Desailly Yann, Pierre Juliette, Couture Olivier, Tanter Mickael
CNRS, INSERM, ESPCI ParisTech, PSL Research University, Institut Langevin, 1 rue Jussieu, F-75005, Paris, France.
Phys Med Biol. 2015 Nov 21;60(22):8723-40. doi: 10.1088/0031-9155/60/22/8723. Epub 2015 Oct 28.
As in other imaging methods based on waves, the resolution of ultrasound imaging is limited by the wavelength. However, the diffraction-limit can be overcome by super-localizing single events from isolated sources. In recent years, we developed plane-wave ultrasound allowing frame rates up to 20,000 fps. Ultrafast processes such as rapid movement or disruption of ultrasound contrast agents (UCA) can thus be monitored, providing us with distinct punctual sources that could be localized beyond the diffraction limit. We previously showed experimentally that resolutions beyond λ/10 can be reached in ultrafast ultrasound localization microscopy (uULM) using a 128 transducer matrix in reception. Higher resolutions are theoretically achievable and the aim of this study is to predict the maximum resolution in uULM with respect to acquisition parameters (frequency, transducer geometry, sampling electronics). The accuracy of uULM is the error on the localization of a bubble, considered a point-source in a homogeneous medium. The proposed model consists in two steps: determining the timing accuracy of the microbubble echo in radiofrequency data, then transferring this time accuracy into spatial accuracy. The simplified model predicts a maximum resolution of 40 μm for a 1.75 MHz transducer matrix composed of two rows of 64 elements. Experimental confirmation of the model was performed by flowing microbubbles within a 60 μm microfluidic channel and localizing their blinking under ultrafast imaging (500 Hz frame rate). The experimental resolution, determined as the standard deviation in the positioning of the microbubbles, was predicted within 6 μm (13%) of the theoretical values and followed the analytical relationship with respect to the number of elements and depth. Understanding the underlying physical principles determining the resolution of superlocalization will allow the optimization of the imaging setup for each organ. Ultimately, accuracies better than the size of capillaries are achievable at several centimeter depths.
与其他基于波的成像方法一样,超声成像的分辨率受波长限制。然而,通过对孤立源的单个事件进行超定位可以克服衍射极限。近年来,我们开发了平面波超声,其帧率可达20000帧/秒。因此,可以监测诸如超声造影剂(UCA)的快速移动或破裂等超快过程,为我们提供可在衍射极限之外进行定位的独特点状源。我们之前通过实验表明,在接收时使用128换能器矩阵的超快超声定位显微镜(uULM)中可以实现超过λ/10的分辨率。理论上可以实现更高的分辨率,本研究的目的是根据采集参数(频率、换能器几何形状、采样电子设备)预测uULM中的最大分辨率。uULM的精度是气泡定位的误差,在均匀介质中气泡被视为点源。所提出的模型包括两个步骤:确定射频数据中微泡回波的定时精度,然后将此时间精度转换为空间精度。简化模型预测,对于由两排64个元件组成的1.75 MHz换能器矩阵,最大分辨率为40μm。通过使微泡在60μm微流体通道内流动并在超快成像(500帧/秒帧率)下定位其闪烁来对模型进行实验验证。实验分辨率确定为微泡定位的标准偏差,预测值与理论值相差6μm(13%)以内,并且遵循与元件数量和深度的解析关系。了解决定超定位分辨率的潜在物理原理将有助于针对每个器官优化成像设置。最终,在几厘米深度处可以实现优于毛细血管尺寸的精度。