首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Automated laser-scanning-microbeam fluorescence/Raman image analysis of human lens with multichannel detection: evidence for metabolic production of a green fluorophor.
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Automated laser-scanning-microbeam fluorescence/Raman image analysis of human lens with multichannel detection: evidence for metabolic production of a green fluorophor.

机译:具有多通道检测功能的人晶状体的自动激光扫描微束荧光/拉曼图像分析:绿色荧光团代谢产生的证据。

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摘要

A laser-microprobe fluorescence/Raman spectrometer with a 700-channel detector has been constructed and applied to the collection of data on the distribution of a green fluorophor throughout the exposed area of a human lens sectioned along the visual axis. The area (approximately 6.5 X 9.5 mm) covering the lens section was scanned automatically by the microprobe programmed to measure the fluorescence intensity at 1200 data points. The spectrometer output was accumulated in a microcomputer and displayed as a three-dimensional perspective view showing the fluorescence intensity at each point on the grid. The method permits the precise and detailed mapping at high resolution of the spatial distribution of a fluorophor or Raman-emissive constituent in a plane of the frozen lens to give results not obtainable by any other feasible procedure. The green fluorophor (441.6 nm, excitation wavelength; 520 nm, peak emission wavelength) has a distribution indicating a metabolic rather than a photochemical mode of production. Moreover, the lower level of fluorophor in the anterior segment suggests the existence of mechanisms in the anterior cortex (including the epithelium) that reduce significantly the accumulation of fluorophor. Such distribution studies are invaluable in clarifying metabolic interrelationships among the different zones of the lens, including especially photochemical reactions postulated to involve the effect of daylight on the lens in human subjects.
机译:具有700通道检测器的激光微探针荧光/拉曼光谱仪已被构建,并用于收集绿色荧光团沿人眼轴的整个曝光区域分布的数据。用微探针自动扫描覆盖透镜部分的区域(约6.5 X 9.5毫米),以测量1200个数据点的荧光强度。光谱仪的输出被存储在微型计算机中,并显示为三维透视图,显示了网格上每个点的荧光强度。该方法允许在荧光透镜或拉曼发射性成分在冷冻晶状体的平面中的空间分布的高分辨率下进行精确而详细的映射,以给出任何其他可行程序都无法获得的结果。绿色荧光团(441.6 nm,激发波长; 520 nm,峰值发射波长)的分布表示代谢而不是光化学生产方式。此外,前段荧光团的水平较低表明前皮质(包括上皮)中存在显着减少荧光团积累的机制。这样的分布研究在阐明晶状体不同区域之间的代谢相互关系方面,尤其是被认为涉及日光对人类受试者晶状体影响的光化学反应方面,具有十分重要的意义。

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