2023
DOI: 10.1039/d3ra03736c
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Sustainable bioactivity enhancement of ZnO–Ag nanoparticles in antimicrobial, antibiofilm, lung cancer, and photocatalytic applications

Gouranga Dutta,
Santosh kumar Chinnaiyan,
Abimanyu Sugumaran
et al.

Abstract: Green synthesized ZnO and ZnO–Ag NPs using a plant extract. SEM image validate the final product. Characterized by FTIR, XRD, zeta, XPS, etc. Following this, their anticancer, antibacterial, and photocatalytic potentials are evaluated.

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Cited by 4 publications
(5 citation statements)
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References 85 publications
(147 reference statements)
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“…It is already established that ZnO nanoparticles (NPs) are toxic to Drosophila and can induce the increased production of reactive oxygen species (ROS), resulting in oxidative stress and genotoxicity. The high generation of ROS may be the cause of both the delay in postembryonic development and the high larval lethality after exposure to ZnO and ZnO:0.5Au [51,53,54]. ZnO NPs cause toxicity because they induce the generation of excess ROS and disrupt the flow of Ca 2+ , leading to cellular distress, which consequently induces a series of cellular damage, such as changes in Nrf2 signaling pathways, reduction of antioxidant proteins such as glutathione (GSH), redox imbalance, and mitochondrial dysfunction, which in the end lead to cell death. , …”
Section: Antimicrobial Activity Assaysmentioning
confidence: 99%
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“…It is already established that ZnO nanoparticles (NPs) are toxic to Drosophila and can induce the increased production of reactive oxygen species (ROS), resulting in oxidative stress and genotoxicity. The high generation of ROS may be the cause of both the delay in postembryonic development and the high larval lethality after exposure to ZnO and ZnO:0.5Au [51,53,54]. ZnO NPs cause toxicity because they induce the generation of excess ROS and disrupt the flow of Ca 2+ , leading to cellular distress, which consequently induces a series of cellular damage, such as changes in Nrf2 signaling pathways, reduction of antioxidant proteins such as glutathione (GSH), redox imbalance, and mitochondrial dysfunction, which in the end lead to cell death. , …”
Section: Antimicrobial Activity Assaysmentioning
confidence: 99%
“…63−66 The high generation of ROS may be the cause of both the delay in postembryonic development and the high larval lethality after exposure to ZnO and ZnO:0.5Au [51,53,54]. ZnO NPs cause toxicity because they induce the generation of excess ROS and disrupt the flow of Ca 2+ , leading to cellular distress, which consequently induces a series of cellular damage, such as changes in Nrf2 signaling pathways, reduction of antioxidant proteins such as glutathione (GSH), 58 redox imbalance, and mitochondrial dysfunction, which in the end lead to cell death. 17,54 We suggest that possible mitochondrial dysfunctions and reduced levels of GSH synthesis are the causes of the alterations in larval development found in this study.…”
Section: Antimicrobial Activity Assaysmentioning
confidence: 99%
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