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Photoacoustic imaging depth comparison at 532- 800- and 1064-nm wavelengths: Monte Carlo simulation and experimental validation

机译:在532、800和1064 nm波长处的光声成像深度比较:蒙特卡洛模拟和实验验证

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摘要

Photoacoustic imaging (PAI) provides high-resolution and high-optical-contrast imaging beyond optical diffusion limit. Further improvement in imaging depth has been achieved by using near-infrared window-I (NIR-I, 700 to 900 nm) for illumination, due to lower scattering and absorption by tissues in this wavelength range. Recently, near-infrared window-II (NIR-II, 900 to 1700 nm) has been explored for PAI. We studied the imaging depths in biological tissues for different illumination wavelengths in visible, NIR-I, and NIR-II regions using Monte Carlo (MC) simulations and validated with experimental results. MC simulations were done to compute fluence in tissue, absorbance in blood vessel, and in a spherical absorber (mimicking sentinel lymph node) embedded at different depths in breast tissue. Photoacoustic tomography and acoustic resolution photoacoustic microscopy experiments were conducted to validate the MC results. We demonstrate that maximum imaging depth is achieved by wavelengths in NIR-I window ( ) when the energy density deposited is same for all wavelengths. However, illumination using wavelengths around 1064 nm (NIR-II window) gives the maximum imaging depth when the energy density deposited is proportional to maximum permissible exposure (MPE) at corresponding wavelength. These results show that it is the higher MPE of NIR-II window that helps in increasing the PAI depth for chromophores embedded in breast tissue.
机译:光声成像(PAI)提供了超出光扩散限制的高分辨率和高光学对比度成像。由于在此波长范围内组织的较低散射和吸收,通过使用近红外窗口I(NIR-I,700至900nm)进行照明,可以实现成像深度的进一步改善。最近,已经研究了用于PAI的近红外window-II(NIR-II,900至1700 nm)。我们使用蒙特卡洛(MC)模拟研究了可见,NIR-I和NIR-II区域中不同照射波长的生物组织中的成像深度,并用实验结果进行了验证。进行了MC模拟以计算组织的通量,血管的吸收率以及嵌入乳房组织不同深度的球形吸收剂(模拟前哨淋巴结)的吸收率。进行了光声层析成像和声学分辨率光声显微镜实验以验证MC结果。我们证明,当沉积的能量密度对于所有波长都相同时,最大成像深度是通过NIR-1窗口中的波长实现的。但是,当沉积的能量密度与相应波长下的最大允许曝光量(MPE)成正比时,使用1064 nm附近的波长的照明(NIR-II窗口)可以提供最大的成像深度。这些结果表明,NIR-II窗口的较高MPE有助于增加嵌入乳房组织中的发色团的PAI深度。

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