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Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model

BACKGROUND: Although there are a number of reports regarding the toxicity evaluation of inorganic nanoparticles, knowledge on biodegradable nanomaterials, which have always been considered safe, is still limited. For example, the toxicity of chitosan nanoparticles, one of the most widely used drug/g...

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Autores principales: Hu, Yu-Lan, Qi, Wang, Han, Feng, Shao, Jian-Zhong, Gao, Jian-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260029/
https://www.ncbi.nlm.nih.gov/pubmed/22267920
http://dx.doi.org/10.2147/IJN.S25853
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author Hu, Yu-Lan
Qi, Wang
Han, Feng
Shao, Jian-Zhong
Gao, Jian-Qing
author_facet Hu, Yu-Lan
Qi, Wang
Han, Feng
Shao, Jian-Zhong
Gao, Jian-Qing
author_sort Hu, Yu-Lan
collection PubMed
description BACKGROUND: Although there are a number of reports regarding the toxicity evaluation of inorganic nanoparticles, knowledge on biodegradable nanomaterials, which have always been considered safe, is still limited. For example, the toxicity of chitosan nanoparticles, one of the most widely used drug/gene delivery vehicles, is largely unknown. In the present study, the zebrafish model was used for a safety evaluation of this nanocarrier. METHODS: Chitosan nanoparticles with two particle sizes were prepared by ionic cross-linking of chitosan with sodium tripolyphosphate. Chitosan nanoparticles of different concentrations were incubated with zebrafish embryos, and ZnO nanoparticles were used as the positive control. RESULTS: Embryo exposure to chitosan nanoparticles and ZnO nanoparticles resulted in a decreased hatching rate and increased mortality, which was concentration-dependent. Chitosan nanoparticles at a size of 200 nm caused malformations, including a bent spine, pericardial edema, and an opaque yolk in zebrafish embryos. Furthermore, embryos exposed to chitosan nanoparticles showed an increased rate of cell death, high expression of reactive oxygen species, as well as overexpression of heat shock protein 70, indicating that chitosan nanoparticles can cause physiological stress in zebrafish. The results also suggest that the toxicity of biodegradable nanocarriers such as chitosan nanoparticles must be addressed, especially considering the in vivo distribution of these nanoscaled particles. CONCLUSION: Our results add new insights into the potential toxicity of nanoparticles produced by biodegradable materials, and may help us to understand better the nanotoxicity of drug delivery carriers.
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spelling pubmed-32600292012-01-20 Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model Hu, Yu-Lan Qi, Wang Han, Feng Shao, Jian-Zhong Gao, Jian-Qing Int J Nanomedicine Original Research BACKGROUND: Although there are a number of reports regarding the toxicity evaluation of inorganic nanoparticles, knowledge on biodegradable nanomaterials, which have always been considered safe, is still limited. For example, the toxicity of chitosan nanoparticles, one of the most widely used drug/gene delivery vehicles, is largely unknown. In the present study, the zebrafish model was used for a safety evaluation of this nanocarrier. METHODS: Chitosan nanoparticles with two particle sizes were prepared by ionic cross-linking of chitosan with sodium tripolyphosphate. Chitosan nanoparticles of different concentrations were incubated with zebrafish embryos, and ZnO nanoparticles were used as the positive control. RESULTS: Embryo exposure to chitosan nanoparticles and ZnO nanoparticles resulted in a decreased hatching rate and increased mortality, which was concentration-dependent. Chitosan nanoparticles at a size of 200 nm caused malformations, including a bent spine, pericardial edema, and an opaque yolk in zebrafish embryos. Furthermore, embryos exposed to chitosan nanoparticles showed an increased rate of cell death, high expression of reactive oxygen species, as well as overexpression of heat shock protein 70, indicating that chitosan nanoparticles can cause physiological stress in zebrafish. The results also suggest that the toxicity of biodegradable nanocarriers such as chitosan nanoparticles must be addressed, especially considering the in vivo distribution of these nanoscaled particles. CONCLUSION: Our results add new insights into the potential toxicity of nanoparticles produced by biodegradable materials, and may help us to understand better the nanotoxicity of drug delivery carriers. Dove Medical Press 2011 2011-12-14 /pmc/articles/PMC3260029/ /pubmed/22267920 http://dx.doi.org/10.2147/IJN.S25853 Text en © 2011 Hu 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
Hu, Yu-Lan
Qi, Wang
Han, Feng
Shao, Jian-Zhong
Gao, Jian-Qing
Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title_full Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title_fullStr Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title_full_unstemmed Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title_short Toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
title_sort toxicity evaluation of biodegradable chitosan nanoparticles using a zebrafish embryo model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260029/
https://www.ncbi.nlm.nih.gov/pubmed/22267920
http://dx.doi.org/10.2147/IJN.S25853
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