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NIR light active ternary modified ZnO nanocomposites for combined cancer therapy

Recent developments in nanomedicine for cancer therapy enable nanoparticles for tumour specific therapeutics. Certain nanoparticles with their inherent physical/chemical properties can themselves act as drugs. Also they can be designed to respond to either tumor microenvironment or externally applie...

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Detalles Bibliográficos
Autores principales: Vasuki, K., Manimekalai, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895759/
https://www.ncbi.nlm.nih.gov/pubmed/31844691
http://dx.doi.org/10.1016/j.heliyon.2019.e02729
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author Vasuki, K.
Manimekalai, R.
author_facet Vasuki, K.
Manimekalai, R.
author_sort Vasuki, K.
collection PubMed
description Recent developments in nanomedicine for cancer therapy enable nanoparticles for tumour specific therapeutics. Certain nanoparticles with their inherent physical/chemical properties can themselves act as drugs. Also they can be designed to respond to either tumor microenvironment or externally applied physical stimuli such as temperature, light, magnetic field, and ultrasound for tumor-targeted and enhanced anticancer efficacy. In this study, a simple design of cost-effective ternary modified zinc oxide nanocomposites possessing near-infrared (NIR) absorbance were synthesized using simple, fast, thermal decomposition route with hydrazine precursors. The in vitro cytotoxicity of these nanocomposites studied on human breast cancer cells (MCF-7) and the human embryonic kidney normal cells (HEK 293) by MTT assay show that they are highly selective and are dose dependent against both the cell lines. The developed nanocomposites can be used for combined photothermal (PTT) and photo dynamic (PDT) cancer therapy.
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spelling pubmed-68957592019-12-16 NIR light active ternary modified ZnO nanocomposites for combined cancer therapy Vasuki, K. Manimekalai, R. Heliyon Article Recent developments in nanomedicine for cancer therapy enable nanoparticles for tumour specific therapeutics. Certain nanoparticles with their inherent physical/chemical properties can themselves act as drugs. Also they can be designed to respond to either tumor microenvironment or externally applied physical stimuli such as temperature, light, magnetic field, and ultrasound for tumor-targeted and enhanced anticancer efficacy. In this study, a simple design of cost-effective ternary modified zinc oxide nanocomposites possessing near-infrared (NIR) absorbance were synthesized using simple, fast, thermal decomposition route with hydrazine precursors. The in vitro cytotoxicity of these nanocomposites studied on human breast cancer cells (MCF-7) and the human embryonic kidney normal cells (HEK 293) by MTT assay show that they are highly selective and are dose dependent against both the cell lines. The developed nanocomposites can be used for combined photothermal (PTT) and photo dynamic (PDT) cancer therapy. Elsevier 2019-11-14 /pmc/articles/PMC6895759/ /pubmed/31844691 http://dx.doi.org/10.1016/j.heliyon.2019.e02729 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Vasuki, K.
Manimekalai, R.
NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title_full NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title_fullStr NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title_full_unstemmed NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title_short NIR light active ternary modified ZnO nanocomposites for combined cancer therapy
title_sort nir light active ternary modified zno nanocomposites for combined cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895759/
https://www.ncbi.nlm.nih.gov/pubmed/31844691
http://dx.doi.org/10.1016/j.heliyon.2019.e02729
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