Quercetin and 3-O-methylquercetin in vitro skin layers permeation/retention from hydrogels: why only a methoxy group difference determines different behaviors?

J Pharm Pharmacol. 2019 May;71(5):733-745. doi: 10.1111/jphp.13050. Epub 2018 Dec 3.

Abstract

Objectives: The present study was designed to verify if quercetin (QCT), a flavonoid with antioxidant and antiviral activity, and 3-O-methylquercetin (3OMQ), a quercetin C3-methoxylated derivative, present differences in their behavior against complexation with β-cyclodextrin (β-CD) and the corresponding permeation/retention trhough porcine ear skin, when incorporated into hydroxypropyl methylcellulose (HPMC) or chitosan (CS) hydrogels.

Methods: The influence of β-CD on the skin permeation/retention of QCT and 3OMQ from hydrogels is comparatively evaluated for both flavonoids using porcine ear skin in Franz cells model. The properties of the two flavonoids using the semi-empirical method Recife Model was studied.

Key findings: Quercetin presented higher skin retention compared with its C3-methoxy derivative 3OMQ. The best permeation/retention of QCT was observed when it was incorporated into CS hydrogel containing 5% β-CD, whereas, for 3OMQ, the HPMC hydrogel containing 5% β-CD was the best formulation. The flavonoids complexation with β-CD in water occurred preferentially with the insertion of the B ring through the secondary OH rim.

Conclusions: The dynamic molecular modeling revealed that the methyl group at C3 in 3OMQ molecule determined significant difference in its complexation with β-CD, in comparison to its analogous QCT and that difference is coincident with the permeation behavior of these flavonoids, denoting a possible relationship with their molecular dynamics.

Keywords: 3-O-methylquercetin; cyclodextrin; molecular modeling; quercetin; skin retention.

MeSH terms

  • Animals
  • Chitosan / administration & dosage
  • Chitosan / chemistry
  • Chitosan / pharmacokinetics
  • Ear, External / metabolism
  • Hydrogels / administration & dosage
  • Hydrogels / chemistry
  • Hydrogels / pharmacokinetics*
  • Models, Molecular
  • Molecular Conformation
  • Quercetin / administration & dosage
  • Quercetin / analogs & derivatives*
  • Quercetin / chemistry*
  • Quercetin / pharmacokinetics*
  • Skin / drug effects
  • Skin / metabolism*
  • Skin Absorption / drug effects*
  • Structure-Activity Relationship
  • Swine
  • beta-Cyclodextrins / chemistry
  • beta-Cyclodextrins / pharmacokinetics

Substances

  • Hydrogels
  • beta-Cyclodextrins
  • 3-methylquercetin
  • Chitosan
  • Quercetin
  • betadex