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Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities
Manganese metallic nanoparticles are attractive materials for various biological and medical applications. In the present study, we synthesized unique Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) (0.01 ≤ x ≤ 0.05) nanoparticles (NPs) by using the hydrothermal approach. The structure and surface morphology...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915425/ https://www.ncbi.nlm.nih.gov/pubmed/31752130 http://dx.doi.org/10.3390/nano9111635 |
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author | Akhtar, Sultan Rehman, Suriya Almessiere, Munirah A. Khan, Firdos Alam Slimani, Yassine Baykal, Abdulhadi |
author_facet | Akhtar, Sultan Rehman, Suriya Almessiere, Munirah A. Khan, Firdos Alam Slimani, Yassine Baykal, Abdulhadi |
author_sort | Akhtar, Sultan |
collection | PubMed |
description | Manganese metallic nanoparticles are attractive materials for various biological and medical applications. In the present study, we synthesized unique Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) (0.01 ≤ x ≤ 0.05) nanoparticles (NPs) by using the hydrothermal approach. The structure and surface morphology of the products were determined by X-ray powder diffraction (XRD), transmission electron and scanning electron microcopies (TEM and SEM), along with energy dispersive X-ray spectroscopy (EDX). We evaluated the impact of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) NPs on both human embryonic stem cells (HEK-293) (normal cells) and human colon carcinoma cells (HCT-116) (cancerous cells). We found that post-48 h of treatment of all products showed a significant decline in the cancer cell population as revealed by microscopically and the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) tetrazolium (MTT) assay. The inhibitory concentration (IC(50)) values of the products ranged between 0.75 and 2.25 µg/mL. When tested on normal and healthy cells (HEK-293), we found that the treatment of products did not produce any effects on the normal cells, which suggests that all products selectively targeted the cancerous cells. The anti-bacterial properties of the samples were also evaluated by Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) assays, which showed that products also inhibited the bacterial growth. |
format | Online Article Text |
id | pubmed-6915425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69154252019-12-24 Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities Akhtar, Sultan Rehman, Suriya Almessiere, Munirah A. Khan, Firdos Alam Slimani, Yassine Baykal, Abdulhadi Nanomaterials (Basel) Article Manganese metallic nanoparticles are attractive materials for various biological and medical applications. In the present study, we synthesized unique Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) (0.01 ≤ x ≤ 0.05) nanoparticles (NPs) by using the hydrothermal approach. The structure and surface morphology of the products were determined by X-ray powder diffraction (XRD), transmission electron and scanning electron microcopies (TEM and SEM), along with energy dispersive X-ray spectroscopy (EDX). We evaluated the impact of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) NPs on both human embryonic stem cells (HEK-293) (normal cells) and human colon carcinoma cells (HCT-116) (cancerous cells). We found that post-48 h of treatment of all products showed a significant decline in the cancer cell population as revealed by microscopically and the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) tetrazolium (MTT) assay. The inhibitory concentration (IC(50)) values of the products ranged between 0.75 and 2.25 µg/mL. When tested on normal and healthy cells (HEK-293), we found that the treatment of products did not produce any effects on the normal cells, which suggests that all products selectively targeted the cancerous cells. The anti-bacterial properties of the samples were also evaluated by Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) assays, which showed that products also inhibited the bacterial growth. MDPI 2019-11-18 /pmc/articles/PMC6915425/ /pubmed/31752130 http://dx.doi.org/10.3390/nano9111635 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Akhtar, Sultan Rehman, Suriya Almessiere, Munirah A. Khan, Firdos Alam Slimani, Yassine Baykal, Abdulhadi Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title | Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title_full | Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title_fullStr | Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title_full_unstemmed | Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title_short | Synthesis of Mn(0.5)Zn(0.5)Sm(x)Eu(x)Fe(1.8−2x)O(4) Nanoparticles via the Hydrothermal Approach Induced Anti-Cancer and Anti-Bacterial Activities |
title_sort | synthesis of mn(0.5)zn(0.5)sm(x)eu(x)fe(1.8−2x)o(4) nanoparticles via the hydrothermal approach induced anti-cancer and anti-bacterial activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915425/ https://www.ncbi.nlm.nih.gov/pubmed/31752130 http://dx.doi.org/10.3390/nano9111635 |
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