TY - JOUR
T1 - CRITICAL APPRAISAL OF TARGETED ULTRASOUND CONTRAST AGENTS FOR MOLECULAR IMAGING IN LARGE ARTERIES
AU - Kornmann, Liselotte M.
AU - Reesink, Koen D.
AU - Reneman, Robert S.
AU - Hoeks, Arnold P. G.
PY - 2010/2
Y1 - 2010/2
N2 - 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. ([email protected])
AB - 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. ([email protected])
KW - Animal models
KW - Contrast agents
KW - Endothelial inflammation
KW - Flow chamber
KW - Molecular imaging
KW - Shear stress
KW - Targeting
KW - Ultrasound
U2 - 10.1016/j.ultrasmedbio.2009.09.009
DO - 10.1016/j.ultrasmedbio.2009.09.009
M3 - Article
C2 - 20018434
SN - 0301-5629
VL - 36
SP - 181
EP - 191
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 2
ER -