| Literature DB >> 29687630 |
Xiaoyuan Li1,2, Yu Wang3, Zigui Wang2, Yanxin Qi1, Linlong Li2,3, Peibiao Zhang3, Xuesi Chen3, Yubin Huang1.
Abstract
3D printing has become an essential part of bone tissue engineering and attracts great attention for the fabrication of bioactive scaffolds. Combining this rapid manufacturing technique with chemical precipitation, biodegradable 3D scaffold composed of polymer matrix (polylactic acid and polyethylene glycol), ceramics (nano hydroxyapatite), and drugs (dexamethasone (Dex)) is prepared. Results of water contact angle, differential scanning calorimeter, and mechanical tests confirm that incorporation of Dex leads to significantly improved wettability, higher crystallinity degree, and tunable degradation rates. In vitro experiment with mouse MC3T3-E1 cells implies that Dex released from scaffolds is not beneficial for early cell proliferation, but it improves late alkaline phosphatase secretion and mineralization significantly. Anti-inflammation assay of murine RAW 264.7 cells proves that Dex released from all the scaffolds successfully suppresses lipopolysaccharide induced interleukin-6 and inducible nitric oxide synthase secretion by M1 macrophages. Further in vivo experiment on rat calvarial defects indicates that scaffolds containing Dex promote osteoinduction and osteogenic response and would be promising candidates for clinical applications.Entities:
Keywords: 3D printing; bone tissue engineering; degradable polymer; dexamethasone; nano hydroxyapatite
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Year: 2018 PMID: 29687630 DOI: 10.1002/mabi.201800068
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979