Ex-vivo confocal Raman microspectroscopy of porcine skin with 633/785-NM laser excitation and optical clearing with glycerol/water/DMSO solution

Author:

Jaafar Ali123,Mahmood Malik H.124,Holomb Roman15,Himics László1,Váczi Tamás1,Sdobnov Anton Y.67,Tuchin Valery V.689,Veres Miklós1

Affiliation:

1. Institute for Solid State Physics and Optics, Wigner Research Centre for Physics, P.O. Box 49, H-1121 Budapest, Hungary

2. Institute of Physics, University of Szeged, Dom ter 9, H-6720 Szeged, Hungary

3. Ministry of Higher Education and Scientific Research, Baghdad 10065, Iraq

4. Physiology Department, College of Medicine, University of Misan, Al-Amarah, Misan 62001, Iraq

5. Uzhhorod National University, Uzhhorod 88015, Transcarpathia, Ukraine

6. Science Medical Center, Saratov State University, 83 Astrakhanskaya Str., Saratov 410012, Russia

7. Optoelectronics and Measurement Techniques Laboratory, University of Oulu, 90570 Oulu, Finland

8. Laboratory of Laser Diagnostics of Technical and Living Systems, Institute of Precision Mechanics and Control of the Russian Academy of Sciences, 24 Rabochaya, Saratov 410028, Russia

9. Interdisciplinary Laboratory of Biophotonics, National Research Tomsk State University, 36 Lenin Avenue, Tomsk 634050, Russia

Abstract

Confocal Raman microspectroscopy (CRM) with 633- and 785-nm excitation wavelengths combined with optical clearing (OC) technique was used for ex-vivo study of porcine skin in the Raman fingerprint region. The optical clearing has been performed on the skin samples by applying a mixture of glycerol and distilled water and a mixture of glycerol, distilled water and chemical penetration enhancer dimethyl sulfoxide (DMSO) during 30[Formula: see text]min and 60[Formula: see text]min of treatment. It was shown that the combined use of the optical clearing technique and CRM at 633[Formula: see text]nm allowed one to preserve the high probing depth, signal-to-noise ratio and spectral resolution simultaneously. Comparing the effect of different optical clearing agents on porcine skin showed that an optical clearing agent containing chemical penetration enhancer provides higher optical clearing efficiency. Also, an increase in treatment time allows to improve the optical clearing efficiency of both optical clearing agents. As a result of optical clearing, the detection of the amide-III spectral region indicating well-distinguishable structural differences between the type-I and type-IV collagens has been improved.

Publisher

World Scientific Pub Co Pte Ltd

Subject

Biomedical Engineering,Atomic and Molecular Physics, and Optics,Medicine (miscellaneous),Electronic, Optical and Magnetic Materials

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