Functional drug targeting to erythrocytes in vivo using antibody bearing liposomes as drug vehicles

Biochem Biophys Res Commun. 1987 Oct 14;148(1):357-61. doi: 10.1016/0006-291x(87)91118-1.

Abstract

Covalent attachment of anti-erythrocyte F(ab')2 to the liposome surface has recently been shown to considerably enhance the liposome binding to erythrocytes in vivo. These antibody bearing liposomes have now been found quite effective as vehicles for delivering the antimalarial drug, chloroquine, to erythrocytes in Plasmodium berghei-infected mice. This demonstrates the usefulness of antibody targeted liposomes as carriers for site-specific drug delivery.

MeSH terms

  • Animals
  • Chloroquine / administration & dosage
  • Chloroquine / blood*
  • Chloroquine / therapeutic use
  • Cholesterol* / blood
  • Erythrocytes / metabolism*
  • Gangliosides* / blood
  • Immunoglobulin Fab Fragments*
  • Lipid Bilayers / administration & dosage
  • Liposomes / administration & dosage*
  • Malaria / blood*
  • Malaria / drug therapy
  • Male
  • Mice
  • Phosphatidylcholines* / blood

Substances

  • Gangliosides
  • Immunoglobulin Fab Fragments
  • Lipid Bilayers
  • Liposomes
  • Phosphatidylcholines
  • Chloroquine
  • Cholesterol