2009
DOI: 10.1016/j.lfs.2008.11.001
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Nanoencapsulation of quercetin enhances its dietary efficacy in combating arsenic-induced oxidative damage in liver and brain of rats

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Cited by 127 publications
(61 citation statements)
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“…Nanoencapsulated quercitin, orally administered before the arsenite injection, prevented the arsenic cerebral oxidative damage. 38 The authors hypothesized the ability of these NPs to cross the BBB via particle uptake mechanism based on an endocytotic pathway by the brain capillary endothelial cells. It is not clear if the treatment of rats with arsenic maintained the BBB integrity, thus it is difficult to give an absolute conclusion on the real efficacy and BBB crossing pathway.…”
Section: Lysosomal Storage Disordersmentioning
confidence: 99%
“…Nanoencapsulated quercitin, orally administered before the arsenite injection, prevented the arsenic cerebral oxidative damage. 38 The authors hypothesized the ability of these NPs to cross the BBB via particle uptake mechanism based on an endocytotic pathway by the brain capillary endothelial cells. It is not clear if the treatment of rats with arsenic maintained the BBB integrity, thus it is difficult to give an absolute conclusion on the real efficacy and BBB crossing pathway.…”
Section: Lysosomal Storage Disordersmentioning
confidence: 99%
“…A number of studies have shown arsenic-induced formation of reactive oxygen and nitrogen species as well as elevated DNA oxidation. Thus, arsenite 12,13 .…”
Section: Introductionmentioning
confidence: 99%
“…Besides, it is widely accepted that the beneficial effects of quercetin against arsenic toxicity are mainly due to its antioxidant properties and also due to regulation of signalling pathway. The preventive role of quercetin encapsulated in nanoparticles against NaAsO 2 -induced acute liver and neuronal toxicity in rats has been shown in our previous work (Ghosh et al 2009) where a single oral dose of nanoformulation was found to be effective against acute arsenic toxicity. Inorganic arsenic when administered for a longer duration (chronic arsenic treatment) of time gets metabolized by a process involving a two-electron reduction of pentavalent arsenic to trivalent arsenic, exerting more oxidative pressure to cellular macromolecules.…”
Section: Discussionmentioning
confidence: 68%
“…Bioavailability of drugs can be improved when they are administered intravenously upon entrapment in liposomes (Gregoriadis et al 1988). Our previous report indicates that nanoencapsulation of drug enhances its dietary efficiency in combating arsenic-induced acute toxicity in liver and brain of rats (Ghosh et al 2009). …”
Section: Drug Deliverymentioning
confidence: 99%
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