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Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats

The present work aims at evaluating the potential gains derived from partially replacing calcium in resorbable β-tricalcium phosphate (β-TCP) by two different molar percentages of strontium (5, 10) and zinc (1, 2), concomitantly with a fixed molar percentage (0.5) of manganese. Synthetic granular co...

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Autores principales: Ferreira, Manuel M., Brito, Ana F., Brazete, Daniela, Pereira, Inês C., Carrilho, Eunice, Abrantes, Ana M., Pires, Ana S., Aguiar, Maria J., Carvalho, Lina, Botelho, Maria F., Ferreira, José M.F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337740/
https://www.ncbi.nlm.nih.gov/pubmed/30577440
http://dx.doi.org/10.3390/ma12010004
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author Ferreira, Manuel M.
Brito, Ana F.
Brazete, Daniela
Pereira, Inês C.
Carrilho, Eunice
Abrantes, Ana M.
Pires, Ana S.
Aguiar, Maria J.
Carvalho, Lina
Botelho, Maria F.
Ferreira, José M.F.
author_facet Ferreira, Manuel M.
Brito, Ana F.
Brazete, Daniela
Pereira, Inês C.
Carrilho, Eunice
Abrantes, Ana M.
Pires, Ana S.
Aguiar, Maria J.
Carvalho, Lina
Botelho, Maria F.
Ferreira, José M.F.
author_sort Ferreira, Manuel M.
collection PubMed
description The present work aims at evaluating the potential gains derived from partially replacing calcium in resorbable β-tricalcium phosphate (β-TCP) by two different molar percentages of strontium (5, 10) and zinc (1, 2), concomitantly with a fixed molar percentage (0.5) of manganese. Synthetic granular composite bone filling grafts consisting of doped β-TCP and an alkali-free bioactive glass were prepared and implanted in ~4 mm diameter bone defects drilled in the calvaria of Wistar rats used as animal models. The animals were sacrificed after 9 weeks of implantation and the calvaria was excised. Non-manipulated bone was used as positive control, while empty defects were used as a negative control group. The von Kossa staining revealed an enhanced new bone formation with increasing doping levels, supporting the therapeutic effects exerted by the doping elements. The percentage of newly formed bone was similar when the defects were filled with autologous bone, BG (previous results) or 3TCP2/7BG, which indicates that the latter two are excellent candidates for replacement of autologous bone as bone regeneration material. This finding confirms that doping with suitable doses of therapeutic ions is a good strategy towards transposing the bone graft materials to biomedical applications in humans.
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spelling pubmed-63377402019-01-22 Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats Ferreira, Manuel M. Brito, Ana F. Brazete, Daniela Pereira, Inês C. Carrilho, Eunice Abrantes, Ana M. Pires, Ana S. Aguiar, Maria J. Carvalho, Lina Botelho, Maria F. Ferreira, José M.F. Materials (Basel) Article The present work aims at evaluating the potential gains derived from partially replacing calcium in resorbable β-tricalcium phosphate (β-TCP) by two different molar percentages of strontium (5, 10) and zinc (1, 2), concomitantly with a fixed molar percentage (0.5) of manganese. Synthetic granular composite bone filling grafts consisting of doped β-TCP and an alkali-free bioactive glass were prepared and implanted in ~4 mm diameter bone defects drilled in the calvaria of Wistar rats used as animal models. The animals were sacrificed after 9 weeks of implantation and the calvaria was excised. Non-manipulated bone was used as positive control, while empty defects were used as a negative control group. The von Kossa staining revealed an enhanced new bone formation with increasing doping levels, supporting the therapeutic effects exerted by the doping elements. The percentage of newly formed bone was similar when the defects were filled with autologous bone, BG (previous results) or 3TCP2/7BG, which indicates that the latter two are excellent candidates for replacement of autologous bone as bone regeneration material. This finding confirms that doping with suitable doses of therapeutic ions is a good strategy towards transposing the bone graft materials to biomedical applications in humans. MDPI 2018-12-20 /pmc/articles/PMC6337740/ /pubmed/30577440 http://dx.doi.org/10.3390/ma12010004 Text en © 2018 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ferreira, Manuel M.
Brito, Ana F.
Brazete, Daniela
Pereira, Inês C.
Carrilho, Eunice
Abrantes, Ana M.
Pires, Ana S.
Aguiar, Maria J.
Carvalho, Lina
Botelho, Maria F.
Ferreira, José M.F.
Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title_full Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title_fullStr Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title_full_unstemmed Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title_short Doping β-TCP as a Strategy for Enhancing the Regenerative Potential of Composite β-TCP—Alkali-Free Bioactive Glass Bone Grafts. Experimental Study in Rats
title_sort doping β-tcp as a strategy for enhancing the regenerative potential of composite β-tcp—alkali-free bioactive glass bone grafts. experimental study in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337740/
https://www.ncbi.nlm.nih.gov/pubmed/30577440
http://dx.doi.org/10.3390/ma12010004
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