Evidence map›Paper›PMID 30253803›Full record

ArticleBMC pharmacology & toxicology2018

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

Rezvan Enteshari Najafabadi, Nasrin Kazemipour, Abolghasem Esmaeili, Siamak Beheshti, Saeed Nazifi

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 84 citations in OpenAlex.

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  15. The blood-brain barrier: structure, regulation, and drug delivery.Signal transduction and targeted therapy · 2023
    Review
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  17. Pharmacokinetics and tumor delivery of nanoparticles.Journal of drug delivery science and technology · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Rezvan Enteshari NajafabadiDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Nasrin KazemipourDepartment of Basic Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Abolghasem EsmaeiliCell, Molecular Biology and Biochemistry Division, Department of Biology, Faculty of Sciences, University of Isfahan, P.O. Box: 8174673441, Isfahan, Iran. aesmaeili@sci.ui.ac.ir.ORCID 0000-0002-8844-4591
Siamak BeheshtiCell, Molecular Biology and Biochemistry Division, Department of Biology, Faculty of Sciences, University of Isfahan, P.O. Box: 8174673441, Isfahan, Iran.
Saeed NazifiDepartment of Clinical Science, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Shiraz University · IRUniversity of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundQuercetin (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.

methodsQuercetin 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.

resultsThe 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.

conclusionThe 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.

Indexed as

Drug Delivery SystemsAnimalsBiological AvailabilityBrainDrug LiberationIronLiverMagnetite NanoparticlesMaleNeuroprotective AgentsQuercetinRats, WistarIronMagnetite NanoparticlesNeuroprotective AgentsQuercetinHPLCNanoparticlesOral drug deliveryQuercetinSPION

Identifiers

PMID30253803
PMCPMC6156978
OpenAlexW2892685702

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.