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In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery

  • Noor Hafizah Arbain
  • Norazlinaliza Salim
  • Hamid Reza Fard Masoumi
  • Tin Wui Wong
  • Mahiran Basri
  • Mohd Basyaruddin Abdul Rahman
Original Article
  • 70 Downloads

Abstract

Bioavailability of quercetin, a flavonoid potentially known to combat cancer, is challenging due to hydrophobic nature. Oil-in-water (O/W) nanoemulsion system could be used as nanocarrier for quercertin to be delivered to lung via pulmonary delivery. The novelty of this nanoformulation was introduced by using palm oil ester/ricinoleic acid as oil phase which formed spherical shape nanoemulsion as measured by transmission electron microscopy and Zetasizer analyses. High energy emulsification method and D-optimal mixture design were used to optimize the composition towards the volume median diameter. The droplet size, polydispersity index, and zeta potential of the optimized formulation were 131.4 nm, 0.257, and 51.1 mV, respectively. The formulation exhibited high drug entrapment efficiency and good stability against phase separation and storage at temperature 4 °C for 3 months. It was discovered that the system had an acceptable median mass aerodynamic diameter (3.09 ± 0.05 μm) and geometric standard deviation (1.77 ± 0.03) with high fine particle fraction (90.52 ± 0.10%), percent dispersed (83.12 ± 1.29%), and percent inhaled (81.26 ± 1.28%) for deposition in deep lung. The in vitro release study demonstrated that the sustained release pattern of quercetin from naneomulsion formulation up to 48 h of about 26.75% release and it was in adherence to Korsmeyer’s Peppas mechanism. The cytotoxicity study demonstrated that the optimized nanoemulsion can potentially induce cyctotoxicity towards A549 lung cancer cells without affecting the normal cells. These results of the study suggest that nanoemulsion is a potential carrier system for pulmonary delivery of molecules with low water solubility like quercetin.

Keywords

Palm oil ester Nanoemulsion Quercetin Pulmonary delivery D-optimal mixture design 

Notes

Acknowledgements

The financial assistance provided from MyBRAIN 15 for Arbain N.H. by Ministry of Higher Education Malaysia (MOHE) and NanoMITe research grant (Vote. No. 5526306) were gratefully acknowledged.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Controlled Release Society 2018

Authors and Affiliations

  • Noor Hafizah Arbain
    • 1
  • Norazlinaliza Salim
    • 1
  • Hamid Reza Fard Masoumi
    • 1
  • Tin Wui Wong
    • 2
  • Mahiran Basri
    • 1
  • Mohd Basyaruddin Abdul Rahman
    • 1
  1. 1.Integrated Chemical BioPhysics Research, Department of Chemistry, Faculty of ScienceUniversiti Putra MalaysiaSerdangMalaysia
  2. 2.Non-Destructive Biomedical and Pharmaceutical Research Centre, iPROMISEUniversiti Teknologi MARAPuncak AlamMalaysia

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