTNs) were rapidly fabricated in 10 min, and their size (around 250-350 nm) and chemical composition were controlled through the TA concentration. In vitro analysis using human adipose derived stem cells (hADSCs) showed that mTNs effectively scavenged reactive oxygen species (ROS) and enhanced osteogenesis of hADSCs by inducing secretion of alkaline phosphatase. mTNs also increased osteogenic marker gene expression even in the presence of ROS, which can generally arrest osteogenesis (OPN: 1.74, RUNX2: 1.90, OCN: 1.47-fold changes relative to cells not treated with mTNs). In vivo analysis using a mouse peritonitis model revealed that mTNs showed anti-inflammatory effects by decreasing levels of pro-inflammatory cytokines in blood (IL-6: 73 +/- 4, TNF-alpha: 42 +/- 2%) and peritoneal fluid (IL-6: 78 +/- 2, TNF-alpha: 21 +/- 6%). We believe that this one-step method for fabrication of multi-functional nanoparticles has considerable potential in tissue engineering approaches that require control of complex microenvironments, as required for tissue regeneration.
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