Evaluation of photocatalytic, antimicrobial and anticancer activities of ZnO/MS (M=Zn, Cd or Pb) core/shell nanoparticles

[Display omitted] •ZnO and ZnO/MS core/shell nanoparticles were synthesized and characterized.•The photodegradation property was investigated using methylene blue.•ZnO/MS core/shell nanoparticles exhibited enhanced photodegradation.•ZnO/MS core/shell nanoparticles showed moderate antimicrobial activ...

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Veröffentlicht in:Materials science & engineering. B, Solid-state materials for advanced technology Solid-state materials for advanced technology, 2017-11, Vol.225, p.20-32
Hauptverfasser: Rehana, Dilaveez, Mahendiran, D., Manigandan, R., Narayanan, V., Kalilur Rahiman, A.
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Sprache:eng
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Zusammenfassung:[Display omitted] •ZnO and ZnO/MS core/shell nanoparticles were synthesized and characterized.•The photodegradation property was investigated using methylene blue.•ZnO/MS core/shell nanoparticles exhibited enhanced photodegradation.•ZnO/MS core/shell nanoparticles showed moderate antimicrobial activity.•Paclitaxel loaded core/shell nanoparticles showed higher anticancer activity. Zinc oxide nanoparticles were synthesized by co-precipitation method followed by covering with MS (M=Zn, Cd, or Pb) to obtain ZnO/MS core/shell nanoparticles using chemical method. The formation of core/shell nanoparticles were authenticated by various spectroscopic techniques. The photocatalytic activity of the synthesized core/shell nanoparticles shows the significant role of the shell layer in the photodegradation of methylene blue. The antimicrobial activity has been evaluated against two Gram (–ve) (E. coli and K. pneumoniae) and two Gram (+ve) (E. faecalis and S. aureus) bacterial, and two fungi (A. niger and C. albicans) strains. In vitro anti-proliferative activity of ZnO and ZnO/MS core/shell nanoparticles at a concentration of 0.06M was evaluated against two human cancerous cell lines such as breast (MCF-7) and lung (A549), and one normal human kidney (HEK-293) cell line by MTT assay. DNA fragmentation analysis proved the inhibition of proliferation through induction of apoptosis.
ISSN:0921-5107
1873-4944
DOI:10.1016/j.mseb.2017.08.003