2015
DOI: 10.1016/j.toxlet.2015.09.013
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Effect of titanium dioxide nanoparticles on the cardiovascular system after oral administration

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Cited by 101 publications
(76 citation statements)
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“…The studies applying the longest exposure of all studies with characterized and uncoated TiO 2 NPs, were those of Chen et al (2015), Wang et al (2013) and the 28-d study in Warheit et al (2015a). Chen et al (2015) focused on cardiac toxicity and inflammatory response in initially young rats (3 weeks old at the start of the study) after 30 and 90 days of exposure.…”
Section: Kinetic Modelmentioning
confidence: 99%
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“…The studies applying the longest exposure of all studies with characterized and uncoated TiO 2 NPs, were those of Chen et al (2015), Wang et al (2013) and the 28-d study in Warheit et al (2015a). Chen et al (2015) focused on cardiac toxicity and inflammatory response in initially young rats (3 weeks old at the start of the study) after 30 and 90 days of exposure.…”
Section: Kinetic Modelmentioning
confidence: 99%
“…Chen et al (2015) focused on cardiac toxicity and inflammatory response in initially young rats (3 weeks old at the start of the study) after 30 and 90 days of exposure. They report decreases of lactate dehydrogenase (LDH), hydroxybutyrate dehydrogenase (HBDH), and triglycerides and increase of white blood cells and granulocytes at 50 mg/kg bw/d after 90 days.…”
Section: Kinetic Modelmentioning
confidence: 99%
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“…However, the inflammatory response in subjects returned to control levels a few days' post exposure (Grassian et al, 2007). After performing an in vivo study in rats investigating the effects of daily oral and gastrointestinal administration of titanium dioxide nanoparticles over the span of 30 to 90 days, Chen et al found significant cardio vascular damage and inflammatory response (Chen et al, 2015).…”
Section: Toxicitymentioning
confidence: 99%
“…[9][10][11][12][13][14] The 2010 American Heart Association scientific statement reached the conclusion that both short-term and chronic exposure to PM 2.5 can trigger cardiovascular disease-related events or increase the risk for cardiovascular mortality, while reductions in PM levels are associated with decreases in cardiovascular mortality. 10 Recent toxicological evaluations of engineered nanoparticles, including nanoparticles of silica 15,16 and titanium dioxide, 17 and carbon nanotube, 18 have demonstrated that exposure to engineered nanoparticles poses risks to cardiovascular functions and causes cardiovascular-related phenotypes in animal models.…”
Section: Introductionmentioning
confidence: 99%