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Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice

BACKGROUND: This study explored the pharmacokinetic parameters and tissue distribution of magnetic iron oxide nanoparticles (Fe(3)O(4) MNPs) in imprinting control region (ICR) mice. METHODS: The Fe(3)O(4) MNPs were synthesized by chemical coprecipitation, and their morphology and appearance were obs...

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Autores principales: Wang, Jun, Chen, Yue, Chen, Baoan, Ding, Jiahua, Xia, Guohua, Gao, Chong, Cheng, Jian, Jin, Nan, Zhou, Ying, Li, Xiaomao, Tang, Meng, Wang, Xue Mei
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963932/
https://www.ncbi.nlm.nih.gov/pubmed/21042548
http://dx.doi.org/10.2147/IJN.S13662
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author Wang, Jun
Chen, Yue
Chen, Baoan
Ding, Jiahua
Xia, Guohua
Gao, Chong
Cheng, Jian
Jin, Nan
Zhou, Ying
Li, Xiaomao
Tang, Meng
Wang, Xue Mei
author_facet Wang, Jun
Chen, Yue
Chen, Baoan
Ding, Jiahua
Xia, Guohua
Gao, Chong
Cheng, Jian
Jin, Nan
Zhou, Ying
Li, Xiaomao
Tang, Meng
Wang, Xue Mei
author_sort Wang, Jun
collection PubMed
description BACKGROUND: This study explored the pharmacokinetic parameters and tissue distribution of magnetic iron oxide nanoparticles (Fe(3)O(4) MNPs) in imprinting control region (ICR) mice. METHODS: The Fe(3)O(4) MNPs were synthesized by chemical coprecipitation, and their morphology and appearance were observed by transmission electron microscopy. ICR mice were divided into a control group and a Fe(3)O(4) MNP-treated group. Probable target organs in ICR mice were observed, and the pharmacokinetic parameters and biodistribution of Fe(3)O(4) MNPs in tissues were identified using atomic absorption spectrophotometry. RESULTS: Fe(3)O(4) MNPs were spherical with a well distributed particle diameter, and were distributed widely in various target organs and tissues including the heart, liver, spleen, lungs, kidneys, brain, stomach, small intestine, and bone marrow. The majority of Fe(3)O(4) MNPs were distributed to the liver and the spleen. Fe(3)O(4) MNP levels in brain tissue were higher in the Fe(3)O(4) MNP-treated group than in the control group, indicating that Fe(3)O(4) MNPs can penetrate the blood–brain barrier. CONCLUSION: These results suggest that the distribution of Fe(3)O(4) MNPs was mostly in the liver and spleen, so the curative effect of these compounds could be more pronounced for liver tumors. Furthermore, Fe(3)O(4) MNPs might be used as drug carriers to overcome physiologic barriers.
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spelling pubmed-29639322010-11-01 Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice Wang, Jun Chen, Yue Chen, Baoan Ding, Jiahua Xia, Guohua Gao, Chong Cheng, Jian Jin, Nan Zhou, Ying Li, Xiaomao Tang, Meng Wang, Xue Mei Int J Nanomedicine Original Research BACKGROUND: This study explored the pharmacokinetic parameters and tissue distribution of magnetic iron oxide nanoparticles (Fe(3)O(4) MNPs) in imprinting control region (ICR) mice. METHODS: The Fe(3)O(4) MNPs were synthesized by chemical coprecipitation, and their morphology and appearance were observed by transmission electron microscopy. ICR mice were divided into a control group and a Fe(3)O(4) MNP-treated group. Probable target organs in ICR mice were observed, and the pharmacokinetic parameters and biodistribution of Fe(3)O(4) MNPs in tissues were identified using atomic absorption spectrophotometry. RESULTS: Fe(3)O(4) MNPs were spherical with a well distributed particle diameter, and were distributed widely in various target organs and tissues including the heart, liver, spleen, lungs, kidneys, brain, stomach, small intestine, and bone marrow. The majority of Fe(3)O(4) MNPs were distributed to the liver and the spleen. Fe(3)O(4) MNP levels in brain tissue were higher in the Fe(3)O(4) MNP-treated group than in the control group, indicating that Fe(3)O(4) MNPs can penetrate the blood–brain barrier. CONCLUSION: These results suggest that the distribution of Fe(3)O(4) MNPs was mostly in the liver and spleen, so the curative effect of these compounds could be more pronounced for liver tumors. Furthermore, Fe(3)O(4) MNPs might be used as drug carriers to overcome physiologic barriers. Dove Medical Press 2010-10-21 2010 /pmc/articles/PMC2963932/ /pubmed/21042548 http://dx.doi.org/10.2147/IJN.S13662 Text en © 2010 Wang et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Wang, Jun
Chen, Yue
Chen, Baoan
Ding, Jiahua
Xia, Guohua
Gao, Chong
Cheng, Jian
Jin, Nan
Zhou, Ying
Li, Xiaomao
Tang, Meng
Wang, Xue Mei
Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title_full Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title_fullStr Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title_full_unstemmed Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title_short Pharmacokinetic parameters and tissue distribution of magnetic Fe(3)O(4) nanoparticles in mice
title_sort pharmacokinetic parameters and tissue distribution of magnetic fe(3)o(4) nanoparticles in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963932/
https://www.ncbi.nlm.nih.gov/pubmed/21042548
http://dx.doi.org/10.2147/IJN.S13662
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