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In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp

Calcium salt precipitation induced by intracanal medicaments contributes to the formation of apical hard tissue during apexification. This study compared the calcium salt-forming ability of a new calcium silicate-based intracanal medicament (Bio-C Temp) with that of two commercial calcium hydroxide...

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Autores principales: Edanami, Naoki, Belal, Razi Saifullah Ibn, Takenaka, Shoji, Yoshiba, Kunihiko, Gutierrez, Rosa Edith Baldeon, Takahara, Shintaro, Yoshiba, Nagako, Ohkura, Naoto, Noiri, Yuichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137445/
https://www.ncbi.nlm.nih.gov/pubmed/37185469
http://dx.doi.org/10.3390/dj11040091
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author Edanami, Naoki
Belal, Razi Saifullah Ibn
Takenaka, Shoji
Yoshiba, Kunihiko
Gutierrez, Rosa Edith Baldeon
Takahara, Shintaro
Yoshiba, Nagako
Ohkura, Naoto
Noiri, Yuichiro
author_facet Edanami, Naoki
Belal, Razi Saifullah Ibn
Takenaka, Shoji
Yoshiba, Kunihiko
Gutierrez, Rosa Edith Baldeon
Takahara, Shintaro
Yoshiba, Nagako
Ohkura, Naoto
Noiri, Yuichiro
author_sort Edanami, Naoki
collection PubMed
description Calcium salt precipitation induced by intracanal medicaments contributes to the formation of apical hard tissue during apexification. This study compared the calcium salt-forming ability of a new calcium silicate-based intracanal medicament (Bio-C Temp) with that of two commercial calcium hydroxide pastes (Calcipex Plane II and Vitapex) in a rat subcutaneous implantation model. Polytetrafluoroethylene tubes containing each of the three materials were subcutaneously implanted in 4-week-old male Wistar rats. After 28 days, the composition and amount of calcium salts formed at the material–tissue interface were assessed using micro-Raman spectroscopy, X-ray diffraction, and elemental mapping. The tested materials produced white precipitates that had Raman spectra with peaks corresponding to hydroxyapatite and calcite. X-ray diffraction detected hydroxyapatite formation on Calcipex Plane II and Vitapex implants, as well as calcite formation on all three materials. Elemental mapping revealed that Bio-C Temp generated significantly smaller calcium- and phosphorus-rich calcified regions within the subcutaneous connective tissue than Vitapex. These results indicate that Bio-C Temp produced less calcium salt in rat subcutaneous tissue than Vitapex, although all materials formed hydroxyapatite and calcite in rat subcutaneous tissue. Bio-C Temp could be less effective than Vitapex in promoting apical hard tissue formation during apexification.
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spelling pubmed-101374452023-04-28 In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp Edanami, Naoki Belal, Razi Saifullah Ibn Takenaka, Shoji Yoshiba, Kunihiko Gutierrez, Rosa Edith Baldeon Takahara, Shintaro Yoshiba, Nagako Ohkura, Naoto Noiri, Yuichiro Dent J (Basel) Brief Report Calcium salt precipitation induced by intracanal medicaments contributes to the formation of apical hard tissue during apexification. This study compared the calcium salt-forming ability of a new calcium silicate-based intracanal medicament (Bio-C Temp) with that of two commercial calcium hydroxide pastes (Calcipex Plane II and Vitapex) in a rat subcutaneous implantation model. Polytetrafluoroethylene tubes containing each of the three materials were subcutaneously implanted in 4-week-old male Wistar rats. After 28 days, the composition and amount of calcium salts formed at the material–tissue interface were assessed using micro-Raman spectroscopy, X-ray diffraction, and elemental mapping. The tested materials produced white precipitates that had Raman spectra with peaks corresponding to hydroxyapatite and calcite. X-ray diffraction detected hydroxyapatite formation on Calcipex Plane II and Vitapex implants, as well as calcite formation on all three materials. Elemental mapping revealed that Bio-C Temp generated significantly smaller calcium- and phosphorus-rich calcified regions within the subcutaneous connective tissue than Vitapex. These results indicate that Bio-C Temp produced less calcium salt in rat subcutaneous tissue than Vitapex, although all materials formed hydroxyapatite and calcite in rat subcutaneous tissue. Bio-C Temp could be less effective than Vitapex in promoting apical hard tissue formation during apexification. MDPI 2023-03-30 /pmc/articles/PMC10137445/ /pubmed/37185469 http://dx.doi.org/10.3390/dj11040091 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Brief Report
Edanami, Naoki
Belal, Razi Saifullah Ibn
Takenaka, Shoji
Yoshiba, Kunihiko
Gutierrez, Rosa Edith Baldeon
Takahara, Shintaro
Yoshiba, Nagako
Ohkura, Naoto
Noiri, Yuichiro
In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title_full In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title_fullStr In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title_full_unstemmed In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title_short In Vivo Assessment of the Calcium Salt-Forming Ability of a New Calcium Silicate-Based Intracanal Medicament: Bio-C Temp
title_sort in vivo assessment of the calcium salt-forming ability of a new calcium silicate-based intracanal medicament: bio-c temp
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137445/
https://www.ncbi.nlm.nih.gov/pubmed/37185469
http://dx.doi.org/10.3390/dj11040091
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