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Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice

With a simple synthesis and easy engineering of physicochemical properties, iron oxide nanoparticles (IONPs) have become widely used in multiple biomedical applications. The study of IONPs toxicity has become an important issue, especially as the results reported so far are contradictory and range f...

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Autores principales: MÎNDRILĂ, BOGDAN, ROGOVEANU, ION, BUTEICĂ, SANDRA-ALICE, CERCELARU, LILIANA, MIHAIESCU, DAN-EDUARD, MĂNESCU, MARINA-DANIELA, MÎNDRILĂ, ION, PIRICI, IONICA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical University Publishing House Craiova 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590356/
https://www.ncbi.nlm.nih.gov/pubmed/36320876
http://dx.doi.org/10.12865/CHSJ.48.02.02
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author MÎNDRILĂ, BOGDAN
ROGOVEANU, ION
BUTEICĂ, SANDRA-ALICE
CERCELARU, LILIANA
MIHAIESCU, DAN-EDUARD
MĂNESCU, MARINA-DANIELA
MÎNDRILĂ, ION
PIRICI, IONICA
author_facet MÎNDRILĂ, BOGDAN
ROGOVEANU, ION
BUTEICĂ, SANDRA-ALICE
CERCELARU, LILIANA
MIHAIESCU, DAN-EDUARD
MĂNESCU, MARINA-DANIELA
MÎNDRILĂ, ION
PIRICI, IONICA
author_sort MÎNDRILĂ, BOGDAN
collection PubMed
description With a simple synthesis and easy engineering of physicochemical properties, iron oxide nanoparticles (IONPs) have become widely used in multiple biomedical applications. The study of IONPs toxicity has become an important issue, especially as the results reported so far are contradictory and range from lack of toxicity to cellular toxicity. The aim of this study was to evaluate the histopathological changes induced in mouse liver by long-term intraperitoneal injection of low doses of IONPs functionalized with salicylic acid (SaIONPs). The study was performed on C57BL/6 mice that received by intraperitoneal injection (IP), every two days, 0.6ml of SaIONPs aqueous suspension (35mg/kg body weight SaIONPs that contained 20mg/kg body weight of Fe3O4) for 28 days. The results of this study showed that the cumulative dose of 105mg/kg body weight SaIONPs (62mg/kg body weight of Fe3O4) induced histopathological changes in the subcapsular region of the mouse liver, possible by the release of salicylic acid into the peritoneal cavity. The cumulative dose of 244mg/kg body weight SaIONPs (145mg/kg body weight of Fe3O4) induced liver centrilobular necrosis, which requires the use of lower doses in biological applications. However, this may prove to be beneficial in the case of targeted accumulation of SaIONPs
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spelling pubmed-95903562022-10-31 Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice MÎNDRILĂ, BOGDAN ROGOVEANU, ION BUTEICĂ, SANDRA-ALICE CERCELARU, LILIANA MIHAIESCU, DAN-EDUARD MĂNESCU, MARINA-DANIELA MÎNDRILĂ, ION PIRICI, IONICA Curr Health Sci J Original Paper With a simple synthesis and easy engineering of physicochemical properties, iron oxide nanoparticles (IONPs) have become widely used in multiple biomedical applications. The study of IONPs toxicity has become an important issue, especially as the results reported so far are contradictory and range from lack of toxicity to cellular toxicity. The aim of this study was to evaluate the histopathological changes induced in mouse liver by long-term intraperitoneal injection of low doses of IONPs functionalized with salicylic acid (SaIONPs). The study was performed on C57BL/6 mice that received by intraperitoneal injection (IP), every two days, 0.6ml of SaIONPs aqueous suspension (35mg/kg body weight SaIONPs that contained 20mg/kg body weight of Fe3O4) for 28 days. The results of this study showed that the cumulative dose of 105mg/kg body weight SaIONPs (62mg/kg body weight of Fe3O4) induced histopathological changes in the subcapsular region of the mouse liver, possible by the release of salicylic acid into the peritoneal cavity. The cumulative dose of 244mg/kg body weight SaIONPs (145mg/kg body weight of Fe3O4) induced liver centrilobular necrosis, which requires the use of lower doses in biological applications. However, this may prove to be beneficial in the case of targeted accumulation of SaIONPs Medical University Publishing House Craiova 2022 2022-06-30 /pmc/articles/PMC9590356/ /pubmed/36320876 http://dx.doi.org/10.12865/CHSJ.48.02.02 Text en Copyright © 2014, Medical University Publishing House Craiova https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Original Paper
MÎNDRILĂ, BOGDAN
ROGOVEANU, ION
BUTEICĂ, SANDRA-ALICE
CERCELARU, LILIANA
MIHAIESCU, DAN-EDUARD
MĂNESCU, MARINA-DANIELA
MÎNDRILĂ, ION
PIRICI, IONICA
Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title_full Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title_fullStr Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title_full_unstemmed Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title_short Liver Histopathological Changes Related to Intraperitoneal Administration of Salicylic Acid/Fe3O4 Nanoparticles to C57BL/6 Mice
title_sort liver histopathological changes related to intraperitoneal administration of salicylic acid/fe3o4 nanoparticles to c57bl/6 mice
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590356/
https://www.ncbi.nlm.nih.gov/pubmed/36320876
http://dx.doi.org/10.12865/CHSJ.48.02.02
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