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Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties

This study effectively reports the influence of experimental incubation period on the sol-gel production of husk-like zinc oxide nanoparticles (ZNPs) and their anti-cancerous abilities. The surface morphology of ZNPs was studied with the help of SEM. With the use of TEM, the diameter range of the ZN...

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Autores principales: Alhoqail, Wardah A., Alothaim, Abdulaziz S., Suhail, Mohd, Iqbal, Danish, Kamal, Mehnaz, Asmari, Majid Mohammed, Jamal, Azfar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953567/
https://www.ncbi.nlm.nih.gov/pubmed/36830857
http://dx.doi.org/10.3390/biomedicines11020320
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author Alhoqail, Wardah A.
Alothaim, Abdulaziz S.
Suhail, Mohd
Iqbal, Danish
Kamal, Mehnaz
Asmari, Majid Mohammed
Jamal, Azfar
author_facet Alhoqail, Wardah A.
Alothaim, Abdulaziz S.
Suhail, Mohd
Iqbal, Danish
Kamal, Mehnaz
Asmari, Majid Mohammed
Jamal, Azfar
author_sort Alhoqail, Wardah A.
collection PubMed
description This study effectively reports the influence of experimental incubation period on the sol-gel production of husk-like zinc oxide nanoparticles (ZNPs) and their anti-cancerous abilities. The surface morphology of ZNPs was studied with the help of SEM. With the use of TEM, the diameter range of the ZNPs was estimated to be ~86 and ~231 nm for ZNP(A) and ZNP(B), prepared by incubating zinc oxide for 2 and 10 weeks, respectively. The X-ray diffraction (XRD) investigation showed that ZNPs had a pure wurtzite crystal structure. On prolonging the experimental incubation, a relative drop in aspect ratio was observed, displaying a distinct blue-shift in the UV-visible spectrum. Furthermore, RBC lysis assay results concluded that ZNP(A) and ZNP(B) both demonstrated innoxious nature. As indicated by MTT assay, reactive oxygen species (ROS) release, and chromatin condensation investigations against the human epidermoid carcinoma (HEC) A431 cells, ZNP(B) demonstrated viable relevance to chemotherapy. Compared to ZNP(B), ZNP(A) had a slightly lower IC(50) against A431 cells due to its small size. This study conclusively describes a simple, affordable method to produce ZNP nano-formulations that display significant cytotoxicity against the skin cancer cell line A431, suggesting that ZNPs may be useful in the treatment of cancer.
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spelling pubmed-99535672023-02-25 Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties Alhoqail, Wardah A. Alothaim, Abdulaziz S. Suhail, Mohd Iqbal, Danish Kamal, Mehnaz Asmari, Majid Mohammed Jamal, Azfar Biomedicines Article This study effectively reports the influence of experimental incubation period on the sol-gel production of husk-like zinc oxide nanoparticles (ZNPs) and their anti-cancerous abilities. The surface morphology of ZNPs was studied with the help of SEM. With the use of TEM, the diameter range of the ZNPs was estimated to be ~86 and ~231 nm for ZNP(A) and ZNP(B), prepared by incubating zinc oxide for 2 and 10 weeks, respectively. The X-ray diffraction (XRD) investigation showed that ZNPs had a pure wurtzite crystal structure. On prolonging the experimental incubation, a relative drop in aspect ratio was observed, displaying a distinct blue-shift in the UV-visible spectrum. Furthermore, RBC lysis assay results concluded that ZNP(A) and ZNP(B) both demonstrated innoxious nature. As indicated by MTT assay, reactive oxygen species (ROS) release, and chromatin condensation investigations against the human epidermoid carcinoma (HEC) A431 cells, ZNP(B) demonstrated viable relevance to chemotherapy. Compared to ZNP(B), ZNP(A) had a slightly lower IC(50) against A431 cells due to its small size. This study conclusively describes a simple, affordable method to produce ZNP nano-formulations that display significant cytotoxicity against the skin cancer cell line A431, suggesting that ZNPs may be useful in the treatment of cancer. MDPI 2023-01-23 /pmc/articles/PMC9953567/ /pubmed/36830857 http://dx.doi.org/10.3390/biomedicines11020320 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alhoqail, Wardah A.
Alothaim, Abdulaziz S.
Suhail, Mohd
Iqbal, Danish
Kamal, Mehnaz
Asmari, Majid Mohammed
Jamal, Azfar
Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title_full Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title_fullStr Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title_full_unstemmed Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title_short Husk-like Zinc Oxide Nanoparticles Induce Apoptosis through ROS Generation in Epidermoid Carcinoma Cells: Effect of Incubation Period on Sol-Gel Synthesis and Anti-Cancerous Properties
title_sort husk-like zinc oxide nanoparticles induce apoptosis through ros generation in epidermoid carcinoma cells: effect of incubation period on sol-gel synthesis and anti-cancerous properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953567/
https://www.ncbi.nlm.nih.gov/pubmed/36830857
http://dx.doi.org/10.3390/biomedicines11020320
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