Engineering erythrocytes for the modulation of drugs' and contrasting agents' pharmacokinetics and biodistribution

Adv Drug Deliv Rev. 2016 Nov 15;106(Pt A):73-87. doi: 10.1016/j.addr.2016.05.008. Epub 2016 May 14.

Abstract

Pharmacokinetics, biodistribution, and biological activity are key parameters that determine the success or failure of therapeutics. Many developments intended to improve their in vivo performance, aim at modulating concentration, biodistribution, and targeting to tissues, cells or subcellular compartments. Erythrocyte-based drug delivery systems are especially efficient in maintaining active drugs in circulation, in releasing them for several weeks or in targeting drugs to selected cells. Erythrocytes can also be easily processed to entrap the desired pharmaceutical ingredients before re-infusion into the same or matched donors. These carriers are totally biocompatible, have a large capacity and could accommodate traditional chemical entities (glucocorticoids, immunossuppresants, etc.), biologics (proteins) and/or contrasting agents (dyes, nanoparticles). Carrier erythrocytes have been evaluated in thousands of infusions in humans proving treatment safety and efficacy, hence gaining interest in the management of complex pathologies (particularly in chronic treatments and when side-effects become serious issues) and in new diagnostic approaches.

Keywords: Delivery of vascular contrasting agents; Dexamethasone; Drug delivery by red blood cells; Enzyme replacement therapy; Erythrocytes; Immunophilins; Tacrolimus.

Publication types

  • Review

MeSH terms

  • Animals
  • Contrast Media / administration & dosage
  • Drug Delivery Systems / adverse effects
  • Drug Delivery Systems / methods*
  • Erythrocyte Transfusion* / adverse effects
  • Erythrocytes / cytology
  • Erythrocytes / metabolism*
  • Humans
  • Pharmaceutical Preparations / administration & dosage*
  • Pharmaceutical Preparations / blood*
  • Tissue Distribution

Substances

  • Contrast Media
  • Pharmaceutical Preparations