Recent Advances in Endocannabinoid System Targeting for Improved Specificity: Strategic Approaches to Targeted Drug Delivery

Int J Mol Sci. 2022 Oct 30;23(21):13223. doi: 10.3390/ijms232113223.

Abstract

Opportunities for developing innovative and intelligent drug delivery technologies by targeting the endocannabinoid system are becoming more apparent. This review provides an overview of strategies to develop targeted drug delivery using the endocannabinoid system (ECS). Recent advances in endocannabinoid system targeting showcase enhanced pharmaceutical therapy specificity while minimizing undesirable side effects and overcoming formulation challenges associated with cannabinoids. This review identifies advances in targeted drug delivery technologies that may permit access to the full pharmacotherapeutic potential of the ECS. The design of optimized nanocarriers that target specific tissues can be improved by understanding the nature of the signaling pathways, distribution in the mammalian body, receptor structure, and enzymatic degradation of the ECS. A closer look at ligand-receptor complexes, endocannabinoid tone, tissue distribution, and G-protein activity leads to a better understanding of the potential of the ECS toolkit for therapeutics. The signal transduction pathways examine the modulation of downstream effector proteins, desensitization, signaling cascades, and biased signaling. An in-depth and overall view of the targeted system is achieved through homology modeling where mutagenesis and ligand binding examine the binding site and allow sequence analysis and the formation of libraries for molecular docking and molecular dynamic simulations. Internalization routes exploring receptor-mediated endocytosis and lipid rafts are also considered for explicit signaling. Furthermore, the review highlights nanotechnology and surface modification aspects as a possible future approach for specific targeting.

Keywords: allosteric modulation; biased signaling; endocannabinoid system; endocannabinoid tone; g-protein coupled receptors; receptor-mediated drug delivery; surface-modified nanoparticles.

Publication types

  • Review

MeSH terms

  • Animals
  • Cannabinoids* / pharmacology
  • Endocannabinoids* / metabolism
  • Ligands
  • Mammals / metabolism
  • Molecular Docking Simulation
  • Signal Transduction

Substances

  • Endocannabinoids
  • Ligands
  • Cannabinoids

Grants and funding

This research was funded by the National Research Foundation, grant number SFH180531338233 and was funded by Rhodes Research Committee (Professor S.M. Khamanga and Professor R.B. Walker).