Lipid microspheres for drug delivery from the pharmaceutical viewpoint

Crit Rev Ther Drug Carrier Syst. 1994;11(4):215-29.

Abstract

Lipid microsphere (LM) preparations of corticosteroid, nonsteroid, anti-inflammatory drugs and prostaglandins all showed more potent activity than free drugs. The LM, with a diameter of 0.2 microns, were drug carriers prepared from soybean oil and lecithin, with the drug being incorporated within the LM. This study suggests that the LM is a very promising carrier in a drug delivery system. Future trends in this field are outlined, followed by a discussion of physicochemical properties in the evaluation of novel emulsion delivery systems.

Publication types

  • Review

MeSH terms

  • Adsorption
  • Alprostadil / administration & dosage*
  • Alprostadil / chemistry
  • Alprostadil / pharmacology
  • Biological Availability
  • Dexamethasone / administration & dosage
  • Dexamethasone / pharmacology
  • Drug Delivery Systems*
  • Emulsions
  • Flurbiprofen / administration & dosage
  • Flurbiprofen / pharmacology
  • Humans
  • Lipids / chemistry*
  • Microspheres
  • Particle Size
  • Phosphatidylcholines / chemistry
  • Phosphatidylcholines / metabolism
  • Soybean Oil / chemistry
  • Soybean Oil / metabolism

Substances

  • Emulsions
  • Lipids
  • Phosphatidylcholines
  • Flurbiprofen
  • Dexamethasone
  • Soybean Oil
  • Alprostadil