Additive manufacturing of bioactive glass in a biodegradable matrix

Detalhes bibliográficos
Autor(a) principal: Pires, Liliana S. O.
Data de Publicação: 2022
Outros Autores: Fernandes, Maria Helena F. V., Oliveira, José Martinho
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/35916
Resumo: Bioactive glass can induce a specific and fast response in the human body that supports tissue regeneration. It is possible to control the design of customized bioapplications with advanced technologies. Although currently used in research, only a few of these technologies have been approved by the FDA to be applied in Tissue Engineering. There is dedicated additive manufacturing equipment to manufacture biomaterials. Since they are emerging technologies in emerging fields of application it is necessary to study and develop formulations with suitable processing characteristics [1]. Formulations of bioactive glass (CaO·P2O5·MgO·SiO2 system) in two different biodegradable matrices (polylactide (PLA) and polycaprolactone (PCL)) were prepared and processed by material extrusion process, namely by Fused Filament Fabrication technique.. The polymer (PLA or PCL) involves bioactive particles in biocompatible media and allows to acquire extrudable skills. The formulations with different solid contents (20–50 wt.%) were prepared using a brabender mixer type and were characterized by different techniques (e.g., X-ray diffraction (XRD), differential scanning calorimetry (DSC), melt flow index (MFI)). The inorganic particles influence the rheological and thermal properties of bioactive glass composites. The viscosity decreases with the increase of bioactive glass content in the polymer matrix. Mechanical standard samples and scaffolds were printed and characterized. Bioactive glass composites until 40 wt.% of solid content can be printed. The bioactive glass improves the mechanical resistance of composites compared to a neat polymer matrix. However, formulations with high bioactive glass solid content (50 wt.%) showed printing limitations by their brittleness and clogging tendency.
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spelling Additive manufacturing of bioactive glass in a biodegradable matrixAdditive manufacturingBioactive glass compositesTissue engineeringBioactive glass can induce a specific and fast response in the human body that supports tissue regeneration. It is possible to control the design of customized bioapplications with advanced technologies. Although currently used in research, only a few of these technologies have been approved by the FDA to be applied in Tissue Engineering. There is dedicated additive manufacturing equipment to manufacture biomaterials. Since they are emerging technologies in emerging fields of application it is necessary to study and develop formulations with suitable processing characteristics [1]. Formulations of bioactive glass (CaO·P2O5·MgO·SiO2 system) in two different biodegradable matrices (polylactide (PLA) and polycaprolactone (PCL)) were prepared and processed by material extrusion process, namely by Fused Filament Fabrication technique.. The polymer (PLA or PCL) involves bioactive particles in biocompatible media and allows to acquire extrudable skills. The formulations with different solid contents (20–50 wt.%) were prepared using a brabender mixer type and were characterized by different techniques (e.g., X-ray diffraction (XRD), differential scanning calorimetry (DSC), melt flow index (MFI)). The inorganic particles influence the rheological and thermal properties of bioactive glass composites. The viscosity decreases with the increase of bioactive glass content in the polymer matrix. Mechanical standard samples and scaffolds were printed and characterized. Bioactive glass composites until 40 wt.% of solid content can be printed. The bioactive glass improves the mechanical resistance of composites compared to a neat polymer matrix. However, formulations with high bioactive glass solid content (50 wt.%) showed printing limitations by their brittleness and clogging tendency.MDPI2023-01-20T10:40:21Z2022-07-05T00:00:00Z2022-07-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/35916eng10.3390/materproc2022008112Pires, Liliana S. O.Fernandes, Maria Helena F. V.Oliveira, José Martinhoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:09:25Zoai:ria.ua.pt:10773/35916Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:06:56.562001Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Additive manufacturing of bioactive glass in a biodegradable matrix
title Additive manufacturing of bioactive glass in a biodegradable matrix
spellingShingle Additive manufacturing of bioactive glass in a biodegradable matrix
Pires, Liliana S. O.
Additive manufacturing
Bioactive glass composites
Tissue engineering
title_short Additive manufacturing of bioactive glass in a biodegradable matrix
title_full Additive manufacturing of bioactive glass in a biodegradable matrix
title_fullStr Additive manufacturing of bioactive glass in a biodegradable matrix
title_full_unstemmed Additive manufacturing of bioactive glass in a biodegradable matrix
title_sort Additive manufacturing of bioactive glass in a biodegradable matrix
author Pires, Liliana S. O.
author_facet Pires, Liliana S. O.
Fernandes, Maria Helena F. V.
Oliveira, José Martinho
author_role author
author2 Fernandes, Maria Helena F. V.
Oliveira, José Martinho
author2_role author
author
dc.contributor.author.fl_str_mv Pires, Liliana S. O.
Fernandes, Maria Helena F. V.
Oliveira, José Martinho
dc.subject.por.fl_str_mv Additive manufacturing
Bioactive glass composites
Tissue engineering
topic Additive manufacturing
Bioactive glass composites
Tissue engineering
description Bioactive glass can induce a specific and fast response in the human body that supports tissue regeneration. It is possible to control the design of customized bioapplications with advanced technologies. Although currently used in research, only a few of these technologies have been approved by the FDA to be applied in Tissue Engineering. There is dedicated additive manufacturing equipment to manufacture biomaterials. Since they are emerging technologies in emerging fields of application it is necessary to study and develop formulations with suitable processing characteristics [1]. Formulations of bioactive glass (CaO·P2O5·MgO·SiO2 system) in two different biodegradable matrices (polylactide (PLA) and polycaprolactone (PCL)) were prepared and processed by material extrusion process, namely by Fused Filament Fabrication technique.. The polymer (PLA or PCL) involves bioactive particles in biocompatible media and allows to acquire extrudable skills. The formulations with different solid contents (20–50 wt.%) were prepared using a brabender mixer type and were characterized by different techniques (e.g., X-ray diffraction (XRD), differential scanning calorimetry (DSC), melt flow index (MFI)). The inorganic particles influence the rheological and thermal properties of bioactive glass composites. The viscosity decreases with the increase of bioactive glass content in the polymer matrix. Mechanical standard samples and scaffolds were printed and characterized. Bioactive glass composites until 40 wt.% of solid content can be printed. The bioactive glass improves the mechanical resistance of composites compared to a neat polymer matrix. However, formulations with high bioactive glass solid content (50 wt.%) showed printing limitations by their brittleness and clogging tendency.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-05T00:00:00Z
2022-07-05
2023-01-20T10:40:21Z
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url http://hdl.handle.net/10773/35916
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dc.relation.none.fl_str_mv 10.3390/materproc2022008112
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