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Spatial distribution of tissue fluorescence

机译:组织荧光的空间分布

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Abstract: Fluorescence signal during tissue LIF-analysis depends on both excitation conditions and tissue optics, registration optics and location of the probe relative to tissue sample as well. To develop reliable fiber optic probes and optimize their position the spatial distribution of tissue fluorescence should be studied. Fluorescence indicatrices of skin of rat were measured in angular range of 80 degrees. Excited light from He-Cd (20 mW, 442 nm) laser was delivered on the cutaneous surface at the angular range from 0 to 60 degrees with the tissue surface. Fluorescence was registered in the spectrum between 530 nm and 700 nm with 1.5 nm resolution. Autofluorescence of the skin of 5 white rats was studied in-vivo. Local application of sensitizer hypericin was used for stimulated fluorescence studies. Fluorescence indicatrices were not corresponded to scattering ones under the same conditions and depended on incident angle of excitative laser beam. No influence of polarization of excitative beam on outside fluorescence distribution was observed. Maximum in-vivo fluorescence yield was registered at the normal incidence. There were observed marked differences between spatial distribution of normal and photosensitized rat skin tissues. !7
机译:摘要:组织LIF分析过程中的荧光信号取决于激发条件和组织光学器件,配准光学器件以及探头相对于组织样品的位置。为了开发可靠的光纤探头并优化其位置,应该研究组织荧光的空间分布。在80度的角度范围内测量大鼠皮肤的荧光指数。来自He-Cd(20 mW,442 nm)激光的激发光以与组织表面成0至60度的角度范围传递到皮肤表面。在530 nm至700 nm之间的光谱中以1.5 nm的分辨率记录了荧光。体内研究了5只白色大鼠皮肤的自发荧光。敏化剂金丝桃素的局部应用用于激发荧光研究。在相同条件下,荧光指示物不对应于散射指示物,而是取决于激发激光束的入射角。没有观察到激发光束的偏振对外部荧光分布的影响。在正常入射下记录了最大的体内荧光产量。观察到正常和光敏大鼠皮肤组织的空间分布之间存在明显差异。 !7

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