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Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
by
Mohammad, Rosfarizan
, Namvar, Farideh
, Rahman, Heshu Sulaiman
, Chartrand, Max Stanley
, Yeap, Swee Keong
, Azizi, Susan
, Tahir, Paridah Mohd
in
Algae
/ Apoptosis
/ Aqueous solutions
/ B cells
/ Cancer
/ Cytotoxicity
/ Fibroblasts
/ Free radicals
/ Laboratories
/ Medical research
/ Methods
/ Protein expression
/ Proteins
/ Veterinary medicine
/ Zinc oxide
/ Zinc oxides
2015
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Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
by
Mohammad, Rosfarizan
, Namvar, Farideh
, Rahman, Heshu Sulaiman
, Chartrand, Max Stanley
, Yeap, Swee Keong
, Azizi, Susan
, Tahir, Paridah Mohd
in
Algae
/ Apoptosis
/ Aqueous solutions
/ B cells
/ Cancer
/ Cytotoxicity
/ Fibroblasts
/ Free radicals
/ Laboratories
/ Medical research
/ Methods
/ Protein expression
/ Proteins
/ Veterinary medicine
/ Zinc oxide
/ Zinc oxides
2015
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Do you wish to request the book?
Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
by
Mohammad, Rosfarizan
, Namvar, Farideh
, Rahman, Heshu Sulaiman
, Chartrand, Max Stanley
, Yeap, Swee Keong
, Azizi, Susan
, Tahir, Paridah Mohd
in
Algae
/ Apoptosis
/ Aqueous solutions
/ B cells
/ Cancer
/ Cytotoxicity
/ Fibroblasts
/ Free radicals
/ Laboratories
/ Medical research
/ Methods
/ Protein expression
/ Proteins
/ Veterinary medicine
/ Zinc oxide
/ Zinc oxides
2015
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Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
Journal Article
Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
2015
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Overview
The aim of this study is to evaluate the in vitro cytotoxic activity and cellular effects of previously prepared ZnO-NPs on murine cancer cell lines using brown seaweed (Sargassum muticum) aqueous extract. Treated cancer cells with ZnO-NPs for 72 hours demonstrated various levels of cytotoxicity based on calculated IC50 values using MTT assay as follows: 21.7 ± 1.3 μg/mL (4T1), 17.45 ± 1.1 μg/mL (CRL-1451), 11.75 ± 0.8 μg/mL (CT-26), and 5.6 ± 0.55 μg/mL (WEHI-3B), respectively. On the other hand, ZnO-NPs treatments for 72 hours showed no toxicity against normal mouse fibroblast (3T3) cell line. On the other hand, paclitaxel, which imposed an inhibitory effect on WEHI-3B cells with IC50 of 2.25 ± 0.4, 1.17 ± 0.5, and 1.6 ± 0.09 μg/mL after 24, 48, and 72 hours treatment, respectively, was used as positive control. Furthermore, distinct morphological changes were found by utilizing fluorescent dyes; apoptotic population was increased via flowcytometry, while a cell cycle block and stimulation of apoptotic proteins were also observed. Additionally, the present study showed that the caspase activations contributed to ZnO-NPs triggered apoptotic death in WEHI-3 cells. Thus, the nature of biosynthesis and the therapeutic potential of ZnO-NPs could prepare the way for further research on the design of green synthesis therapeutic agents, particularly in nanomedicine, for the treatment of cancer.
Publisher
Hindawi Publishing Corporation,John Wiley & Sons, Inc
Subject
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