首页> 美国卫生研究院文献>Journal of Biomedical Optics >Noninvasive evaluation of hemodynamics and light scattering property during two-stage mouse cutaneous carcinogenesis based on multispectral diffuse reflectance images at isosbestic wavelengths of hemoglobin
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Noninvasive evaluation of hemodynamics and light scattering property during two-stage mouse cutaneous carcinogenesis based on multispectral diffuse reflectance images at isosbestic wavelengths of hemoglobin

机译:基于血红蛋白等吸收波长的多光谱漫反射图像对两阶段小鼠皮肤癌变过程中的血流动力学和光散射特性进行非侵入性评估

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摘要

We investigate a multispectral imaging method to evaluate spatiotemporal changes in both cutaneous hemoglobin concentration and light scattering parameter in mouse skin through diffuse reflectance spectroscopy using the reflectance images acquired at isosbestic wavelengths of hemoglobin (420, 450, 500, and 585 nm). In the proposed approach, Monte Carlo simulation-based empirical formulas are introduced to extract the scattering power representing the wavelength dependence of light scattering spectrum of skin tissue, as well as the total hemoglobin concentration in dermal vasculatures. The use of isosbestic wavelengths of hemoglobin enables the values of and to be estimated independently of the oxygenation of hemoglobin. Experiments using mice two-stage chemical carcinogenesis model are performed to confirm the feasibility of the proposed method for evaluating the changes in cutaneous vasculatures and tissue morphology during tumor initiation, promotion, and progression processes. The experimental results reveal that the changes in scattering power of back skin are significantly reduced and followed by the increase in total hemoglobin concentration in the carcinogenesis mice group, which indicates morphological changes in skin tissue such as edema and cell swelling caused by tumor promotion and successive angiogenesis along with tumor progression. The results suggest that the potential of the present method to detect cutaneous carcinogenesis in an early stage and monitor physiological changes during promotion and progression process of nonmelanoma tumors.
机译:我们研究了一种多光谱成像方法,通过使用在血红蛋白等渗波长(420、450、500和585 nm)上获得的反射率图像的漫反射光谱法,评估小鼠皮肤中皮肤血红蛋白浓度和光散射参数的时空变化。在提出的方法中,引入了基于蒙特卡罗模拟的经验公式来提取代表皮肤组织光散射光谱的波长依赖性的散射能力,以及皮肤脉管系统中的总血红蛋白浓度。血红蛋白的等渗波长的使用使得的值和可以独立于血红蛋白的氧合而估计。进行了使用小鼠两阶段化学致癌模型的实验,以证实所提出的方法在评估肿瘤发生,促进和进展过程中皮肤脉管系统和组织形态变化的可行性。实验结果表明,在致癌小鼠组中,背面皮肤的散射能力变化明显降低,然后总血红蛋白浓度增加,这表明肿瘤组织和继发性肿瘤引起的皮肤组织形态变化,例如水肿和细胞肿胀血管生成以及肿瘤进展。结果表明,本方法在早期检测皮肤癌变和监测非黑素瘤肿瘤的促进和发展过程中的生理变化的潜力。

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