Nanocarriers enhance the transdermal bioavailability of resveratrol: In-vitro and in-vivo study

Colloids Surf B Biointerfaces. 2016 Dec 1:148:650-656. doi: 10.1016/j.colsurfb.2016.09.045. Epub 2016 Sep 28.

Abstract

The aim of this study was to develop and assess the potential of nanostructured emulsion carriers for resveratrol topical application. Different compositions of resveratrol-loaded nanostructured emulsions were prepared using different types and amounts of surfactants and oily phases (isopropyl myristate and caproyl 90). The produced nanostructured emulsions were within the nanosized range 23.4-422.2nm with low viscosity range 2.15-17.53cps. The transdermal amount and deposition amount in the skin after 24 applications of resveratrol-loaded nanostructured emulsion were significantly increased about 896.2-fold and 10.2-fold respectively, when compared to the drug-saturated solution-treated group. Nanostructured emulsion containing IPM and low amounts of mixed surfactant of Tween80/Span 20 showed highest permeation capacity. In vivo study showed that the plasma concentration of resveratrol could be maintained at high levels for a long time after topical application of drug-loaded nanostructured emulsion. The histological examination demonstrated that the free drug- and drug-loaded nanostructured emulsion demonstrated considerably less irritation than the standard irritation group (0.8% paraformaldehyde-treated). The residual contents of resveratrol in the tested formulations after 3 months of storage at 25°C and 40°C were more than 99.97±3.90%. The results of present work confirm the high potential of nanostructured emulsion as carriers for drug topical application.

Keywords: Deposition amount; Resveratrol; Skin irritation; Stability; Topical application; Transdermal amount.

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
  • Biological Availability
  • Drug Carriers / chemistry*
  • Drug Stability
  • Emulsions / chemistry
  • Nanostructures / chemistry*
  • Particle Size
  • Rats, Sprague-Dawley
  • Resveratrol
  • Skin / metabolism*
  • Skin Absorption
  • Skin Tests
  • Stilbenes / administration & dosage
  • Stilbenes / chemistry
  • Stilbenes / pharmacokinetics*
  • Thermodynamics
  • Viscosity

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Drug Carriers
  • Emulsions
  • Stilbenes
  • Resveratrol