The effect of supplementing the calcium phosphate cement containing poloxamer 407 on cellular activities

被引:1
作者
Kim, Yeeun [1 ]
Hamada, Kenichi [1 ]
Sekine, Kazumitsu [1 ,2 ]
机构
[1] Tokushima Univ, Dept Biomat & Bioengn, Grad Sch Biomed Sci, Tokushima, Japan
[2] Tokushima Univ, Grad Sch Biomed Sci, Dept Biomat & Bioengn, 3-18-15 Kuramoto, Tokushima 7708504, Japan
基金
日本学术振兴会;
关键词
calcium phosphate cement; cell adhesion; cytotoxicity; Poloxamer; 407; beta-TCP; IN-VITRO; BONE; DIFFERENTIATION; HYDROXYAPATITE; STRENGTH; CHITOSAN; INJECTABILITY; RELEASE; CELLS;
D O I
10.1002/jbm.b.35335
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Calcium phosphate cement (CPC) is generally used for bone repair and augmentation. Poloxamers are tri-block copolymers that are used as surfactants but have applications in drug and antibiotic delivery. However, their biological effects on bone regeneration systems remain unelucidated. Here, we aimed to understand how supplementing the prototype CPC with poloxamer would impact cellular activity and its function as a bone-grafting material. A novel CPC, modified beta-tricalcium phosphate (m beta-TCP) powder, was developed through a planetary ball-milling process using a beta-tricalcium phosphate (beta-TCP). The m beta-TCP dissolves rapidly and accelerates hydroxyapatite precipitation; successfully shortening the cement setting time and enhancing the strength. Furthermore, the addition of poloxamer 407 to m beta-TCP could reduce the risk of leakage from bone defects and improve fracture toughness while maintaining mechanical properties. In this study, the poloxamer addition effects (0.05 and 0.1 g/mL) on the cellular activities of MC3T3-E1 cells cultured in vitro were investigated. The cell viability of m beta-TCP containing poloxamer 407 was similar to that of m beta-TCP. All specimens showed effective cell attachment and healthy polygonal extension of the cytoplasm firmly attached to hydroxyapatite (HA) crystals. Therefore, even with the addition of poloxamer to m beta-TCP, it does not have a negative effect to osteoblast growth. These data demonstrated that the addition of poloxamer 407 to m beta-TCP might be considered a potential therapeutic application for the repair and regeneration of bone defects.
引用
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页数:10
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