October 1998
Volume 39, Issue 11
Free
Articles  |   October 1998
Raman detection of macular carotenoid pigments in intact human retina.
Author Affiliations
  • P S Bernstein
    Department of Ophthalmology, Moran Eye Center, University of Utah School of Medicine, Salt Lake City 84132, USA.
  • M D Yoshida
    Department of Ophthalmology, Moran Eye Center, University of Utah School of Medicine, Salt Lake City 84132, USA.
  • N B Katz
    Department of Ophthalmology, Moran Eye Center, University of Utah School of Medicine, Salt Lake City 84132, USA.
  • R W McClane
    Department of Ophthalmology, Moran Eye Center, University of Utah School of Medicine, Salt Lake City 84132, USA.
  • W Gellermann
    Department of Ophthalmology, Moran Eye Center, University of Utah School of Medicine, Salt Lake City 84132, USA.
Investigative Ophthalmology & Visual Science October 1998, Vol.39, 2003-2011. doi:
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    • Get Citation

      P S Bernstein, M D Yoshida, N B Katz, R W McClane, W Gellermann; Raman detection of macular carotenoid pigments in intact human retina.. Invest. Ophthalmol. Vis. Sci. 1998;39(11):2003-2011.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: To develop and test a novel noninvasive optical technique suitable for the objective measurement of macular carotenoid levels in human retina. METHODS: A resonance Raman scattering apparatus was constructed to measure carotenoid levels in flat-mounted human retinas and eyecups and in experimental animal eyes. Light from an argon laser was used to resonantly excite the electronic absorption of the carotenoid pigments, and scattered light was collected and analyzed by a Raman spectrometer. After carotenoid Raman measurements were completed on the retinal samples, macular carotenoid levels were determined by high-performance liquid chromatography (HPLC). RESULTS: Carotenoid resonance Raman scattering proved to be a highly sensitive and specific method for the noninvasive measurement of macular pigments in the human retina. Signal strength scaled linearly with actual macular carotenoid content as measured by HPLC. Our apparatus was also used to record resonance Raman signals from xanthophyll carotenoids stored in the retinal pigment epithelium of intact frog eyes. CONCLUSIONS: This new noninvasive optical method will facilitate studies of ocular carotenoid distributions and their role in degenerative diseases of the eye and may allow for the rapid screening of carotenoid levels in large populations at risk for vision loss from age-related macular degeneration, the leading cause of blindness in the elderly in the United States. A prototype clinical instrument is under development.

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