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Histological Injury to Rat Brain, Liver, and Kidneys by Gold Nanoparticles is Dose-Dependent
[Image: see text] Gold nanoparticles (GNPs) possess various interesting plasmonic properties that can provide a variety of diagnostic and therapeutic functionalities for biomedical applications. Compared to other inorganic metal nanoparticles (NPs), GNPs are less toxic and more biocompatible. Howeve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219072/ https://www.ncbi.nlm.nih.gov/pubmed/35755394 http://dx.doi.org/10.1021/acsomega.2c00727 |
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author | Fadia, Bekhti Sari Mokhtari-Soulimane, Nassima Meriem, Bensalah Wacila, Nacer Zouleykha, Badi Karima, Rouigueb Soulimane, Tewfik Tofail, Syed A. M. Townley, Helen Thorat, Nanasaheb D. |
author_facet | Fadia, Bekhti Sari Mokhtari-Soulimane, Nassima Meriem, Bensalah Wacila, Nacer Zouleykha, Badi Karima, Rouigueb Soulimane, Tewfik Tofail, Syed A. M. Townley, Helen Thorat, Nanasaheb D. |
author_sort | Fadia, Bekhti Sari |
collection | PubMed |
description | [Image: see text] Gold nanoparticles (GNPs) possess various interesting plasmonic properties that can provide a variety of diagnostic and therapeutic functionalities for biomedical applications. Compared to other inorganic metal nanoparticles (NPs), GNPs are less toxic and more biocompatible. However, the in vivo toxicity of gold nanoparticles on humans can be significant due to the size effect. This work aims to study the effect of multiple doses of small-size (≈20 nm) GNPs on the vital organs of Wistar rats. The study includes the oxidative stress in vital organs (liver, brain, and kidney) caused by GNPs and histopathology analysis. The rats were given a single caudal injection of NPs dispersed in PBS at 25, 50, 100, and 250 mg/kg of body weight. After sacrifice, both plasma and organs were collected for the determination of oxidant/antioxidant markers and histological studies. Our data show the high sensitivity of oxidative stress parameters to the GNPs in the brain, liver, and kidneys. However, the response to this stress is different between the organs and depends upon the antioxidant defense, where GSH levels control the MDA and PCO levels. Histological alterations are mild at 25, 50, and 100 mg/kg but significant at higher concentrations of 250 mg/kg. Therefore, histological impairments are shown to be dependent on the dose of GNPs. The results contribute to the understanding of oxidative stress and cellular interaction induced by nanoparticles. |
format | Online Article Text |
id | pubmed-9219072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92190722022-06-24 Histological Injury to Rat Brain, Liver, and Kidneys by Gold Nanoparticles is Dose-Dependent Fadia, Bekhti Sari Mokhtari-Soulimane, Nassima Meriem, Bensalah Wacila, Nacer Zouleykha, Badi Karima, Rouigueb Soulimane, Tewfik Tofail, Syed A. M. Townley, Helen Thorat, Nanasaheb D. ACS Omega [Image: see text] Gold nanoparticles (GNPs) possess various interesting plasmonic properties that can provide a variety of diagnostic and therapeutic functionalities for biomedical applications. Compared to other inorganic metal nanoparticles (NPs), GNPs are less toxic and more biocompatible. However, the in vivo toxicity of gold nanoparticles on humans can be significant due to the size effect. This work aims to study the effect of multiple doses of small-size (≈20 nm) GNPs on the vital organs of Wistar rats. The study includes the oxidative stress in vital organs (liver, brain, and kidney) caused by GNPs and histopathology analysis. The rats were given a single caudal injection of NPs dispersed in PBS at 25, 50, 100, and 250 mg/kg of body weight. After sacrifice, both plasma and organs were collected for the determination of oxidant/antioxidant markers and histological studies. Our data show the high sensitivity of oxidative stress parameters to the GNPs in the brain, liver, and kidneys. However, the response to this stress is different between the organs and depends upon the antioxidant defense, where GSH levels control the MDA and PCO levels. Histological alterations are mild at 25, 50, and 100 mg/kg but significant at higher concentrations of 250 mg/kg. Therefore, histological impairments are shown to be dependent on the dose of GNPs. The results contribute to the understanding of oxidative stress and cellular interaction induced by nanoparticles. American Chemical Society 2022-06-07 /pmc/articles/PMC9219072/ /pubmed/35755394 http://dx.doi.org/10.1021/acsomega.2c00727 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Fadia, Bekhti Sari Mokhtari-Soulimane, Nassima Meriem, Bensalah Wacila, Nacer Zouleykha, Badi Karima, Rouigueb Soulimane, Tewfik Tofail, Syed A. M. Townley, Helen Thorat, Nanasaheb D. Histological Injury to Rat Brain, Liver, and Kidneys by Gold Nanoparticles is Dose-Dependent |
title | Histological Injury to Rat Brain, Liver, and Kidneys
by Gold Nanoparticles is Dose-Dependent |
title_full | Histological Injury to Rat Brain, Liver, and Kidneys
by Gold Nanoparticles is Dose-Dependent |
title_fullStr | Histological Injury to Rat Brain, Liver, and Kidneys
by Gold Nanoparticles is Dose-Dependent |
title_full_unstemmed | Histological Injury to Rat Brain, Liver, and Kidneys
by Gold Nanoparticles is Dose-Dependent |
title_short | Histological Injury to Rat Brain, Liver, and Kidneys
by Gold Nanoparticles is Dose-Dependent |
title_sort | histological injury to rat brain, liver, and kidneys
by gold nanoparticles is dose-dependent |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219072/ https://www.ncbi.nlm.nih.gov/pubmed/35755394 http://dx.doi.org/10.1021/acsomega.2c00727 |
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