“…where q is the molecular charge, N is the number of molecules per unit volume, m is the molecular mass, ω is the probing light frequency, ω 0 is the central frequency of molecular absorption band, and γ is the attenuation coefficient. [21][22][23][24][25] Over the last decades, various techniques to determine RI of biological tissues were developed; they include confocal microscopy, 1,6 optical fiber cladding method, 27 minimum deviation angle method, 28,29 optical coherent tomography with multiple modifications, 6,9,[30][31][32][33][34][35][36] total internal reflection method, 26,37,38 measurement of the intensity profile of diffuse light refracted into the prism around the critical angle, 39 various modifications of nonlinear phase microscopy, [40][41][42] and quantitative phase imaging techniques. 12,43,44 Because of the strong hemoglobin absorption, direct measurements of the real part of RI using conventional refractometers (for example, an Abbe refractometer) have proven to be difficult, and data are available at a few wavelengths only.…”