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Oral Biofilm Formation on Different Materials for Dental Implants
Published on: June 24, 2018
Zinc and metformin co-functionalized polyetheretherketone: A novel dental implant material tailored for the elderly
Zhengwei Liu1, Enze Zhao2, Yansong Wang3
1Department of Orthopedics, Northern Jiangsu People's Hospital, Clinical Teaching Hospital of Medical School, Nanjing University, Yangzhou, Jiangsu, PR China.
Introduction:
The rising demand for dental implants among the elderly population is challenged by age-related impairments in osteogenic regeneration, such as Wnt/β-catenin signaling decline, ROS-mediated cellular senescence (compromising osteoblast differentiation), and elevated pro-inflammatory cytokines (e.g. IL-6, TNF-α). Senescent osteoblasts establishes a pathological triad: (1) cell-cycle arrest-mediated osteogenic impairment, (2) SASP-fueled chronic inflammation, and (3) immune-bone uncoupling-collectively driving alveolar bone deterioration in the elderly. Polyetheretherketone (PEEK), with its elastic modulus similar to that of alveolar bone, emerges as a promising implant material. However, its bioinert nature limits its osseointegration capabilities.
Objectives:
This study aimed to develop a functionalized PEEK derivative, ZnMet@PEEK, by integrating zinc (Zn) and metformin (Met) into PEEK. to enhance osseointegration with alveolar bone in elderly patients.
Methods:
In this study, we combined the anti-inflammatory and osteogenic properties of Zn with the anti-senescence effects of Met using dopamine-assisted physical adhesion to prepare ZnMet@PEEK, aiming to enhance PEEK's osseointegration with alveolar bone in elderly patients. We examined the biocompatibility and osteoblast differentiation-inducing ability of ZnMet@PEEK in vitro by CCK8, live/dead cell staining, RT-qPCR, immunofluorescence staining and Enzyme-Linked Immunosorbent Assay for osteogenesis-related proteins. Further, we constructed an animal model and detected the bone regeneration ability of ZnMet@PEEK in vivo by micro-CT and histological analysis.
Results:
Material characterization confirmed the incorporation of ZnMet onto PEEK. in vitro and in vivo evaluations demonstrated that ZnMet@PEEK exhibited excellent biocompatibility, significantly inhibited inflammation, promoted bone formation, and inhibited cellular senescence, ultimately resulting in enhanced osseointegration in aged rats.
Conclusions:
In this study, we successfully developed a new functionalized PEEK derivative, ZnMet@PEEK, with tailored bioactivities including anti-inflammatory, osteogenic, and anti-senescence properties, as a dental implant for the elderly population. Therefore, we believe that ZnMet@PEEK, specifically tailored for elderly patients, is a promising dental implant material offering a novel solution to the multifaceted challenges of osseointegration.
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