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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Published in:Bioinorganic Chemistry and Applications
Main Author: Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
Format: Article
Language:English
Published: Hindawi Limited 2022
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85139287018&doi=10.1155%2f2022%2f8546079&partnerID=40&md5=073ce8ee9f9f65d2e67727703f34bd74
id 2-s2.0-85139287018
spelling 2-s2.0-85139287018
Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
2022
Bioinorganic Chemistry and Applications
2022

10.1155/2022/8546079
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85139287018&doi=10.1155%2f2022%2f8546079&partnerID=40&md5=073ce8ee9f9f65d2e67727703f34bd74
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 IC50 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. © 2022 Musthahimah Muhamad et al.
Hindawi Limited
15653633
English
Article
All Open Access; Gold Open Access
author Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
spellingShingle Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
author_facet Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
author_sort Muhamad M.; Ab.rahim N.; Wan Omar W.A.; Nik Mohamed Kamal N.N.S.
title 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_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_sort Cytotoxicity and Genotoxicity of Biogenic Silver Nanoparticles in A549 and BEAS-2B Cell Lines
publishDate 2022
container_title Bioinorganic Chemistry and Applications
container_volume 2022
container_issue
doi_str_mv 10.1155/2022/8546079
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85139287018&doi=10.1155%2f2022%2f8546079&partnerID=40&md5=073ce8ee9f9f65d2e67727703f34bd74
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 IC50 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. © 2022 Musthahimah Muhamad et al.
publisher Hindawi Limited
issn 15653633
language English
format Article
accesstype All Open Access; Gold Open Access
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