Physicochemical and pharmacokinetic characterization of a spray-dried malotilate emulsion

Int J Pharm. 2011 Jul 29;414(1-2):186-92. doi: 10.1016/j.ijpharm.2011.05.032. Epub 2011 May 17.

Abstract

Malotilate (MT) is a hepatoprotective drug administered orally. However, MT was found to be a poorly water-soluble drug with low oral bioavailability. In the present investigation, a novel spray-dried emulsion (SDE) loaded with MT was prepared, and its physicochemical properties were characterized by rheological evaluation, particle size measurement, in vitro release, and surface morphology. The pharmacokinetic study of SDE, in comparison to MT suspension with the pure MT powder homogeneously dispersed in 0.5% CMC-Na solution, was also performed in rats after a single oral dose. It was found that SDE exhibited a 2.9-fold higher peak plasma concentration (C(max)) and 2.3-fold higher area under the curve (AUC) than MT suspension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Drug Carriers
  • Drug Compounding
  • Drug Delivery Systems*
  • Emulsions
  • Excipients
  • Liver Diseases / metabolism
  • Male
  • Malonates / blood*
  • Malonates / chemistry
  • Malonates / pharmacokinetics*
  • Malonates / pharmacology
  • Particle Size
  • Powders
  • Protective Agents / analysis*
  • Protective Agents / chemistry
  • Protective Agents / pharmacokinetics*
  • Protective Agents / pharmacology
  • Rats
  • Solubility

Substances

  • Drug Carriers
  • Emulsions
  • Excipients
  • Malonates
  • Powders
  • Protective Agents
  • diisopropyl 1,3-dithiol-2-ylidenemalonate