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角膜中荧光素体内测量的校准。

Calibration of measurements in vivo of fluorescein in the cornea.

作者信息

Taarnhøj J, Schlecht L, McLaren J W, Brubaker R F

机构信息

Department of Ophthalmology, Mayo Clinic, Rochester, MN 55905.

出版信息

Exp Eye Res. 1990 Aug;51(2):113-8. doi: 10.1016/0014-4835(90)90062-y.

Abstract

Quenching of fluorescence of fluorescein is not observed with broad field fluorophotometers. Fluorophotometric equipment which measures the fluorescence in a tiny spot has, however, been reported to underestimate the molarity of fluorescein in the rabbit corneal stroma by as much as a factor of two. In this experiment, quenching was measured in the rabbit cornea with two scanning fluorophotometers. The quenching was measured by four different techniques: (1) by elution of fluorescein, (2) by elution of albumin, (3) by polarization of fluorescence, and (4) by spectrofluorophotometry. It was estimated by all four methods that quenching in the living rabbit cornea with these instruments is approximately 20%. Taken together, the four experiments suggest that the quenching of fluorescence of fluorescein can be explained entirely on the basis of the interaction of fluorescein and albumin in the stroma.

摘要

宽视野荧光光度计未观察到荧光素荧光的淬灭现象。然而,据报道,测量微小光斑中荧光的荧光光度设备会低估兔角膜基质中荧光素的摩尔浓度,低估幅度高达两倍。在本实验中,使用两台扫描荧光光度计测量兔角膜中的淬灭情况。通过四种不同技术测量淬灭:(1)通过荧光素洗脱,(2)通过白蛋白洗脱,(3)通过荧光偏振,(4)通过荧光分光光度法。通过所有四种方法估计,使用这些仪器时,活兔角膜中的淬灭约为20%。综合来看,这四个实验表明,荧光素荧光的淬灭完全可以基于基质中荧光素与白蛋白的相互作用来解释。

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