Gong Yukang, Niu Yanan, Wang Chenhao, Ye Gaoqi, Chen Menghang, Hu Gaokai, Hu Yang, Xue Yuhan, Guo Tao, Yin Wenjuan, Zhang Yuangong, Gao Zheng, Liu Feng, Gao Wenshan
School of Clinical Medicine, Hebei University, Baoding 071002, Hebei, China.
Affiliated Hospital of Hebei University, Hebei University, Baoding 071002, Hebei, China.
Biomater Res. 2025 Jun 9;29:0213. doi: 10.34133/bmr.0213. eCollection 2025.
Although brushite calcium phosphate cements (Bru-CPCs) possess good bioactivity and biocompatibility, their low compressive strength hinders their effective application in osteoporotic bone defect treatment. Therefore, the aim of this study was to improve the compressive strength without sacrificing the osteogenesis properties of Bru-CPCs. Montmorillonite (MMT) was added into Bru-CPCs to get Bru-CPCs/1.5% MMT. The compressive strength of Bru-CPCs/1.5% MMT increased to 13.31 MPa, but the interfacial interactions between MMT and Bru-CPCs (inorganic-inorganic phase) limited further improvement in compressive strength. Inspired by the adhesive proteins in mussels, MMT was coated with a polydopamine (PDA) layer to get MMT@PDA. The compressive strength of Bru-CPCs/1.5% MMT@PDA further increased to 16.58 MPa. Then, the surface morphology, adhesiveness, biocompatibility, and bioactivity of CPCs/1.5% MMT@PDA were evaluated. All data indicated that by adding MMT@PDA, the compressive strength was improved without sacrificing the osteogenesis properties of Bru-CPCs.
虽然透钙磷石磷酸钙骨水泥(Bru-CPCs)具有良好的生物活性和生物相容性,但其较低的抗压强度阻碍了它们在骨质疏松性骨缺损治疗中的有效应用。因此,本研究的目的是在不牺牲Bru-CPCs成骨特性的前提下提高其抗压强度。将蒙脱石(MMT)添加到Bru-CPCs中以得到Bru-CPCs/1.5% MMT。Bru-CPCs/1.5% MMT的抗压强度提高到了13.31 MPa,但MMT与Bru-CPCs之间的界面相互作用(无机-无机相)限制了抗压强度的进一步提高。受贻贝中粘附蛋白的启发,用聚多巴胺(PDA)层包覆MMT以得到MMT@PDA。Bru-CPCs/1.5% MMT@PDA的抗压强度进一步提高到了16.58 MPa。然后,对CPCs/1.5% MMT@PDA的表面形态、粘附性、生物相容性和生物活性进行了评估。所有数据表明,通过添加MMT@PDA,在不牺牲Bru-CPCs成骨特性的情况下提高了抗压强度。