Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study

Aim: Intracanal medicaments are often recommended during endodontic sessions to eliminate the necrotic debris and microorganisms. The aim of the present study was to observe the cytotoxicity of calcium hydroxide (CH) and colchicine (COL), at different concentrations, on human gingival fibroblast cel...

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Main Authors: Behnaz Barakatein, Alireza Farhad, Elham Shadmehr, Hamidreza Mohammad Sharifi, Masoud Mohammadi Hamidreza Mohamad Sharif, Amin Davoudi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Endodontology
Subjects:
Online Access:http://www.endodontologyonweb.org/article.asp?issn=0970-7212;year=2022;volume=34;issue=2;spage=76;epage=79;aulast=Barakatein
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author Behnaz Barakatein
Alireza Farhad
Elham Shadmehr
Hamidreza Mohammad Sharifi
Masoud Mohammadi Hamidreza Mohamad Sharif
Amin Davoudi
author_facet Behnaz Barakatein
Alireza Farhad
Elham Shadmehr
Hamidreza Mohammad Sharifi
Masoud Mohammadi Hamidreza Mohamad Sharif
Amin Davoudi
author_sort Behnaz Barakatein
collection DOAJ
description Aim: Intracanal medicaments are often recommended during endodontic sessions to eliminate the necrotic debris and microorganisms. The aim of the present study was to observe the cytotoxicity of calcium hydroxide (CH) and colchicine (COL), at different concentrations, on human gingival fibroblast cells. Materials and Methods: Human gingival fibroblasts were cultured on plastic flasks containing RPMI 1640 media and fetal calf serum 10% supplemented with antibiotic agents. Trypsin/ethylenediaminetetraacetic acid 0.2% enzyme was used to isolate the cells, and the suspension was transferred to tubes for centrifuging. Conventional CH and COL were separately mixed with sterile saline solution to prepare a stock media. By serial dilution of stock media, desired concentrations were prepared at 2, 1.75, 1.5, and 1.25 mg/ml, separately. After considering a control group, the cells were exposed to test materials. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was conducted at 24 h, 72 h, and 7 days later. Optical density (OD) was evaluated to attain cell viability percentage. Finally, the recorded data were analyzed by Kruskal–Wallis and Mann–Whitney tests using SPSS software version 19 at a significant level of 0.05. Results: The highest (1.40 ± 0.66) and lowest (0.15 ± 0.00) ODs were observed in CH 1.25 mg/ml and COL 1.5 mg/ml after 72 h, respectively. All of the concentrations of both CH and COL showed significant OD differences with the control group (all P = 0.001). Conclusion: Both CH and COL manifested similar cytotoxicity on human gingival fibroblast cells.
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spelling doaj.art-a24a31f8e3104628976a1a493424a9ac2022-12-22T03:00:50ZengWolters Kluwer Medknow PublicationsEndodontology0970-72122022-01-01342767910.4103/endo.endo_107_20Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory studyBehnaz BarakateinAlireza FarhadElham ShadmehrHamidreza Mohammad SharifiMasoud Mohammadi Hamidreza Mohamad SharifAmin DavoudiAim: Intracanal medicaments are often recommended during endodontic sessions to eliminate the necrotic debris and microorganisms. The aim of the present study was to observe the cytotoxicity of calcium hydroxide (CH) and colchicine (COL), at different concentrations, on human gingival fibroblast cells. Materials and Methods: Human gingival fibroblasts were cultured on plastic flasks containing RPMI 1640 media and fetal calf serum 10% supplemented with antibiotic agents. Trypsin/ethylenediaminetetraacetic acid 0.2% enzyme was used to isolate the cells, and the suspension was transferred to tubes for centrifuging. Conventional CH and COL were separately mixed with sterile saline solution to prepare a stock media. By serial dilution of stock media, desired concentrations were prepared at 2, 1.75, 1.5, and 1.25 mg/ml, separately. After considering a control group, the cells were exposed to test materials. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was conducted at 24 h, 72 h, and 7 days later. Optical density (OD) was evaluated to attain cell viability percentage. Finally, the recorded data were analyzed by Kruskal–Wallis and Mann–Whitney tests using SPSS software version 19 at a significant level of 0.05. Results: The highest (1.40 ± 0.66) and lowest (0.15 ± 0.00) ODs were observed in CH 1.25 mg/ml and COL 1.5 mg/ml after 72 h, respectively. All of the concentrations of both CH and COL showed significant OD differences with the control group (all P = 0.001). Conclusion: Both CH and COL manifested similar cytotoxicity on human gingival fibroblast cells.http://www.endodontologyonweb.org/article.asp?issn=0970-7212;year=2022;volume=34;issue=2;spage=76;epage=79;aulast=Barakateincalcium hydroxidecolchicinecytotoxicity testfibroblast
spellingShingle Behnaz Barakatein
Alireza Farhad
Elham Shadmehr
Hamidreza Mohammad Sharifi
Masoud Mohammadi Hamidreza Mohamad Sharif
Amin Davoudi
Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
Endodontology
calcium hydroxide
colchicine
cytotoxicity test
fibroblast
title Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
title_full Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
title_fullStr Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
title_full_unstemmed Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
title_short Cytotoxicity of two different intercanal medicaments on human gingival fibroblasts - A Laboratory study
title_sort cytotoxicity of two different intercanal medicaments on human gingival fibroblasts a laboratory study
topic calcium hydroxide
colchicine
cytotoxicity test
fibroblast
url http://www.endodontologyonweb.org/article.asp?issn=0970-7212;year=2022;volume=34;issue=2;spage=76;epage=79;aulast=Barakatein
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AT hamidrezamohammadsharifi cytotoxicityoftwodifferentintercanalmedicamentsonhumangingivalfibroblastsalaboratorystudy
AT masoudmohammadihamidrezamohamadsharif cytotoxicityoftwodifferentintercanalmedicamentsonhumangingivalfibroblastsalaboratorystudy
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