Enhanced Osteogenesis of Dental Pulp Stem Cells In Vitro Induced by Chitosan-PEG-Incorporated Calcium Phosphate Cement

被引:12
作者
Kim, Jae Eun [1 ]
Park, Sangbae [2 ]
Lee, Woong-Sup [3 ]
Han, Jinsub [1 ,4 ]
Lim, Jae Woon [2 ]
Jeong, Seung [2 ]
Lee, Myung Chul [5 ]
Yang, Woo-Young [6 ]
Seonwoo, Hoon [7 ,8 ]
Kim, B. Moon [3 ]
Choung, Yun-Hoon [9 ]
Jang, Kyoung-Je [10 ,11 ]
Chung, Jong Hoon [1 ,4 ,12 ,13 ]
机构
[1] Seoul Natl Univ, Dept Biosyst Engn, Seoul 08826, South Korea
[2] Seoul Natl Univ, Dept Biosyst & Biomat Sci & Engn, Seoul 08826, South Korea
[3] Seoul Natl Univ, Coll Nat Sci, Dept Chem, Seoul 08826, South Korea
[4] Seoul Natl Univ, BK21 Global Smart Farm Educ Res Ctr, Seoul 08826, South Korea
[5] Harvard Med Sch, Div Engn Med, Dept Brigham & Womens Hosp, Cambridge, MA 02139 USA
[6] Seoul Natl Univ, Dent Res Inst, Seoul 08826, South Korea
[7] Sunchon Natl Univ, Coll Life Sci & Nat Resources, Dept Ind Machinery Engn, Sunchon 57922, South Korea
[8] Sunchon Natl Univ, Interdisciplinary Program IT Bio Convergence Syst, Sunchon 57922, South Korea
[9] Ajou Univ, Dept Otolaryngol, Sch Med, Suwon 16499, South Korea
[10] Gyeongsang Natl Univ, Coll Agr & Life Sci, Div Agrosyst Engn, Jinju 52828, South Korea
[11] Gyeongsang Natl Univ, Inst Agr & Life Sci, Jinju 52828, South Korea
[12] Seoul Natl Univ, Seoul 08826, South Korea
[13] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
calcium phosphate cement; chitosan-poly (ethylene glycol) (CS; PEG); dental pulp stem cell; osteogenesis; bone substitute; STRENGTH IMPROVEMENT; HYPODERMIC INJECTION; IONIC MODIFICATION; BONE SUBSTITUTES; PART I; DIFFERENTIATION; BIOMATERIALS; SCAFFOLDS; CHEMISTRY; VISCOSITY;
D O I
10.3390/polym13142252
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The use of bone graft materials is required for the treatment of bone defects damaged beyond the critical defect; therefore, injectable calcium phosphate cement (CPC) is actively used after surgery. The application of various polymers to improve injectability, mechanical strength, and biological function of injection-type CPC is encouraged. We previously developed a chitosan-PEG conjugate (CS/PEG) by a sulfur (VI) fluoride exchange reaction, and the resulting chitosan derivative showed high solubility at a neutral pH. We have demonstrated the CPC incorporated with a poly (ethylene glycol) (PEG)-grafted chitosan (CS/PEG) and developed CS/PEG CPC. The characterization of CS/PEG CPC was conducted using Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). The initial properties of CS/PEG CPCs, such as the pH, porosity, mechanical strength, zeta potential, and in vitro biocompatibility using the WST-1 assay, were also investigated. Moreover, osteocompatibility of CS/PEG CPCs was carried out via Alizarin Red S staining, immunocytochemistry, and Western blot analysis. CS/PEG CPC has enhanced mechanical strength compared to CPC, and the cohesion test also demonstrated in vivo stability. Furthermore, we determined whether CS/PEG CPC is a suitable candidate for promoting the osteogenic ability of Dental Pulp Stem Cells (DPSC). The elution of CS/PEG CPC entraps more calcium ion than CPC, as confirmed through the zeta potential test. Accordingly, the ion trapping effect of CS/PEG is considered to have played a role in promoting osteogenic differentiation of DPSCs. The results strongly suggested that CS/PEG could be used as suitable additives for improving osteogenic induction of bone substitute materials.
引用
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页数:16
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