Ultrasound active nanoscaled lipid formulations for thrombus lysis

Eur J Pharm Biopharm. 2011 Apr;77(3):424-9. doi: 10.1016/j.ejpb.2010.12.003. Epub 2010 Dec 17.

Abstract

In the present study, we investigated the sonothrombolytic effect of new nanoscaled lipid formulations in human blood clots, using diagnostic ultrasound. Human blood clots of 1 ml were incubated with 1 μl of the different lipid dispersions DPPC/CH, DPPC/PEG40S, DSPC/PEG40S and the commercially available ultrasound contrast agent SonoVue®. Clots were stored for 3 days at 5 °C to obtain maximal clot retraction and lytic resistance. Each clot weight was determined before and after continuous insonation for 1h of insonation at 1.4 MHz. The pressure in the insonation chamber was 80 mm Hg to mimic middle arterial blood pressure. There were no significant differences in thrombus weight before insonation. All nanoscaled formulations and SonoVue® were able to reduce thrombus weight compared to the weight loss of clots that were not insonated but kept under pressure for one hour (p < 0.001). We found a highly significant weight reduction with DSPC/PEG40S compared to SonoVue® (p = 0.007). Nanoscaled DSPC/PEG40S dispersion could be a promising formulation in ultrasound enhanced thrombolysis even without thrombolytic drugs. Stable cavitation is a crucial parameter in fragmentation of thrombus architecture. Further studies of physicochemical properties of DSPC/PEG40S are necessary to corroborate our hypothesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Equipment Design
  • Fibrinolysis / drug effects*
  • Fibrinolytic Agents / administration & dosage
  • Fibrinolytic Agents / chemistry
  • Fibrinolytic Agents / pharmacology*
  • Humans
  • In Vitro Techniques
  • Intracranial Thrombosis / blood
  • Intracranial Thrombosis / drug therapy
  • Intracranial Thrombosis / therapy
  • Microbubbles / therapeutic use
  • Microscopy, Atomic Force
  • Models, Biological*
  • Nanostructures / chemistry*
  • Phospholipids / administration & dosage
  • Phospholipids / chemistry
  • Phospholipids / pharmacology*
  • Phospholipids / therapeutic use
  • Sulfur Hexafluoride / administration & dosage
  • Sulfur Hexafluoride / therapeutic use
  • Surface Properties
  • Thrombolytic Therapy / methods
  • Ultrasonic Therapy / methods
  • Ultrasonics*

Substances

  • Fibrinolytic Agents
  • Phospholipids
  • contrast agent BR1
  • Sulfur Hexafluoride