4.7 Article

Matlodextrin-cinnamon essential oil nanoformulation as a potent protective against titanium nanoparticles-induced oxidative stress, genotoxicity, and reproductive disturbances in male mice

期刊

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
卷 28, 期 29, 页码 39035-39051

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SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-13518-0

关键词

Titanium dioxide nanoparticles; Encapsulated cinnamon oil; Oxidative stress; Genotoxicity; Reproductive toxicity; Antioxidants

资金

  1. Deanship of Scientific Research (DSR) at the University of Jeddah, Jeddah, Saudi Arabia

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This study found that encapsulated cinnamon oil (ECO) could potentially protect against adverse effects induced by titanium oxide nanoparticles (TiO2NPs), reducing oxidative stress, DNA damage, chromosomal aberrations, and reproductive disturbances. Co-administration of TiO2NPs and ECO showed dose-dependent alleviation of these disturbances, suggesting ECO as a promising and safe candidate for protecting against the health hazards of TiO2NPs.
Recently, bio-nanofabrication becomes one of the widest methods for synthesizing nanoparticles (NPs); however, there is scanty literature exploring the toxicity of these green NPs against living organisms. This study aimed to evaluate the potential protective role of encapsulated cinnamon oil (ECO) against titanium oxide nanoparticle (TiO2NP)-induced oxidative stress, DNA damage, chromosomal aberration, and reproductive disturbances in male mice. Sixty male Balb/c mice were distributed into six groups treated orally for 3 weeks and included control group, TiO2NP-treated group (25 mg/kg b.w), ECO at low or high dose-treated groups (50 or 100 mg/kg b.w), and the groups that received TiO(2)NPs plus ECO at a low or high dose. The results of GC-MS revealed the isolation of 21 compounds and the majority was cinnamaldehyde. The average size zeta potential of TiO(2)NPs and ECO were 28.9 and 321 nm and -33.97 and -17.35 mV, respectively. TiO2NP administration induced significant changes in liver and kidney function, decreased antioxidant capacity, and increased oxidative stress markers in liver and kidney, DNA damage in the hepatocytes, the number of chromosomal aberrations in the bone marrow and germ cells, and sperm abnormalities along with histological changes in the liver, kidney, and testis. Co-administration of TiO(2)NPs and ECO could alleviate these disturbances in a dose-dependent manner. It could be concluded that ECO is a promising and safe candidate for the protection against the health hazards of TiO(2)NPs.

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