Background
Type: Article

Using superparamagnetic iron oxide nanoparticles to enhance bioavailability of quercetin in the intact rat brain

Journal: BMC Pharmacology and Toxicology (20506511)Year: 25 September 2018Volume: 19Issue:
Enteshari Najafabadi R.Kazemipour N.Esmaeili A.aBeheshti S.a Nazifi S.
Gold • GreenDOI:10.1186/s40360-018-0249-7Language: English

Abstract

Background: Quercetin (QT) as a bioactive flavonoid has a potential therapeutic activity for numerous neuronal injuries and neurodegenerative diseases. However, the low absorption rate of QT, especially through the blood-brain barrier, restricts its bioactivity in the body. The current research took the advantage of superparamagnetic iron oxide nanoparticles (SPIONs) to enhance the bioavailability of quercetin. Methods: Quercetin conjugated with SPIONs was prepared by means of nanoprecipitation method and was characterized by X-ray diffractometer, scanning electron microscope, and Fourier transformed infrared spectrometer analyses. Wistar male rats were orally fed by gavage with QT and QT-SPION at 50 and 100 mg/kg daily doses for 7 days. Using high-performance liquid chromatography (HPLC) method, biodistribution of QT was evaluated in plasma and brain tissue. Results: The outcomes of this research revealed a higher concentration in the plasma and brain of the rats fed with QT-SPION in comparison to free QT. Conclusion: The results of this study confirm that SPION as a targeted drug delivery system enhances the bioavailability of quercetin in the brain about ten folds higher than free quercetin and could be used for the treatment of neurodegenerative disorders. © 2018 The Author(s).


Author Keywords

HPLCNanoparticlesOral drug deliveryQuercetinSPION

Other Keywords

AnimalsBiological AvailabilityBrainDrug Delivery SystemsDrug LiberationIronLiverMagnetite NanoparticlesMaleNeuroprotective AgentsQuercetinRats, Wistarsuperparamagnetic iron oxide nanoparticlemagnetite nanoparticleneuroprotective agentadultanimal experimentanimal tissueArticlecontrolled studydrug bioavailabilitydrug blood leveldrug brain leveldrug delivery systemdrug distributiondrug dosage form comparisondrug releaseFourier transform infrared spectroscopyhigh performance liquid chromatographyhistologyiron blood levelnonhumanratanatomy and histologyanimalbioavailabilitychemistrydrug effectmetabolismWistar rat