Intravenously administered nanoparticles increase survival following blast trauma

Proc Natl Acad Sci U S A. 2014 Jul 15;111(28):10293-8. doi: 10.1073/pnas.1406979111. Epub 2014 Jun 30.

Abstract

Explosions account for 79% of combat-related injuries, leading to multiorgan hemorrhage and uncontrolled bleeding. Uncontrolled bleeding is the leading cause of death in battlefield traumas as well as in civilian life. We need to stop the bleeding quickly to save lives, but, shockingly, there are no treatments to stop internal bleeding. A therapy that halts bleeding in a site-specific manner and is safe, stable at room temperature, and easily administered is critical for the advancement of trauma care. To address this need, we have developed hemostatic nanoparticles that are administered intravenously. When tested in a model of blast trauma with multiorgan hemorrhaging, i.v. administration of the hemostatic nanoparticles led to a significant improvement in survival over the short term (1 h postblast). No complications from this treatment were apparent out to 3 wk. This work demonstrates that these particles have the potential to save lives and fundamentally change trauma care.

Keywords: clot; lung; medic; polytrauma; synthetic platelets.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Administration, Intravenous
  • Animals
  • Blast Injuries / drug therapy*
  • Blast Injuries / pathology
  • Disease Models, Animal
  • Hemorrhage / drug therapy*
  • Hemorrhage / pathology
  • Hemostatics / pharmacology*
  • Male
  • Mice
  • Nanoparticles*
  • Time Factors
  • Warfare

Substances

  • Hemostatics