Evidence map›Paper›PMID 37111527›Full record

ArticlePharmaceutics2023

Synthesis and Characterization of Quercetin-Iron Complex Nanoparticles for Overcoming Drug Resistance.

Lucas Prestianni, Eric R Espinal, Sarah F Hathcock, Nadine Vollmuth, Pixiang Wang, Robert A Holler, Shaoyang Liu, Brandon J Kim, Yuping Bao

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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

9 authors.

Lucas PrestianniChemical and Biological Engineering, The University of Alabama, Tuscaloosa, AL 35487, USA.ORCID 0000-0003-1410-3628
Eric R EspinalDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
Sarah F HathcockDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
Nadine VollmuthDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
Pixiang WangDepartment of Chemistry and Physics, Center for Materials and Manufacturing Sciences, Troy University, Troy, AL 36082, USA.
Robert A HollerAlabama Analytical Research Center, The University of Alabama, Tuscaloosa, AL 35487, USA.
Shaoyang LiuDepartment of Chemistry and Physics, Center for Materials and Manufacturing Sciences, Troy University, Troy, AL 36082, USA.ORCID 0000-0002-3863-0812
Brandon J KimDepartment of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA.
Yuping BaoChemical and Biological Engineering, The University of Alabama, Tuscaloosa, AL 35487, USA.ORCID 0000-0003-2829-4082

Funding

National Science Foundation 1915873US Department of Education P200A210069
6 · The paper itself

Abstract

Quercetin, one of the major natural flavonoids, has demonstrated great pharmacological potential as an antioxidant and in overcoming drug resistance. However, its low aqueous solubility and poor stability limit its potential applications. Previous studies suggest that the formation of quercetin-metal complexes could increase quercetin stability and biological activity. In this paper, we systematically investigated the formation of quercetin-iron complex nanoparticles by varying the ligand-to-metal ratios with the goal of increasing the aqueous solubility and stability of quercetin. It was found that quercetin-iron complex nanoparticles could be reproducibly synthesized with several ligand-to-iron ratios at room temperature. The UV-Vis spectra of the nanoparticles indicated that nanoparticle formation greatly increased the stability and solubility of quercetin. Compared to free quercetin, the quercetin-iron complex nanoparticles exhibited enhanced antioxidant activities and elongated effects. Our preliminary cellular evaluation suggests that these nanoparticles had minimal cytotoxicity and could effectively block the efflux pump of cells, indicating their potential for cancer treatment.

Indexed as

drug resistanceefflux pumpflavonoidsiron complexquercetin

Identifiers

PMID37111527
PMCPMC10144594

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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.