Ultrasound-targeted transfection of tissue-type plasminogen activator gene carried by albumin nanoparticles to dog myocardium to prevent thrombosis after heart mechanical valve replacement

Int J Nanomedicine. 2012:7:2911-9. doi: 10.2147/IJN.S32363. Epub 2012 Jun 19.

Abstract

Background: There are more than 300,000 prosthetic heart valve replacements each year worldwide. These patients are faced with a higher risk of thromboembolic events after heart valve surgery and long-term or even life-long anticoagulative and antiplatelet therapies are necessary. Some severe complications such as hemorrhaging or rebound thrombosis can occur when the therapy ceases. Tissue-type plasminogen activator (t-PA) is a thrombolytic agent. One of the best strategies is gene therapy, which offers a local high expression of t-PA over a prolonged time period to avoid both systemic hemorrhaging and local rebound thrombosis. There are some issues with t-PA that need to be addressed: currently, there is no up-to-date report on how the t-PA gene targets the heart in vivo and the gene vector for t-PA needs to be determined.

Aims: To fabricate an albumin nano-t-PA gene ultrasound-targeted agent and investigate its targeting effect on prevention of thrombosis after heart mechanic valve replacement under therapeutic ultrasound.

Methods: A dog model of mechanical tricuspid valve replacement was constructed. A highly expressive t-PA gene plasmid was constructed and packaged by nanoparticles prepared with bovine serum albumin. This nanopackaged t-PA gene plasmid was further cross-linked to ultrasonic microbubbles prepared with sucrose and bovine serum albumin to form the ultrasonic-targeted agent for t-PA gene transfection. The agent was given intravenously followed by a therapeutic ultrasound treatment (1 MHz, 1.5 w/cm(2), 10 minutes) of the heart soon after valve replacement had been performed. The expression of t-PA in myocardium was detected with multiclonal antibodies to t-PA by the indirect immunohistochemical method. Venous blood t-PA and D-dimer contents were tested before and 1, 2, 4, and 8 weeks after the operation.

Results: The high expression of t-PA could be seen in myocardium with increases in blood t-PA and D-dimer contents and thrombosis was prevented 8 weeks after operation.

Conclusion: We successfully fabricated an albumin nano-t-PA gene ultrasound-targeted agent that could prevent dog thrombosis after mechanical heart valve replacement. Our study provides an experimental basis for prevention of human thrombosis-related diseases.

Keywords: albumin nanoparticles; ultrasonic microbubbles; valve replacement.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cattle
  • Coronary Thrombosis / prevention & control*
  • Cricetinae
  • Cricetulus
  • Dogs
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Heart Valve Prosthesis Implantation / methods*
  • Humans
  • Immunohistochemistry
  • Male
  • Microbubbles
  • Myocardium / chemistry
  • Myocardium / metabolism*
  • Nanoparticles / administration & dosage*
  • Nanoparticles / chemistry
  • Plasmids / administration & dosage
  • Plasmids / genetics
  • Plasmids / metabolism
  • Postoperative Complications / prevention & control
  • Prothrombin Time
  • Serum Albumin, Bovine / administration & dosage
  • Serum Albumin, Bovine / chemistry
  • Tissue Plasminogen Activator / blood
  • Tissue Plasminogen Activator / genetics*
  • Tissue Plasminogen Activator / metabolism
  • Transfection / methods*
  • Ultrasonography / methods*

Substances

  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D
  • Serum Albumin, Bovine
  • Tissue Plasminogen Activator