Delivery Efficacy Differences of Intravenous and Intraperitoneal Injection of Exosomes: Perspectives from Tracking Dye Labeled and MiRNA Encapsulated Exosomes

Curr Drug Deliv. 2020;17(3):186-194. doi: 10.2174/1567201817666200122163251.

Abstract

Background: Exosomes are cell-derived nanovesicles that play vital roles in intercellular communication. Recently, exosomes are recognized as promising drug delivery vehicles. Up till now, how the in vivo distribution of exosomes is affected by different administration routes has not been fully understood.

Methods: In the present study, in vivo distribution of exosomes following intravenous and intraperitoneal injection approaches was systemically analyzed by tracking the fluorescence-labeled exosomes and qPCR analysis of C. elegans specific miRNA abundance delivered by exosomes in different organs.

Results: The results showed that exosomes administered through tail vein were mostly taken up by the liver, spleen and lungs while exosomes injected intraperitoneally were more dispersedly distributed. Besides the liver, spleen, and lungs, intraperitoneal injection effectively delivered exosomes into the visceral adipose tissue, making it a promising strategy for obesity therapy. Moreover, the results from fluorescence tracking and qPCR were slightly different, which could be explained by systemic errors.

Conclusion: Together, our study reveals that different administration routes cause a significant differential in vivo distribution of exosomes, suggesting that optimization of the delivery route is prerequisite to obtain rational delivery efficiency in detailed organs.

Keywords: Exosomes; administration route; efficiency; in vivo delivery; intraperitoneal injection; intravenous injection..

Publication types

  • Comparative Study

MeSH terms

  • Adipose Tissue / metabolism
  • Administration, Intravenous
  • Animals
  • Caenorhabditis elegans
  • Exosomes*
  • Fluorescent Dyes / administration & dosage*
  • Fluorescent Dyes / pharmacokinetics
  • HEK293 Cells
  • Humans
  • Injections, Intraperitoneal
  • Liver / metabolism
  • Lung / metabolism
  • Male
  • Mice, Inbred C57BL
  • MicroRNAs / administration & dosage*
  • MicroRNAs / pharmacokinetics
  • Microscopy, Confocal
  • Optical Imaging
  • Spleen / metabolism
  • Tissue Distribution

Substances

  • Fluorescent Dyes
  • MicroRNAs