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Ultrafast ultrasound localization microscopy for deep super-resolution vascular imaging

机译:超快速超声定位显微镜用于深度超高分辨率血管成像

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摘要

Non-invasive imaging deep into organs at microscopic scales remains an open quest in biomedical imaging. Although optical microscopy is still limited to surface imaging owing to optical wave diffusion and fast decorrelation in tissue, revolutionary approaches such as fluorescence photo-activated localization microscopy led to a striking increase in resolution by more than an order of magnitude in the last decade(1). In contrast with optics, ultrasonic waves propagate deep into organs without losing their coherence and are much less affected by in vivo decorrelation processes. However, their resolution is impeded by the fundamental limits of diffraction, which impose a long-standing trade-off between resolution and penetration. This limits clinical and preclinical ultrasound imaging to a sub-millimetre scale. Here we demonstrate in vivo that ultrasound imaging at ultrafast frame rates (more than 500 frames per second) provides an analogue to optical localization microscopy by capturing the transient signal decorrelation of contrast agents-inert gas microbubbles. Ultrafast ultrasound localization microscopy allowed both non-invasive sub-wavelength structural imaging and haemodynamic quantification of rodent cerebral microvessels (less than ten micrometres in diameter) more than ten millimetres below the tissue surface, leading to transcranial whole-brain imaging within short acquisition times (tens of seconds). After intravenous injection, single echoes from individual microbubbles were detected through ultrafast imaging. Their localization, not limited by diffraction, was accumulated over 75,000 images, yielding 1,000,000 events per coronal plane and statistically independent pixels of ten micrometres in size. Precise temporal tracking of microbubble positions allowed us to extract accurately in-plane velocities of the blood flow with a large dynamic range (from one millimetre per second to several centimetres per second). These results pave the way for deep non-invasive microscopy in animals and humans using ultrasound. We anticipate that ultrafast ultrasound localization microscopy may become an invaluable tool for the fundamental understanding and diagnostics of various disease processes that modify the microvascular blood flow, such as cancer, stroke and arteriosclerosis.
机译:在微观尺度上深入器官深处的非侵入性成像仍然是生物医学成像中的一个开放任务。尽管由于光学波的扩散和组织中快速的去相关性,光学显微镜仍然仅限于表面成像,但在过去十年中,革命性的方法(例如荧光光激活定位显微镜)使分辨率显着提高了一个数量级以上(1) )。与光学器件相比,超声波可以深入器官内传播而不会失去其相干性,并且受体内去相关过程的影响要小得多。但是,衍射的基本局限性阻碍了它们的分离度,这在分离度和穿透力之间存在着长期的权衡。这将临床和临床前超声成像限制在亚毫米范围内。在这里,我们在体内证明了超声成像以超快的帧速率(每秒超过500帧)通过捕获造影剂惰性气体微泡的瞬态信号去相关性,提供了光学定位显微镜的类似物。超快超声定位显微镜可以对组织表面以下十毫米以上的啮齿动物脑微血管(直径小于十微米)进行无创性亚波长结构成像和血流动力学定量分析,从而在较短的采集时间内实现经颅全脑成像(数十秒)。静脉内注射后,通过超快速成像检测到单个微气泡的单个回波。它们的定位不受衍射限制,累积了75,000张图像,每个冠状平面产生了1,000,000个事件,并且统计独立的像素大小为10微米。对微气泡位置的精确时间跟踪使我们能够以较大的动态范围(从每秒1毫米到每秒几厘米)准确地提取血流的平面速度。这些结果为使用超声波在动物和人类中进行深层非侵入式显微镜扫清了道路。我们预计,超快速超声定位显微镜可能会成为宝贵的工具,可用于对各种改变微血管血流(例如癌症,中风和动脉硬化)的疾病过程进行基本了解和诊断。

著录项

  • 来源
    《Nature》 |2015年第7579期|499-502|共4页
  • 作者单位

    INSERM, Inst Langevin, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Inst Langevin, F-75005 Paris, France|CNRS, UMR 7587, F-75005 Paris, France;

    INSERM, Inst Langevin, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Inst Langevin, F-75005 Paris, France|CNRS, UMR 7587, F-75005 Paris, France;

    CNRS, UMR 8249, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Brain Plast Unit, F-75005 Paris, France;

    INSERM, Inst Langevin, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Inst Langevin, F-75005 Paris, France|CNRS, UMR 7587, F-75005 Paris, France;

    CNRS, UMR 8249, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Brain Plast Unit, F-75005 Paris, France;

    INSERM, Inst Langevin, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Inst Langevin, F-75005 Paris, France|CNRS, UMR 7587, F-75005 Paris, France;

    INSERM, Inst Langevin, F-75005 Paris, France|PSL Res Univ, ESPCI ParisTech, Inst Langevin, F-75005 Paris, France|CNRS, UMR 7587, F-75005 Paris, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 02:52:44

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