Doyle Timothy E, Warnick Keith H, Carruth Brent L
Department of Physics, Utah State University, Logan, Utah 84322-4415, USA.
J Acoust Soc Am. 2007 Dec;122(6):EL210-6. doi: 10.1121/1.2800894.
Ultrasonic spectroscopy may offer an alternative to imaging methods for the in vivo detection of microscopic cancer. To investigate this potential, a numerical model that incorporates multiple scattering, wave-mode conversion, and hierarchical microstructures was developed to simulate ultrasonic interactions in biological tissue at the microscopic level. Simulated high-frequency (20-75 MHz) spectra of up to 2137 cells displayed significant correlations to nucleus diameter and malignant cell infiltration, and indicated as few as 300 malignant cells may be detectable in normal tissue. The results suggest that ultrasonic spectroscopy combined with simulation-based interpretive models may provide real-time histopathology during surgeries, biopsies, and endoscopies.
超声光谱学可能为体内微观癌症检测提供一种替代成像方法。为了研究这种潜力,开发了一个包含多重散射、波模转换和分层微观结构的数值模型,以在微观层面模拟生物组织中的超声相互作用。对多达2137个细胞的模拟高频(20 - 75兆赫)光谱显示出与细胞核直径和恶性细胞浸润有显著相关性,并表明在正常组织中少至300个恶性细胞也可能被检测到。结果表明,超声光谱学与基于模拟的解释模型相结合,可能在手术、活检和内窥镜检查期间提供实时组织病理学信息。