Literature DB >> 21855616

Rutile TiO₂ particles exert size and surface coating dependent retention and lesions on the murine brain.

Lili Zhang1, Ru Bai, Bai Li, Cuicui Ge, Jiangfeng Du, Ying Liu, Laurent Le Guyader, Yuliang Zhao, Yanchuan Wu, Shida He, Yongmei Ma, Chunying Chen.   

Abstract

The rising commercial use and large-scale production of engineered nanoparticles (NPs) may lead to unintended exposure to humans. The central nervous system (CNS) is a potential susceptible target of the inhaled NPs, but so far the amount of studies on this aspect is limited. Here, we focus on the potential neurological lesion in the brain induced by the intranasally instilled titanium dioxide (TiO₂) particles in rutile phase and of various sizes and surface coatings. Female mice were intranasally instilled with four different types of TiO₂ particles (i.e. two types of hydrophobic particles in micro- and nano-sized without coating and two types of water-soluble hydrophilic nano-sized particles with silica surface coating) every other day for 30 days. Inductively coupled plasma mass spectrometry (ICP-MS) were used to determine the titanium contents in the sub-brain regions. Then, the pathological examination of brain tissues and measurements of the monoamine neurotransmitter levels in the sub-brain regions were performed. We found significant up-regulation of Ti contents in the cerebral cortex and striatum after intranasal instillation of hydrophilic TiO₂ NPs. Moreover, TiO₂ NPs exposure, in particular the hydrophilic NPs, caused obvious morphological changes of neurons in the cerebral cortex and significant disturbance of the monoamine neurotransmitter levels in the sub-brain regions studied. Thus, our results indicate that the surface modification of the NPs plays an important role on their effects on the brain. In addition, the difference in neurotoxicity of the two types of hydrophilic NPs may be induced by the shape differences of the materials. The present results suggest that physicochemical properties like size, shape and surface modification of the nanomaterials should be considered when evaluating their neurological effects.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21855616     DOI: 10.1016/j.toxlet.2011.08.001

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  15 in total

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Authors:  Tobias A Mattei; Azeem A Rehman
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Journal:  Mol Neurobiol       Date:  2015-07-02       Impact factor: 5.590

4.  Alternating magnetic field-induced hyperthermia increases iron oxide nanoparticle cell association/uptake and flux in blood-brain barrier models.

Authors:  Mo Dan; Younsoo Bae; Thomas A Pittman; Robert A Yokel
Journal:  Pharm Res       Date:  2014-11-07       Impact factor: 4.200

Review 5.  Neurotoxicology of Nanomaterials.

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Journal:  Chem Res Toxicol       Date:  2020-04-14       Impact factor: 3.739

6.  Induction of size-dependent breakdown of blood-milk barrier in lactating mice by TiO2 nanoparticles.

Authors:  Chengke Zhang; Shumei Zhai; Ling Wu; Yuhong Bai; Jianbo Jia; Yi Zhang; Bin Zhang; Bing Yan
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Review 7.  Central nervous system toxicity of metallic nanoparticles.

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Journal:  Int J Nanomedicine       Date:  2015-07-03

8.  Health effects of exposure to nano-TiO2: a meta-analysis of experimental studies.

Authors:  Xuhong Chang; Yu Zhang; Meng Tang; Bei Wang
Journal:  Nanoscale Res Lett       Date:  2013-01-25       Impact factor: 4.703

Review 9.  Interactions between nanosized materials and the brain.

Authors:  M Simkó; Mats-Olof Mattsson
Journal:  Curr Med Chem       Date:  2014       Impact factor: 4.530

10.  A review on potential neurotoxicity of titanium dioxide nanoparticles.

Authors:  Bin Song; Jia Liu; Xiaoli Feng; Limin Wei; Longquan Shao
Journal:  Nanoscale Res Lett       Date:  2015-08-26       Impact factor: 4.703

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