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Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines

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 bas...

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Autores principales: Namvar, Farideh, Rahman, Heshu Sulaiman, Mohamad, Rosfarizan, Azizi, Susan, Tahir, Paridah Mohd, Chartrand, Max Stanley, Yeap, Swee Keong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345278/
https://www.ncbi.nlm.nih.gov/pubmed/25784947
http://dx.doi.org/10.1155/2015/593014
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author Namvar, Farideh
Rahman, Heshu Sulaiman
Mohamad, Rosfarizan
Azizi, Susan
Tahir, Paridah Mohd
Chartrand, Max Stanley
Yeap, Swee Keong
author_facet Namvar, Farideh
Rahman, Heshu Sulaiman
Mohamad, Rosfarizan
Azizi, Susan
Tahir, Paridah Mohd
Chartrand, Max Stanley
Yeap, Swee Keong
author_sort Namvar, Farideh
collection PubMed
description 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 IC(50) 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 IC(50) 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.
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spelling pubmed-43452782015-03-17 Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines Namvar, Farideh Rahman, Heshu Sulaiman Mohamad, Rosfarizan Azizi, Susan Tahir, Paridah Mohd Chartrand, Max Stanley Yeap, Swee Keong Evid Based Complement Alternat Med Research Article 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 IC(50) 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 IC(50) 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. Hindawi Publishing Corporation 2015 2015-02-16 /pmc/articles/PMC4345278/ /pubmed/25784947 http://dx.doi.org/10.1155/2015/593014 Text en Copyright © 2015 Farideh Namvar et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Namvar, Farideh
Rahman, Heshu Sulaiman
Mohamad, Rosfarizan
Azizi, Susan
Tahir, Paridah Mohd
Chartrand, Max Stanley
Yeap, Swee Keong
Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title_full Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title_fullStr Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title_full_unstemmed Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title_short Cytotoxic Effects of Biosynthesized Zinc Oxide Nanoparticles on Murine Cell Lines
title_sort cytotoxic effects of biosynthesized zinc oxide nanoparticles on murine cell lines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345278/
https://www.ncbi.nlm.nih.gov/pubmed/25784947
http://dx.doi.org/10.1155/2015/593014
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