In vivo biodistribution and efficacy of peptide mediated delivery

Trends Pharmacol Sci. 2010 Nov;31(11):528-35. doi: 10.1016/j.tips.2010.07.006. Epub 2010 Sep 7.

Abstract

To transverse the plasma membrane and gain access to the cellular interior is one of the major obstacles for many novel pharmaceutical molecules. Since the late 1990s, cell-penetrating peptides (CPPs) have been utilized as transport vectors for a broad spectrum of 'biological cargoes', ranging from inert gold particles to multifaceted macromolecules such as proteins and plasmids. Numerous studies have shown that CPPs are efficient carriers for bioactive cargoes in vitro. However, even though CPPs are versatile transport vectors, this does not guarantee they can be developed into useful pharmaceutical molecules. Nevertheless, recent progress in the field has shown CPPs to be effective for in vivo delivery with retained biological activity of a wide variety of bioactive cargoes into virtually any mammalian tissue. This review will focus on recent developments and applications for CPP delivery and distribution in vivo.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / pharmacokinetics
  • Cell Membrane / metabolism
  • Cell Membrane Permeability
  • Cell-Penetrating Peptides / adverse effects
  • Cell-Penetrating Peptides / pharmacokinetics*
  • Cell-Penetrating Peptides / toxicity
  • Drug Carriers
  • Humans
  • Inflammation / drug therapy
  • Neoplasms / drug therapy
  • Oligonucleotides / administration & dosage*
  • Oligonucleotides / pharmacokinetics
  • Protein Transport
  • Proteins / metabolism
  • Proteins / pharmacology
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Tissue Distribution

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antineoplastic Agents
  • Cell-Penetrating Peptides
  • Drug Carriers
  • Oligonucleotides
  • Proteins
  • RNA, Small Interfering