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3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p

The object was to enhance the bioactivity of pure polyether-ether-ketone (PEEK) by incorporating nano-TiO(2) (n-TiO(2)) and investigate its potential mechanism. PEEK/n-TiO(2) composite was manufactured using a 3D PEEK printer and characterized by scanning electron microscopy (SEM), 3D profiler, ener...

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Autores principales: Li, Zhikun, Li, Yifan, Xu, Wei, Yu, Jimin, Tong, Shichao, Zhang, Xiangyang, Ye, Xiaojian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885016/
https://www.ncbi.nlm.nih.gov/pubmed/36760721
http://dx.doi.org/10.1515/med-2023-0636
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author Li, Zhikun
Li, Yifan
Xu, Wei
Yu, Jimin
Tong, Shichao
Zhang, Xiangyang
Ye, Xiaojian
author_facet Li, Zhikun
Li, Yifan
Xu, Wei
Yu, Jimin
Tong, Shichao
Zhang, Xiangyang
Ye, Xiaojian
author_sort Li, Zhikun
collection PubMed
description The object was to enhance the bioactivity of pure polyether-ether-ketone (PEEK) by incorporating nano-TiO(2) (n-TiO(2)) and investigate its potential mechanism. PEEK/n-TiO(2) composite was manufactured using a 3D PEEK printer and characterized by scanning electron microscopy (SEM), 3D profiler, energy-dispersive spectroscopy, and Fourier-transform infrared (FT-IR) analyses. Cytocompatibility was tested using SEM, fluorescence, and cell counting kit-8 assays. Osteogenic differentiation was evaluated by osteogenic gene and mineralized nodule levels. The expression of the candidate miRNAs were detected in composite group, and its role in osteogenic differentiation was studied. As a results the 3D-printed PEEK/n-TiO(2) composite (Φ = 25 mm, H = 2 mm) was successfully fabricated, and the TiO(2) nanoparticles were well distributed and retained the nanoscale size of the powder. The Ra value of the composite surface was 2.69 ± 0.29, and Ti accounted for 22.29 ± 12.09% (in weight), and FT-IR analysis confirmed the characteristic peaks of TiO(2). The cells in the composite group possessed better proliferation and osteogenic differentiation abilities than those in the PEEK group. miR-154-5p expression was decreased in the composite group, and the inhibition of miR-154-5p significantly enhanced the proliferation and osteogenic differentiation abilities. In conclusion, 3D-printed PEEK/n-TiO(2) composite enhanced cytocompatibility and osteogenic induction ability by downregulating miR-154-5p, which provides a promising solution for improving the osteointegration of PEEK.
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spelling pubmed-98850162023-02-08 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p Li, Zhikun Li, Yifan Xu, Wei Yu, Jimin Tong, Shichao Zhang, Xiangyang Ye, Xiaojian Open Med (Wars) Research Article The object was to enhance the bioactivity of pure polyether-ether-ketone (PEEK) by incorporating nano-TiO(2) (n-TiO(2)) and investigate its potential mechanism. PEEK/n-TiO(2) composite was manufactured using a 3D PEEK printer and characterized by scanning electron microscopy (SEM), 3D profiler, energy-dispersive spectroscopy, and Fourier-transform infrared (FT-IR) analyses. Cytocompatibility was tested using SEM, fluorescence, and cell counting kit-8 assays. Osteogenic differentiation was evaluated by osteogenic gene and mineralized nodule levels. The expression of the candidate miRNAs were detected in composite group, and its role in osteogenic differentiation was studied. As a results the 3D-printed PEEK/n-TiO(2) composite (Φ = 25 mm, H = 2 mm) was successfully fabricated, and the TiO(2) nanoparticles were well distributed and retained the nanoscale size of the powder. The Ra value of the composite surface was 2.69 ± 0.29, and Ti accounted for 22.29 ± 12.09% (in weight), and FT-IR analysis confirmed the characteristic peaks of TiO(2). The cells in the composite group possessed better proliferation and osteogenic differentiation abilities than those in the PEEK group. miR-154-5p expression was decreased in the composite group, and the inhibition of miR-154-5p significantly enhanced the proliferation and osteogenic differentiation abilities. In conclusion, 3D-printed PEEK/n-TiO(2) composite enhanced cytocompatibility and osteogenic induction ability by downregulating miR-154-5p, which provides a promising solution for improving the osteointegration of PEEK. De Gruyter 2023-01-28 /pmc/articles/PMC9885016/ /pubmed/36760721 http://dx.doi.org/10.1515/med-2023-0636 Text en © 2023 the author(s), published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Li, Zhikun
Li, Yifan
Xu, Wei
Yu, Jimin
Tong, Shichao
Zhang, Xiangyang
Ye, Xiaojian
3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title_full 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title_fullStr 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title_full_unstemmed 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title_short 3D-printed polyether-ether-ketone/n-TiO(2) composite enhances the cytocompatibility and osteogenic differentiation of MC3T3-E1 cells by downregulating miR-154-5p
title_sort 3d-printed polyether-ether-ketone/n-tio(2) composite enhances the cytocompatibility and osteogenic differentiation of mc3t3-e1 cells by downregulating mir-154-5p
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885016/
https://www.ncbi.nlm.nih.gov/pubmed/36760721
http://dx.doi.org/10.1515/med-2023-0636
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