Razansky Daniel, Baeten John, Ntziachristos Vasilis
Institute for Biological and Medical Imaging, Technical University of Munich and Helmholtz Center Munich, Ingolstädter Landstrasse 1, D-85764 Neuherberg, Germany.
Med Phys. 2009 Mar;36(3):939-45. doi: 10.1118/1.3077120.
Optoacoustic imaging is emerging as a noninvasive imaging modality that can resolve optical contrast through several millimeters to centimeters of tissue with the resolution achieved by ultrasound imaging. More recently, applied at multiple illumination wavelengths, multispectral optoacoustic tomography (MSOT) offered the ability to effectively visualize tissue biomarkers by resolving their distinct spectral signatures. While the imaging potential of the method has been demonstrated, little is known on the sensitivity performance in resolving chromophoric and fluorescent substances, such as optical functional and molecular reporters. Herein the authors investigate the detection capacity and physical limits of tomographic optoacoustic imaging by simulating signals originating from absorbing spheres in tissue-mimicking media. To achieve this, a modified optoacoustic equation is employed to incorporate wavelength-dependent propagation and attenuation of diffuse light and ultrasound. The theoretical predictions are further validated in phantom experiments involving Cy5.5, a common near-infrared fluorescent molecular agent.
光声成像正在成为一种非侵入性成像方式,它能够以超声成像所达到的分辨率,在几毫米到几厘米的组织中分辨出光学对比度。最近,多光谱光声断层扫描(MSOT)应用于多个照明波长,通过解析不同的光谱特征,具备了有效可视化组织生物标志物的能力。虽然该方法的成像潜力已得到证明,但对于分辨发色团和荧光物质(如光学功能和分子报告物)时的灵敏度性能却知之甚少。在此,作者通过模拟组织模拟介质中吸收球体产生的信号,研究断层光声成像的检测能力和物理极限。为实现这一目标,采用了一个经过修改的光声方程,以纳入漫射光和超声的波长依赖性传播和衰减。理论预测在涉及常见近红外荧光分子试剂Cy5.5的体模实验中得到了进一步验证。