Ultrasound in Medicine and Biology
Volume 36, Issue 2 , Pages 181-191, February 2010

Critical Appraisal of Targeted Ultrasound Contrast Agents for Molecular Imaging in Large Arteries

  • Liselotte M. Kornmann

      Affiliations

    • Department of Biophysics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands
  • ,
  • Koen D. Reesink

      Affiliations

    • Department of Biophysics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands
  • ,
  • Robert S. Reneman

      Affiliations

    • Department of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands
  • ,
  • Arnold P.G. Hoeks

      Affiliations

    • Department of Biophysics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands
    • Corresponding Author InformationAddress correspondence to: Prof. Dr. Arnold P. G. Hoeks, Department of Biomedical Engineering/Biophysics, Maastricht University, PO Box 616, 6200 MD, Maastricht, The Netherlands.

Received 23 June 2009; received in revised form 26 August 2009; accepted 21 September 2009. published online 17 December 2009.

Abstract 

Molecular imaging may provide new insights into the early detection and development of atherosclerosis before first symptoms occur. One of the techniques in use employs noninvasive ultrasound. In the past decade, experimental and clinical validation studies showed that for the microcirculation targeted ultrasound contrast agents, such as echogenic liposomes, microbubbles and perfluorocarbon emulsions, do improve visualization of specific structures. For large arteries, however, successful application is less obvious. In this review, we will address the challenges for molecular imaging of large arteries. We will discuss the problems encountered in the use of targeted ultrasound contrast agents presently available, mainly based on data obtained in flow chambers and animal studies because clinical studies are lacking. We conclude that molecular imaging of activated endothelium in large- and middle-sized arteries by site-specific accumulation of contrast material is still difficult to achieve due to wall shear stress conditions in these vessels. (A.Hoeks@bf.unimaas.nl)

Key Words: Animal models, Contrast agents, Endothelial inflammation, Flow chamber, Molecular imaging, Shear stress, Targeting, Ultrasound

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PII: S0301-5629(09)01537-3

doi:10.1016/j.ultrasmedbio.2009.09.009

Ultrasound in Medicine and Biology
Volume 36, Issue 2 , Pages 181-191, February 2010