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Artemia salina as a model organism in toxicity assessment of nanoparticles.

作者信息

Rajabi Somayeh, Ramazani Ali, Hamidi Mehrdad, Naji Tahereh

机构信息

Cell and Molecular Biology Departments, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.

Biotechnology Departments, School of Pharmacy, Zanjan University of Medical Sciences, Zanjan, Iran.

出版信息

Daru. 2015 Feb 24;23(1):20. doi: 10.1186/s40199-015-0105-x.


DOI:10.1186/s40199-015-0105-x
PMID:25888940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4344789/
Abstract

BACKGROUND: Because of expanding presence of nanomaterials, there has been an increase in the exposure of humans to nanoparticles that is why nanotoxicology studies are important. A number of studies on the effects of nanomatrials in in vitro and in vivo systems have been published. Currently cytotoxicity of different nanoparticles is assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay on different cell lines to determine cell viability, a tedious and expensive method. The aim of this study was to evaluate the Artemia salina test in comparison with the MTT assay in the assessment of cytotoxicity of nanostructures because the former method is more rapid and convenient and less expensive. METHODS: At the first stage, toxicity of different nanoparticles with different concentrations (1.56-400 μg/mL) was measured by means of the brine shrimp lethality test. At the second stage, the effect of nanoparticles on the viability of the L929 cell line was assessed using the MTT assay. Experiments were conducted with each concentration in triplicate. RESULTS: The results obtained from both tests (A. salina test and MTT assay) did not have statistically significant differences (P>0.05). CONCLUSIONS: These findings suggest that the A. salina test may expedite toxicity experiments and decrease costs, and therefore, may be considered an alternative to the in vitro cell culture assay.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/4344789/a8b118af3e91/40199_2015_105_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/4344789/a8b118af3e91/40199_2015_105_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f7a/4344789/a8b118af3e91/40199_2015_105_Fig1_HTML.jpg

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本文引用的文献

[1]
Toxicity of nanomaterials; an undermined issue.

Daru. 2014-8-15

[2]
Ecotoxicity of pristine graphene to marine organisms.

Ecotoxicol Environ Saf. 2014-1-15

[3]
Antiplasmodial activity of ethanolic extracts of some selected medicinal plants from the northwest of Iran.

Parasitol Res. 2013-8-7

[4]
Nanotoxicology using the sea anemone Nematostella vectensis: from developmental toxicity to genotoxicology.

Nanotoxicology. 2013-6-3

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Different biokinetics of nanomedicines linking to their toxicity; an overview.

Daru. 2013-2-22

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In vivo-in vitro comparison of acute respiratory tract toxicity using human 3D airway epithelial models and human A549 and murine 3T3 monolayer cell systems.

Toxicol In Vitro. 2012-10-22

[7]
Anti-leishmanial and toxicity activities of some selected Iranian medicinal plants.

Parasitol Res. 2012-8-9

[8]
Effects of aqueous suspensions of titanium dioxide nanoparticles on Artemia salina: assessment of nanoparticle aggregation, accumulation, and toxicity.

Environ Monit Assess. 2012-7-19

[9]
Silica-encapsulated magnetic nanoparticles: enzyme immobilization and cytotoxic study.

Int J Biol Macromol. 2012-1-16

[10]
Nanotoxicology and in vitro studies: the need of the hour.

Toxicol Appl Pharmacol. 2011-12-2

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