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3D printing of PLA:CaP:GO scaffolds for bone tissue applications

Graphene oxide (GO) has attracted increasing interest for biomedical applications owing to its outstanding properties such as high specific surface area, ability to bind functional molecules for therapeutic purposes and solubility, together with mechanical resistance and good thermal conductivity. T...

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Autores principales: González-Rodríguez, L., Pérez-Davila, S., Lama, R., López-Álvarez, M., Serra, J., Novoa, B., Figueras, A., González, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227527/
https://www.ncbi.nlm.nih.gov/pubmed/37260570
http://dx.doi.org/10.1039/d3ra00981e
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author González-Rodríguez, L.
Pérez-Davila, S.
Lama, R.
López-Álvarez, M.
Serra, J.
Novoa, B.
Figueras, A.
González, P.
author_facet González-Rodríguez, L.
Pérez-Davila, S.
Lama, R.
López-Álvarez, M.
Serra, J.
Novoa, B.
Figueras, A.
González, P.
author_sort González-Rodríguez, L.
collection PubMed
description Graphene oxide (GO) has attracted increasing interest for biomedical applications owing to its outstanding properties such as high specific surface area, ability to bind functional molecules for therapeutic purposes and solubility, together with mechanical resistance and good thermal conductivity. The combination of GO with other biomaterials, such as calcium phosphate (CaP) and biodegradable polymers, presents a promising strategy for bone tissue engineering. Presently, the development of these advanced biomaterials benefits from the use of additive manufacturing techniques, such as 3D printing. In this study, we develop a 3D printed PLA:CaP:GO scaffold for bone tissue engineering. First, GO was characterised alone by XPS to determine its main bond contributions and C : O ratio. Secondly, we determined the GO dose which ensures the absence of toxicity, directly exposed in vitro (human osteoblast-like cells MG-63) and in vivo (zebrafish model). In addition, GO was microinjected in the zebrafish to evaluate its effect on immune cells, quantifying the genetic expression of the main markers. Results indicated that the GO tested (C : O of 2.14, 49.50% oxidised, main bonds: C–OH, C–O–C) in a dose ≤0.25 mg mL(−1) promoted MG63 cells viability percentages above 70%, and in a dose ≤0.10 mg mL(−1) resulted in the absence of toxicity in zebrafish embryos. The immune response evaluation reinforced this result. Finally, the optimised GO dose (0.10 mg mL(−1)) was combined with polylactic acid (PLA) and CaP to obtain a 3D printed PLA:CaP:GO scaffold. Physicochemical characterisation (SEM/EDS, XRD, FT-Raman, nano-indentation) was performed and in vivo tests confirmed its biocompatibility, enabling a novel approach for bone tissue-related applications.
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spelling pubmed-102275272023-05-31 3D printing of PLA:CaP:GO scaffolds for bone tissue applications González-Rodríguez, L. Pérez-Davila, S. Lama, R. López-Álvarez, M. Serra, J. Novoa, B. Figueras, A. González, P. RSC Adv Chemistry Graphene oxide (GO) has attracted increasing interest for biomedical applications owing to its outstanding properties such as high specific surface area, ability to bind functional molecules for therapeutic purposes and solubility, together with mechanical resistance and good thermal conductivity. The combination of GO with other biomaterials, such as calcium phosphate (CaP) and biodegradable polymers, presents a promising strategy for bone tissue engineering. Presently, the development of these advanced biomaterials benefits from the use of additive manufacturing techniques, such as 3D printing. In this study, we develop a 3D printed PLA:CaP:GO scaffold for bone tissue engineering. First, GO was characterised alone by XPS to determine its main bond contributions and C : O ratio. Secondly, we determined the GO dose which ensures the absence of toxicity, directly exposed in vitro (human osteoblast-like cells MG-63) and in vivo (zebrafish model). In addition, GO was microinjected in the zebrafish to evaluate its effect on immune cells, quantifying the genetic expression of the main markers. Results indicated that the GO tested (C : O of 2.14, 49.50% oxidised, main bonds: C–OH, C–O–C) in a dose ≤0.25 mg mL(−1) promoted MG63 cells viability percentages above 70%, and in a dose ≤0.10 mg mL(−1) resulted in the absence of toxicity in zebrafish embryos. The immune response evaluation reinforced this result. Finally, the optimised GO dose (0.10 mg mL(−1)) was combined with polylactic acid (PLA) and CaP to obtain a 3D printed PLA:CaP:GO scaffold. Physicochemical characterisation (SEM/EDS, XRD, FT-Raman, nano-indentation) was performed and in vivo tests confirmed its biocompatibility, enabling a novel approach for bone tissue-related applications. The Royal Society of Chemistry 2023-05-30 /pmc/articles/PMC10227527/ /pubmed/37260570 http://dx.doi.org/10.1039/d3ra00981e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
González-Rodríguez, L.
Pérez-Davila, S.
Lama, R.
López-Álvarez, M.
Serra, J.
Novoa, B.
Figueras, A.
González, P.
3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title 3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title_full 3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title_fullStr 3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title_full_unstemmed 3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title_short 3D printing of PLA:CaP:GO scaffolds for bone tissue applications
title_sort 3d printing of pla:cap:go scaffolds for bone tissue applications
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227527/
https://www.ncbi.nlm.nih.gov/pubmed/37260570
http://dx.doi.org/10.1039/d3ra00981e
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