Effect of Surface Modification of PEEK Artificial Phalanx by 3D Printing on its Biological Activity

Objective: Polyetheretherketone (PEEK) is widely used as an orthopedic implant material owing to its good biocompatibility and mechanical strength; however, PEEK implants are biologically inert, resulting in suboptimal cellular responses after implantation. The aim of this study was to enhance the b...

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Veröffentlicht in:Coatings (Basel) 2023-02, Vol.13 (2), p.400
Hauptverfasser: Shi, Yun, Deng, Ting, Peng, Yu, Qin, Zugan, Ramalingam, Murugan, Pan, Yang, Chen, Cheng, Zhao, Feng, Cheng, Lijia, Liu, Juan
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container_end_page
container_issue 2
container_start_page 400
container_title Coatings (Basel)
container_volume 13
creator Shi, Yun
Deng, Ting
Peng, Yu
Qin, Zugan
Ramalingam, Murugan
Pan, Yang
Chen, Cheng
Zhao, Feng
Cheng, Lijia
Liu, Juan
description Objective: Polyetheretherketone (PEEK) is widely used as an orthopedic implant material owing to its good biocompatibility and mechanical strength; however, PEEK implants are biologically inert, resulting in suboptimal cellular responses after implantation. The aim of this study was to enhance the biological activity of PEEK through sulfonation treatment. Methods: In this study, distal phalangeal implants of PEEK were customized by fused deposition modeling (FDM) printing technology and soaked in concentrated sulfuric acid at different times to obtain sulfonated PEEK (SPEEK). The groups were divided into five groups according to the sulfonation time as follows: 0 min (control group), 1 min (group SPEEK1), 2 min (group SPEEK2), 4 min (group SPEEK4), and 8 min (group SPEEK8). Then the physicochemical characteristics of implants were determined by SEM, XRD, EDS, etc. The implants were co-cultured with stem cells from human exfoliated deciduous teeth (SHED), and then the cell proliferation, adhesion, alkaline phosphatase (ALP) activity, and alizarin red staining were performed to detect the biological activity, biocompatibility, and osteogenic activity of the SPEEK implants. Results: The sulfonation time range of 1 to 8 min could promote the formation of micropores on the surface of PEEK implants, while slightly affecting the composition and compression performance of the implants. Compared with the control group, the hydrophilicity of PEEK materials was not improved after sulfonation treatment. Tests for adhesion and proliferation of SHED indicated that SPEEK2 showed superior biocompatibility. Furthermore, ALP activity and semi-quantitative analysis of Alizarin red staining showed that the osteogenic activity of SPEEK2 phalanges exhibited significantly stronger osteogenic activity than the other groups. Conclusions: The method presented here provides a promising approach to improve the surface bioactivity of PEEK implants prepared by FDM, providing a shred of primary evidence to support the application of SPEEK in orthopedics.
doi_str_mv 10.3390/coatings13020400
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The aim of this study was to enhance the biological activity of PEEK through sulfonation treatment. Methods: In this study, distal phalangeal implants of PEEK were customized by fused deposition modeling (FDM) printing technology and soaked in concentrated sulfuric acid at different times to obtain sulfonated PEEK (SPEEK). The groups were divided into five groups according to the sulfonation time as follows: 0 min (control group), 1 min (group SPEEK1), 2 min (group SPEEK2), 4 min (group SPEEK4), and 8 min (group SPEEK8). Then the physicochemical characteristics of implants were determined by SEM, XRD, EDS, etc. The implants were co-cultured with stem cells from human exfoliated deciduous teeth (SHED), and then the cell proliferation, adhesion, alkaline phosphatase (ALP) activity, and alizarin red staining were performed to detect the biological activity, biocompatibility, and osteogenic activity of the SPEEK implants. Results: The sulfonation time range of 1 to 8 min could promote the formation of micropores on the surface of PEEK implants, while slightly affecting the composition and compression performance of the implants. Compared with the control group, the hydrophilicity of PEEK materials was not improved after sulfonation treatment. Tests for adhesion and proliferation of SHED indicated that SPEEK2 showed superior biocompatibility. Furthermore, ALP activity and semi-quantitative analysis of Alizarin red staining showed that the osteogenic activity of SPEEK2 phalanges exhibited significantly stronger osteogenic activity than the other groups. Conclusions: The method presented here provides a promising approach to improve the surface bioactivity of PEEK implants prepared by FDM, providing a shred of primary evidence to support the application of SPEEK in orthopedics.</description><identifier>ISSN: 2079-6412</identifier><identifier>EISSN: 2079-6412</identifier><identifier>DOI: 10.3390/coatings13020400</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>3-D printers ; 3D printing ; Alizarin ; Alkaline phosphatase ; Analysis ; Biocompatibility ; Biological activity ; Biological effects ; Contact angle ; Fused deposition modeling ; Implants, Artificial ; Orthopaedic implants ; Orthopedics ; Polyether ether ketones ; Prosthesis ; Software ; Staining ; Stem cells ; Sulfuric acid ; Surgical implants ; Three dimensional printing</subject><ispartof>Coatings (Basel), 2023-02, Vol.13 (2), p.400</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-c00755aee8d296c1e08f5e161fcc12d80ddff6dc53015afcae39b89e06ce68a3</citedby><cites>FETCH-LOGICAL-c380t-c00755aee8d296c1e08f5e161fcc12d80ddff6dc53015afcae39b89e06ce68a3</cites><orcidid>0000-0002-4412-6807 ; 0000-0001-7260-7379 ; 0000-0001-6498-9792</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Shi, Yun</creatorcontrib><creatorcontrib>Deng, Ting</creatorcontrib><creatorcontrib>Peng, Yu</creatorcontrib><creatorcontrib>Qin, Zugan</creatorcontrib><creatorcontrib>Ramalingam, Murugan</creatorcontrib><creatorcontrib>Pan, Yang</creatorcontrib><creatorcontrib>Chen, Cheng</creatorcontrib><creatorcontrib>Zhao, Feng</creatorcontrib><creatorcontrib>Cheng, Lijia</creatorcontrib><creatorcontrib>Liu, Juan</creatorcontrib><title>Effect of Surface Modification of PEEK Artificial Phalanx by 3D Printing on its Biological Activity</title><title>Coatings (Basel)</title><description>Objective: Polyetheretherketone (PEEK) is widely used as an orthopedic implant material owing to its good biocompatibility and mechanical strength; however, PEEK implants are biologically inert, resulting in suboptimal cellular responses after implantation. 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however, PEEK implants are biologically inert, resulting in suboptimal cellular responses after implantation. The aim of this study was to enhance the biological activity of PEEK through sulfonation treatment. Methods: In this study, distal phalangeal implants of PEEK were customized by fused deposition modeling (FDM) printing technology and soaked in concentrated sulfuric acid at different times to obtain sulfonated PEEK (SPEEK). The groups were divided into five groups according to the sulfonation time as follows: 0 min (control group), 1 min (group SPEEK1), 2 min (group SPEEK2), 4 min (group SPEEK4), and 8 min (group SPEEK8). Then the physicochemical characteristics of implants were determined by SEM, XRD, EDS, etc. The implants were co-cultured with stem cells from human exfoliated deciduous teeth (SHED), and then the cell proliferation, adhesion, alkaline phosphatase (ALP) activity, and alizarin red staining were performed to detect the biological activity, biocompatibility, and osteogenic activity of the SPEEK implants. Results: The sulfonation time range of 1 to 8 min could promote the formation of micropores on the surface of PEEK implants, while slightly affecting the composition and compression performance of the implants. Compared with the control group, the hydrophilicity of PEEK materials was not improved after sulfonation treatment. Tests for adhesion and proliferation of SHED indicated that SPEEK2 showed superior biocompatibility. Furthermore, ALP activity and semi-quantitative analysis of Alizarin red staining showed that the osteogenic activity of SPEEK2 phalanges exhibited significantly stronger osteogenic activity than the other groups. Conclusions: The method presented here provides a promising approach to improve the surface bioactivity of PEEK implants prepared by FDM, providing a shred of primary evidence to support the application of SPEEK in orthopedics.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/coatings13020400</doi><orcidid>https://orcid.org/0000-0002-4412-6807</orcidid><orcidid>https://orcid.org/0000-0001-7260-7379</orcidid><orcidid>https://orcid.org/0000-0001-6498-9792</orcidid><oa>free_for_read</oa></addata></record>
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source MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects 3-D printers
3D printing
Alizarin
Alkaline phosphatase
Analysis
Biocompatibility
Biological activity
Biological effects
Contact angle
Fused deposition modeling
Implants, Artificial
Orthopaedic implants
Orthopedics
Polyether ether ketones
Prosthesis
Software
Staining
Stem cells
Sulfuric acid
Surgical implants
Three dimensional printing
title Effect of Surface Modification of PEEK Artificial Phalanx by 3D Printing on its Biological Activity
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