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

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 introduce...

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Published in:Drug Delivery and Translational Research
Main Author: Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
Format: Article
Language:English
Published: Springer Verlag 2019
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85063647007&doi=10.1007%2fs13346-018-0509-5&partnerID=40&md5=1ca22f8a79e4faf30a72be06095f457a
id 2-s2.0-85063647007
spelling 2-s2.0-85063647007
Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
2019
Drug Delivery and Translational Research
9
2
10.1007/s13346-018-0509-5
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85063647007&doi=10.1007%2fs13346-018-0509-5&partnerID=40&md5=1ca22f8a79e4faf30a72be06095f457a
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. © 2018, Controlled Release Society.
Springer Verlag
2190393X
English
Article

author Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
spellingShingle Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
author_facet Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
author_sort Arbain N.H.; Salim N.; Masoumi H.R.F.; Wong T.W.; Basri M.; Abdul Rahman M.B.
title In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
title_short In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
title_full In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
title_fullStr In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
title_full_unstemmed In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
title_sort In vitro evaluation of the inhalable quercetin loaded nanoemulsion for pulmonary delivery
publishDate 2019
container_title Drug Delivery and Translational Research
container_volume 9
container_issue 2
doi_str_mv 10.1007/s13346-018-0509-5
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85063647007&doi=10.1007%2fs13346-018-0509-5&partnerID=40&md5=1ca22f8a79e4faf30a72be06095f457a
description 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. © 2018, Controlled Release Society.
publisher Springer Verlag
issn 2190393X
language English
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