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Optics and Spectroscopy, 2024 Volume 132, Issue 4, Pages 383–392 (Mi os1181)

Proceedings of the International Conference The XXVII Annual International Conferences Saratov Fall Meeting 2023, September 25 - 29, 2023, Saratov, Russia
Biophotonics

Differentiation methods of rat brain tissues and glioma model 101.8 ex vivo using optical coherence tomography

P. V. Aleksandrovaab, K. I. Zaitseva, P. V. Nikitinc, A. I. Alekseevad, A. A. Nebezheve, V. I. Polshinae, P. A. Karalkine, I. N. Dolganovab

a Prokhorov General Physics Institute of the Russian Academy of Sciences, 119991 Moscow, Russia
b Osipyan Institute of Solid State Physics, Russian Academy of Sciences, 142432 Chernogolovka, Russia
c University of Houston, Houston, Texas, the USA
d Avtsyn Research Institute of Human Morphology of Federal State Budgetary Scientific Institution "Petrovsky National Research Centre of Surgery", 117418 Moscow, Russia
e Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia

Abstract: The article considers two methods of image analysis obtained by using optical coherence tomography (OCT): analysis of attenuation coefficient and speckle-structures of images as regards differentiation of intact tissues and rat brain tumors. The glioma model 101.8 was used for extracting information from speckle structures using wavelet analysis method of OCT images and calculating the power of local brightness fluctuations in speckles. Applying linear discriminant analysis, the effectiveness of the developed approach consisting of two methods was evaluated on the basis of sensitivity, specificity and precision values in differentiation of glioma model and intact tissues. The results of the study showed the advantages of the developed OCT image analysis method for neurosurgery.

Keywords: optical coherence tomography, glioma, wavelet analysis, Fisher linear discriminant analysis, speckle structure, attenuation coefficient.

Received: 09.02.2024
Revised: 20.02.2024
Accepted: 05.03.2024

DOI: 10.61011/OS.2024.04.58216.41-24



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