Bioavailability of an R-α-Lipoic Acid/γ-Cyclodextrin Complex in Healthy Volunteers

Int J Mol Sci. 2016 Jun 15;17(6):949. doi: 10.3390/ijms17060949.

Abstract

R-α-lipoic acid (R-LA) is a cofactor of mitochondrial enzymes and a very strong antioxidant. R-LA is available as a functional food ingredient but is unstable against heat or acid. Stabilized R-LA was prepared through complexation with γ-cyclodextrin (CD), yielding R-LA/CD. R-LA/CD was orally administered to six healthy volunteers and showed higher plasma levels with an area under the plasma concentration-time curve that was 2.5 times higher than that after oral administration of non-complexed R-LA, although the time to reach the maximum plasma concentration and half-life did not differ. Furthermore, the plasma glucose level after a single oral administration of R-LA/CD or R-LA was not affected and no side effects were observed. These results indicate that R-LA/CD could be easily absorbed in the intestine. In conclusion, γ-CD complexation is a promising technology for delivering functional but unstable ingredients like R-LA.

Keywords: R-α-lipoic acid; bioavailability; clinical study; cyclodextrin; healthy volunteers; oral administration; pharmacokinetics.

MeSH terms

  • Adult
  • Antioxidants / administration & dosage
  • Antioxidants / pharmacokinetics
  • Biological Availability
  • Drug Combinations
  • Healthy Volunteers
  • Humans
  • Male
  • Thioctic Acid / administration & dosage*
  • Thioctic Acid / adverse effects
  • Thioctic Acid / chemistry
  • Thioctic Acid / pharmacokinetics*
  • gamma-Cyclodextrins / administration & dosage*
  • gamma-Cyclodextrins / adverse effects
  • gamma-Cyclodextrins / chemistry
  • gamma-Cyclodextrins / pharmacokinetics*

Substances

  • Antioxidants
  • Drug Combinations
  • gamma-Cyclodextrins
  • Thioctic Acid