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Proceedings Paper

Optical properties extracted from 3D confocal images to assay 3D-printed scleroderma disease model (Conference Presentation)

Paper Abstract

With the highest mortality rate among rheumatic diseases, scleroderma leads to the painful formation of thick skin and organs. The cause of this thickening is the overproduction of collagen protein in the skin. The pathogenesis scleroderma is not fully understood and there exist no good disese models to provide context for drug discovery. To tackle this problem, we created a disease model of scleroderma with 3D printed collagen containing fibroblasts, MATLAB and confocal microscopy to observe optical properties mu and rho, which can be directly mapped to the scattering coefficient and scattering anisotropy. These optical properties varied with collagen levels and served as our metric for disease model severity. Our observations were based on the correlation between Rho and Mu values in the decay -- Signal = Rho*e(-Mu*Z) -- of the light absorbed over the depth of the tissue. We found that in our scleroderma model the Rho and Mu values increased with age and collagen concentration.

Paper Details

Date Published: 9 March 2020
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Proc. SPIE 11238, Optical Interactions with Tissue and Cells XXXI, 112380R (9 March 2020); doi: 10.1117/12.2549948
Show Author Affiliations
Daniel S. Gareau, The Rockefeller Univ. (United States)
Bart Halibart, The Rockefeller Univ. (United States)
Julia Adelman, The Rockefeller Univ. (United States)
James Krueger, The Rockefeller Univ. (United States)
Noa Kalfus, The Rockefeller Univ. (United States)


Published in SPIE Proceedings Vol. 11238:
Optical Interactions with Tissue and Cells XXXI
Bennett L. Ibey; Norbert Linz, Editor(s)

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