Research Article  Open Access
V. A. Ushenko, N. D. Pavlyukovich, L. Trifonyuk, "SpatialFrequency Azimuthally Stable Cartography of Biological Polycrystalline Networks", International Journal of Optics, vol. 2013, Article ID 683174, 7 pages, 2013. https://doi.org/10.1155/2013/683174
SpatialFrequency Azimuthally Stable Cartography of Biological Polycrystalline Networks
Abstract
A new azimuthally stable polarimetric technique processing microscopic images of optically anisotropic structures of biological tissues histological sections is proposed. It has been used as a generalized model of phase anisotropy definition of biological tissues by using superposition of Mueller matrices of linear birefringence and optical activity. The matrix element has been chosen as the main information parameter, whose value is independent of the rotation angle of both sample and probing beam polarization plane. For the first time, the technique of concerted spatialfrequency filtration has been used in order to separate the manifestation of linear birefringence and optical activity. Thereupon, the method of azimuthally stable spatialfrequency cartography of biological tissues histological sections has been elaborated. As the analyzing tool, complex statistic, correlation, and fractal analysis of coordinate distributions of element has been performed. The possibility of using the biopsy of the uterine wall tissue in order to differentiate benign (fibromyoma) and malignant (adenocarcinoma) conditions has been estimated.
1. Introduction
The state of the art in medical science demands from the experts not only certain practical skills but also knowledge of general pathologic processes, their nomenclature and definitions, causes, pathogenesis, and results as well as their importance for human. The pathologic processes on a cellular and tissue level can be detected by means of light microscope.
Samples preparation for microscopic investigations is a complex process that involves degradation of image quality of histological samples. In order to overcome the problems connected with image deformation (artifacts), the high professionalism and complex chore are necessary for results correction. The usage of computing for the mentioned tasks allows facilitating the work with medical images.
The methods and algorithms of objects isolation in the microscopic images—segmentation of histological objects in grayscale and color images—are mainly developing at present time. The algorithms of segmentation of extended (vessels, fibers) and areal (cells and their structures) objects are being elaborated [1–8].
A new medicalphysical method, namely, laser polarimetry of biological tissues histological sections, becomes an extension and an addition to the techniques of microscopic images structure processing [9–11]. The background of such method consists in measurements of coordinate distributions of polarization states (polarization maps) in the plane of microscopic images of biological tissues histological sections. Such method allows obtaining a new, inaccessible measurement for histological and mathematical methods of analysis and information about optical anisotropy (linear and circular birefringence [11]) of nonuniformly scaled structural elements of different biological objects. At the same time, a complex analysis of the polarization maps of a tissue specimen is azimuthally dependent on the probing beam polarization plane and sample rotation angle. Such a condition complicates using such a method during the comparative investigations of groups of histological sections with different pathologies.
Thus, further progress of laser polarimetry may be connected with the development of azimuthally stable methods of direct measurement of the parameters of linear and circular birefringences.
The solution of this task is the use of Muellermatrix cartography with the socalled rotational invariants. The Mueller matrix elements appear to be azimuthally stable and sample rotation angle () independent [12–15].
It has been determined that, in the case of optically thin (attenuation coefficient ) layers, the value is preferably defined by phase anisotropy mechanisms—linear and circular birefringences [16].
The separation of such mechanisms is possible with the help of spatialfrequency Fourier selection [17].
Our research is aimed at designing the experimental method of azimuthally stable Fourier polarimetry and spatialfrequency selection of parameter distributions of linear and circular birefringences of the biopsy of the uterine wall tissue in order to differentiate benign (fibromyoma) and malignant (adenocarcinoma) conditions.
2. The Theory of Method
The following model concepts have been assumed [9–11] by us as the basis for an analysis of the processes of modulation of laser radiation by the polycrystalline network of biological crystals with linear and circular birefringences:(i)the uterine wall tissue consists of two optical anisotropic layers of the muscular (myometrium) and connective (endometrium) layers;(ii)the optical anisotropic myometrium network is formed by largescale (the range of the transverse dimensions ) filiform myosin fibrils with a prevalence by linear birefringence;(iii)the optical anisotropy of such structures is characterized by coordinate distribution of the matrix element in the plane of histological section, where is a direction of fibrils packing and is a phase shift between linearly polarized orthogonal components of the light beam amplitude;(iv)the optical anisotropic component of the endometrium is formed by collagen fibers regulated according to the direction of optic axes (; ) with predominantly circular birefringence , where is polarization plane rotation angle.
From the medical point of view, “optical separation” of the polarization manifestations of linear and circular birefringences of optical anisotropic layers of the uterine wall is the topical task.
The fact is that, at the initial, early stages, the pathological changes in the human organism are accompanied by a concentration increase of optically active proteins in case of the generalized preservation of the morphological macrostructures of polycrystalline protein network of the myometrium and endometrium [16, 17].
Fibrillar structural changes—the formation of the growth direction of tumors shoots and so on—correspond to a more developed pathological condition.
With the purpose of a selection of such conditions, we have applied the method of spatialfrequency filtration of the polarization inhomogeneous field of laser radiation in Fourier plane [18, 19].
The main idea of such approach is that spatialfrequency structure of Fourier form of laser image of the tissue of the uterine wall is different for its largescale (myosin) and smallscale (collagen) protein structures. Proceeding from this, using spatialfrequency filtration, it is mainly possible to isolate either lowfrequency (with linear birefringence) or highfrequency (with circular birefringence) components, which by means of Fourier conversion transform into, respectively, “separated” laser images.
3. Optical Realization of Spatial Frequency of Fourier Selection of the Uterine Tissue Optical Anisotropy of Protein Networks
Figure 1 presents a diagram of modified laser Fourier polarimeter with spatialfrequency filtration [20].
Illumination of a sample under study was performed by the parallel () laser beam of HeNe (?µm, ?mW). The polarization light source consisted of quarterwave plates 3 and 5 and polarizer 4; it formed a right circularly polarized beam. The histological sections of the biopsy of the uterine wall tissue were placed in the focal plane of polarization microobjective 7 (focal distance—, aperture—0.1, magnification—). Behind the Fourier focal plane, the vignetting diaphragm was located; its size changed within the range of 2? to . Polarization microobjective 8 (focal distance—?mm, aperture—0.1, and magnification—) was located at the focal length forming the frequency plane of lens 7 and, thus, performed inverse Fourier transform of a filtered image outside the polarization field of laser radiation. The coordinate distribution of intensity of such fields, polarizationally filtered by quarterwave plate 9 and polarizer 10, was registered in the plane of CCDcamera 11 (the Imaging Source DMK 41AU02.AS, monochrome CCD, Sony ICX205AL (progressive scan); resolution—; light sensitive area size—?µm; sensitivity—0.05?lx; dynamic range—8?bit; SNR—9?bit, deviation of photosensitive characteristics from linear no more than 15%). It provided the range of measuring the structural elements of polycrystalline network with the resolution of 2–2000?µm.
The matrix element was calculated for each probing beam within every pixel () as follows:
Here, and are the intensities of spatialfrequency filtered image for each polarization states of probing beams (; 0°; 90°).
In order to get a quantitative estimation of coordinate distributions , we have used, as in the case of traditional laser polarimetry [9–11, 16, 17], three mutually complementary techniques of mathematical analysis, namely, statistic, autocorrelation, and fractal.
We have calculated a set of statistical moments of the 1st–4th orders using the following algorithms:
The obtained data characterizes the histogram of the element of optically anisotropic structures in the plane of histological section.
The method of autocorrelation with the use of function was assumed as the basis of an analysis of the coordinate structure of distributions
Here, is the step of changing the coordinates () of a distribution of a set of polarization distributions for a specific horizontal line of the pixel digital camera. The resultant expression for the autocorrelation function is obtained by averaging expression (3) along all lines
The obtained dependency characterizes the coordinate interconnection between the optically anisotropic structures in the plane of histological section.
We have selected correlation moments and that determine a distribution and the excess of the autocorrelation function as quantitative parameters that characterize autocorrelation dependences .
A fractal analysis of distributions was performed using a calculation of logarithmic dependences for the power spectra with following evaluation of dispersion.
Dependences are approximated using the leastsquares method into curves and are classified in such a way:(i) are fractal on condition that the value of the slope is constant for 23 decades of a change of sizes ;(ii) are multifractal, on condition of the presence of several slopes in ;(iii) are random, in case of the absence of stable slopes over the whole range of a change sizes .
The obtained results characterize the scale selfsimilarity of the distribution of optically anisotropic structures in the plane of histological section.
4. Experimental Results and Discussion
As objects of investigation, we chose two groups of opticallythin (attenuation coefficient ), single scattered histological sections of the biopsy of benign (16 samples) and malignant (14 samples) tumors of the uterus.
The samples were prepared on a freezing microtome, using a standard technique. From the optical point of view, such samples characterized by transformation of polarization without depolarization.
The conventional microscopic images of the samples of both groups are presented in Figure 2.
(a)
(b)
As it can be seen from Figure 2, the coordinate and scale structures of such conventional microscopic images are similar. This fact considerably complicates the histological differentiation of benign and malignant states of uterus tissue.
4.1. SpatialFrequency Fourier Polarimetry of Linear Birefringence of the Fibrillar Matrices of the Uterine Tissue
For the purpose of choosing the optimal conditions of spatialfrequency filtration, the following range of possible sizes of the vignetting diaphragm was used.
The criterion for diaphragm size choosing is a simultaneous change of the set of statistic moments (4) of . In our case, the optimal size was .
Such geometric size was chosen for comparative investigations of optical anisotropy of the fibrillar networks of the uterine tissue with benign and malignant changes, which characterize coordinate distributions of rotational invariant —Figure 3.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
A comparative analysis of aggregate parameters that characterize matrix maps of linear birefringence of largescale optically anisotropic fibrillar networks of the uterine tissue samples revealed some discrepancies between them. Namely, the main extrema of histograms of the distributions of random matrix maps, values for histological sections of both types are localized in different areas. Thus, the most probable value is for a benign tumor (Figure 3(b)), for a malignant one it is (Figure 3(f)). The revealed peculiarity, in our opinion, is connected with a more developed structure of newly formed fibers of malignant tumor than with benign fibromyoma of the similar optical anisotropic network.
Dependences of autocorrelation functions (4) of distribution of both uterine tissue samples smoothly and monotonously, (Figure 3, fragments (c) and (g)) indicate a coordinately homogeneous structure of the corresponding matrix maps formed by the mechanisms of linear birefringence of myosin fibrils. Besid such maps, a dimensionally selfsimilar construction has been deleted—logarithmic dependences of power distributions spectra are characterized by a similar slope (Figure 3, fragments (d), (h)).
Thus, matrix maps (Figure 3, fragments (a) and (e)) of linear birefringence of the polycrystalline network of myosin fibrils are characterized by a sufficiently similar correlation and homogeneous (fractal) structure. The main indication of oncologic changes is the formation of a developed optically anisotropic network with an increased level of linear birefringence index and a transformation of a histogram of the distribution of .
Quantitative differences between matrix maps of the protein matrices of the uterine tissue of both types illustrate average values and standard deviations of the set of statistic , correlative (), and fractal () parameters, illustrated in Table 1. Also, let us introduce the specificity parameter (—the number of the correct and incorrect diagnoses within a group) in differentiation of benign and malignant uterine tumors.

A comparative analysis of the data of laserfrequency Fourierpolarimetry of linear birefringence of protein polycrystalline networks of histological section of benign and malignant uterine tumors biopsy revealed sensibility to a differentiation of such states of all statistic moments of the 1st through the 4th orders with specificity level Sp ~ 60%–77% (printed in bold in Table 1).
4.2. SpatialFrequency Fourier Polarimetry of Circular Birefringence of the Fibrillar Networks of Uterine Tissue
Diagnostic possibilities of differentiating of pathologically changed samples of the uterine tissue, using the method of highfrequency spatialfrequency Fourierdomain—polarimetry of circular birefringence employing opaque filter illustrates probable (fragments (b), (f)), autocorrelation (fragments (c), (g)), and spectral (fragments (d), (h)) dependences of matrix maps (fragments (a), (e)), adduced in a series in Figure 4.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
On comparing the findings about the structure of the distributions of circular birefringence index (Figure 4, fragments (a) and (e)) under the conditions of high frequency filtration of laser field radiation, transformed by polycrystalline collagen fibrils of a layer of the endometrial tissue are the following characteristics of the oncologic state, detected. Firstly, it is a range expansion of random values that changes for a histogram of the matrix map at the expense of a “pathologic” increase of the concentrations and the size of the collagenous fibrils (Figure 4, fragments (b), (f)). Secondly, the formation of growth orientations leads to the transformation of the multifractal (Figure 4, fragment (d)) distribution into a selfsimilar—inherent fixed inclination (Figure 4, fragment (h) for approximate curve ).
Quantitative differences between matrix maps of circular birefringence of polycrystalline collagenous networks of the endometrium with pathology of both types illustrate average values and standard deviations of statistic set , correlative (), and fractal () parameters, presented in Table 2.

A comparative analysis revealed the following oncologic condition, with a high level of specificity () of uterus parameters (printed in bold in Table 2):(i)statistic moments of the 1st and the 2nd orders ; differences between values are from 2 to 3, 5 times;(ii)correlation moments of the 4th order of the autocorrelation function of distributions ; differences between the values reach 2 times;(iii)transformation of multifractal distributions into fractal ones.
5. Conclusions
A model of generalized optic anisotropy of the fibrillar protein matrices has been suggested, and the method of Fourier polarimetry for the parameters of linear (phase shift between orthogonal components of the laser wave amplitude) and circular (the rotation angle of the polarization plane) birefringences of the tissue biopsy of the uterine wall a spatial frequency selection of such coordinate distributions for a differentiation of benign (fibromyoma) and malignant (adenocarcinoma) conditions has been substantiated.
A set of criteria for a polarizationphase differentiation of benign (fibromyoma) and malignant (adenocarcinoma) conditions of the uterine has been revealed and substantiated as follows:(i)statistical moments of the 1st–4th order which characterize a distribution of azimuthally stable matrix element , stipulated by linear birefringence of myosin fibrils of the endometrium layer;(ii)statistical moments of the 1st–4th orders which characterize a distribution of azimuthally stable matrix element , stipulated by circular birefringence of the network of collagenous fibrils of the endometrium layer;(iii)correlation moments of the 4th order, which characterize autocorrelation functions of the distributions for , stipulated by circular birefringence of the network of collagenous fibrils; (iv)a slope change of approximate curve of loglog dependency for the power spectra of distribution of and transformed by optical anisotropic protein matrices.
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Copyright
Copyright © 2013 V. A. Ushenko et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.