A self-microemulsifying drug delivery system to overcome intestinal resveratrol toxicity and presystemic metabolism

J Pharm Sci. 2014 Nov;103(11):3491-3500. doi: 10.1002/jps.24114. Epub 2014 Aug 7.

Abstract

A mixed lipid-mixed surfactant self-microemulsifying drug delivery system (SMEDDS) was developed to exploit the health benefits of resveratrol, a Biopharmaceutical Classification System Class 2 natural polyphenol, subject to extensive intestinal presystemic metabolism. SMEDDS with a mixed lipid phase (castor oil/Capmul MCM 1:1) and a mixed surfactant phase (Kolliphor EL/Kolliphor RH 40 1:1) was developed and evaluated for its self-emulsifying properties and in vitro dispersion. The impact of SMEDDS on the permeability properties of resveratrol and its metabolite fluxes through the rat intestine and Caco-2 cells was monitored. The inhibitory effect of selected SMEDDS components on the efflux transporters multidrug resistance-associated protein and P-gp as well as cytotoxicity was assessed on Caco-2 cells. The formulation allowed for high resveratrol loading (122.5 mg/g SMEDDS), excellent self-emulsifying properties, and very rapid release. When formulated in SMEDDS, resveratrol metabolite efflux significantly declined. The formulation (SMEDDS without incorporated resveratrol) and its individual components did not compromise in vitro cell vitality and integrity. Mixed lipid-mixed surfactant SMEDDS is a prospective formulation to improve resveratrol biopharmaceutical, pharmacokinetic, and toxicological properties, leading the way to resveratrol use not only as a supplement but also as a pharmacological drug.

Keywords: Caco-2 cells; dissolution; drug delivery systems; gastrointestinal; lipids; phase diagram; self-emulsifying; solubility; surfactants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Animals
  • Caco-2 Cells
  • Caprylates / chemistry*
  • Castor Oil / chemistry*
  • Chemistry, Pharmaceutical
  • Drug Carriers*
  • Emulsions
  • Glycerides / chemistry*
  • Humans
  • Intestinal Absorption
  • Jejunum / metabolism*
  • Male
  • Multidrug Resistance-Associated Proteins / metabolism
  • Permeability
  • Rats
  • Rats, Sprague-Dawley
  • Resveratrol
  • Solubility
  • Stilbenes / administration & dosage
  • Stilbenes / chemistry
  • Stilbenes / metabolism*
  • Stilbenes / toxicity
  • Surface-Active Agents / chemistry*
  • Technology, Pharmaceutical / methods
  • Viscosity

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Caprylates
  • Drug Carriers
  • Emulsions
  • Glycerides
  • Multidrug Resistance-Associated Proteins
  • Stilbenes
  • Surface-Active Agents
  • Castor Oil
  • Resveratrol
  • monooctanoin