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Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration

OBJECTIVE: The primary objective of this research was to develop a poly(l‐lactic acid) (PLLA) scaffold and evaluate critical characteristics essential for its biologic use as a craniofacial implant. MATERIALS AND METHODS: PLLA scaffolds were designed and fabricated using fused deposition modeling te...

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Autores principales: Karanth, Divakar, Puleo, David, Dawson, Dolph, Holliday, L. S., Sharab, Lina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098282/
https://www.ncbi.nlm.nih.gov/pubmed/36779270
http://dx.doi.org/10.1002/cre2.712
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author Karanth, Divakar
Puleo, David
Dawson, Dolph
Holliday, L. S.
Sharab, Lina
author_facet Karanth, Divakar
Puleo, David
Dawson, Dolph
Holliday, L. S.
Sharab, Lina
author_sort Karanth, Divakar
collection PubMed
description OBJECTIVE: The primary objective of this research was to develop a poly(l‐lactic acid) (PLLA) scaffold and evaluate critical characteristics essential for its biologic use as a craniofacial implant. MATERIALS AND METHODS: PLLA scaffolds were designed and fabricated using fused deposition modeling technology. The surface morphology and microarchitecture were analyzed using scanning electron microscopy (SEM) and microCT, respectively. Crystallography, compressive modulus, and the piezoelectric potential generated upon mechanical distortion were characterized. Hydrolytic degradation was studied. MG63 osteoblast‐like cell proliferation and morphology were assessed. RESULTS: The porosity of the scaffolds was 73%, with an average pore size of 450 µm and an average scaffold fiber thickness of 130 µm. The average compressive modulus was 244 MPa, and the scaffolds generated an electric potential of 25 mV upon cyclic/repeated loading. The crystallinity reduced from 27.5% to 13.9% during the 3D printing process. The hydrolytic degradation was minimal during a 12‐week period. Osteoblast‐like cells did not attach to the uncoated scaffold but attached well after coating the scaffold with fibrinogen. They then proliferated to cover the complete scaffold by Day 14. CONCLUSION: The PLLA scaffolds were designed and printed, proving the feasibility of 3D printing as a method of fabricating PLLA scaffolds. The elastic modulus was comparable to that of trabecular bone, and the piezoelectric properties of the PLLA were retained after 3D printing. The scaffolds were cytocompatible. These 3D‐printed PLLA scaffolds showed promising properties akin to the natural bone, and they warrant further investigation for bone regeneration.
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spelling pubmed-100982822023-04-14 Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration Karanth, Divakar Puleo, David Dawson, Dolph Holliday, L. S. Sharab, Lina Clin Exp Dent Res Original Articles OBJECTIVE: The primary objective of this research was to develop a poly(l‐lactic acid) (PLLA) scaffold and evaluate critical characteristics essential for its biologic use as a craniofacial implant. MATERIALS AND METHODS: PLLA scaffolds were designed and fabricated using fused deposition modeling technology. The surface morphology and microarchitecture were analyzed using scanning electron microscopy (SEM) and microCT, respectively. Crystallography, compressive modulus, and the piezoelectric potential generated upon mechanical distortion were characterized. Hydrolytic degradation was studied. MG63 osteoblast‐like cell proliferation and morphology were assessed. RESULTS: The porosity of the scaffolds was 73%, with an average pore size of 450 µm and an average scaffold fiber thickness of 130 µm. The average compressive modulus was 244 MPa, and the scaffolds generated an electric potential of 25 mV upon cyclic/repeated loading. The crystallinity reduced from 27.5% to 13.9% during the 3D printing process. The hydrolytic degradation was minimal during a 12‐week period. Osteoblast‐like cells did not attach to the uncoated scaffold but attached well after coating the scaffold with fibrinogen. They then proliferated to cover the complete scaffold by Day 14. CONCLUSION: The PLLA scaffolds were designed and printed, proving the feasibility of 3D printing as a method of fabricating PLLA scaffolds. The elastic modulus was comparable to that of trabecular bone, and the piezoelectric properties of the PLLA were retained after 3D printing. The scaffolds were cytocompatible. These 3D‐printed PLLA scaffolds showed promising properties akin to the natural bone, and they warrant further investigation for bone regeneration. John Wiley and Sons Inc. 2023-02-13 /pmc/articles/PMC10098282/ /pubmed/36779270 http://dx.doi.org/10.1002/cre2.712 Text en © 2023 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Karanth, Divakar
Puleo, David
Dawson, Dolph
Holliday, L. S.
Sharab, Lina
Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title_full Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title_fullStr Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title_full_unstemmed Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title_short Characterization of 3D printed biodegradable piezoelectric scaffolds for bone regeneration
title_sort characterization of 3d printed biodegradable piezoelectric scaffolds for bone regeneration
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098282/
https://www.ncbi.nlm.nih.gov/pubmed/36779270
http://dx.doi.org/10.1002/cre2.712
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