Improved cationic lipid formulations for in vivo gene therapy

Ann N Y Acad Sci. 1995 Nov 27;772:126-39. doi: 10.1111/j.1749-6632.1995.tb44738.x.

Abstract

The problem of assessing in vivo activity of gene delivery systems is complex. The reporter gene must be carefully chosen depending on the application. Plasmids with strong promoters, enhancers and other elements that optimize transcription and translation should be employed, such as the CMVint and pCIS-CAT constructs. Formulation aspects of cationic lipid-DNA complexes are being studied in several laboratories, and the physical properties and molecular organization of the complexes are being elucidated. Likewise, studies on the mechanism of DNA delivery with cationic lipids are accumulating which support the basic concept that the complexes fuse with biological membranes leading to the entry of intact DNA into the cytoplasm. Naked plasmid DNA administered by various routes is expressed at significant levels in vivo. This observation is not restricted to skeletal and heart muscle, but has been observed in lung, dermis, and in undefined tissues following intravenous administration. Most of the widely available cationic lipids, including Lipofectin, Lipofectamine and DC-cholesterol have a very poor ability to enhance DNA expression above the baseline naked DNA level, at least in lung. In this report we have revealed a novel cationic lipid, DLRIE, which can significantly enhance CAT expression in mouse lung by 25-fold above the naked DNA level. Other compounds are currently being evaluated which can enhance the naked DNA expression even higher. Plasmid vector improvements have led to further increase in in vivo lung expression, so that the net improvement is > 5,000-fold. Results of this nature are advancing the pharmaceutical gene therapy opportunities for synthetic cationic lipid based gene delivery systems.

Publication types

  • Review

MeSH terms

  • Animals
  • Cation Exchange Resins / administration & dosage
  • Cation Exchange Resins / chemistry
  • Cations
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Chloramphenicol O-Acetyltransferase / genetics
  • DNA, Recombinant / administration & dosage*
  • Dodecanol / administration & dosage
  • Dodecanol / analogs & derivatives
  • Dodecanol / chemistry
  • Drug Administration Routes
  • Drug Carriers
  • Genes, Reporter
  • Genetic Therapy*
  • Genetic Vectors*
  • Lipids* / administration & dosage
  • Lipids* / chemistry
  • Liposomes / chemistry*
  • Luciferases / biosynthesis
  • Luciferases / genetics
  • Macromolecular Substances
  • Mice
  • Mice, Inbred BALB C
  • Myristic Acids / administration & dosage
  • Myristic Acids / chemistry
  • Phosphatidylethanolamines / administration & dosage
  • Phosphatidylethanolamines / chemistry
  • Quaternary Ammonium Compounds / administration & dosage
  • Quaternary Ammonium Compounds / chemistry
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / genetics
  • Transfection / methods*
  • beta-Galactosidase / biosynthesis
  • beta-Galactosidase / genetics

Substances

  • Cation Exchange Resins
  • Cations
  • DNA, Recombinant
  • Drug Carriers
  • Lipids
  • Lipofectamine
  • Liposomes
  • Macromolecular Substances
  • Myristic Acids
  • N-(2-hydroxyethyl)-N,N-dimethyl-2,3-bis(dodecyloxy)-1-propanaminium bromide
  • Phosphatidylethanolamines
  • Quaternary Ammonium Compounds
  • Recombinant Fusion Proteins
  • N-(1-(2,3-dioleyloxy)propyl)-N,N,N-trimethylammonium
  • (3-dimyristyloxypropyl)(dimethyl)(hydroxyethyl)ammonium
  • Dodecanol
  • 1,2-dielaidoylphosphatidylethanolamine
  • Luciferases
  • Chloramphenicol O-Acetyltransferase
  • beta-Galactosidase