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Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament

OBJECTIVE: The aim of this study is to compare the cytotoxicity of triple antibiotic paste (TAP) with an anti-inflammatory drug (TAP+Catafast-TAPC) in nano and regular formulations versus calcium hydroxide as intracanal medicaments. METHODS: The TAPC drugs extraction were made in cell culture media...

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Autores principales: Nashaat, Yousra, Sabry, Hadil, Hassan, Soha Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056808/
https://www.ncbi.nlm.nih.gov/pubmed/33762529
http://dx.doi.org/10.14744/eej.2020.29292
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author Nashaat, Yousra
Sabry, Hadil
Hassan, Soha Ahmed
author_facet Nashaat, Yousra
Sabry, Hadil
Hassan, Soha Ahmed
author_sort Nashaat, Yousra
collection PubMed
description OBJECTIVE: The aim of this study is to compare the cytotoxicity of triple antibiotic paste (TAP) with an anti-inflammatory drug (TAP+Catafast-TAPC) in nano and regular formulations versus calcium hydroxide as intracanal medicaments. METHODS: The TAPC drugs extraction were made in cell culture media MEM-E (Eagle’s minimal essential medium) using concentration of 10 mg/mL of each sample for seven days. Inhibitory concentrations (IC50 values) were determined for each extract. A human fibroblasts cell line was used to evaluate the cytotoxicity of different concentrations (10, 0.625 and 0.07 mg/mL) using MTT essay. The cell viability was measured after 24 h, 48 h and 7 days for all concentrations of the drugs. Flow cytometry analysis was carried out to identify the effect of materials on apoptosis/necrosis. Statistical analysis for the obtained results was done by one-way ANOVA. RESULTS: The results revealed that cell viability was inversely proportional to the duration of treatment in all of the groups. Calcium hydroxide (Control group) demonstrated a significantly greater cytotoxic effect, followed by Nano Triple Antibiotic Paste with Catafast as an anti-inflamatory drug (Nano TAPC), while Triple Antibiotic Paste with Catafast (TAPC) had the least cytotoxic effect. Nano TAPC has the greatest apoptotic value, while TAPC had the least when compared with the reference group, with no significant difference between groups (P<0.05). CONCLUSION: The cytotoxic effect of Nano TAPC was lower than that of calcium hydroxide and higher than that of TAPC. Although Nano TAPC has the highest apoptotic value when compared to TAPC and calcium hydroxide but still there is no statistically significant difference between them.
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spelling pubmed-80568082021-04-21 Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament Nashaat, Yousra Sabry, Hadil Hassan, Soha Ahmed Eur Endod J Original Article OBJECTIVE: The aim of this study is to compare the cytotoxicity of triple antibiotic paste (TAP) with an anti-inflammatory drug (TAP+Catafast-TAPC) in nano and regular formulations versus calcium hydroxide as intracanal medicaments. METHODS: The TAPC drugs extraction were made in cell culture media MEM-E (Eagle’s minimal essential medium) using concentration of 10 mg/mL of each sample for seven days. Inhibitory concentrations (IC50 values) were determined for each extract. A human fibroblasts cell line was used to evaluate the cytotoxicity of different concentrations (10, 0.625 and 0.07 mg/mL) using MTT essay. The cell viability was measured after 24 h, 48 h and 7 days for all concentrations of the drugs. Flow cytometry analysis was carried out to identify the effect of materials on apoptosis/necrosis. Statistical analysis for the obtained results was done by one-way ANOVA. RESULTS: The results revealed that cell viability was inversely proportional to the duration of treatment in all of the groups. Calcium hydroxide (Control group) demonstrated a significantly greater cytotoxic effect, followed by Nano Triple Antibiotic Paste with Catafast as an anti-inflamatory drug (Nano TAPC), while Triple Antibiotic Paste with Catafast (TAPC) had the least cytotoxic effect. Nano TAPC has the greatest apoptotic value, while TAPC had the least when compared with the reference group, with no significant difference between groups (P<0.05). CONCLUSION: The cytotoxic effect of Nano TAPC was lower than that of calcium hydroxide and higher than that of TAPC. Although Nano TAPC has the highest apoptotic value when compared to TAPC and calcium hydroxide but still there is no statistically significant difference between them. Kare Publishing 2021-03-12 /pmc/articles/PMC8056808/ /pubmed/33762529 http://dx.doi.org/10.14744/eej.2020.29292 Text en Copyright: © 2021 European Endodontic Journal https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Original Article
Nashaat, Yousra
Sabry, Hadil
Hassan, Soha Ahmed
Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title_full Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title_fullStr Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title_full_unstemmed Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title_short Evaluation of the Cytotoxicity and Apoptotic Effects of Nano Triple Antibiotic Paste with Nano Anti-Inflammatory Drug as an Intracanal Medicament
title_sort evaluation of the cytotoxicity and apoptotic effects of nano triple antibiotic paste with nano anti-inflammatory drug as an intracanal medicament
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056808/
https://www.ncbi.nlm.nih.gov/pubmed/33762529
http://dx.doi.org/10.14744/eej.2020.29292
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