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Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line

Among nanoparticles used for medical applications, palladium nanoparticles (PdNPs) are among the least investigated. This study was undertaken to develop PdNPs by green synthesis using white tea (W.tea; Camellia sinensis) extract to produce the Pd@W.tea NPs. The Pd@W.tea NPs were characterized by UV...

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Autores principales: Azizi, Susan, Mahdavi Shahri, Mahnaz, Rahman, Heshu Sulaiman, Rahim, Raha Abdul, Rasedee, Abdullah, Mohamad, Rosfarizan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734231/
https://www.ncbi.nlm.nih.gov/pubmed/29276385
http://dx.doi.org/10.2147/IJN.S149371
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author Azizi, Susan
Mahdavi Shahri, Mahnaz
Rahman, Heshu Sulaiman
Rahim, Raha Abdul
Rasedee, Abdullah
Mohamad, Rosfarizan
author_facet Azizi, Susan
Mahdavi Shahri, Mahnaz
Rahman, Heshu Sulaiman
Rahim, Raha Abdul
Rasedee, Abdullah
Mohamad, Rosfarizan
author_sort Azizi, Susan
collection PubMed
description Among nanoparticles used for medical applications, palladium nanoparticles (PdNPs) are among the least investigated. This study was undertaken to develop PdNPs by green synthesis using white tea (W.tea; Camellia sinensis) extract to produce the Pd@W.tea NPs. The Pd@W.tea NPs were characterized by UV–vis spectroscopy and X-ray diffractometry, and evaluated with transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The Pd@W.tea NPs were spherical (size 6–18 nm) and contained phenols and flavonoids acquired from the W.tea extract. Pd@W.tea NPs has good 1-diphenyl-2-picrylhydrazyl (DPPH), OH, and NO-scavenging properties as well as antibacterial effects toward Staphylococcus epidermidis and Escherichia coli. MTT assay showed that Pd@W.tea NPs (IC(50) =0.006 μM) were more antiproliferative toward the human leukemia (MOLT-4) cells than the W.tea extract (IC(50) =0.894 μM), doxorubicin (IC(50) =2.133 μM), or cisplatin (IC(50) =0.013 μM), whereas they were relatively innocuous for normal human fibroblast (HDF-a) cells. The anticancer cell effects of Pd@W.tea NPs are mediated through the induction of apoptosis and G2/M cell-cycle arrest.
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spelling pubmed-57342312017-12-22 Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line Azizi, Susan Mahdavi Shahri, Mahnaz Rahman, Heshu Sulaiman Rahim, Raha Abdul Rasedee, Abdullah Mohamad, Rosfarizan Int J Nanomedicine Original Research Among nanoparticles used for medical applications, palladium nanoparticles (PdNPs) are among the least investigated. This study was undertaken to develop PdNPs by green synthesis using white tea (W.tea; Camellia sinensis) extract to produce the Pd@W.tea NPs. The Pd@W.tea NPs were characterized by UV–vis spectroscopy and X-ray diffractometry, and evaluated with transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The Pd@W.tea NPs were spherical (size 6–18 nm) and contained phenols and flavonoids acquired from the W.tea extract. Pd@W.tea NPs has good 1-diphenyl-2-picrylhydrazyl (DPPH), OH, and NO-scavenging properties as well as antibacterial effects toward Staphylococcus epidermidis and Escherichia coli. MTT assay showed that Pd@W.tea NPs (IC(50) =0.006 μM) were more antiproliferative toward the human leukemia (MOLT-4) cells than the W.tea extract (IC(50) =0.894 μM), doxorubicin (IC(50) =2.133 μM), or cisplatin (IC(50) =0.013 μM), whereas they were relatively innocuous for normal human fibroblast (HDF-a) cells. The anticancer cell effects of Pd@W.tea NPs are mediated through the induction of apoptosis and G2/M cell-cycle arrest. Dove Medical Press 2017-12-14 /pmc/articles/PMC5734231/ /pubmed/29276385 http://dx.doi.org/10.2147/IJN.S149371 Text en © 2017 Azizi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Azizi, Susan
Mahdavi Shahri, Mahnaz
Rahman, Heshu Sulaiman
Rahim, Raha Abdul
Rasedee, Abdullah
Mohamad, Rosfarizan
Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title_full Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title_fullStr Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title_full_unstemmed Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title_short Green synthesis palladium nanoparticles mediated by white tea (Camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (MOLT-4) cell line
title_sort green synthesis palladium nanoparticles mediated by white tea (camellia sinensis) extract with antioxidant, antibacterial, and antiproliferative activities toward the human leukemia (molt-4) cell line
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734231/
https://www.ncbi.nlm.nih.gov/pubmed/29276385
http://dx.doi.org/10.2147/IJN.S149371
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