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Molecular acoustic angiography: Demonstration of in vivo feasibility for high resolution superharmonic ultrasound molecular imaging

机译:分子声血管造影:演示高分辨率超谐波超声分子成像的体内可行性

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Ultrasound molecular imaging utilizes targeted microbubbles to image molecular targets such as integrins, selectins, and other extracellular binding domains. Targeted microbubbles have typically been imaged using contrast-specific multi-pulse imaging sequences. Here we present an alternative strategy for ultrasound molecular imaging based on superharmonic signals produced by microbubbles. Bound bubbles were insonified near resonance using a low frequency (4 MHz) and superharmonic echoes were received at high frequencies (30 MHz). The feasibility of superharmonic molecular imaging was shown using microbubbles targeted to the αβ integrin in a rat fibrosarcoma model (n=5) and combined with superharmonic images of free microbubbles to produce high contrast, high resolution 3D volumes of both microvascular anatomy and molecular targeting. Anatomical localization of molecular markers may prove easier using ultrasound-based acoustic angiography images as a reference rather than conventional B-mode images.
机译:超声分子成像利用靶向微泡对分子靶标(例如整联蛋白,选择蛋白和其他细胞外结合域)进行成像。通常使用对比度特定的多脉冲成像序列对目标微气泡进行成像。在这里,我们提出了一种基于微气泡产生的超谐波信号的超声分子成像的替代策略。使用低频(4 MHz)在接近共振的状态下对绑定的气泡进行声化,并在高频(30 MHz)处接收超谐波回声。在大鼠纤维肉瘤模型(n = 5)中使用针对αβ整联蛋白的微气泡并结合游离微气泡的超谐波图像来产生高对比度,高分辨率的3D体积的微血管解剖结构和分子靶向,证明了超谐波分子成像的可行性。使用基于超声的声学血管造影图像作为参考,而不是常规的B模式图像,可以证明分子标记的解剖定位更容易。

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