Quercetin-loaded PLGA nanoparticles: a highly effective antibacterial agent in vitro and anti-infection application in vivo
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  • 作者:Dongdong Sun ; Nuan Li ; Weiwei Zhang ; Endong Yang…
  • 关键词:PLGA ; Quercetin ; Histological study ; Antibacterial agent ; Nanomedicine ; Health effects
  • 刊名:Journal of Nanoparticle Research
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:18
  • 期:1
  • 全文大小:8,540 KB
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  • 作者单位:Dongdong Sun (1)
    Nuan Li (1)
    Weiwei Zhang (1)
    Endong Yang (1)
    Zhipeng Mou (1)
    Zhiwei Zhao (1)
    Haiping Liu (1)
    Weiyun Wang (1)

    1. School of Life Sciences, Anhui Agricultural University, Hefei, 230036, China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Nanotechnology
    Inorganic Chemistry
    Characterization and Evaluation Materials
    Physical Chemistry
    Applied Optics, Optoelectronics and Optical Devices
  • 出版者:Springer Netherlands
  • ISSN:1572-896X
文摘
Nanotechnology-based approaches have tremendous potential for enhancing efficacy against infectious diseases. PLGA-based nanoparticles as drug delivery carrier have shown promising potential, owing to their sizes and related unique properties. This article aims to develop nanosized poly (d, l-lactide-co-glycolide) PLGA nanoparticle formulation loaded with quercetin (QT). QT is an antioxidant and antibacterial compound isolated from Chinese traditional medicine with low skin permeability and extreme water insolubility. The quercetin-loaded PLGA nanoparticles (PQTs) were synthesized by emulsion–solvent evaporation method and stabilized by coating with poly (vinyl alcohol). The characteristics of PQTs were analyzed by Fourier transform infrared spectroscopy, Ultraviolet–Visible spectroscopy, scanning electron microscope, transmission electron microscopy, and atomic force microscopy, respectively. The PQTs showed a spherical shape with an average size of 100–150 nm. We compared the antibacterial effects of PQTs against Escherichia coli (E. coli) and Micrococcus tetragenus (M. tetragenus).The PQTs produced stronger antibacterial activity to E. coli than that to M. tetragenus through disrupting bacterial cell wall integrity. The antibacterial ratio was increased with the increasing dosages and incubation time. Next, we tested the in vivo antibacterial activity in mice. No noticeable organ damage was captured from H&E-staining organ slices, suggesting the promise of using PQTs for in vivo applications. The results of this study demonstrated the interaction between bacteria and PLGA-based nanoparticles, providing encouragement for conducting further investigations on properties and antimicrobial activity of the PQTs in clinical application.

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