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Comparing the effective attenuation lengths for long wavelength in vivo imaging of the mouse brain

机译:比较小鼠大脑长波长体内成像的有效衰减长度

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摘要

Light attenuation in thick biological tissues, caused by a combination of absorption and scattering, limits the penetration depth in multiphoton microscopy (MPM). Both tissue scattering and absorption are dependent on wavelengths, which makes it essential to choose the excitation wavelength with minimum attenuation for deep imaging. Although theoretical models have been established to predict the wavelength dependence of light attenuation in brain tissues, the accuracy of these models in experimental settings needs to be verified. Furthermore, the water absorption contribution to the tissue attenuation, especially at 1450 nm where strong water absorption is predicted to be the dominant contributor in light attenuation, has not been confirmed. Here we performed a systematic study of in vivo three-photon imaging at different excitation wavelengths, 1300 nm, 1450 nm, 1500 nm, 1550 nm, and 1700 nm, and quantified the tissue attenuation by calculating the effective attenuation length at each wavelength. The experimental data show that the effective attenuation length at 1450 nm is significantly shorter than that at 1300 nm or 1700 nm. Our results provide unequivocal validation of the theoretical estimations based on water absorption and tissue scattering in predicting the effective attenuation lengths for long wavelength in vivo imaging.
机译:吸收和散射的结合导致厚生物组织中的光衰减,限制了多光子显微镜(MPM)的穿透深度。组织的散射和吸收都取决于波长,这使得必须选择具有最小衰减的激发波长进行深度成像。尽管已经建立了理论模型来预测脑组织中光衰减的波长依赖性,但仍需要验证这些模型在实验环境中的准确性。此外,尚未证实吸水对组织衰减的贡献,特别是在1450 nm处,其中强吸水被预测是光衰减的主要贡献者,尚未得到证实。在这里,我们对1300 nm,1450 nm,1500 nm,1550 nm和1700 nm不同激发波长下的体内三光子成像进行了系统研究,并通过计算每个波长下的有效衰减长度来量化组织衰减。实验数据表明,在1450 nm处的有效衰减长度明显短于1300 nm或1700 nm处的衰减长度。我们的结果为预测长波长体内成像的有效衰减长度提供了基于吸水和组织散射的理论估计值的明确验证。

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