To be targeted: is the magic bullet concept a viable option for synthetic nucleic acid therapeutics?

Hum Gene Ther. 2011 Jul;22(7):799-807. doi: 10.1089/hum.2011.065. Epub 2011 Jun 17.

Abstract

Nucleic acids offer the possibility of tailor-made, individualized treatments for genetic disorders, infectious diseases, and cancer. As an alternative to viral vectors, synthetic delivery systems have a potentially improved safety profile, but often lack sufficient efficiency especially when applied in vivo. Receptor targeting of synthetic vectors can improve the specificity of the vector and increase the efficiency of nucleic acid delivery to the target site. This review covers recent concepts for targeted DNA and RNA delivery to organs like liver and lung, and also to solid cancers. Syntheses and applications of delivery systems targeted with proteins, peptides, and small molecules as ligands coupled to polymeric or lipidic nucleic acid carriers are reviewed. Therapeutic concepts for treatment of genetic and infectious diseases are explained. Systemic treatment regimens of metastasized malignancies in combination with chemotherapy and radiation have already been successfully applied in preclinical studies. In addition, a first clinical study in the human application of a targeted synthetic carrier has been performed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Drug Carriers / administration & dosage
  • Drug Delivery Systems / methods*
  • Genetic Therapy
  • Humans
  • Ligands
  • Lipids / administration & dosage
  • Lipids / genetics
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Nucleic Acids / administration & dosage*
  • Nucleic Acids / genetics*
  • Peptides / administration & dosage
  • Peptides / genetics
  • Polymers / administration & dosage
  • RNA, Small Interfering / administration & dosage

Substances

  • Drug Carriers
  • Ligands
  • Lipids
  • Nucleic Acids
  • Peptides
  • Polymers
  • RNA, Small Interfering