Targeted spectroscopy in the eye fundus.

Significance: The assessment of biomarkers in the eye is rapidly gaining traction for the screening, diagnosis, and monitoring of ocular and neurological diseases. Targeted ocular spectroscopy is a technology that enables concurrent imaging of the eye fundus and analysis of high-quality spectra from a targeted region within the imaged area. This provides structural, compositional, and functional information of specific regions of the eye fundus from a non-invasive approach to ocular biomarker detection. Aim: The aim of our study was to demonstrate the multimodal functionality and validation of targeted ocular spectroscopy. This was done in vitro, using a reference target and a model eye, and in vivo. Approach: Images and spectra from different regions of a reference target and a model eye were acquired and analyzed to validate the system. Targeted ocular fluorescence spectroscopy was also demonstrated with the same model. Subsequently, in vivo imaging and diffuse reflectance spectra were acquired to assess blood oxygen saturation in the optic nerve head and the parafovea of healthy subjects. Results: Tests conducted with the reference target showed accurate spectral analysis within specific areas of the imaging space. In the model eye, distinct spectral signatures were observed for the optic disc, blood vessels, the retina, and the macula, consistent with the variations in tissue composition and functions between these regions. An ocular oximetry algorithm was applied to in vivo spectra from the optic nerve head and parafovea of healthy patients, showing significant differences in blood oxygen saturation. Finally, targeted fluorescence spectral analysis was performed in vitro. Conclusions: Diffuse reflectance and fluorescence spectroscopy in specific regions of the eye fundus open the door to a whole new range of monitoring and diagnostic capabilities, from assessment of oxygenation in glaucoma and diabetic retinopathy to photo-oxidation and photodegradation in age-related macular degeneration.

Blood oxygenation measurements by multichannel reflectometry on the venous and arterial structures of the retina.

The aim of the present study was to propose a model and a method to derive the oxyhemoglobin blood content in the retinal veins and arteries by full spectrum reflectometry measurements in the spectral zone from 430 to 680 nm. We proposed a mathematical equation expressed as a linear combination of two terms S(OHb)(λ) and S(Hb)(λ) representing the normalized spectral absorption functions of the hemoglobin and the oxyhemoglobin, one term λ(-n) representing the ocular media absorption with scattering, and a family of multi-Gaussian functions, which usefully compensate for the noncompatibility of the model and the experimental data in the red spectral zone. The present paper suggests that the spectral reflection function in the area from 520 to 580 nm is optimal in calculating the oxyhemoglobin concentration of the blood contained in the endothelial structures of retinal vessels. The model calculation needs a function (1/λ)(-n) that corrects for the ocular media absorption and light scattering on the vessels' structures. For the spectral area of lights with wavelength larger than 580 nm, the reflected light represents mainly the light scattering on the red blood cells.

Biocompatibility and light transmission of liposomal lenses.

PURPOSE: To validate the biocompatibility and transmittance properties of contact lenses bearing intact liposomes. These liposomal lenses loaded with therapeutics can be used as ophthalmic drug delivery systems. METHODS: The biocompatibility of soft contact lenses, coated with liposomes was evaluated through in vitro direct and indirect cytocompatibility assays on human corneal epithelial cells, on reconstructed human corneas and on ex vivo rabbit corneas. The direct and indirect transmission spectra of liposome-covered lenses were also evaluated to test if they transmit all wavelengths of the ultraviolet-visible spectrum, to thereby fulfill their optical function, without gross alteration of the colors perception and with a minimum of light dispersion. RESULTS: Contact lenses bearing layers of stable liposomes did not induce any significant changes in cell viability and in cell growth, compared with lenses bearing no liposome. Elution assays revealed that no cytotoxic compound leaks from the lenses whether bearing liposomes or not. Histological analyses of reconstructed human corneas and ex vivo rabbit corneas directly exposed to liposomal lenses revealed neither alteration to the cell nor to the tissue structures. Contact lenses bearing layers of liposomes did not significantly affect light transmission compared with control lenses without liposome at the wavelength of maximal photopic sensitivity, i.e., 550 nm. In addition, the contact lenses afford more eye protection in the ultraviolet spectrum, compared with the control lenses. CONCLUSIONS: Liposomal contact lenses are biocompatible and their transmittance properties are not affected in the visible light range.