Molecular Ultrasound Imaging

被引:48
|
作者
Koese, Gurbet [1 ]
Darguzyte, Milita [1 ]
Kiessling, Fabian [1 ,2 ]
机构
[1] Univ Hosp Aachen, Inst Expt Mol Imaging, Forckenbeckstr 55, D-52074 Aachen, Germany
[2] Fraunhofer MEVIS, Inst Med Image Comp, Forckenbeckstr 55, D-52074 Aachen, Germany
关键词
molecular ultrasound; nanobubbles; active targeting; targeted microbubbles; angiogenesis; inflammation; thrombosis; clinical translation; molecular imaging; ENDOTHELIAL GROWTH-FACTOR; ACOUSTIC RADIATION FORCE; TARGETED CONTRAST AGENT; INFLAMMATORY-BOWEL-DISEASE; ACUTE CORONARY SYNDROMES; P-SELECTIN EXPRESSION; TUMOR ANGIOGENESIS; IN-VIVO; BREAST-CANCER; ANTIANGIOGENIC THERAPY;
D O I
10.3390/nano10101935
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the last decade, molecular ultrasound imaging has been rapidly progressing. It has proven promising to diagnose angiogenesis, inflammation, and thrombosis, and many intravascular targets, such as VEGFR2, integrins, and selectins, have been successfully visualized in vivo. Furthermore, pre-clinical studies demonstrated that molecular ultrasound increased sensitivity and specificity in disease detection, classification, and therapy response monitoring compared to current clinically applied ultrasound technologies. Several techniques were developed to detect target-bound microbubbles comprising sensitive particle acoustic quantification (SPAQ), destruction-replenishment analysis, and dwelling time assessment. Moreover, some groups tried to assess microbubble binding by a change in their echogenicity after target binding. These techniques can be complemented by radiation force ultrasound improving target binding by pushing microbubbles to vessel walls. Two targeted microbubble formulations are already in clinical trials for tumor detection and liver lesion characterization, and further clinical scale targeted microbubbles are prepared for clinical translation. The recent enormous progress in the field of molecular ultrasound imaging is summarized in this review article by introducing the most relevant detection technologies, concepts for targeted nano- and micro-bubbles, as well as their applications to characterize various diseases. Finally, progress in clinical translation is highlighted, and roadblocks are discussed that currently slow the clinical translation.
引用
收藏
页码:1 / 28
页数:28
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