Fabrication of Submicro-Nano Structures on Polyetheretherketone Surface by Femtosecond Laser for Exciting Cellular Responses of MC3T3-E1 Cells/Gingival Epithelial Cells

被引:21
作者
Xie, Dong [1 ,2 ]
Xu, Chenhui [1 ]
Ye, Cheng [1 ]
Mei, Shiqi [3 ]
Wang, Longqing [1 ]
Zhu, Qi [1 ]
Chen, Qing [1 ]
Zhao, Qi [1 ]
Xu, Zhiyan [3 ]
Wei, Jie [3 ]
Yang, Lili [1 ]
机构
[1] Second Mil Med Univ, Shanghai Changzheng Hosp, Spine Ctr, Dept Orthopaed, Shanghai 200003, Peoples R China
[2] PLA Navy 905 Hosp, Dept Orthopaed, Shanghai 200052, Peoples R China
[3] East China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2021年 / 16卷
基金
中国国家自然科学基金;
关键词
polyetheretherketone; PEEK; surface modification; submicro-nano structures; functional group; cell responses; IN-VITRO; OSTEOGENIC DIFFERENTIATION; TITANIUM SURFACE; PROLIFERATION; OSTEOBLASTS; PEEK; OSSEOINTEGRATION; BIOMATERIALS; TOPOGRAPHY; COMPOSITE;
D O I
10.2147/IJN.S303411
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: Polyetheretherketone (PEEK) exhibits high mechanical strengths and outstanding biocompatibility but biological inertness that does not excite the cell responses and stimulate bone formation. The objective of this study was to construct submicro-nano structures on PEEK by femtosecond laser (FSL) for exciting the responses of MC3T3-E1 cells and gingival epithelial (GE) cells, which induce regeneration of bone/gingival tissues for long-term stability of dental implants. Materials and Methods: In this study, submicro-nano structures were created on PEEK surface by FSL with power of 80 mW (80FPK) and 160 mW (160FPK). Results: Compared with PEEK, both 80FPK and 160FPK with submicro-nano structures exhibited elevated surface performances (hydrophilicity, surface energy, roughness and protein absorption). Furthermore, in comparison with 80FPK, 160FPK further enhanced the surface performances. In addition, compared with PEEK, both 80FPK and 160FPK significantly excited not only the responses (adhesion, proliferation, alkaline phosphatase [ALP] activity and osteogenic gene expression) of MC3T3-E1 cells but also responses (adhesion as well as proliferation) of GE cells of human in vitro. Moreover, in comparison with 80FPK, 160FPK further enhanced the responses of MC3T3-E1 cells/GE cells. Conclusion: FSL created submicro-nano structures on PEEK with elevated surface performances, which played crucial roles in exciting the responses of MC3T3-E1 cells/GE cells. Consequently, 160FPK with elevated surface performances and outstanding cytocompatibility would have enormous potential as an implant for dental replacement.
引用
收藏
页码:3201 / 3216
页数:16
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