A survey on "Trojan Horse" peptides: opportunities, issues and controlled entry to "Troy"

J Control Release. 2014 Nov 28:194:53-70. doi: 10.1016/j.jconrel.2014.08.014. Epub 2014 Aug 23.

Abstract

Cell-penetrating peptides (CPPs), often vividly termed as the "Trojan Horse" peptides, have attracted considerable interest for the intracellular delivery of a wide range of cargoes, such as small molecules, peptides, proteins, nucleic acids, contrast agents, nanocarriers and so on. Some preclinical and clinical developments of CPP conjugates demonstrate their promise as therapeutic agents for drug discovery. There is increasing evidence to suggest that CPPs have the potential to cross several bio-barriers (e.g., blood-brain barriers, intestinal mucosa, nasal mucosa and skin barriers). Despite revolutionary process in many aspects, there are a lot of basic issues unclear for these entities, such as internalization mechanisms, translocation efficiency, translocation kinetics, metabolic degradation, toxicity, side effect, distribution and non-specificity. Among them, non-specificity remains a major drawback for the in vivo application of CPPs in the targeted delivery of cargoes. So far, diverse organelle-specific CPPs or controlled delivery strategies have emerged and improved their specificity. In this review, we will look at the opportunities of CPPs in clinical development, bio-barriers penetration and nanocarriers delivery. Then, a series of basic problems of CPPs will be discussed. Finally, this paper will highlight the use of various controlled strategies in the organelle-specific delivery and targeted delivery of CPPs. The purpose of this review will be to emphasize most influential advance in this field and present a fundamental understanding for challenges and utilizations of CPPs. This will accelerate their translation as efficient vectors from the in vitro setting into the clinic arena, and retrieve the entry art to "Troy".

Keywords: Cell-penetrating peptides; Clinical development; Controlled delivery strategies; Non-specificity; Organelle-specific delivery.

Publication types

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

MeSH terms

  • Animals
  • Cell-Penetrating Peptides / administration & dosage*
  • Cell-Penetrating Peptides / pharmacokinetics
  • Cell-Penetrating Peptides / therapeutic use*
  • Cells / metabolism
  • Drug Carriers
  • Drug Delivery Systems / methods*
  • Humans
  • Nanotechnology

Substances

  • Cell-Penetrating Peptides
  • Drug Carriers