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Igor Ermakov Phones & Addresses

  • 1669 Downington Ave, Salt Lake Cty, UT 84105 (801) 534-0692
  • 515 6Th Ave, Salt Lake City, UT 84103 (801) 534-0692
  • Cottonwood Heights, UT

Work

Company: University of utah Dec 1997 to Apr 2015 Position: Scientist, biomedical optics

Industries

Higher Education

Resumes

Resumes

Igor Ermakov Photo 1

Senior Research Scientist

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Location:
Salt Lake City, UT
Industry:
Higher Education
Work:
University of Utah Dec 1997 - Apr 2015
Scientist, Biomedical Optics

Longevity Link Corporation Dec 1997 - Apr 2015
Senior Research Scientist

Publications

Us Patents

Methods And Apparatus For Detection Of Carotenoids In Macular Tissue

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US Patent:
20060134004, Jun 22, 2006
Filed:
Dec 21, 2004
Appl. No.:
11/018403
Inventors:
Werner Gellermann - Salt Lake City UT, US
Mohsen Sharifzadeh - Salt Lake City UT, US
Igor Ermakov - Salt Lake City UT, US
Paul Bernstein - Salt Lake City UT, US
International Classification:
A61K 49/00
A61B 10/00
US Classification:
424009600, 600315000
Abstract:
Methods and apparatus are provided for the noninvasive detection and measurement of macular pigments such as carotenoids in macular tissue. In one technique, lipoftiscin autofluorescence spectroscopy is utilized for macular pigment measurements. In autofluorescence spectroscopy, the emission of lipoftiscin is excited at two wavelengths: one wavelength that overlaps both the macular pigment and lipofuscin absorption and another wavelength that lies outside the macular pigment absorption range but that still excites the lipofuscin emission. The macular pigment absorption is then derived from the different lipoftiscin emission intensities in the macula and peripheral retina. In another technique, both autofluorescence spectroscopy, as described above, and resonance Raman spectroscopy are used to identify and quantify the presence of carotenoids in macular tissue. In using resonance Raman spectroscopy, laser light is directed onto the eye tissue and the scattered light is then spectrally filtered and detected. The frequency difference between the laser light and the Raman scattered light is known as the Raman shift. The magnitude of the Raman shift is an indication of the type of chemical present, and the intensities of the Raman signal peaks correspond directly to the chemical concentration.

Noninvasive Measurement Of Carotenoids In Biological Tissue

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US Patent:
20090306521, Dec 10, 2009
Filed:
Jun 6, 2008
Appl. No.:
12/134667
Inventors:
Igor V. Ermakov - Salt Lake City UT, US
Werner Gellerman - Salt Lake City UT, US
Assignee:
Longevity Link, Inc. - Salt Lake City UT
International Classification:
A61B 6/00
A61B 5/103
US Classification:
600477, 600587
Abstract:
A method and apparatus are provided for the determination of carotenoid antioxidants and similar chemical compounds in biological tissue such as living skin. The method and apparatus provide a noninvasive, rapid, accurate, and safe determination of carotenoid levels which in turn can provide diagnostic information of the antioxidant status of tissue. Reflection spectroscopy is used to measure the concentrations of carotenoids and similar substances in tissue. White light is directed upon the area of tissue that is of interest. A small fraction of diffusively scattered light is collected and measured. The tissue is pressured to temporarily squeeze blood out of the measured tissue volume while the reflection spectrum is continuously monitored, displayed, and analyzed in near real time. After an optimal time period of typically 15 seconds, the influence of the dominating hemoglobin and oxyhemoglobin tissue absorptions on the reflection spectra are minimized.

Noninvasive Measurement Of Flavonoid Compounds In Biological Tissue

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US Patent:
20100179435, Jul 15, 2010
Filed:
Jan 13, 2009
Appl. No.:
12/352702
Inventors:
Mohsen Sharifzadeh - Salt Lake City UT, US
Igor V. Ermakov - Salt Lake City UT, US
Werner Gellermann - Salt Lake City UT, US
International Classification:
A61B 6/00
US Classification:
600476
Abstract:
Methods and apparatus are disclosed which facilitate the rapid, noninvasive and quantitative measurement of the concentration of flavonoid compounds, as well as their isomers and metabolites, in biological tissue such as human skin. Low-intensity, visible-light illumination of intact tissue provides for high spatial resolution, and allows for precise quantification of the flavonoid levels in the tissue. The preferred embodiments malce use of a previously unknown, low-oscillator strength, optical absorption transition of flavonoids. This malces it possible to optically excite flavonoids in living human tissue outside the absorption range of other, potentially confounding skin chromophores. A system constructed in accordance with the invention includes a source of light for illuminating a localized region of tissue with light that overlaps the absorption bands of a flavonoid compound; a device for detecting the fluorescence emitted by the flavonoid compound resulting from the illumination; and a processor for determining the concentration level of the flavonoid compound based upon the detected fluorescence.

Noninvasive Measurement Of Carotenoids In Biological Tissue

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US Patent:
20120330164, Dec 27, 2012
Filed:
Sep 4, 2012
Appl. No.:
13/602798
Inventors:
Igor V. Ermakov - Salt Lake City UT, US
Werner Gellerman - Salt Lake City UT, US
Assignee:
Longevity Link, Inc. - Salt Lake City UT
International Classification:
A61B 6/00
US Classification:
600476
Abstract:
A method and apparatus are provided for the determination of carotenoid antioxidants and similar chemical compounds in biological tissue such as living skin. The method and apparatus provide a noninvasive, rapid, accurate, and safe determination of carotenoid levels which in turn can provide diagnostic information of the antioxidant status of tissue. Reflection spectroscopy is used to measure the concentrations of carotenoids and similar substances in tissue. White light is directed upon the area of tissue that is of interest. A small fraction of diffusively scattered light is collected and measured. The tissue is pressured to temporarily squeeze blood out of the measured tissue volume while the reflection spectrum is continuously monitored, displayed, and analyzed in near real time. After an optimal time period of typically 15 seconds, the influence of the dominating hemoglobin and oxyhemoglobin tissue absorptions on the reflection spectra are minimized.

Optical Detection Of Carotenoid-Related Compounds In Human Bone And Surrounding Tissues

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US Patent:
20140200419, Jul 17, 2014
Filed:
Jan 17, 2013
Appl. No.:
13/744260
Inventors:
Igor V. Ermakov - Salt Lake City UT, US
Thomas D. Rosenberg - Holladay UT, US
Werner Gellermann - Salt Lake City UT, US
International Classification:
A61B 5/00
US Classification:
600306, 600476
Abstract:
The present invention is directed to measuring the levels of carotenoids and other similar chemical compounds that are present in varying degrees in human bone and surrounding tissues. The invention permits non-contact, quantitative measurements of carotenoid levels of tissues, exposed during surgery, from a safe distance. Light reflected from an exposed bone or surrounding tissue is captured and processed to accurately quantify the carotenoid content of the bone or tissue.

Isbn (Books And Publications)

Islam V Russkoi Literature XV-XX V.V.

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Author

Igor Ermakov

ISBN #

5934060465

Igor V Ermakov from Salt Lake City, UT, age ~54 Get Report