Biological Fixation of Bioactive Bone Cement in Vertebroplasty: The First Clinical Investigation of Borosilicate Glass (BSG) Reinforced PMMA Bone Cement

PMMA bone cement has been clinically used for decades in vertebroplasty due to its high mechanical strength and satisfactory injectability. However, the interface between bone and PMMA is fragile and more prone to refracture in situ because PMMA lacks a proper biological response from the host bone...

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Veröffentlicht in:ACS applied materials & interfaces 2022-11, Vol.14 (46), p.51711-51727
Hauptverfasser: Zhang, Hao, Cui, Yinglin, Zhuo, Xianglong, Kim, Jua, Li, Honglong, Li, Shuaijie, Yang, Hongsheng, Su, Kun, Liu, Chunyu, Tian, Pengfei, Li, Xian, Li, Li, Wang, Deping, Zhao, Limin, Wang, Jianyun, Cui, Xu, Li, Bing, Pan, Haobo
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Sprache:eng
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Zusammenfassung:PMMA bone cement has been clinically used for decades in vertebroplasty due to its high mechanical strength and satisfactory injectability. However, the interface between bone and PMMA is fragile and more prone to refracture in situ because PMMA lacks a proper biological response from the host bone with minimal bone integration and dense fibrous tissue formation. Here, we modified PMMA by incoporating borosilicate glass (BSG) with a dual glass network of [BO3] and [SiO4], which spontaneously modulates immunity and osteogenesis. In particular, the BSG modified PMMA bone cement (abbreviated as BSG/PMMA cement) provided an alkaline microenvironment that spontaneously balanced the activities between osteoclasts and osteoblasts. Furthermore, the trace elements released from the BSGs enhanced the osteogenesis to strengthen the interface between the host bone and the implant. This study shows the first clinical case after implantation of BSG/PMMA for three months using the dual-energy CT, which found apatite nucleation around PMMA instead of fibrous tissues, indicating the biological interface was formed. Therefore, BSG/PMMA is promising as a biomaterial in vertebroplasty, overcoming the drawback of PMMA by improving the biological response from the host bone.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.2c15250