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Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts

BACKGROUND. Polylactic-co-glycolic acid and zinc oxide (PLGA-ZnO) nanocomposite has been investigated for its antibacterial properties, which could be beneficial for adding to wound dressings after periodontal surgery. However, its cytotoxicity against human gingival fibroblasts (HGFs) remains uncle...

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Autores principales: Mozaffari, Asieh, Mirzapour, Samira Mohammad, Rad, Motahare Sharifi, Ranjbaran, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460777/
https://www.ncbi.nlm.nih.gov/pubmed/37645553
http://dx.doi.org/10.34172/japid.2023.010
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author Mozaffari, Asieh
Mirzapour, Samira Mohammad
Rad, Motahare Sharifi
Ranjbaran, Mehdi
author_facet Mozaffari, Asieh
Mirzapour, Samira Mohammad
Rad, Motahare Sharifi
Ranjbaran, Mehdi
author_sort Mozaffari, Asieh
collection PubMed
description BACKGROUND. Polylactic-co-glycolic acid and zinc oxide (PLGA-ZnO) nanocomposite has been investigated for its antibacterial properties, which could be beneficial for adding to wound dressings after periodontal surgery. However, its cytotoxicity against human gingival fibroblasts (HGFs) remains unclear and should be evaluated. METHODS. ZnO nanoparticles were synthesized using the hydrothermal method. These metallic nanoparticles were incorporated into the PLGA matrix by the solvent/non-solvent process. The nanomaterial was evaluated by field emission scanning electron microscopy (FESEM), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), and x-ray diffraction (XRD) analyses. HGF cells were acquired from the National Cell Bank and categorized into four groups: ZnO, PLGA, ZnO-PLGA, and control. The cells were exposed to different ZnO (1, 20, 40, 60, 80, and 100 µg/mL) and PLGA (0.2, 4, 8, 12, 16, and 20 µg/mL) concentrations for 24 and 48 hours. The cytotoxicity was tested using the MTT assay. The data were analyzed using SPSS 25, and P<0.05 was considered statistically significant. RESULTS. ZnO nanoparticles exhibited significant toxicity at≥40 µg/mL concentrations after 24 hours. Cell viability decreased significantly at all the tested concentrations after 48 hours of exposure. PLGA-ZnO cell viability in 24 hours was similar to the control group for all the concentrations up to 80 µg/mL. CONCLUSION. ZnO nanoparticles could be toxic against HGF in high concentrations and with prolonged exposure. Therefore, incorporating ZnO nanoparticles into a biocompatible polymer such as PLGA could be a beneficial strategy for reducing their toxicity.
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spelling pubmed-104607772023-08-29 Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts Mozaffari, Asieh Mirzapour, Samira Mohammad Rad, Motahare Sharifi Ranjbaran, Mehdi J Adv Periodontol Implant Dent Research Article BACKGROUND. Polylactic-co-glycolic acid and zinc oxide (PLGA-ZnO) nanocomposite has been investigated for its antibacterial properties, which could be beneficial for adding to wound dressings after periodontal surgery. However, its cytotoxicity against human gingival fibroblasts (HGFs) remains unclear and should be evaluated. METHODS. ZnO nanoparticles were synthesized using the hydrothermal method. These metallic nanoparticles were incorporated into the PLGA matrix by the solvent/non-solvent process. The nanomaterial was evaluated by field emission scanning electron microscopy (FESEM), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), and x-ray diffraction (XRD) analyses. HGF cells were acquired from the National Cell Bank and categorized into four groups: ZnO, PLGA, ZnO-PLGA, and control. The cells were exposed to different ZnO (1, 20, 40, 60, 80, and 100 µg/mL) and PLGA (0.2, 4, 8, 12, 16, and 20 µg/mL) concentrations for 24 and 48 hours. The cytotoxicity was tested using the MTT assay. The data were analyzed using SPSS 25, and P<0.05 was considered statistically significant. RESULTS. ZnO nanoparticles exhibited significant toxicity at≥40 µg/mL concentrations after 24 hours. Cell viability decreased significantly at all the tested concentrations after 48 hours of exposure. PLGA-ZnO cell viability in 24 hours was similar to the control group for all the concentrations up to 80 µg/mL. CONCLUSION. ZnO nanoparticles could be toxic against HGF in high concentrations and with prolonged exposure. Therefore, incorporating ZnO nanoparticles into a biocompatible polymer such as PLGA could be a beneficial strategy for reducing their toxicity. Tabriz University of Medical Sciences 2023-06-03 /pmc/articles/PMC10460777/ /pubmed/37645553 http://dx.doi.org/10.34172/japid.2023.010 Text en © 2023 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mozaffari, Asieh
Mirzapour, Samira Mohammad
Rad, Motahare Sharifi
Ranjbaran, Mehdi
Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title_full Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title_fullStr Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title_full_unstemmed Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title_short Cytotoxicity of PLGA-zinc oxide nanocomposite on human gingival fibroblasts
title_sort cytotoxicity of plga-zinc oxide nanocomposite on human gingival fibroblasts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460777/
https://www.ncbi.nlm.nih.gov/pubmed/37645553
http://dx.doi.org/10.34172/japid.2023.010
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