Finlay Jarod C, Foster Thomas H
Department of Radiology and of Physics and Astronomy, University of Rochester, 601 Elmwood Avenue, Box 648, Rochester, New York 14642, USA.
Med Phys. 2004 Jul;31(7):1949-59. doi: 10.1118/1.1760188.
We present a method for the analysis of steady state diffuse reflectance spectra obtained from vascularized tissue or from tissue simulating phantoms at a single, short source-detector separation. This method uses reasonable assumptions about the structure of the reduced scattering spectrum and basis absorption spectra for oxy- and deoxyhemoglobin, which dominate tissue absorption in the visible region of the spectrum. Using a hybrid P3-diffusion description of light propagation, described originally by Hull and Foster [J. Opt. Soc. Am. A 18, 584-599 (2001)] and suitable for short (approximately 1 mm) source-detector separations and optical properties of tissue at visible wavelengths, we create a forward model of the diffuse reflectance with four free parameters. We demonstrate that this model is able to recover accurately the hemoglobin concentrations and scattering properties from synthetic data generated by Monte Carlo simulation and from reflectance spectra acquired from tissue-simulating phantoms containing intact human erythrocytes. We show also that the method is capable of monitoring carbogen-induced changes in murine tumor oxygenation in vivo. The successful implementation of single, short detector separations enables the measurement of intratumor heterogeneities in hemoglobin oxygen saturation and responses to carbogen using a simple fiber-based probe design.
我们提出了一种用于分析稳态漫反射光谱的方法,该光谱是在单一、短源探测器间距下从血管化组织或组织模拟体模中获得的。此方法对约化散射光谱的结构以及氧合血红蛋白和脱氧血红蛋白的基础吸收光谱采用了合理假设,这些在光谱的可见光区域主导着组织吸收。利用最初由赫尔和福斯特[《美国光学学会杂志A》18, 584 - 599 (2001)]描述的、适用于短(约1毫米)源探测器间距以及可见光波长下组织光学特性的光传播混合P3 - 扩散描述,我们创建了一个具有四个自由参数的漫反射正向模型。我们证明,该模型能够从蒙特卡罗模拟生成的合成数据以及从含有完整人类红细胞的组织模拟体模获取的反射光谱中准确恢复血红蛋白浓度和散射特性。我们还表明,该方法能够在体内监测卡波金诱导的小鼠肿瘤氧合变化。成功实施单一、短探测器间距使得能够使用简单的基于光纤的探头设计测量肿瘤内血红蛋白氧饱和度的异质性以及对卡波金的反应。