The effects of particle size, shape, density and flow characteristics on particle margination to vascular walls in cardiovascular diseases

Expert Opin Drug Deliv. 2018 Jan;15(1):33-45. doi: 10.1080/17425247.2017.1316262. Epub 2017 Apr 13.

Abstract

Introduction: Vascular-targeted drug delivery is a promising approach for the treatment of atherosclerosis, due to the vast involvement of endothelium in the initiation and growth of plaque, a characteristic of atherosclerosis. One of the major challenges in carrier design for targeting cardiovascular diseases (CVD) is that carriers must be able to navigate the circulation system and efficiently marginate to the endothelium in order to interact with the target receptors.

Areas covered: This review draws on studies that have focused on the role of particle size, shape, and density (along with flow hemodynamics and hemorheology) on the localization of the particles to activated endothelial cell surfaces and vascular walls under different flow conditions, especially those relevant to atherosclerosis.

Expert opinion: Generally, the size, shape, and density of a particle affect its adhesion to vascular walls synergistically, and these three factors should be considered simultaneously when designing an optimal carrier for targeting CVD. Available preliminary data should encourage more studies to be conducted to investigate the use of nano-constructs, characterized by a sub-micrometer size, a non-spherical shape, and a high material density to maximize vascular wall margination and minimize capillary entrapment, as carriers for targeting CVD.

Keywords: Particle physical properties; atherosclerosis; cardiovascular diseases; flow characteristics; margination; particle density; particle shape; particle size.

Publication types

  • Review

MeSH terms

  • Coronary Artery Disease / drug therapy*
  • Coronary Artery Disease / physiopathology
  • Coronary Vessels / physiology*
  • Densitometry
  • Drug Carriers / therapeutic use
  • Drug Delivery Systems*
  • Endothelium, Vascular / metabolism*
  • Hemodynamics / physiology
  • Humans
  • Particle Size*

Substances

  • Drug Carriers