Measurements of endogeous fluorophores open the possibility for evaluation of metabolic state at the eye. For
interpretation of 2-dimensional measurements of time-resolved auto fluorescence in 2 separate spectral ranges at the
human eye, comparing measurements were performed on porcine eyes. Determining excitation and emission spectra,
attention was drawn of proof of coenzymes NADH and FAD in isolated anatomical structures cornea, aqueous
humor, lens, vitreous, neuronal retina, retinal pigment epithelium (RPE), choroid, and sclera. All these structures
exhibit auto fluorescence, highest in lens. Excitation at 350 nm results in local fluorescence maxima at 460 nm,
corresponding to NADH, in all structures. This short-wave excitation allows metabolic studies only at the anterior
eye, because of the limited transmission of the ocular media. During excitation at 446 nm the existence of FAD is
expressed by local fluorescence maxima at 530 nm. The composition fluorescence spectra allow no discrimination
between single ocular structures. Approximating the dynamic fluorescence by a double exponential function, the
shortest lifetimes were detected in RPE and neuronal retina. The histograms of mean lifetime tM cover each other on
lens with cornea and also on sclera with choroid. Despite the lifetimes are close between RPE and neuronal retina,
the relative contributions Q1 are wide different. The gradient of trend lines in cluster diagrams of amplitudes α2 vs.
α1 allows a discrimination of ocular structures.
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