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

Author:

Prestianni Lucas1ORCID,Espinal Eric R.2,Hathcock Sarah F.2,Vollmuth Nadine2,Wang Pixiang3,Holler Robert A.4,Liu Shaoyang3ORCID,Kim Brandon J.2567,Bao Yuping167ORCID

Affiliation:

1. Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, AL 35487, USA

2. Department of Biological Sciences, The University of Alabama, Tuscaloosa, AL 35487, USA

3. Department of Chemistry and Physics, Center for Materials and Manufacturing Sciences, Troy University, Troy, AL 36082, USA

4. Alabama Analytical Research Center, The University of Alabama, Tuscaloosa, AL 35487, USA

5. Department of Microbiology, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, AL 35487, USA

6. Center for Convergent Biosciences and Medicine, The University of Alabama, Tuscaloosa, AL 35487, USA

7. Alabama Life Research Institute, The University of Alabama, Tuscaloosa, AL 35487, USA

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.

Funder

NSF-CBET

Breast Cancer Research Foundation of Alabama

U.S. Department of Education

Publisher

MDPI AG

Subject

Pharmaceutical Science

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