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Cancer is a life-threatening disease that has claimed the lives of many people worldwide. With the current diagnostic methods, it is hard to determine cancer at an early stage, due to its versatile nature and lack of genomic biomarkers. The rapid development of biophotonics has emerged as a potential tool in cancer detection and diagnosis. Using the fluorescence, scattering, and absorption characteristics of cells and tissues, it is possible to detect cancer at an early stage. The diagnostic techniques addressed in this review are highly sensitive to the chemical and morphological changes in the cell and tissue during disease progression. These changes alter the fluorescence signal of the cell/tissue and are detected using spectroscopy and microscopy techniques including confocal and two-photon fluorescence (TPF). Further, second harmonic generation (SHG) microscopy reveals the morphological changes that occurred in non-centrosymmetric structures in the tissue, such as collagen. Again, Raman spectroscopy is a non-destructive method that provides a fingerprinting technique to differentiate benign and malignant tissue based on Raman signal. Photoacoustic microscopy and spectroscopy of tissue allow molecule-specific detection with high spatial resolution and penetration depth. In addition, terahertz spectroscopic studies reveal the variation of tissue water content during disease progression. In this review, we address the applications of spectroscopic and microscopic techniques for cancer detection based on the optical properties of the tissue. The discussed state-of-the-art techniques successfully determines malignancy to its rapid diagnosis.

Azopolymers are highly efficient materials, able to register the polarization state of light. They have broad range of applications from diffractive optical elements with unique polarization properties to biophysics. We present a study of birefringence kinetics, induced with five different pump lasers with wavelengths 355, 442, 491, 514 and 532 nm in thin films of widely used amorphous azopolymer PAZO – poly[1-[4-(3-carboxy-4-hydroxyphenylazo)benzene sulfon amido]-1,2-ethanediyl, sodium salt]. During the real-time measurement, the value of the photoinduced birefringence (Δn) is determined at 635 nm, using a DPSS laser. When saturation is reached, the spectrum of the birefringence is measured. Our results indicate that the investigated azopolymer can be used for applications in a wide wavelength range.

Tissue polarimetry holds great promise to improve the effectiveness of conventional cancer diagnostics and staging, being a fast, minimally invasive, and low-cost optical technique. We introduce an enhanced diagnostic method for ex vivo colon specimens assessment by utilizing Stokes and Mueller matrix polarimetry. The proposed method makes use of experimental Mueller matrices, measured from healthy and tumor zones of a colon specimen, as input data for post-processing algorithms that include physical realisability filtering, symmetric decomposition and estimation of various polarization and depolarization metrics for colon specimen diagnostics. We validated our results with the gold standard histological diagnostics provided by pathologists. It was found that the Stokes-Mueller matrix polarimetry, combined with the appropriate filtering, decomposition algorithms and polarization/depolarization metrics calculations provides relevant optical markers of the colon tissue pathological conditions (healthy versus cancer), as confirmed by histopathology analysis. This approach potentially provides physicians with valuable and complementary information that holds promises in helping with the diagnostics of colon tissue specimens.

Tissue polarimetry could be identified as a complementary optical and non-invasive technique to assist the gold standard histopathology analysis of tissue. In general, polarimetric diagnostics is based on tracing different polarimetric responses (including light depolarization) in tissue zones with structure altered by the benign and pre/cancerous formations. In this manuscript, both healthy and malignant tissue zones of a thick formalin-fixed colon specimen were used for Mueller matrix measurements. Additionally, two more Mueller matrices from Monte Carlo simulation and tissue mimicking phantom were also evaluated, in order to assess polarimetric char- acterization and modeling of turbid media. Symmetric decomposition algorithm of Mueller matrices developed in house was adopted to extract both polarization and depolarization properties, encoded in the Mueller matrix elements. The decomposition products allowed to reveal important information about the internal tissue struc- ture and morphology. The depolarization and polarization parameters were found to follow the particular trends that depend on a choice of parametric space.

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This work is dedicated to the diagnosis and grading of colon cancer by a combined use of Poincaré sphere and 2D Stokes vector polarimetry mapping approaches. The major challenge consists in exploring the applicability of polarized light for noninvasive screening of the histological abnormalities within the samples of biological tissues. Experimental studies were conducted in ex vivo colon sample, excised after surgical procedure for colon tumor removal of G2-adenocarcinoma lesion. Polarimetric measurements in linear and circular regime were carried via personally developed polarimetric, optical set-up, using supercontinuous fiber laser with irradiation fixed at 635 nm. We apply the Poincaré sphere and two-dimensional Stokes vector scanning approach for screening the corresponding tissue samples. A comparison between linear and circular polarization states is made both for quantitative and qualitative evaluations. It is shown that circular polarization has better diagnostic capabilities than linear polarization, with higher dynamic ranges of the polarimetric parameters and better values of the diagnostic quantities. In addition to the standard polarimetry parameters, utilized as essential diagnostic markers, we apply statistical analysis to obtain more detailed information in frame of the applied diagnostic approach.

Regretfully, because of her sudden demise, Assoc. Prof. Ekaterina Borisova is no longer amongst us. COVID-19 pulled away a brilliant scientist during the peak of her scientific career (see Fig. 1). All authors would like to express deepest condolences and sincere support to her family, friends, relatives and colleagues! We, therefore, rightfully commemorate her dedicated and devoted contribution to biophotonics, her readiness to always support, help, motivate and inspire all her colleagues and collaborators., We would like to acknowledge the support from the National Science Fund of the Bulgarian Ministry of Education and Science (NSFB-MES) under all current projects involving Assoc. Prof. Ekaterina Borisova, which are grant numbers: #DN 18-8; #КP06-N29/11/18.12.18; #KP06-N28/11/14.12.2018; #KP06-Russia-9/2020; #KP-06-N23/8; #KP-06/N38/13; #KP06-India-8/07.08.2019; #KP-06-KOST-6. Also, projects under NRRI #DO1-401/18.12.2020 and #D01-392/18.12.2020.

Upon polarimetry the polarization state of light can be obtained for different depolarizing or non-depolarizing medias such as biological specimens. Tissue polarimetry can facilitate a differentiation between healthy and (pre)cancerous tissues, without using any contrast agents and ionizing radiation. Early cancer detection is vital to increase the life expectancy of patients. Turbid medias like biological tissues can change the state and/or decrease the initial polarization of light. Circularly polarized light is preferred as found to possess better ability to detect abnormal changes in tissues, compared to linearly polarized light. In this paper we analyse polarimetric parameters, measured with Thorlabs Stokes meter included in tissue polarimetric experimental set- up in reflection geometry and multiple ex vivo colon samples. The polarimetric device operates in the spectral range between 400 nm and 700 nm, where all experiments had been conducted with wavelength of 635 nm. By reaching reference values for the polarimetric parameters we can propose a theoretical Mueller matrix, that can be used to describe the depolarization properties of the colon samples used in the experiments. The proposed Mueller matrix is to be modelled and experimentally validated to find out if it matches the theory and can be further decomposed to three matrices of depolarization, diattenuation and retardance. All of the aforementioned experimental approaches are a step closer to a pre-clinical trial, which is a bridge to the final and the most challenging goal - tissue polarimetric set-up for in vivo diagnostics.

Tissue polarimetry provides a non-invasive, fast and relatively cheap differentiation of healthy from tumor tissues. This approach uses the different manner in which healthy tissues depolarize light, compared to the tumor ones. In extremely scattering optical media, such as biological tissues, light undergoes multiples scattering events, leading to changes in the two orthogonal components of the electric field Ex, Ey and a phase shift between them, which partially or fully depolarizes the initial polarization. When the size of the scattering particles is less than the wavelength of light (d < λ), then the linear polarization is preserved better. On the contrary, when the size of the scattering particles is greater than the wavelength of light (d > λ), then the circular polarization is preserved better. Measuring the Stokes parameters of light with linear and circular polarization and wavelength λ = 635 nm, diagnostic conclusions might be obtained for the histological condition of the samples, which are in agreement with the analysis of the pathologists. Moreover, this approach optimizes the differentiation based on polarization properties for the investigated soft tissues samples.

Apart from the huge physiological importance of hemo-, myo- globin and hemin, they play also an important role as robust and effective recognition agents in chemical and biological sensors. In this aspect the key factor in developing a reliable biosensor is the immobilization on the transducer. Usually immobilization can be produced by chemical methods, but there is frequently a need for homogeneous films of well-controlled thickness or films which can be deposited in a dry environment. The film thickness is of main importance for the optical transducer detected by Surface Plasmon Resonance (SPR) what is used in our study. Hundreds of immobilization protocols have been developed in an effort to ensure high performance sensing. All of them are focused on finding and deposition of appropriate matrices in which the recognition medium can be incorporated. However, the matrix always deteriorates the effectiveness of recognition. It seems that the best approach is to perform direct immobilization of the recognition medium. However, this is not always possible regarding the organic materials – the problem is whether the deposition retains the bioactivity of the recognition agent. On the other hand, the type of the transducer also imposes constrains. For example, the direct immobilization of the proteins is not possible for electrochemical sensors, because of the distance between the redox center and electrodes is too long. Evaluating the pros and cons of organic (protein) film deposition we have considered to study the possibility for direct immobilization of myoglobin, hemoglobin and hemin on SPR transducer. To best of our knowledge, SPR biochip with immobilized myoglobin, hemoglobin and hemin has never been constructed before. We have used spin coating, for direct immobilization and matrix-assisted pulsed-laser evaporation (MAPLE) for elaboration of the SPR biochip. The performance of both SPR chips – direct and MAPLE immobilized, was studied by SPR registration of the binding activity of myo- and hemo- globin ligands with carbon monoxide (CO), carbon dioxide (CO2) and nitride oxide (NO).

The implementation of tissue polarimetry in medicine arises mainly for the need of non-invasive and highly sensitive discrimination between healthy and tumor tissues. This fast, relatively cheap method may be useful for better histological diagnostics by the physicians. Although, the most challenging goal is to apply tissue polarimetric optical system for in vivo measurements, initially one have to optimize the optical system using ex vivo histological samples, phantoms and etc. This paper is focused on the polarimetric parameters from lower gastrointestinal tract histological samples, by using polarized light with several wavelengths, namely 444 nm, 488 nm, 514 nm, 594 nm and 635 nm, detected and processed by commercially available polarimeter. Our experimental results reveal the best wavelength choice in favor of 635 nm for all colon samples used. Light with circular polarization was used in the experiments, as found to survive more scattering events, compared to linearly polarized light. Furthermore, circularly polarized light carries additional information about the phase difference between the two orthogonal components of the electric field (Ex and Ey) and in the case of reflection, the incident state of polarization undergoes a ip of its helicity. By this way, a better detection of histological changes in tissues, related to abnormal tissue structure can be made. Furthermore, the multiwavelength, polarimetric analysis may provide better insight for future in vivo implementation and the results from the ex vivo biological samples presented in this study, contribute to better discrimination based on optical measurements, applicable for tumor detection.

Experimental validation of a previously reported depolarizing Mueller matrix model is crucial to understanding the light-tissue interactions and the morphological alterations originating in malignant tissue zones in terms of their optical properties. This manuscript is a continuation of a previously reported case study, where a theoretical model was introduced with an additional Monte Carlo simulation. The main aim of this study is to empirically validate both theory and modelling. Once extracted from an experimental Mueller matrix via symmetric decomposition, the polarimetric quantities were compared with the corresponding parameters previously determined from polarized Monte Carlo simulations. Our results were obtained from an ex vivo colon sample and indicate a potential capability to provide supplementary polarimetric data to physicians and the gold standard histopathology analysis.

The microstructural analysis of tissues plays a crucial role in the early detection of abnormal tissue morphology. Polarization microscopy, an optical tool for studying the anisotropic properties of biomolecules, can distinguish normal and malignant tissue features even in the absence of exogenous labelling. To facilitate the quantitative analysis, we developed a polarization-sensitive label-free imaging system based on the Stokes-Mueller calculus. Polarization images of ductal carcinoma tissue samples were obtained using various input polarization states and Stokes-Mueller images were reconstructed using Matlab software. Further, polarization properties, such as degree of linear and circular polarization and anisotropy, were reconstructed from the Stokes images. The Mueller matrix obtained was decomposed using the Lu-Chipman decomposition method to acquire the individual polarization properties of the sample, such as depolarization, diattenuation and retardance. By using the statistical parameters obtained from the polarization images, a support vector machine (SVM) algorithm was trained to facilitate the tissue classification associated with its pathological condition.

Polarization holographic gratings (PHG) were recorded using a laser emitting a wavelength of 491 nm in thin films of the (poly[1-[4-(3-carboxy-4-hydroxyphenylazo)benzenesulfonamido]-1,2-ethanediyl, sodium salt]) azopolymer, shortly denoted as PAZO. Thin azopolymer films with various thicknesses were spin-coated on plastic and glass substrates. Four different polarization states of the recording beams were used, and the results compared: a) two vertical linear polarizations, b) horizontal and vertical linear polarizations, c) linear polarizations at +45° and –45° relative to the recording plane, and d) two orthogonal circular polarizations – left- and right-handed (LCP and RCP). The diffraction efficiency in the +1 diffraction order was monitored in real time by a probing laser beam at the wavelength of 635 nm. The results indicate that the highest diffraction efficiency is achieved when recording with orthogonal polarizations – linear at ±45° or left and right circular. This is explained by the ability of the azopolymer material to record the variations in the polarization state of light better than the variations in its intensity. The holographic gratings obtained can be used to enhance the light-extraction efficiency of an OLED device.