Liu Dachuan, Shi Jiaxu, Ni Youhao, Dong Li, Cui Chen, Wang Lijie, Zhang Yu, Xu Jingxi, Chen Weicheng, Lu Kai, Lukic Miodrag J, Xia Wei, Chen Song, Li Bin
Orthopedic Institute, Department of Orthopedic Surgery, Medical 3D Printing Center, The First Affiliated Hospital, MOE Key Laboratory of Geriatric Diseases and Immunology, School of Basic Medical Sciences, Suzhou Medical College, Soochow University, Suzhou, Jiangsu 215000, China.
Key Laboratory of C&PC Structures of Ministry of Education, Southeast University, Nanjing 211189, China.
Research (Wash D C). 2025 Jul 10;8:0776. doi: 10.34133/research.0776. eCollection 2025.
In orthopedic minimally invasive surgeries (MIS) such as percutaneous vertebroplasty (PVP) and percutaneous kyphoplasty (PKP), calcium phosphate cements (CPCs) are an attractive alternative to bioinert polymethyl methacrylate (PMMA) due to their superior biocompatibility and osteoconductivity. However, the mechanical strength and injectability of CPCs often remain insufficient for load-bearing applications, limiting their broader use in these critical procedures. To address this challenge, we introduce a machine learning-assisted approach to enhance both the mechanical strength and injectability of CPCs by identifying specific polymers as superplasticizers. By optimizing its concentration and the liquid-to-powder (L/P) ratio, we developed an injectable brushite-based cement with an exceptional compressive strength of 79.5 ± 4.3 MPa, surpassing both traditional CPCs and PMMA in orthopedic applications. Zeta potential and adsorption studies reveal that these superplasticizers enhance cement paste dispersion via electrostatic repulsion. In vitro assays demonstrate excellent biocompatibility and osteogenic properties, while in vivo experiments further confirm the cement's superior osteoinductive capability. The brushite cement regulates cellular metabolism and stem cell differentiation by enhancing energy metabolism and activating key signaling pathways such as phosphatidylinositol 3-kinase-AKT and mitogen-activated protein kinase-extracellular signal-regulated kinase. These findings offer a novel approach to fabricating CPCs with enhanced mechanical strength and osteogenic potential, addressing long-standing challenges in orthopedic MIS.
在诸如经皮椎体成形术(PVP)和经皮后凸成形术(PKP)等骨科微创手术(MIS)中,磷酸钙骨水泥(CPC)由于其优异的生物相容性和成骨传导性,是生物惰性聚甲基丙烯酸甲酯(PMMA)的一种有吸引力的替代品。然而,CPC的机械强度和可注射性通常仍不足以用于承重应用,限制了它们在这些关键手术中的更广泛应用。为应对这一挑战,我们引入了一种机器学习辅助方法,通过识别特定聚合物作为高效减水剂来提高CPC的机械强度和可注射性。通过优化其浓度和液粉比(L/P),我们开发了一种可注射的透钙磷石基骨水泥,其抗压强度高达79.5±4.3MPa,在骨科应用中超过了传统CPC和PMMA。zeta电位和吸附研究表明,这些高效减水剂通过静电排斥增强水泥浆体的分散性。体外试验证明了其优异的生物相容性和成骨特性,而体内实验进一步证实了该骨水泥具有卓越的骨诱导能力。透钙磷石骨水泥通过增强能量代谢和激活关键信号通路(如磷脂酰肌醇3激酶 - AKT和丝裂原活化蛋白激酶 - 细胞外信号调节激酶)来调节细胞代谢和干细胞分化。这些发现为制造具有增强机械强度和成骨潜力的CPC提供了一种新方法,解决了骨科MIS中长期存在的挑战。