Bougainvillea flower extract mediated zinc oxide’s nanomaterials for antimicrobial and anticancer activity

[Display omitted] •Bougainvillea flower extract mediated zinc oxide nanomaterial fabrication•Biogenic nanomaterial characterization by standard characterization techniques•ZnO-MNs employed for the de-stabilization of biofilm formation and antimicrobial properties•ZnO-MNs used as an anticancer agent...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2019-08, Vol.116, p.108983-108983, Article 108983
Hauptverfasser: Ahmar Rauf, Mohd, Oves, Mohammad, Ur Rehman, Fawad, Rauf Khan, Abdur, Husain, Nazim
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container_end_page 108983
container_issue
container_start_page 108983
container_title Biomedicine & pharmacotherapy
container_volume 116
creator Ahmar Rauf, Mohd
Oves, Mohammad
Ur Rehman, Fawad
Rauf Khan, Abdur
Husain, Nazim
description [Display omitted] •Bougainvillea flower extract mediated zinc oxide nanomaterial fabrication•Biogenic nanomaterial characterization by standard characterization techniques•ZnO-MNs employed for the de-stabilization of biofilm formation and antimicrobial properties•ZnO-MNs used as an anticancer agent against MCF-7 cells with biocompatibility testing The zinc oxide nanomaterials (ZnO-NMs), owing to their broad biomedical applications have lately attracted the incredible interest in the development of therapeutic agents against microbial infections. In this contribution, we have biosynthesized ZnO-NMs with a size of ˜ 40 nm from the Bougainvillea flower extracts. The FTIR and SEM-EDX mapping analysis confirmed the size, shape and biogenic origin of ZnO-NPs. Furthermore, the purified ZnO-NMs were applied for antibacterial studies against susceptible and resistant bacterial strains and to elucidate the possible mechanism of their activity. The XTT assay and confocal imaging confirmed the ZnO-NMs materials anti-biofilm activities against medically important pathogens, i.e., S. aureus and E. coli. Moreover, the absence of cytotoxicity against healthy kidney cells (HEK-293) and erythrocytes confirmed their biocompatible nature. Furthermore, the biosynthesized ZnO-NMs showed potent anticancer activity against the breast cancer cell line (MCF-7). These biosynthesized ZnO-NMs are having excellent antimicrobial and anticancer activities and are highly biocompatible due to biogenic nature. During antimicrobial study, Zno-NMs showed excellent minimum inhibitory concentration 16 μg concentration againt E. coli, P. aeruginosa and S. aureus. While in anticancer activity, of ZnO-NMs with 15 μg/ml dose showed good response against MCF-7 cell line. Further, this killing was mechanically confirmed by ROS generation by the ZnO-NMs, which cause cell lysis by the peroxidation of membrane lipid. So, this biogenic ZnO-NMs can be used in the future for nanomaterial-based drug development.
doi_str_mv 10.1016/j.biopha.2019.108983
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In this contribution, we have biosynthesized ZnO-NMs with a size of ˜ 40 nm from the Bougainvillea flower extracts. The FTIR and SEM-EDX mapping analysis confirmed the size, shape and biogenic origin of ZnO-NPs. Furthermore, the purified ZnO-NMs were applied for antibacterial studies against susceptible and resistant bacterial strains and to elucidate the possible mechanism of their activity. The XTT assay and confocal imaging confirmed the ZnO-NMs materials anti-biofilm activities against medically important pathogens, i.e., S. aureus and E. coli. Moreover, the absence of cytotoxicity against healthy kidney cells (HEK-293) and erythrocytes confirmed their biocompatible nature. Furthermore, the biosynthesized ZnO-NMs showed potent anticancer activity against the breast cancer cell line (MCF-7). These biosynthesized ZnO-NMs are having excellent antimicrobial and anticancer activities and are highly biocompatible due to biogenic nature. During antimicrobial study, Zno-NMs showed excellent minimum inhibitory concentration 16 μg concentration againt E. coli, P. aeruginosa and S. aureus. While in anticancer activity, of ZnO-NMs with 15 μg/ml dose showed good response against MCF-7 cell line. Further, this killing was mechanically confirmed by ROS generation by the ZnO-NMs, which cause cell lysis by the peroxidation of membrane lipid. 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In this contribution, we have biosynthesized ZnO-NMs with a size of ˜ 40 nm from the Bougainvillea flower extracts. The FTIR and SEM-EDX mapping analysis confirmed the size, shape and biogenic origin of ZnO-NPs. Furthermore, the purified ZnO-NMs were applied for antibacterial studies against susceptible and resistant bacterial strains and to elucidate the possible mechanism of their activity. The XTT assay and confocal imaging confirmed the ZnO-NMs materials anti-biofilm activities against medically important pathogens, i.e., S. aureus and E. coli. Moreover, the absence of cytotoxicity against healthy kidney cells (HEK-293) and erythrocytes confirmed their biocompatible nature. Furthermore, the biosynthesized ZnO-NMs showed potent anticancer activity against the breast cancer cell line (MCF-7). These biosynthesized ZnO-NMs are having excellent antimicrobial and anticancer activities and are highly biocompatible due to biogenic nature. 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subjects Anti-Bacterial Agents - pharmacology
Anti-biofilm
Anti-Infective Agents - pharmacology
Antibacterial
Anticancer
Apoptosis - drug effects
bcl-2-Associated X Protein - metabolism
Biofilms - drug effects
Bougainvillea flower
Caspase 9 - metabolism
Cell Cycle - drug effects
Cell Membrane - drug effects
Cell Membrane - metabolism
DNA - metabolism
DNA Damage
Escherichia coli - drug effects
Escherichia coli - ultrastructure
Flowers - chemistry
HEK293 Cells
Hemolysis - drug effects
Humans
Hydrophobic and Hydrophilic Interactions
MCF-7 cell
MCF-7 Cells
Nanostructures - chemistry
Nanostructures - ultrastructure
Nyctaginaceae - chemistry
Plant Extracts - pharmacology
Reactive Oxygen Species - metabolism
Staphylococcus aureus - drug effects
Staphylococcus aureus - ultrastructure
Tumor Suppressor Protein p53 - metabolism
Zinc Oxide - pharmacology
ZnO-NMs
title Bougainvillea flower extract mediated zinc oxide’s nanomaterials for antimicrobial and anticancer activity
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