{"id":83,"count":0,"description":"<style>\r\n.archive p{text-align:left !important;}\r\n<\/style>\r\n<div style=\"width: 60%;  margin: 50px auto 0; padding: 10px;  border: 1px solid #00ffff;\">\r\n<p class=\"style5\" align=\"left\"><strong><h1 class=\"\" style=\"text-align:center;\">Frequency Infused Water<\/h1><\/strong><\/p>\r\n\r\n<ul class=\"nav nav-tabs\">\r\n  <li role=\"presentation\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/\">Water Home<\/a><\/li>\r\n  <li role=\"presentation\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/benifits\/\">Benefit<\/a><\/li>\r\n  <li role=\"presentation\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/research-gia-water-frequency-infusion-device\/\">Research<\/a><\/li>\r\n\r\n<li role=\"presentation\" class=\"active\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/test-results\/\">Test Results<\/a><\/li>\r\n  <li role=\"presentation\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/testimonial\/\">Testimonial<\/a><\/li>\r\n  <li role=\"presentation\"><a href=\"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/order\/\">Order<\/a><\/li>\r\n<\/ul>\r\n\r\n\r\n<p style=\"font-weight:bold; padding-top:20px;\" align=\"center\"><span class=\"style112\">Biological Tests Results<\/span><\/p>\r\n<p align=\"center\">\r\n<strong>MRET ACTIVATED WATER AND ITS SUCCESFUL APPLICATION FOR PREVENTIVE TREATMENT AND ENHANCED TUMOR RESISTANCE IN ONCOLOGY<\/strong><\/p>\r\nThe goal of this investigation was to study on mice the effect of MRET activated water as a potential agent for the prevention and treatment of two kinds of oncology diseases (laboratory models of Ehrlich's ascites tumor and Sarcoma ascites form). Significant positive effect of MRET activated water regarding the tumor resistance on animals was observed in the experiments conducted on 500 mice (22 groups with 20 mice in each group and 10 groups with 5 mice in each group). The best results were observed in the groups of mice on MRET water activated for 30 minutes (optimal regime of activation). The substantial anti-tumor efficacy was confirmed by very high level of reduction of Total Number of Viable Tumor Cells by 76% in \u201cpreventive treatment\u201d and by 55% in \u201ctherapeutic treatment\u201d regime. The life span of mice which received optimal activated water increased by 61% in \u201cpreventive treatment\u201d and by 43% in \u201ctherapeutic treatment\u201d regime. The significant anti-tumor effect of MRET Activated Water on mice was close to the action of the chemotherapy agents and allowed to avoid the side effects that typically follow chemotherapy treatment in oncology.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/oncology_fig_1.jpg\" alt=\"\" \/><\/p>\r\nFig 1: The effect of preventive (1\u20135) and therapeutic (6\u201310) application of MRET activated water on average total number of viable cells <C> in an ascetic tumor, obtained from mice inoculated intraperitoneally with tumor cells of Ehrlich carcinoma.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/oncology_fig_2.jpg\" alt=\"\" \/><\/p>\r\nFig 2: The change of the percentage increase of life span of tumor-bearing mice with ascitic Ehrlich carcinoma which received different types of MRET activated water in \u201cpreventive treatment\u201d and \u201ctherapeutic treatment\u201d regimes. The digits under the charts correspond with the duration of water activation in minutes.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/oncology_fig_3.jpg\" alt=\"\" \/><\/p>\r\nFig 3: The effect of MRET activated water on cytotoxic activity of lymphocytes containing NK-cells. Activated water was applied for mice without tumors in two regimes (for 21 and 14 days), called \u201cpreventive\u201d (1\u20135) and \u201ctherapeutic\u201d (6\u201310).\r\n\r\nThe results of investigation of the application of water activated by non-ionizing Molecular Resonance Effect Technology (MRET) process for prevention treatment and enhancement of tumor resistance of animals to two types of oncology diseases in vivo on 500 mice are presented. The research conducted on physical parameters of water confirmed that MRET activation process contributed to substantial modification of the basic physical-molecular properties of distilled water (substantial reduction of viscosity as a function of applied tangent pressure, as well as substantial decrease of electrical conductivity and dielectric permittivity as functions of the frequencies of applied electromagnetic field). The significant positive effect of MRET activated water on tumor resistance of animals was observed in the process of this investigation in all groups of mice on different fractions of activated water. The best results were observed in the groups of mice on MRET water activated for 30 minutes (optimal regime of activation). The results were better in \u201cpreventive treatment\u201d regime compare to \u201ctherapeutic treatment\u201d regime. Additionally, this investigation confirmed that the long-term preservation of activated water at low temperature (around 0\u00b0C) for 45 days decreased its anti-tumor efficacy but left it on the significantly high level compare to other fractions. The test results point at the dual mechanism of MRET water effect on tumors: the prevention and inhibition of tumor growth together with the reduction of quantity of viable tumor cells. The significant anti-tumor effect of MRET activated distilled water on mice was close to the action of the chemotherapy agents and allowed to avoid the side effects that typically follow chemotherapy treatment of oncology.\r\n\r\nIn the process of investigation of cytotoxic activity of NK-cells the significant increase of lymphocyte cytotoxicity levels was observed when donor mice were treated with MRET water activated for 30 minutes. The results also showed that the extension of the application of MRET water from 14 days to 21 days significantly increased the value of cytotoxicity index. It is possible to admit that the extension of time of application of MRET water will lead to higher levels of enhancement in NK-cells activity. Thus, the application of MRET activated water can be quite promising approach for non-drug stimulation of NK-cells immunization vaccines.\r\n\r\nThe detailed description of this investigation is presented in \u201cBENEFITS MRET WATER\u201d.\r\n\r\n<strong>THE EFFECT OF MRET ACTIVATED MEDIUM ON CELL MORPHOLOGY<\/strong>\r\n\r\nThe in vitro investigations on normal PMBC cells (peripheral blood mononuclear cell) and on HeLa cancer cells (cell line ATCC # CCL-2 cervical adenocarcinoma) and were conducted under the supervision of Patrick Pezzoli, Ph.D. at AltheaDx Technologies, San Diego, USA. The experiments analyzed: cells lysed at 0 hour, cells cultured for 24 hours in untreated medium and cells cultured for 24 hours in medium treated with MRET activator for 30 minutes. DNA samples from each batch were processed and the resultant data was analyzed using Affymetrix Genotyping Console 3.0 to obtain genotype calls and copy number calls. Cell counts and % viability were obtained using the Trypan Blue exclusion technique.\r\n\r\nThe experimental data revealed no difference between the zero hour (control), MRET treated and untreated samples in term of genotypes and copy number calls. Thus, MRET activation of water based medium did not induce any changes in cells on genetic level.\r\n\r\nThe studies showed that in MRET activated medium the viability of normal cells (PBMC) was higher (Table 1), and the viability of cancer cells (HeLa) was lower (Table 2) compared to their viability in untreated medium.\r\n<table border=\"1\" width=\"200\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td colspan=\"4\">Table 1: PBMC cell counts and % viability<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Sample<\/td>\r\n<td>Cell Count<\/td>\r\n<td>% Viability<\/td>\r\n<td>Viable cells<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>0 hour<\/td>\r\n<td>3.27x106<\/td>\r\n<td>91.5<\/td>\r\n<td>2.99x106<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Untreated<\/td>\r\n<td>8.70x105<\/td>\r\n<td>83.4<\/td>\r\n<td>0.73x106<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Treated<\/td>\r\n<td>7.73x105<\/td>\r\n<td>88.8<\/td>\r\n<td>0.69x106<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n\u00a0\r\n<table border=\"1\" width=\"266\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td colspan=\"4\">Table 2: HeLa cell counts and % viability<\/td>\r\n<\/tr>\r\n<tr>\r\n<td width=\"60\">Sample<\/td>\r\n<td width=\"40\">Cell Count<\/td>\r\n<td width=\"50\">% Viability<\/td>\r\n<td width=\"88\">Viable cells<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>0 hour<\/td>\r\n<td>3x106<\/td>\r\n<td>92<\/td>\r\n<td>3.27x106<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Untreated<\/td>\r\n<td>7x106<\/td>\r\n<td>97<\/td>\r\n<td>6.79x106<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Treated<\/td>\r\n<td>5x106<\/td>\r\n<td>92<\/td>\r\n<td>4.60x106<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nFor normal cells (PBMC) the changes in cell counts were similar for untreated and MRET treated medium (Fig 1). Thus, MRET treatment did not affect the growth of normal cells.\r\n\r\nFor cancer cells (HeLa) the experimental data revealed significant inhibition of cancer cells growth in MRET treated medium. The growth of viable cancer cells was inhibited by 54% in MRET treated medium compared to untreated medium (Fig 2).\r\n<table border=\"1\" width=\"382\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"180\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/graph1.gif\" alt=\"\" \/><\/div><\/td>\r\n<td width=\"186\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/graph2.gif\" alt=\"\" \/><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Fig 1: Viable PBMC cell counts after 24 hours of incubation<\/td>\r\n<td>Fig 2: Viable HeLa cell counts after 24 hours of incubation<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nThe results of AltheaDx research on HeLa cancer cells in vitro support the results obtained earlier in the investigation regarding the effects of MRET water on tumor resistance in animal model. The study on 500 mice was conducted under the supervision of Professor V. Vysotskii, S. Olishevsky, Ph.D. and Y. Yanish, Ph.D. at Kyiv Institute of Experimental Pathology, Oncology and Radiobiology of Ukrainian Academy of Science. It showed substantial inhibition of growth of viable tumor cells following the consumption of MRET water. In the course of this investigation the groups of mice in \u201cpreventive regime\u201d ingested MRET water for 2 weeks prior to the inoculation of Ehrlich carcinoma cancer cells and for 3 weeks after the inoculation. The groups of mice in \u201ctherapeutic regime\u201d ingested MRET water only during 3 weeks after the inoculation of Ehrlich carcinoma cancer cells. Following the consumption of MRET water activated for 30 minutes (the optimal time of activation) the growth of viable tumor cells was inhibited by 76% in \u201cpreventive regime\u201d and by 55% in \u201ctherapeutic regime.\u201d\r\n\r\nAs a conclusion it is possible to say that the studies conducted at AltheaDx Technology confirmed that MRET activated water did not affect the cells on genetic level; it affected the morphology of normal cells in positive way increasing their viability and promoted significant inhibition of growth of cancer cells.\r\n\r\nMRET Rebounding Effect on White Blood Cell Counts\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Picture_20.png\" alt=\"\" \/><\/p>\r\nA clinical observation was conducted on a patient undergoing chemotherapy treatment for metastasized naso-pharyngeal cancer. On a regular basis, WBC counts usually decrease to very low level. The rebounding of WBC from this low range takes about 3-5 weeks. The ingestion of MRET water prevented the decrease of WBC counts to their lowest level and helped to regain the pre-chemotherapy level within unusually short period of time of 3 days.\r\n\r\n\u00a0\r\n\r\nThus, the clinical observation revealed that on the 10th day after the beginning of chemotherapy (in 3 days after WBC counts dropped to 10% of pre-chemotherapy level) WBC counts rebounded to 93% of their pre-chemotherapy level. In compliance with Student\u2019s Distribution criteria the rebounding of WBC was higher than 70% of pre-chemotherapy level with p=0.05.\r\n\r\n<strong>ANTIBACTERIAL EFFECT OF MRET WATER<\/strong>\r\n\r\nTesting conducted at C.A.I. Environmental Laboratory, Carlsbad, USA revealed the significant reduction of the amount of total coliforms following the process of MRET activation. In the rainwater activated for 30 minutes the amount of total coliforms decreased by 86% after the process of water activation. This test confirms that MRET water acts as antibacterial agent, providing sterilization effect.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/germicidal_1.jpg\" alt=\"\" \/><\/p>\r\nThe effect of MRET activated water on Escherichia coli K-12 and on Complex Microbiological Associations\r\n\r\nThe research was conducted at Kiev Institute of Microbiology and Virology of Ukrainian Academy of Science.\r\n\r\nI. MRET activated water inhibitory effect on growth of conditionally pathogenic bacteria Escherichia coli K-12 in aerobic environment\r\n\r\nThe investigation revealed the significant effect of MRET-activated nutrient medium in aerobic environment on the process of growth and reproduction of E.coli microorganisms, their division, the size of colonies and the modification of forms of culture cells. It was observed that at low initial concentration of cells of investigated culture Escherichia coli K-12 MRET nutrient medium activated during 30 minutes and 60 minutes inhibited the growth of culture 27 and 303 times respectively during the 25 hours of experiment.\r\n\r\nInitial view of Petri dishes with different fractions of nutrient medium at the beginning of experiment is presented on Fig 1.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Ecoli_1.jpg\" alt=\"\" \/><\/p>\r\nFig 1: Petri dishes at the beginning of experiment. Identical very small amount of Escherichia coli K-12 cells was introduced on a surface of non-activated nutrient medium of control dishes and on a surface of dishes with nutrient medium MRET-activated for 30 and 60 minutes(tact=0.5h and tact=1.0h) in aerobic environment. There are no colonies of microorganisms in Petri dishes in the beginning of experiment.\r\n\r\nPetri dishes with grown colonies and statistical parameters of the colonies after 23 hours of experiments are presented on Fig 2: (a) non-activated nutrient medium (control); (b) nutrient medium activated for 30 minutes; (c) nutrient medium activated for 60 minutes. Petri dishes after 29 hours of experiment are shown on Fig 3. The significant inhibition of growth of E.coli in activated samples was revealed and it confirmed the strong bacteriostatic effect of MRET-activated medium.\r\n<table border=\"1\" width=\"200\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig2a.jpg\" alt=\"\" \/><\/td>\r\n<td><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig2b.jpg\" alt=\"\" \/><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>(a) Control:\r\nNumber of colonies NC = 1.7x108 CFU\/ml.\r\nAverage diameter of grown colonies d = 1.1 mm.<\/td>\r\n<td>(b) MRET-activated, tact = 30 minutes:\r\nNumber of colonies N0.5 = 6.4x106 CFU\/ml.\r\nAverage diameter of grown colonies d = 1.8 mm.<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<table border=\"1\" width=\"200\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig2c.jpg\" alt=\"\" \/><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>(c) MRET-activated, tact = 60 minutes:\r\nNumber of colonies N1.0 = 5.2x105 CFU\/ml.\r\nAverage diameter of grown colonies is d = 1.5 mm.\r\nFig 2: Petri dishes after 23 hours of experiment.<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n\u00a0\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Ecoli_3.jpg\" alt=\"\" \/><\/p>\r\n\u00a0\r\n\r\nFig 3: Selected Petri dishes with grown colonies of E.coli K-12 after 29 hours of experiment.\r\n\r\nThis experiment shows that MRET-activation process has very strong bacteriostatic effect on conditionally pathogenic E.coli microorganisms and that the inhibition of E.coli growth is more effective when activation time is increased. It was observed that at low initial concentration of cells of E.coli in nutrient medium MRET-activation during 30 minutes and 60 minutes period of time inhibited the culture growth NC\/N0.5 = 27 and NC\/N1.0 = 303 times respectively after 25 hours of experiment (Fig 4). Consequently, the level of bacteriostatic activity was 96% in 30 minutes activated nutrient medium and 99.7% in 60 minutes activated medium. Thus, the direct correlation between bacteriostatic activity of MRET-activated nutrient medium and the time of activation was confirmed.\r\n\r\nInhibition of E.coli bacteria growth in aerobic environment\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig4.jpg\" alt=\"\" \/><\/p>\r\nFig 4: The inhibition of E.coli growth in aerobic environment: 303 times (tact=1.0 hour) and 27 times (tact=0.5hour) after 25 hours of experiment (blue color - control, red - 30 minutes and green - 60 minutes MRET-activated medium).\r\n\r\nThis experiment also revealed the strong effect of MRET-activated water on the process of division of E.coli microorganisms, the modification of forms of culture cells and the size of colonies. It was observed that one of the reasons of abnormally low growth of E.coli bacteria was related to the modification of the process of cell division in MRET-activated nutrient medium. In the process of growth and reproduction a large number of cells did not separate from each other and the linear line-ups consisting of 2-3 sequentially paired cells were formed. The culture cells grown in non-activated and MRET activated medium are shown on Fig 5 and Fig 6 respectively.\r\n<table border=\"1\" width=\"200\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig5.jpg\" alt=\"\" \/><\/td>\r\n<td><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig6.jpg\" alt=\"\" \/><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>Fig 5: Cells of Escherichia coli K-12 grown in non-activated medium.<\/td>\r\n<td>Fig 6: Cells of Escherichia coli K-12 grown in MRET-activated medium (tact =1 hour).<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nII. The effect of MRET water on metabolic activity of E.coli bacteria in aerobic and anaerobic environment\r\n\r\nReductant activity is an integral characteristic of metabolic activity of microorganisms and it is measured with the help of Sodium Resasurine color indicator in the percentage degree of discoloration (purple = 0%, red = 50%, transparent = 100%). The reductant activity of E.coli bacteria reduced up to 3 times in 30 minutes MRET-activated water and up to 1.6 times in 60 minutes activated water during the first 6 hours of experiment in aerobic environment (Fig 7 and 8).\r\n\r\n<img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig7a.jpg\" alt=\"\" \/><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig7b.jpg\" alt=\"\" \/>\r\n\r\nK \u2013 Control;\r\n0.5 \u2013 0.5 hour MRET-activated water;\r\n1.0 \u2013 1 hour MRET-activated water\r\n<table border=\"1\" width=\"445\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"243\">RC = 0.2, R0.5 = 0.1, R1.0 = 0.4\r\nK0.5 = 0.5, K1.0 = 2.0\r\nDC = D0.5 = D1.0<\/td>\r\n<td width=\"186\">RC = 25, R0.5 = 9, R1.0 = 19\r\nK0.5 = 0.36, K1.0 = 0.76\r\nDC = D0.5 = D1.0<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nFig 7: Comparative test on metabolic (reductant) activity of E.coli (control samples, 30 and 60 minutes MRET- activated water) in aerobic environment: R - reductant activity (in Control, 0.5 hour and 1.0 hour MRET-activated water), K - relative reductant activity, D - optical density.\r\n\r\nRelative Reductant Activity of E.coli bacteria in aerobic environment\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig8.gif\" alt=\"\" \/><\/p>\r\nFig 8: Relative Reductant Activity of E.coli in MRET water activated for 0.5 hour (K0.5=R0.5\/RC - red color) and for 1.0 hour (K1.0=R1.0\/RC - green color) compare to control non-activated samples (KC=1 - blue color) in aerobic environment.\r\n\r\nThis experiment showed that there was no direct correlation between the inhibition of metabolic (reductant) activity and the inhibition of growth of E.coli (bacteriostatic activity) in MRET activated water. The bacteriostatic effect is substantially higher in 60 minutes activated water and the inhibition of reductant activity during the first 3 hours is higher in 30 minutes activated water. Thus, this experiment revealed that the optimum time of activation for the maximum inhibition of metabolic activity of E.coli bacteria in aerobic environment is 30 minutes. The same optimum time of activation was found in the process of another investigation regarding the application of MRET activated water for preventive treatment and enhancement of tumor resistance in vivo on 500 mice for two types of cancer conducted at Kiev Institute of Experimental Pathology, Oncology and Radiobiology of Ukrainian Academy of Science.\r\n\r\nTaking in consideration that a small population of pathogenic bacteria, such as E.coli, is usually presented in complex microbial associations in the intestine of the body, the test on metabolic activity of E.coli bacteria in anaerobic environment was conducted. Anaerobic environment simulates the environmental conditions similar to the conditions in the intestine of humans and animals. The investigation showed that the reductant activity of E.coli bacteria in anaerobic environment practically did not change (Fig 9 and 10).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig9.jpg\" alt=\"\" \/><\/p>\r\nK \u2013 Control; 0.5 \u2013 0.5 hour MRET-activated water; 1.0 \u2013 1 hour MRET-activated water; KSTER \u2013 reference to sterility\r\n\r\nFig 9: Comparative test on metabolic (reductant) activity of E.coli (control samples, 0.5 hour and 1.0 hour MRET- activated water, KSTER - reference to sterility) in anaerobic environment: R - reductant activity (in Control, 0.5 hour and 1.0 hour MRET-activated water), K - relative reductant activity, D - optical density, V - gas volume in the bottles.\r\n\r\nReductant Activity of E.coli bacteria in anaerobic environment\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig10.gif\" alt=\"\" \/><\/p>\r\nFig 10: Reductant Activity of E.coli in 30 and 60 minutes MRET-activated water and in Control non-activated samples (R0.5 - red color, R1.0 - green color, RC - blue color) in anaerobic environment.\r\n\r\nThis experiment revealed that the process of MRET activation did not have any significant effect on reductant activity of E.coli bacteria in anaerobic environment.\r\n\r\nIII. The stimulating effect of MRET water on metabolic activity of Complex Microbial Associations in anaerobic environment\r\n\r\nIn order to simulate the environmental conditions similar to the conditions in the intestine of humans and animals the test on metabolic activity of microbial associations was conducted in anaerobic environment. It was found that MRET-activated water substantially increased reductant activity of complex microbial associations during the first several hours of experiment (Fig 11).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig11.jpg\" alt=\"\" \/><\/p>\r\n1.0 \u2013 1 hour MRET-activated water; 0.5 \u2013 0.5 hour MRET-activated water; K \u2013 Control\r\n\r\nFig 11: Comparative test on metabolic (reductant) activity of microbial associations (1.0 hour and 0.5 hour MRET- activated water and Control samples) in anaerobic environment: R - reductant activity (in Control, 0.5 hour and 1.0 hour MRET-activated water), K - relative reductant activity, V - gas volume in the bottles.\r\n\r\nThis experiment revealed that the optimum time of activation for the maximum increase of metabolic activity of microbial associations in anaerobic environment was 30 minutes. The same optimum time of activation was found in the process of inhibition of metabolic activity of E.coli in aerobic environment and in another investigation regarding the application of MRET activated water for preventive treatment and enhancement of tumor resistance in vivo.\r\n\r\n<strong>CONCLUSIONS<\/strong>\r\n\r\nThis investigation revealed that at low initial concentration of cells of conditionally pathogenic microbiological culture Escherichia coli K-12 in water based nutrient medium activated for 30 minutes and 60 minutes the growth of culture was inhibited 27 and 303 times respectively after the 25 hours of experiment in aerobic environment. This experiment also revealed the strong effect of MRET activated water on the process of division of E.coli microorganisms, the modification of forms of culture cells and the size of colonies. It was observed that one of the reasons of abnormally low growth of E.coli population was related to the modification of the process of cell division in MRET-activated nutrient medium. These results allow admitting that the process of MRET activation and the sterilization effect of MRET water can be applied in food industry and for water purification.\r\n\r\nThe second stage of investigation revealed that the metabolic (reductant) activity of E.coli bacteria reduced up to 3 times in 30 minutes activated water and up to 1.6 times in 60 minutes activated water during the first 6 hours of experiment in aerobic environment. Another experiment showed that the process of MRET-activation did not affect the reductant activity of E.coli bacteria in anaerobic environment and, consequently, should not affect a small population of conditionally pathogenic bacteria, such as E.coli, usually presented in microbial associations in the intestine of the body.\r\n\r\nIn order to simulate the environmental conditions similar to the conditions in the intestine of humans and animals the test on metabolic activity of complex microbial associations was conducted in anaerobic environment. It was discovered that MRET activated process substantially increased reductant activity of complex microbial associations during the first hours of experiment. The same 30 minutes optimum time of activation was observed in the process of inhibition of metabolic activity of conditionally pathogenic E.coli bacteria in aerobic environment and for the maximum increase of metabolic activity of complex microbial associations in anaerobic environment (presented in the intestine). The previous investigation regarding the application of MRET activated water for preventive treatment and enhancement of tumor resistance in oncology in vivo on 500 mice also showed the best results on 30 minutes MRET-activated water. Thus, this investigation shows that the ingestion of MRET water is beneficial for the process of digestion and can enhance metabolism of the body.\r\n\r\nThe Effect of MRET Activated Water on Staphylococcal Infection in vivo in Animal Model (on the cells of immune system) and in vitro on the Culture of Staphylococcus aureus Wood-46\r\n\r\nI. The Effect of MRET Water on Staphylococcal Infection in vivo in Animal Model\r\n\r\nThe research was conducted at Kiyv National Shevchenko University, Ukraine on 400 mice. The mice-male of line BALB in the age of 11 \u2013 13 weeks and of the weight 18 \u2013 21 grams were used. In the process of investigation all mice were divided in three groups. Prior to the inoculation of Staphylococcus aureus Wood-46 culture one group of mice consumed MRET water during 4 weeks (Group 1), another group consumed MRET water during 2 weeks (Group 2), the control group consumed non-activated ordinary distilled water. During the following 2 weeks of experiment the first two groups continued to consume MRET water and the control group consumed ordinary distilled water. The first line of experiments was conducted on 225 mice in order to analyze the persistence of pathogen in homogenate of kidneys of mice comparing 5 groups of mice (two Group 1 and two Group 2 on 15 minutes and 30 minutes MRET activated water and Control). After preliminary experiments the optimal 30 minutes MRET activated water (distilled) was chosen for the main line of investigation.\r\n\r\n<strong>RESULTS:<\/strong>\r\n\r\n1. Significant protective properties of MRET water.\r\n\r\nThe significant protective properties of MRET water were confirmed by substantial decrease of Staphylococcus CFU (colony forming units) in homogenate of kidneys of mice on MRET water compare to control group of mice following the intra-peritoneal staphylococcal infection after the first 24 hours. The analysis of data in the beginning of experiments leads to the conclusion that significant decrease of pathogen\u2019s colonies in homogenate of kidneys of mice on MRET water begins only after 24 hours following the inoculation of Staphylococcus culture. The results on 30 minutes activated water were much better than on 15 minutes activated water and all further experiments were conducted on 30 minute activated water.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Aureus_Wood_table1.png\" alt=\"\" \/><\/p>\r\n2. The consumption of MRET water eliminated the death rate from 30% (control group) to 0% (MRET group) during the first 9 days of experiment.\r\n\r\nThere was no case of animal death in all investigated groups within the first 24 hours after intra-peritoneal inoculation of Staphylococcus culture, which is a pretty standard result. During the next 8 days 30% of animals died in control group which also is a standard result. But there were no death cases in both groups of mice that ingested MRET activated water and it is a remarkable result. Nevertheless, the main consequences of Staphylococcus infection do not manifest in death of animals as in case of oncology diseases. Staphylococcus virus affects the live systems and organs of the body. These pathogenic microorganisms cause inflammations, suppurations, abscesses, furuncles, quinsy, cepsical conditions, etc. That\u2019s why a detailed investigation of the process of stimulation by MRET water of phagocytes and of lymphoid organs of immune system of mice infected with Staphylococcus aureus culture was conducted and is presented in this report.\r\n\r\n3. The development of the local acute inflammation is essentially suppressed in case of ingestion of MRET activated water.\r\n\r\nThe local inflammation was induced with the help of the inoculation of Staphylococcus aureus culture into the hinder left paw. The ordinary inflammatory reaction was observed in the group of mice on non-activated water: the intensive reddening of the hinder left paw (Fig 1). Both groups of mice on MRET water did not develop any reddening the hinder left paw inoculated with Staphylococcus aureus culture (Fig 2). The results of this experiment confirm the fact of the substantial inhibition of inflammatory infection in case of the regular consumption of MRET water.\r\n\r\n4. The consumption of MRET water stimulates the activity of phagocytic system and the level of natural resistance of animals to pathogenic microorganisms.\r\n\r\nFor the following series of experiments the inoculation of Staphylococcus aureus Wood-46 was conducted intra-peritoneal in dose LD30 in order to spread infection all over the body.\r\n\r\nThe phagocytic system is one of the main factors of natural non-specific cellular resistance to infections and inflammations. It is the first line of protection of an organism against penetration and reproduction of pathogenic microorganisms. The protective role of phagocytic cells is based on their capacity to identify, engulf and utilize the alien agents penetrated into internal environment of a macro-organism. Phagocytosis is the main mechanism of natural resistance especially at the first stage of contagious process; it is a regular part of formation of the specific immune response.\r\n\r\nThe most common methodology applied in the studies of the functional activity of phagocytes is the examination of their phagocytic (engulfing of alien cells) and oxygen-dependent bactericidal activity. Phagocytic activity of neutrophils and macrophages is estimated based on Index of Phagocytosis (percentage of the phagocytes which engulfed test-bacteria) and on Phagocytic Number (average number of test-bacteria engulfed by one phagocyte). The cultures of Staphylococcus aureus and Latex are usually used as test-bacteria. The oxygen-dependent bactericidal activity of phagocytes is studied with the help of NBT-test: an oxygen-dependent reduction of Nitro Blue Tetrazolium into an insoluble Diformazan of Nitro Blue Tetrazolium derivative by phagocytes. With the help of NBT-test it is possible to distinguish the activated phagocytes from the non-activated ones.\r\n\r\nMRET water stimulated the phagocytic capacities of neutrophils of a peripheral blood and peritoneal macrophages increasing their phagocytic activity, particularly Phagocytic Indexs (Fig 3A) and Phagocytic Number (Fig 3B). It also stimulated their oxygen-dependent bactericidal activity, particularly the increase of quantity of NBT-positive phagocytes (Fig 4).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Aureus_Wood_fig3a.gif\" alt=\"\" \/><\/p>\r\nFig 3A: Phagocytic Index of neutrophils and macrophages in two weeks of experiment (object of phagocytosis - Staphylococcus aureus): 1 \u2013 Control group; 2 \u2013 Mice on MRET water (preventive for 4 weeks); 3 \u2013 Mice on MRET water (preventive for 2 weeks).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Aureus_Wood_fig3b.gif\" alt=\"\" \/><\/p>\r\nFig 3B: Phagocytic Number of neutrophils and macrophags in two weeks of experiment (object of phagocytosis \u2013 Staphylococcus aureus): 1 \u2013 Control group; 2 \u2013 Mice on MRET water (preventive for 4 weeks); 3 \u2013 Mice on MRET water (preventive for 2 weeks).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/Aureus_Wood_fig4.gif\" alt=\"\" \/><\/p>\r\nFig 4: Oxygen-depended bactericidal activity (NBT-test) of neutrophils and macrophages in two weeks of experiment:\r\n1 \u2013 Control group; 2 \u2013 Mice on MRET water (preventive for 4 weeks); 3 \u2013 Mice on MRET water (preventive for 2 weeks).\r\n\r\nThese experiments confirmed the increase of effective potentials of phagocytes which constitute one of the main factors of natural protection of an organism and initiate the immune response.\r\n\r\nThe analysis of data in the beginning of experiments leads to the conclusion that significant intensification of phagocytic and bactericidal activity of macrophages and neutraphils of mice on MRET water begins only after 24 hours following the intra-peritoneal inoculation of Staphylococcus culture. At the end of two weeks of experiment the mean values of studied parameters in both groups of mice on MRET water substantially increased compare to the control group. The differences in mean values of the parameters of functional activity of phagocytes of groups of mice consuming MRET water compare to the control group of mice on non-activated water were statistically significant with p<0.05 (for Phagocytic Index and NBT-test). These results confirm the significant intensification of phagocytic and bactericidal activity and of immune system response following the consumption of MRET water.\r\n\r\nThe differences in mean values of studied parameters for the groups of mice on MRET water compare to each other were statistically insignificant, which confirms the similarity of the level of beneficial effect of MRET water in both groups. This fact also confirms that the regular consumption of MRET water provides health benefits in rather short time (2 weeks in case of the animal mice model).\r\n\r\n5. The consumption of MRET water substantially enhances the immune activity of lymphoid organs.\r\n\r\nBy the end of another series of experiments in both groups of mice on MRET water was observed substantial statistically significant (p<0.05) increase of the weight and the cellularity (quantity of cells) of a spleen and lymph nodes as well as the insignificant increase of weight and cellularity of thymus (Fig 5 and Fig 6).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig5.gif\" alt=\"\" \/><\/p>\r\nFig 5: The weight of lymphoid organs in two weeks of experiment: 1 \u2013 Control group; 2 \u2013 Mice on MRET water (preventive for 4 weeks); 3 \u2013 Mice on MRET water (preventive for 2 weeks).\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/fig6.gif\" alt=\"\" \/><\/p>\r\nFig 6: The cellularity of lymphoid organs in two weeks of experiment: 1 \u2013 Control group; 2 \u2013 Mice on MRET water (preventive for 4 weeks); 3 \u2013 Mice on MRET water (preventive for 2 weeks).\r\n\r\nThese results confirm the fact of significant intensification of immune system response in animals on MRET water subject to Staphylococcus infection. The difference in studied parameters between the groups of mice on MRET water (4 weeks and 2 weeks of preventive consumption of MRET water) was insignificant which confirms quite fast beneficial effect of MRET water on the immune activity of lymphoid organs.\r\n\r\nIn the beginning of experiment the cellularity and the weight of lymphoid organs in MRET groups did not show the distinct tendency to modifications. It is reasonable to admit that the consumption of MRET water affects the weight and the cellularity of lymphoid organs only during the infection period.\r\n\r\n<strong>CONCLUSIONS:<\/strong>\r\n\r\nThe consumption of MRET activated water significantly enhances the factors of natural resistance of the body which constitute the first line of protection of an organism against the penetration and reproduction of pathogenic microorganisms.\r\n\r\nThe analysis of data in the beginning of experiment leads to the conclusion that significant changes in all studied parameters of mice on MRET water (decrease of pathogen colonies in homogenate of kidneys, increase of the weight and the cellularity of lymphoid organs, intensification of the phagocytic and bactericidal activity of macrophages and neutraphils) begins only after 24 hours following the inoculation of Staphylococcus culture. Another words the consumption of MRET water increases the potentials of immune capacities of the body to counteract the infections without any changes in the vital parameters of immune organs and functions prior to the penetration of infectious pathogens in the body.\r\n\r\nAt the end of two weeks of experiment the mean values of studied parameters in both groups of mice on MRET water (preventive for 4 and 2 weeks respectively) significantly increased compare to the control group. The differences in mean values of the studied parameters of the groups of mice consuming MRET water compare to the control group of mice on non-activated water were statistically significant with p<0.05 (for most of the parameters). These results confirm the significant intensification of phagocytic activity and of immune system response following the consumption of MRET water.\r\n\r\nThe differences in mean values of studied parameters for the groups of mice on MRET water compare to each other were statistically insignificant, which confirms the similarity of the level of the beneficial effect of MRET water in both groups. This fact also confirms that the regular consumption of MRET water provides health benefits in rather short period of time (2 weeks in case of the animal mice model).\r\n\r\nII. The Effect of MRET Activation on the Process of Growth of Staphylococcal Culture in Nutrient Medium\r\n\r\nThe following experiments were designed to study the effect of MRET activation on the process of growth and development of Staphylococcus aureus Wood-46 culture in vitro in nutrient medium (MPA \u2013 meat-peptone agar). The bacterial culture was grown overnight to stationary phase and then platted on MPA in the form of suspension at different inoculation densities. The MPA with culture was MRET activated during the different periods of time (activation for 15 minutes, 30 minutes, 45 minutes, and 60 minutes respectively) following the requirements of sterility. Petri dishes with activated and non-activated medium (MPA with culture) were covered with glass caps (aerobic environment) and placed in the thermostat for cultivation at a temperature of 37oC during 18-24 hours.\r\n\r\nAfter the cultivation the morphological and tinctorial properties of cultures were observed and the numbers of colonies grown on MPA were counted. The bacteriostatic activity of MRET activated nutrient medium (MPA) was measured as an Index of Bacteriostatic Activity (IBA). An Index of Bacteriostatic Activity is defined as a coefficient of the inhibition of growth and reproduction of pathogens in bacteriostatic medium, particularly in MRET activated nutrient medium. It is calculated as reduction of the number of colonies (CFU \u2013 Colony Forming Units) in MRET activated medium related to the control samples not exposed to the activation:\r\n\r\nIBA = (Ncontrol \u2013 Nact)\/Ncontrol\r\nwhere N \u2013 number of bacteria colonies (CFU) in Control (non-activated) and MRET activated nutrient medium, respectively.\r\n\r\nIn order to verify the sterility of experiments Petri dishes with nutrient medium (MPA) without staphylococcal culture were exposed to the process of activation and then were kept in the thermostat. No colonies of culture were observed that confirms the sterility of environment.\r\n\r\n<strong>RESULTS: <\/strong>\r\n\r\nFollowing the investigation the direct correlation between times of activation (tact), initial concentrations of staphylococcal culture (N0) and a number of colonies grown on MRET activated medium were observed. The results are presented below in the form of a series of photos of Petri dishes with the colonies grown on MPA surfaces and the following diagrams based on the data of these experiments (Fig 7 \u2013 12).\r\n\r\nIn the process of investigation the effect of MRET activation on the growth of staphylococcal culture at rather small initial concentration of pathogens was analyzed. The data corresponding to higher initial concentrations N0 > 103 bacteria\/ml were not analyzed due to the difficulties related to calculation of very high values of a number of colonies, despite the fact of the high bacteriostatic activity of MRET activated nutrient medium in case of high initial concentrations.\r\n\r\nThe highly significant bacteriostatic effect of 92 \u2013 93% was observed after MRET activation for 30 minutes and more of cultures with initial concentration N0 = 103 bacteria\/ml (Fig 7 and 8) and of 70 \u2013 90% with initial concentration of N0 = 102 bacteria\/ml (Fig 9 and 10). In case of cultures with low initial concentration N0 = 10 bacteria\/ml the bacteriostatic activity in 15 minutes activated nutrient medium exceeded 93% and in 30 minutes activated nutrient medium was observed 100% inhibition of staphylococcal colonies (Fig 11 and 12).\r\n\r\n\u00a0\r\n<table border=\"1\" width=\"530\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"268\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig7a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<td width=\"197\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig7b.jpg\" alt=\"\" \/><\/div>\r\n<div align=\"center\"><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 103 bacteria\/ml, Control<\/td>\r\n<td>\r\nN0 = 103 bacteria\/ml, tact = 15 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<table border=\"1\" width=\"532\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"252\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig7a.jpg\" alt=\"\" align=\"middle\" \/><\/div><\/td>\r\n<td width=\"264\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig7b.jpg\" alt=\"\" \/><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 103 bacteria\/ml, tact = 30 min<\/td>\r\n<td>\r\nN0 = 103 bacteria\/ml, tact = 45 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<table border=\"1\" width=\"268\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"258\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig7a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 103 bacteria\/ml, tact = 60 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nFig 7: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 103 bacteria\/ml.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig8.gif\" alt=\"\" \/><\/p>\r\nFig 8: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 103 bacteria\/ml. IBA \u2013 Index of Bacteriostatic Activity (reduction of the number of colonies related to the control samples not exposed to activation).\r\n<table border=\"1\" width=\"530\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"268\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig9a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<td width=\"197\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig9b.jpg\" alt=\"\" \/><\/div>\r\n<div align=\"center\"><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 102 bacteria\/ml, Control<\/td>\r\n<td>\r\nN0 = 102 bacteria\/ml, tact = 15 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<table border=\"1\" width=\"532\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"252\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig9a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<td width=\"264\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig9b.jpg\" alt=\"\" \/><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 102 bacteria\/ml, tact = 30 min<\/td>\r\n<td>\r\nN0 = 102 bacteria\/ml, tact = 45 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<table border=\"1\" width=\"268\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"258\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig9a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 102 bacteria\/ml, tact = 60 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nFig 9: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 102 bacteria\/ml.\r\n\r\nFig 10: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 102 bacteria\/ml. IBA \u2013 Index of Bacteriostatic Activity (reduction of the number of colonies related to the control samples not exposed to activation).\r\n<table border=\"1\" width=\"530\" align=\"center\">\r\n<tbody>\r\n<tr>\r\n<td width=\"268\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig11a.jpg\" alt=\"\" \/><\/div><\/td>\r\n<td width=\"197\">\r\n<div align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig11b.jpg\" alt=\"\" \/><\/div>\r\n<div align=\"center\"><\/div><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>N0 = 10 bacteria\/ml, Control<\/td>\r\n<td>\r\nN0 = 10 bacteria\/ml, tact = 15 min<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nFig 11: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 10 bacteria\/ml.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/aw_fig12.gif\" alt=\"\" \/><\/p>\r\nFig 12: The effect of time duration of MRET activation on the inhibition of growth of culture of Staphylococcus aureus Wood-46 with initial concentration of culture N0 = 10 bacteria\/ml. IBA \u2013 Index of Bacteriostatic Activity (reduction of the number of colonies related to the control samples not exposed to activation).\r\n\r\n<strong>CONCLUSIONS:<\/strong>\r\n\r\n1. MRET activation of the water based nutrient medium with suspended staphylococcal culture leads to the origination of high bacteriostatic activity of nutrient medium which depends on the time duration of activation and initial concentration of culture cells.\r\n\r\n2. The bacteriostatic activity increases following the increase of time of activation (the times of activation up to 60 minutes were studied).\r\n\r\n3. The efficacy of bacteriostatic activity increases following the decrease of initial concentration of the suspension of staphylococcal culture. The process of MRET activation is most effective on culture suspensions with the concentration not more than 103 bacteria\/ml.\r\n\r\n4. The results of investigation provide the evidence regarding the high efficacy of MRET activation on the inhibition of growth of colonies and reproduction of staphylococcal microorganisms in vitro. These results allow admitting that the process of MRET activation and the sterilization effect of MRET water can be applied in food industry and for water purification.\r\n\r\nLive Blood Cell Analysis\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/lbt1.jpg\" alt=\"\" \/><\/p>\r\nIn this particular case, the blood sample of the subject before Activated Water ingestion shows free radical attack on cells. Note the \u201cspiky\u201d blood cells that take almost 90% of specimen. 30 minutes later, after Activated Water ingestion, the blood specimen shows non free radical environment.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/lbt2.jpg\" alt=\"\" \/><\/p>\r\nIn this particular case, the blood sample of the subject before Activated Water ingestion shows so called Rouleau formation when blood cells are stacked, forming a worm-like pattern. 30 minutes later, after Activated Water ingestion, most of the worm-like patterns broke up, forming individual patterns of nicely round spheres.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/mret_synopsis_test_7.jpg\" alt=\"\" \/><\/p>\r\n<strong>MRET water effect on seed germination and growth of plants<\/strong>\r\n\r\nThe examinations of influence of MRET activated water on plants was conducted during 3 months period at Kiev Institute of Plants Genetics of Ukrainian Academy of Sciences under supervision of Prof. V. Vysotskii, Kiev National University. MRET activated water accelerated the process of seed germination of several plants (particularly of cabbage, pumpkin, string bean, garden radish and peas) and enhanced their growth cycle.\r\n<p align=\"center\"><img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/mret_synopsis_test_8.jpg\" alt=\"\" \/>\r\n<img src=\"https:\/\/soundhealingcenter.com\/store\/wp-content\/uploads\/2020\/06\/mret_synopsis_test_9.jpg\" alt=\"\" \/><\/p>\r\n\r\n<\/div>","link":"https:\/\/soundhealingcenter.com\/store\/consciousness\/gia\/test-results\/","name":"Test Results","slug":"test-results","taxonomy":"product_cat","parent":34,"meta":[],"menu_order":0,"_links":{"self":[{"href":"https:\/\/soundhealingcenter.com\/store\/wp-json\/wp\/v2\/product_cat\/83","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/soundhealingcenter.com\/store\/wp-json\/wp\/v2\/product_cat"}],"about":[{"href":"https:\/\/soundhealingcenter.com\/store\/wp-json\/wp\/v2\/taxonomies\/product_cat"}],"up":[{"embeddable":true,"href":"https:\/\/soundhealingcenter.com\/store\/wp-json\/wp\/v2\/product_cat\/34"}],"wp:post_type":[{"href":"https:\/\/soundhealingcenter.com\/store\/wp-json\/wp\/v2\/product?product_cat=83"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}