Bone tissue engineering is a promising treatment for bone loss that requires a combination of porous scaffold and osteogenic cells. The aim of this study was to evaluate and develop a tricomposite, biomimetic scaffold consisting of marine-derived biomaterials, namely, chitosan and fucoidan with hydroxyapatite (HA). The effects of chitosan, fucoidan and HA individually and in combination on the proliferation and differentiation of human mesenchymal stem cells (MSCs) were investigated. According to the SEM results, the tricomposite scaffold had a uniform porous structure, which is a key requirement for cell migration, proliferation and vascularisation. The presence of HA and fucoidan in the chitosan tricomposite scaffold was confirmed using FTIR, which showed a slight decrease in porosity and an increase in the density of the tricomposite scaffold compared to other formulations. Fucoidan was found to inhibit cell proliferation at higher concentrations and at earlier time points when applied as a single treatment, but this effect was lost at later time points. Similar results were observed with HA alone. However, both HA and fucoidan increased MSC mineralisation as measured by calcium deposition. Differentiation was significantly enhanced in MSCs cultured on the tricomposite, with increased alkaline phosphatase activity on days 17 and 25. In conclusion, the tricomposite is biocompatible, promotes osteogenesis, and has the structural and compositional properties required of a scaffold for bone tissue engineering. This biomaterial could provide an effective treatment for small bone defects as an alternative to autografts or be the basis for cell attachment and differentiation in ex vivo bone tissue engineering.
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Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USAUniv Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USA
Ryan, Katherine S.
Gulder, Tobias A. M.
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Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USAUniv Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USA
Gulder, Tobias A. M.
Moore, Bradley S.
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Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USAUniv Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, San Diego, CA 92103 USA
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Korea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South KoreaKorea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea
Jeon, Eun Young
Um, Seung-Hoon
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Korea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South KoreaKorea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea
Um, Seung-Hoon
Park, Jaeho
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Korea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea
Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 08826, South KoreaKorea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea
Park, Jaeho
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Jung, Youngmee
Cheon, Cheol-Hong
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Korea Univ, Dept Chem, Seoul 02841, South KoreaKorea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea
Cheon, Cheol-Hong
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Jeon, Hojeong
Chung, Justin J.
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Seoul Natl Univ Hosp, Transdisciplinary Dept Med & Adv Technol, Seoul 03080, South Korea
Seoul Natl Univ, Coll Med, Dept Med, Seoul 03080, South KoreaKorea Inst Sci & Technol, Biomat Res Ctr, Biomed Res Div, Seoul 02792, South Korea