Nonviral vectors for in vivo gene delivery: Physicochemical and pharmacokinetic considerations

Ram I. Mahato, Yoshinobu Takakura, Mitsuru Hashida

Research output: Contribution to journalReview article

142 Citations (Scopus)

Abstract

The use of nonviral vectors is an attractive in vivo gene delivery strategy that is simpler than, and lacks some risks inherent in, viral systems. Liposomes and receptor-mediated polycation systems are promising carriers for delivery and expression of plasmid DNA encoding genes into the target cells. Many barriers need to be overcome for successful in vivo DNA delivery using these carrier systems. Such factors as extent of DNA condensation, particle size of the DNA complex, route of administration, stability against nucleases, target sites, in vivo disposition, binding to cell surface receptor and internalization, and intracellular trafficking affect in vivo gene delivery and expression. This review will provide a critical discussion of the merits and limitations of liposomal and polycationic carrier systems for gene transfer from the viewpoints of their physicochemical and pharmacokinetic properties.

Original languageEnglish (US)
Pages (from-to)133-172
Number of pages40
JournalCritical Reviews in Therapeutic Drug Carrier Systems
Volume14
Issue number2
StatePublished - Apr 29 1997

Fingerprint

Pharmacokinetics
DNA
Genes
Cell Surface Receptors
Particle Size
Liposomes
Plasmids
Gene Expression

Keywords

  • gene delivery
  • liposomes
  • pharmacokinetics
  • plasmid DNA
  • polycation/ligand conjugate

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

Cite this

Nonviral vectors for in vivo gene delivery : Physicochemical and pharmacokinetic considerations. / Mahato, Ram I.; Takakura, Yoshinobu; Hashida, Mitsuru.

In: Critical Reviews in Therapeutic Drug Carrier Systems, Vol. 14, No. 2, 29.04.1997, p. 133-172.

Research output: Contribution to journalReview article

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