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Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer

Green chemistry approaches for designing therapeutically significant nanomedicine have gained considerable attention in the past decade. Herein, we report for the first time on anticancer potential of phytogenic platinum nanoparticles (PtNPs) and palladium nanoparticles (PdNPs) using a medicinal pla...

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Autores principales: Rokade, Shalaka S., Joshi, Komal A., Mahajan, Ketakee, Patil, Saniya, Tomar, Geetanjali, Dubal, Dnyanesh S., Parihar, Vijay Singh, Kitture, Rohini, Bellare, Jayesh R., Ghosh, Sougata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051271/
https://www.ncbi.nlm.nih.gov/pubmed/30057593
http://dx.doi.org/10.1155/2018/4924186
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author Rokade, Shalaka S.
Joshi, Komal A.
Mahajan, Ketakee
Patil, Saniya
Tomar, Geetanjali
Dubal, Dnyanesh S.
Parihar, Vijay Singh
Kitture, Rohini
Bellare, Jayesh R.
Ghosh, Sougata
author_facet Rokade, Shalaka S.
Joshi, Komal A.
Mahajan, Ketakee
Patil, Saniya
Tomar, Geetanjali
Dubal, Dnyanesh S.
Parihar, Vijay Singh
Kitture, Rohini
Bellare, Jayesh R.
Ghosh, Sougata
author_sort Rokade, Shalaka S.
collection PubMed
description Green chemistry approaches for designing therapeutically significant nanomedicine have gained considerable attention in the past decade. Herein, we report for the first time on anticancer potential of phytogenic platinum nanoparticles (PtNPs) and palladium nanoparticles (PdNPs) using a medicinal plant Gloriosa superba tuber extract (GSTE). The synthesis of the nanoparticles was completed within 5 hours at 100°C which was confirmed by development of dark brown and black colour for PtNPs and PdNPs, respectively, along with enhancement of the peak intensity in the UV-visible spectra. High-resolution transmission electron microscopy (HRTEM) showed that the monodispersed spherical nanoparticles were within a size range below 10 nm. Energy dispersive spectra (EDS) confirmed the elemental composition, while dynamic light scattering (DLS) helped to evaluate the hydrodynamic size of the particles. Anticancer activity against MCF-7 (human breast adenocarcinoma) cell lines was evaluated using MTT assay, flow cytometry, and confocal microscopy. PtNPs and PdNPs showed 49.65 ± 1.99% and 36.26 ± 0.91% of anticancer activity. Induction of apoptosis was most predominant in the underlying mechanism which was rationalized by externalization of phosphatidyl serine and membrane blebbing. These findings support the efficiency of phytogenic fabrication of nanoscale platinum and palladium drugs for management and therapy against breast cancer.
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spelling pubmed-60512712018-07-29 Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer Rokade, Shalaka S. Joshi, Komal A. Mahajan, Ketakee Patil, Saniya Tomar, Geetanjali Dubal, Dnyanesh S. Parihar, Vijay Singh Kitture, Rohini Bellare, Jayesh R. Ghosh, Sougata Bioinorg Chem Appl Research Article Green chemistry approaches for designing therapeutically significant nanomedicine have gained considerable attention in the past decade. Herein, we report for the first time on anticancer potential of phytogenic platinum nanoparticles (PtNPs) and palladium nanoparticles (PdNPs) using a medicinal plant Gloriosa superba tuber extract (GSTE). The synthesis of the nanoparticles was completed within 5 hours at 100°C which was confirmed by development of dark brown and black colour for PtNPs and PdNPs, respectively, along with enhancement of the peak intensity in the UV-visible spectra. High-resolution transmission electron microscopy (HRTEM) showed that the monodispersed spherical nanoparticles were within a size range below 10 nm. Energy dispersive spectra (EDS) confirmed the elemental composition, while dynamic light scattering (DLS) helped to evaluate the hydrodynamic size of the particles. Anticancer activity against MCF-7 (human breast adenocarcinoma) cell lines was evaluated using MTT assay, flow cytometry, and confocal microscopy. PtNPs and PdNPs showed 49.65 ± 1.99% and 36.26 ± 0.91% of anticancer activity. Induction of apoptosis was most predominant in the underlying mechanism which was rationalized by externalization of phosphatidyl serine and membrane blebbing. These findings support the efficiency of phytogenic fabrication of nanoscale platinum and palladium drugs for management and therapy against breast cancer. Hindawi 2018-07-02 /pmc/articles/PMC6051271/ /pubmed/30057593 http://dx.doi.org/10.1155/2018/4924186 Text en Copyright © 2018 Shalaka S. Rokade et al. http://creativecommons.org/licenses/by/4.0/ 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
Rokade, Shalaka S.
Joshi, Komal A.
Mahajan, Ketakee
Patil, Saniya
Tomar, Geetanjali
Dubal, Dnyanesh S.
Parihar, Vijay Singh
Kitture, Rohini
Bellare, Jayesh R.
Ghosh, Sougata
Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title_full Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title_fullStr Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title_full_unstemmed Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title_short Gloriosa superba Mediated Synthesis of Platinum and Palladium Nanoparticles for Induction of Apoptosis in Breast Cancer
title_sort gloriosa superba mediated synthesis of platinum and palladium nanoparticles for induction of apoptosis in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051271/
https://www.ncbi.nlm.nih.gov/pubmed/30057593
http://dx.doi.org/10.1155/2018/4924186
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