Effect of the micro/nanostructured topography of polyetheretherketone on the behavior of MC3T3‐E1 preosteoblasts

Author:

Zhao Yuqing1ORCID,Wang Jing2,Wu Fan3,Liu Lipeng4,Wu Gaoyi5,Zhou Libo1ORCID

Affiliation:

1. Heilongjiang Key Lab of Oral Biomedical Materials and Clinical Application & Experimental Center for Stomatology Engineering, Department of Stomatology Jiamusi University Affiliated Stomatological Hospital, Jiamusi University Jiamusi People's Republic of China

2. State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, National Clinical Research Center for Oral Diseases, Shaanxi Engineering Research Center for Dental Materials and Advanced Manufacture, Department of Oral Implants, School of Stomatology The Fourth Military Medical University Xi'an People's Republic of China

3. Key Laboratory of Microecology‐Immunomodulatory Network and Related Diseases, School of Basic Medical Sciences Jiamusi University Jiamusi People's Republic of China

4. State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, National Clinical Research Center for Oral Diseases, Shaanxi Clinical Research Center for Oral Diseases, Department of Pediatric Dentistry, School of Stomatology The Fourth Military Medical University Xi'an People's Republic of China

5. Heilongjiang Key Lab of Oral Biomedical Materials and Clinical Application & Experimental Center for Stomatology Engineering, Jiamusi University Affiliated Stomatological Hospital Jiamusi University Jiamusi People's Republic of China

Abstract

AbstractPolyetheretherketone (PEEK) is of interest because of its excellent mechanical properties. However, the bioinert nature of PEEK limits its use in clinical applications. In this study, a series of micro/nanostructures combining nano‐, submicron‐, and microscale on PEEK were fabricated with 0.5, 1, 4, and 6 min of sulfonation time (S1, S2, S3, and S4). Compared to the flat surface on PEEK, the micro/nanostructure of different sizes all significantly promote cell adhesion, proliferation, and osteogenic differentiation of MC3T3‐E1 cells. It is shown that micro/nano‐porous structures with smaller size and lower roughness of S1 enabled faster cell propagation. The results of alkaline phosphatase staining, alizarin red staining, and quantitative real‐time PCR reveal that the osteogenic activity of MC3T3‐E1 cells gradually decreases with the increasement of pore size, indicating that the micro/nanostructured topography of S1 generated substantially increased matrix mineralization and bone‐like nodule formation, compared to the 3D network surface. This work provides an effective strategy for designing biomaterials with potential clinical applications.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Heilongjiang Province

University Nursing Program for Young Scholar with Creative Talents in Heilongjiang Province

Publisher

Wiley

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