This research is aimed to investigate the reliability of Mueller-matrix differentiation of birefringence change of optically thick layers of biological liquid crystals at the early stages of the change in their physiological state. This is performed by measuring the set of skewness and kurtosis values of Mueller matrix image of the phase element M 44 in various points of the object under investigation.
The paper deals with investigation of the processes of laser radiation transformation by biological crystals networks using the singular optics techniques. The results obtained showed a distinct correlation between the points of “characteristic” values of coordinate distributions of Mueller matrix () elements and polarization singularities (L- and C-points) of laser transformation of biological crystals networks with the following possibility of Mueller-matrix selection of polarization singularity. The technique of Mueller-matrix diagnostics of pathological changes of skin derma is proposed.
The efficiency of using the statistical and fractal analyses for distributions of wavelet coefficients for Mueller matrix images of biological crystal networks inherent to human tissues is theoretically grounded in this work. The authors found interrelations between statistical moments and power spectra for distributions of wavelet coefficients as well as orientation-phase changes in networks of biological crystals. Also determined are the criteria for statistical and fractal diagnostics of changes in the birefringent structure of biological crystal network, which corresponds to pathological changes in tissues.
The anticarcinogenic effects and mechanisms of the biotechnological drugs of Panax ginseng C.A. Meyer cultivated in Russia, bioginseng, panaxel and panaxel-5, were studied. Bioginseng was produced from a tissue culture of ginseng root cultured on standard medium, whereas panaxel and panaxel-5 were produced from ginseng tissue root cultures using standard mediums enriched with 2-carboxyethylgermanium sesquioxide and 1-hydroxygermatran-monohydrate respectively. All three ginseng drugs inhibited the development of mammary tumors induced by intramammary injections of N-methyl-N-nitrosourea (MNU) in rats, the development of the brain and spinal cord tumors induced by transplacental administration of N-ethyl-N-nitrosourea (ENU) in rats, and the development of uterine, cervical and vaginal tumors induced by intravaginal applications of 7,12-dimethylbenz(a)anthracene (DMBA) in mice. The ginseng drugs induced the cytotoxic activity of macrophages in mice, enhanced T-lymphocyte rosette formation in guinea pigs exposed to cyclophosphamide, and stimulated the production of thyroid hormones in rats. These mechanisms may contribute to the anticarcinogenic action of the ginseng drugs. The organic germanium compounds present in panaxel and panaxel-5 did not potentiate the anticarcinogenic or immuno-stimulatory effects as much as biogeinseng. Preliminary clinical trials with panaxel and bioginseng were carried out in patients with precancerous lesions of the esophagus and endometrium. Panaxel was found to have a strong therapeutic effect in patients suffering from chronic erosive esophagitis. Bioginseng induced the regression of adenomatous-cystic hyperplasia of the endometrium in some patients. Thus, we conclude that the drugs of ginseng appear to hold considerable promise for future cancer chemoprevention.
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