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Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines

INTRODUCTION: Biogenic silver nanoparticles (AgNPs-GA) were successfully synthesised using Garcinia atroviridis leaf extract as a reducing agent, which has ethnopharmacological claims against various diseases including cancer. Aim of the Study. Aim of the study is to discover whether AgNPs-GA has cy...

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Autores principales: Muhamad, Musthahimah, Ab.Rahim, Nurhidayah, Wan Omar, Wan Adnan, Nik Mohamed Kamal, Nik Nur Syazni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525761/
https://www.ncbi.nlm.nih.gov/pubmed/36193250
http://dx.doi.org/10.1155/2022/8546079
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author Muhamad, Musthahimah
Ab.Rahim, Nurhidayah
Wan Omar, Wan Adnan
Nik Mohamed Kamal, Nik Nur Syazni
author_facet Muhamad, Musthahimah
Ab.Rahim, Nurhidayah
Wan Omar, Wan Adnan
Nik Mohamed Kamal, Nik Nur Syazni
author_sort Muhamad, Musthahimah
collection PubMed
description INTRODUCTION: Biogenic silver nanoparticles (AgNPs-GA) were successfully synthesised using Garcinia atroviridis leaf extract as a reducing agent, which has ethnopharmacological claims against various diseases including cancer. Aim of the Study. Aim of the study is to discover whether AgNPs-GA has cytotoxic and genotoxic effects on cancerous (A549) and noncancerous (BEAS-2B) human lung cells. MATERIALS AND METHODS: The cytotoxicity profiles of AgNPs-GA were characterized by MTT assay, intracellular reactive oxygen species (ROS) assay, and DAPI and AOPI double staining, whilst genotoxicity was assessed using Comet Assay analysis. The level of silver ions (Ag(+)) and cellular uptake of AgNPs-GA were evaluated by ICP-OES and TEM analyses, respectively. RESULTS: A significant cytotoxic effect was observed by AgNPs-GA on both A549 and BEAS-2B cell lines, with IC(50) values of 20–28 μg/ml and 12–35 μg/ml, respectively. The cytotoxicity profile of AgNPs-GA was also accompanied by a pronounced increase in ROS production, DNA damage, and apoptosis. Moreover, Ag(+) was also detected in cells exposed to AgNPs-GA threefold higher compared to controls. In this study, AgNPs-GA were endocytosed within lysosomes, which may direct to secondary toxicity effects including oxidative stress, impairment of the cell membrane, DNA fragmentation, and cell death. CONCLUSIONS: Taken together, novel toxicological-related mechanisms by AgNPs-GA were proposed involving the generation of ROS that causes DNA damage which led to programmed cell death in both A549 and BEAS-2B cells. Therefore, a combination of scientific assessments is constantly needed to ensure that the quality of biosynthesized nanoparticles is controlled and their safe development is promoted.
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spelling pubmed-95257612022-10-02 Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines Muhamad, Musthahimah Ab.Rahim, Nurhidayah Wan Omar, Wan Adnan Nik Mohamed Kamal, Nik Nur Syazni Bioinorg Chem Appl Research Article INTRODUCTION: Biogenic silver nanoparticles (AgNPs-GA) were successfully synthesised using Garcinia atroviridis leaf extract as a reducing agent, which has ethnopharmacological claims against various diseases including cancer. Aim of the Study. Aim of the study is to discover whether AgNPs-GA has cytotoxic and genotoxic effects on cancerous (A549) and noncancerous (BEAS-2B) human lung cells. MATERIALS AND METHODS: The cytotoxicity profiles of AgNPs-GA were characterized by MTT assay, intracellular reactive oxygen species (ROS) assay, and DAPI and AOPI double staining, whilst genotoxicity was assessed using Comet Assay analysis. The level of silver ions (Ag(+)) and cellular uptake of AgNPs-GA were evaluated by ICP-OES and TEM analyses, respectively. RESULTS: A significant cytotoxic effect was observed by AgNPs-GA on both A549 and BEAS-2B cell lines, with IC(50) values of 20–28 μg/ml and 12–35 μg/ml, respectively. The cytotoxicity profile of AgNPs-GA was also accompanied by a pronounced increase in ROS production, DNA damage, and apoptosis. Moreover, Ag(+) was also detected in cells exposed to AgNPs-GA threefold higher compared to controls. In this study, AgNPs-GA were endocytosed within lysosomes, which may direct to secondary toxicity effects including oxidative stress, impairment of the cell membrane, DNA fragmentation, and cell death. CONCLUSIONS: Taken together, novel toxicological-related mechanisms by AgNPs-GA were proposed involving the generation of ROS that causes DNA damage which led to programmed cell death in both A549 and BEAS-2B cells. Therefore, a combination of scientific assessments is constantly needed to ensure that the quality of biosynthesized nanoparticles is controlled and their safe development is promoted. Hindawi 2022-09-23 /pmc/articles/PMC9525761/ /pubmed/36193250 http://dx.doi.org/10.1155/2022/8546079 Text en Copyright © 2022 Musthahimah Muhamad et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Muhamad, Musthahimah
Ab.Rahim, Nurhidayah
Wan Omar, Wan Adnan
Nik Mohamed Kamal, Nik Nur Syazni
Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title_full Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title_fullStr Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title_full_unstemmed Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title_short Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
title_sort cytotoxicity and genotoxicity of biogenic silver nanoparticles in a549 and beas-2b cell lines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525761/
https://www.ncbi.nlm.nih.gov/pubmed/36193250
http://dx.doi.org/10.1155/2022/8546079
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