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A design strategy for long-term stability of porous PEEK implants by regulation of porous structure and in vivo mechanical stimulation

摘要The bioinert nature of polyether ether ketone(PEEK)material limits the widespread clinical application of PEEK implants.Although the porous structure is considered to improve osseointegration of PEEK implants,it is hardly used due to its mechani-cal properties.This study investigated the combined influence of the porous structure and in vivo mechanical stimulation on implantation safety and bone growth based on finite element analysis of the biomechanical behavior of the implantation system.The combined control of pore size and screw preloads allows the porous PEEK implant to achieve good osseointegration while maintaining a relatively high safety level.A pore size of 600 μm and a preload of 0.05 N·m are the optimal combina-tion for the long-term stability of the implant,with which the safety factor of the implant is>2,and the predicted percentage of effective bone growth area of the bone-implant interface reaches 97%.For further clinical application,PEEK implants were fabricated with fused filament fabrication(FFF)three-dimensional(3D)printing,and clinical outcomes demonstrated better bone repair efficacy and long-term stability of porous PEEK implants compared to solid PEEK implants.Moreover,good osteointegration performance of 3D-printed porous PEEK implants was observed,with an average bone volume frac-tion>40%three months after implantation.In conclusion,3D-printed porous PEEK implants have great potential for clinical application,with validated implantation safety and good osseointegration.

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作者 Yingjie Liu [1] Ling Wang [1] Jie Zhang [2] Shuguang Liu [3] Jibao Zheng [1] Jianfeng Kang [4] Enchun Dong [1] Changning Sun [1] Ruhan A [5] Chaozong Liu [6] Chuncheng Yang [7] Dichen Li [1] 学术成果认领
作者单位 State Key Laboratory for Manufacturing Systems Engineering,School of Mechanical Engineering,Xi'an Jiaotong University,Xi'an 710049,China;National Medical Products Administration(NMPA)Key Laboratory for Research and Evaluation of Additive Manufacturing Medical Devices,Xi'an Jiaotong University,Xi'an 710049,China [1] Stomatological Hospital of Southern Medical University,Guangzhou 510280,China;Department of Oral and Maxillofacial Surgery,Center of Stomatology,Xiangya Hospital,Central South University,Changsha 410000,China [2] Stomatological Hospital of Southern Medical University,Guangzhou 510280,China [3] School of Mechatronic Engineering and Automation,Foshan University,Foshan 528225,China [4] Center for Medical Device Evaluation of NMPA,Beijing 100076,China [5] Institute of Orthopaedic&Musculoskeletal Science,University College London,Royal National Orthopaedic Hospital,Stanmore HA7 4LP,UK [6] Shaanxi Jugao-AM Technology Co.,Ltd.,Xi'an 714026,China [7]
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DOI 10.1631/bdm.2400259
发布时间 2025-04-02(万方平台首次上网日期,不代表论文的发表时间)
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生物设计与制造(英文版)

生物设计与制造(英文版)

2025年8卷2期

275-287页

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