利用光学产生和检测超声的组织显微术

S. Ashkenazi, R. Witte, K. Kim, Y. Hou, M. O’Donnell
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引用次数: 0

摘要

超声光学检测提供了一种独特而吸引人的方式来形成探测器阵列(1D或2D)。基于标准隆的光学技术特别令人感兴趣,因为它们在共振结构内的多次光学反射产生了相对较高的灵敏度。基于标准子技术形成的探测器阵列具有元件密度高、元件活性面积小的特点,能够在高超声频率(通常为10-50 MHz)下实现高分辨率成像。近年来,利用光声效应产生的激光超声已被证明是一种强大的医学和生物成像方式。短激光脉冲照射组织,产生快速热膨胀和声发射。通过检测器阵列检测所产生的声场,可以使用超声成像方法对组织光学吸收进行成像。光声成像最吸引人的特点之一是,它提供了在分子水平上使用多波长照明的组织组成。元件很容易通过光学聚焦来实现。这些技术的典型特点是带宽平坦。激光产生超声波的研究和证明了几十年,但获得了新的兴趣,因为90年代后期在医学成像的应用(7-10)。该方法是基于用短激光脉冲照射组织。光脉冲被组织吸收,使其迅速升温。温度升高后,热膨胀产生声发射。对产生的声场的检测允许重建热沉积的初始分布,从而重建组织中光吸收的分布。这种方法最吸引人的特点是图像对比度是基于组织的光学特性。这使得超声成像在分子水平上探测组织组成成为可能,并促进了与光学造影剂的相互作用,用于功能成像(11,12)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue microscopy using optical generation and detection of ultrasound
Optical detection of ultrasound provides a unique and appealing way of forming detector arrays (1D or 2D). Etalon based optical techniques are of particular interest, due to their relatively high sensitivity resulting from multiple optical reflections within the resonance structure. Detector arrays formed by etalon based techniques are characterized by high element density and small element active area, which enables high resolution imaging at high ultrasonic frequencies (typically 10-50 MHz). Laser generated ultrasound using the photoacoustic effect has been demonstrated in recent years as a powerful imaging modality for medical and biological applications. A short laser pulse illuminates a tissue creating rapid thermal expansion and acoustic emission. Detection of the resulting acoustic field by a detector array enables the imaging of the tissue optical absorption using ultrasonic imaging methods. One of the most appealing features of photoacoustic imaging is that it provides access to tissue composition at the molecular level using multiple wavelength illumination. elements are easily accomplished by optical focusing. These techniques are typically characterized by a flat bandwidth. Laser generation of ultrasound was studied and demonstrated for several decades but gained renewed interest since the late nineties for applications in medical imaging (7-10). The method is based on illuminating tissue with a short laser pulse. The optical pulse is absorbed by the tissue causing it to heat rapidly. The temperature rise is followed by thermal expansion producing acoustic emission. Detection of the resulting acoustic field allows reconstructing the initial distribution of heat deposition and therefore the distribution of optical absorption in the tissue. The most appealing feature of this method is that image contrast is based on the optical properties of tissue. This makes it possible for ultrasonic imaging to probe tissue composition at the molecular level and facilitates the interaction with optical based contrast agents for functional imaging (11, 12).
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