Title of Invention | DEVICE FOR RECORDING POLARIZED ELECTROMAGNETIC RADIATION OF INACTIVATED STRAIN OF PATHOGENIC MICROORGANISMS ONTO A CRYSTAL, DEVICE FOR CHANGING ACTIVITY OF STRAIN OFPATHOGENIC MICROORGANISMS. |
---|---|
Abstract | TITLE: DEVICE FOR RECORDING POLARIZED ELECTROMAGNETIC RADIATION OF INACTIVATED STRAIN OF PATHOGENIC MICROORGANISMS ONTO A CRYSTAL, DEVICE FOR CHANGING ACTIVITY OF STRAIN OFPATHOGENIC MICROORGANISMS. The present invention relates to a device for recording polarized electromagnetic radiation of an inactivated strain of pathohgenic microorganisms onto a crystal and a device for changing the activity of a strin of pathogenic microorganisms. The invention may be used for inactivation and subsequent elimination of pathogenic and conditionally pathogenic microorganisms in a human or animal organism. |
Full Text | The present invention relates to medical engineering, and more exactly to a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms onto a crystal and a device for changing the activity of a strain of pathogenic microorganisms. The invention may be used for inactivation and subsequent elimination of pathogenic and conditionally pathogenic microorganisms from a human pr animal organism. The discovery "Phenomenon of intracellular distanced electromagnetic interactions in a system of two tissue cultures" (registered in the USSR State Register of Discoveries of 15 February 1966, diploma 122, authors V.P. Kaznacheev, S.P. Shurin, L.P. Mikhailova) was placed at the base of the present invention. An earlier unknown phenomenon of distant intracellular electromagnetic interactions between two identical tissue cultures during the action of factors on one of them, the factors being of biological, chemical or physical nature, with a characteristic reaction of another culture in the form of a "mirror" cytopathic effect, which determines the cellular system as a detector of the modulation features of electromagnetic radiation, was experimentally established. Thus, a new information channel in biological systems was detected, and an approach to evaluation of quantum phenomenon in the mechanisms of functioning of a genetic cell program and processes of encoding information in specialized cellular systems was also experimentally developed. The possibility appeared for investigation of means for acting on pathological processes via correction of interference occurring in the photon channel of information transmission. It is presumed that this may be related to selection of chemical compounds, converting the initial light flux of a cell into monochromatic radiation. The possibility of using a new principle for treatment of a number of diseases appeared. New methods for diagnosis of the states and prognosis of the behavior of biological objects were developed on the basis of a study of the modulation characteristics of electromagnetic radiation of biosystems. A device for generating electromagnetic radiation for controlling and improving the state of live organisms is also known (see, for example, U.S.A. patent No. 5792184, 1998), the device comprising a source of energy and a generator of biofrequency spectrum, comprising an energy converter and one of the following elements or compounds thereof: Co, Cu, Mo, Li, Be, Mg, Al, Si, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Zn, Ge, Sr, Zr, Nb, Ta, Hf, Se, Tn, W, Au and Y. The device comprises a source of energy, an energy converter, an element ensuring generation of the biofrequency spectrum being imitated. This element is made in the form of a monomer or compounds consisting of one or several chemical elements. After excitation by the energy of transition of energetic levels, electromagnetic radiation is formed in the element in the form of a physical field of the biofrequency spectrum being imitated, which acts on live organisms. Where there is agreement with the poles of intensive absorption of the organism, a large part of the radiation energy carried by electromagnetic waves is absorbed, causing changes in the energy of molecules, atoms or electrons in live organisms, which then causes oscillation, increases biooxidation and improves the energetic state of cells, resulting in an increase of the permeability of cellular membranes. The generator of the biofrequency spectrum being imitated comprises a substrate of non- metals or ceramic, a radiating layer applied onto the substrate and consisting of borides, nitrides, carbides, sulfides or fluorides, mixed with a liquid binder., and an energy converter in the form of a electrical heating wire disposed in the substrate and arranged at the end faces of the substrate to convert electrical energy into thermal energy. The heat formed by the heating wire is used to excite chemical elements in the radiation layer. This device radiates signals of a bioresonant spectrum with wavelengths in the range of from 0.2 mm to 10 mm. The device has the following main characteristics. In the first place, the device provides for generation of a very wide spectrum of electromagnetic radiation, which covers the visible light band, the near and far IR band, the millimeter wave band and the centimeter wave band, i.e. completely covers the band of frequencies inherent to the natural radiation frequencies of the organism. In the second place, it is known that electromagnetic radiation differs in respect to intensity in different bands of the spectrum, wherein more than 90% of the radiated energy is in the visual light band of the near, middle and far IR bands. Wherein the ultralongwave portion of the IR band, submillimeter and millimeter bands occupy a very wide band, but only a very small amount of the radiated energy is contained therein. In the process of operation, the energy converter converts the electromagnetic electrical energy into thermal energy and maintains a predetermined temperature of the components, ensuring the generation of electromagnetic oscillations in the range of from 0.2 to 10000 mm. It should be noted that even though this device ensures generation of electromagnetic radiation in the range of radiation of live organisms of from 0.2 mm to 10 mm, it is not capable, in the first place, of effectively changing the conformation of the transmembrane molecules located on the plasmatic membrane of pathogenic and conditionally pathogenic microbes, since thermal radiation of a component of the substrate is unpolarized or weakly-polarized and, in the second place, of selectively acting on cells of the organism, for example, to reduce the activity of pathogenic microbes in the organism without changing the activity of the organism"s own cells and the cells of the commensal microflora of this organism. Some of the aspects of the discovery made by Alexander Gurich are disclosed in the publication by Fritz Albert Pope - "Some Properties of Biophotons and Their Interpretation under Conditions of Coherent States" in a magazine of the International Institute of Biophysics, Germany, 1999. Gurvich called the emission of photons from live cells "mitogenetic radiation," which was not accepted by his contemporaries, but at the present time has been put at the base of many works. The energy of activation encompasses the whole electromagnetic spectrum of radiation from radio waves, microwaves, infrared radiation up to the visual and even ultraviolet radiation. And there is only one carrier for the transfer of energy to millions of reactions per second and to each cell - this is unheated photons. A coherent photon field is the source of such photons. Therefore a weak flow of photons from a biological object, which is well known at present and includes the whole spectrum of radiation from ultraviolet to infrared, is called with biophotons and may be quite sufficient to carry out the role of controlling the biochemistry and biology of a live organism. The therrnoluminescence, or more exactly - thermostimulated luminescence, phenomenon is also known (see, for example, "Thermoluminescence of Lithium Fluoride," pp. 212-215 in the monograph "Radiation Physics," v. 5, "Luminescence and Defects of Ionic Crystals," published by Zinatie, Riga, 1967). This phenomenon is based on absorption by the crystal of photons of the gamma band, roentgen and ultraviolet bands and the creation in the crystal of stable energetic states or coloring centers which carry information on the band and the dose of electromagnetic action. This phenomenon is widely used in thermoluminescence dosimetry. Alkali halogen crystals, for example, lithium fluoride, are used as the sensitive element. A recording of the electromagnetic action is carried out at a constant temperature of the crystal in the range of from 70°K to 300°K. Reading the information recorded on the crystal is carried out by changing the temperature of the crystal in the range of from 110°K to 800°K, wherein the spectrum of the information signal radiated by the crystal is primarily in the visual region of the spectrum from 0.3 to 0.7 mm. These crystals makes it possible to retain the recorded information only within several weeks or months, to carry out the reading of the recorded information by changing the temperature of the crystal within the range of from 110°K to 800°K with the radiation spectrum within the range of from 0.3 to 0.7 mm. A device is known for changing the activity of a biological cell (see, for example, RF patent No. 2055604, 1993), comprising a unit for action which carries out reception and transmission of electromagnetic waves and which is positioned adjacent the biological cell. The unit for action is made in the form of a single element and carries out the storage of received electromagnetic waves. A unit for changing the temperature is connected to the unit for action. The devices makes it possible to change the activity of biological cells of one type without changing the activity of biological cells of other types as a result of the resonant interaction of electromagnetic waves of low intensity of the device and cells on its bioresonant frequency. The device operates in the following manner. At first information is recorded in a memory on the metabolic activity of deposited cells, changed in any known manner. With the aid of the unit for changing temperature, a single element is heated. Wherein information on a changed metabolic activity of deposited cells at a bioresonant frequency is recorded in the memory. Heating is carried out with subsequent forced or natural cooling. Cooling may first be carried out, and then heating, which composes a cycle of changing the temperature of a single element. Then a patient - a carrier of pathogenic microorganisms, the activity of which should be changed, is placed directly adjacent a single element and a temperature change cycle is carried out. Wherein, the generator radiates electromagnetic waves of low intensity at the bioresonant frequency of the cells. As a result of the radiation the metabolic activity of the cell being irradiated is set similar to that deposited with a changed metabolic activity. In order to maintain the predetermined metabolic activity of the cells being irradiated for a lengthy period of time, repeated sessions of irradiation are carried out at certain intervals of time. The device does not provide a high degree of inactivation of pathogenic microorganisms and does not make it possible to effectively eliminate different pathogenic and conditionally pathogenic microorganisms which are in the organism of a human being or animal. The efficiency of operation of this device rapidly falls in the process of conducting therapeutic sessions, and furthermore, the device in the process of operation constantly accumulates parasitic polarized radiation from other strains of pathogenic microorganisms which are in an active state in the live organism being irradiated-. It should be noted that as regards modern physics any electromagnetic field is the photonic, corpuscular one, where photon has energy, mass, kinetic momentum and angular momentum - spin. Any electromagnetic field may be always considered as a set of linearly-polarized waves, and the linearly-polarized wave can be considered as a set of left-and right-polarized waves. Thus, the non-polarized radiation always is a set of polarized waves, and for this reason the bioelectromagnetic fields, biophotons and mitogenetic radiation also represent the polarized electromagnetic radiation. This is well explained in Zhvirblis V.E. "Asymmetry versus Chaos, or What the Biofield Is". In an ordinary electromagnetic wave, electrical vector E that determines result of interaction of radiation with a substance, fluctuates in single plane, perpendicular to a direction of wave propagation. Such wave is termed as the plane-polarized one. In all researches of the biological action exerted by electromagnetic radiations: either non-polarized or plane-polarized radiation, or a radiation polarized in an unknown way were used. But electromagnetic radiation can be polarized not only in plane, but circumferentially as well. It means that vector E rotates either clockwise or counter- clockwise so that the wave becomes asymmetric. Addition of two such right and left- polarized waves of one frequency and one amplitude produces the plane-polarized radiation having the symmetry plane; conversely, any plane-polarized wave cannot be represented as the sum of left and right-polarized waves of one frequency and one amplitude. Such is the theory, long supported by experiments. In principle, the whole foregoing discussion can apply to any electromagnetic radiation too. The first successful attempts to discover emission of cells using the photoelectric effect were made by Rayevskiy who employed a modified Geiger-Mueller counter, see: "Fisher H., Photons as transmitter for biochemical communication. The construction of a hypothesis." Based on the results obtained by him, Rayevskiy assesses intensively of the radiation emitted by biological objects (an onion root, muscle carcinoma) within the limits about 1010...10-9 erg/cm-2/s-1, which range corresponds to 100...200 quantum s/s. F.Popp, considering the biological radiation as a possible regulator of biological functions, and analyzing results of measurements of superweak emission of photons by the live cells made by him, believes that biological systems may be considered as the coupled nonlinear oscillators; each oscillator can be considered as a new resonator, and when resonance is involved, then an high polarization and conductivity with greatly efficient transformation and utilization of energy, and also ability of a biological systems to store information for long time should be assumed. So, the foregoing shows that polarizability (i.e. that photon has angular momentum- spin) is one of the parameters that describes the physical state of any electromagnetic wave. It should be also noted that presently the possibility of emission of electromagnetic waves by a biological object (including both cells of animals and microbes), and that of increasing intensity of the electromagnetic waves emission by biological objects, after their exposure to an extreme agent, have been proved experimentally. Consequently, the above-discussed physical phenomenon underlying the technical solution of the claimed invention is well known in science. Reference "Kaznacheyev V.P., Mikhaylova L.P. Bionformational function of natural electromagnetic fields" notes that by use of mercury-dichloride sublimate in dose of 8- 10 mct/ml as an extreme agent to affect the tested cells, which agent causes the cell to perish in first several hours of exposure, intensity of the radiation exceeds the background level and sharply increases immediately after said sublimate is administered, and then decreases back to the background level after 3-5 hours; and by use of said sublimate in dose of 4-5 mct/ml causing the cellular monolayer to perish after 2-3 days due to blockage of respiratory enzymes - the radiation intensity growth maintained for 8-12 hours was determined. The author emphasizes that "prospects for assessing biosystems and controlling them without application of chemical, preventive and medicinal preparations is to be the future remote-control biophysical therapy. Its premises do exist, and they are becoming indispensable for life in view of the ever increasing medicinal, chemical and environmental intoxication." So, the foregoing shows that polarizability (i.e. that photon has angular momentum-spin is one of the parameters that describes the physical state of any electromagnetic wave. It should be also noted that presently the possibility of emission of electromagnetic waves by a biological object (including both cells of animals and microbes), and that of increasing intensity of the electromagnetic waves emission by biological objects, after their exposure to an extreme agent, have been proved experimentally. Consequently, the above-discussed physical phenomenon underlying the technical solution of the claimed invention is well known in science. Capability of a substance-carrier of information (in this case - a crystal) to emit similar polarized electromagnetic waves is discussed as follows. Some proofs to confirm said capability are given below. Example 1. Known is a method for reproducing non-synthetic diagnostic preparations (see: Patent RU No. 2014080, 1992). The essence of the invention consists in that reproduction (recording and reproduction of electromagnetic radiation) of non-synthetic diagnostic means (nosodes, member- extracted preparations) is effected on liquid crystals have the phase transition temperature over 60°C, which crystals, prior to reproduction, are heated hotter than the transition point, with subsequent decrease of temperature back to the initial value thereof during reproduction. The method is implemented as follows: On one of two conductive sites (the entry site) of a known device, positioned is a preparation whose properties are to be transferred onto a carrier placed on a second site(the exit site). As the latter, used is a liquid-crystal film, a layer of liquid crystal on a substance or a solution thereof; the liquid crystal having the phase transition temperature over 60°C (the most preferred value is 70°C-100°C). Before the carrier is placed on the second site, its temperature is increased by 10-20oC higher than the relative point of phase transition, and then on the carrier is quickly placed on the exit site of a re-write device, where the carrier remains until its own temperature falls below the transition point. Fidelity of reproduction of spectrum of electromagnetic radiation by liquid crystals was confirmed by diagnoses of 128 patients using R Fall method by comparison of the effect of ampouled nosodes and liquid crystals whereon electromagnetic radiation of said nosodes had been recorded. Example 2. Reference "Korenbaum V.I. et al, Matters relating to physical mechanisms of change of a patient"s strength in muscle testing with use of homeopathic nosodes", describes one of diagnostic techniques of applied kinesiology, said technique consisting of the contactless action to be extended on a patient by homeopathic nosodes, and of registration of the human organism responses thereto, which response appears in the form of the muscle weakness phenomenon. Authors mention that "Presently there is no doubt as to the existence of the biological field in living organisms [Kozhevnikov Yu. P. Matters relating to the concept of photogenic field]. Its electromagnetic component is registered by up-to-date devices. Thus, existence of specific, sufficiently broadband, electromagnetic perturbations near body of a human is the actual reality. On the other hand, the homeopathic nosode substances, being the product of dilution of microdoses of substances in distilled water, have the long-employed and clinically confirmed [Linde K et al, Are the clinical effects of homeopathy placebo effects? A meta-analysis of placebo-controlled trials] effect of "memory" of the initial preparations. The surmise is that said property is carried by the newly-discovered stable crystalline nanosized formations (rod-like clusters) [Shui-Yin Lo. Anomalous state of ice]. These structures are hardly able to emit themselves. It seems more probable [Shaub U.B. Actual medical research using novel physical techniques] that they would create a selective oscillating system having its own resonant frequency being unique to an initial substance. When in the biological field there are proximate-frequency perturbations, then excitation of the forced electromagnetic oscillations of these structures occurs, which oscillations are emitted into environment. Of course, intensity of such radiation is small, but if beside (in the proximate field) there are resonant oscillating systems turned to the same frequency, then the secondary excitation of the forced oscillations may occur (the effect of "two tune-forks"). Basing on the claimed invention [IN application], in Russia at Izhevsk Mechanical Engineering Works, since 1999, the "Biofon"-series of antimicrobial devices [official Web-site of "Biofon"- series devices"] have been serially produced, which device aids the human organism in freeing from microorganisms, among which are: clamydia, ureaplasm, mycoplasm, viruses of herpes, influenza, staphylococci, streptococci, tubercle bacillus, candidiasis fungi, Trichomonas fungi, amoebas, lamblia and other microorganisms. This device is successfully employed for treatment of diseases of kidneys, urinary bladder, genitalia, infertility, venereal and parasitic infections, pneumonia, angina, bronchitis, maxillary sinusitis, otitis, tick-bome encephalitis, as well as for normalization of microflora and for making a human organism healthier in general. Below are given some examples on the basis of which applicability and patentability of the claimed invention can be affirmed, and which support its efficiency and the physical phenomenon underlying the features of the invention. Example 3. Reference "Mordovskoy G.G., Investigation of the action of "Biofon" medical device exerted on mycrobacteria and assessment of efficiency thereof. Sverdlovsk regional scientific-practical association "Phthisiopulmonology" describes investigations of the action provided by electromagnetic radiation in the IR range of "Biofon" antimicrobial device, wherein as the means for recording and reproducing the spectrum of changes of biological cells used were microcircuit transistors based on silicon crystal whereon electromagnetic radiation of inactivated strains of pathogenic mycobacteria (M. tuberculosis) was recorded. Results of said investigation are represented in Table No. 1. The study revealed: suppression of growth of the deposited virulent strains of tuberculosis bacterially H37Rv, Bovines and Avium, and strains, extracted from tuberculosis patients Nos.1, 2, 3; and activation of growth of avirulent strains H37Rv and Smegmatis saprophytic strain. As regards treatment of tuberculosis patients, [ibid] notes that after one month of treatment, abacillation (destruction of tuberc le bacillus) using "Biofon" device was achieved for 74.2% of the patients, and only for 33.3% of the control group patients. Thus, based on the foregoing, it can be asserted that there are indisputable facts concerning capability of "a means for recording and reproducing " to emit the polarized electromagnetic waves of an inactivated strain, to inactivate similar strains and facilitate freeing of human organism from them. An high medical-biological efficiency of the devices based on the claimed invention should be mentioned. Example 4. Reference "Assessment of the anti-virus effect of "ORVI-Biofon" devices in case of the experimental influenza infection introduced into white mongrel mice. RAMS Research Institute for influenza" cites investigations for assessing the action produced by "ORVU-Biofon" devices on influenza viruses. In said "ORVI-Biofon" device, radiation emitted by inactivated strains of influenza viruses was recorded beforehand. In the course of said investigation, two series of experiments were carried out. First, the anti-influenza action of "ORVI-Biofon" device was assessed basing on the data of lethality of white mice due to the experimental influenza infection introduced via strains of viruses of A/Puerto Rico/8/3/34(HINI) influenza, which are virulent for said animals. Second, action of the same device was investigated in respect of reproduction of influenza viruses in lungs of white mice, and the anti-influenza action of said device was assessed. After they had been infected by the influenza virus, the animals every 3-4 hours were subjected to irradiation emitted from "ORVI-Biofon" devices for 10 days. On the 10th day after the infection, among 30 control animals only 9 mice remained alive (survivability being 33.3%), and in the experimental group 28 mice remained alive (survivability being 93.3%). Comparative assessment of the influenza virus" capability of reproduction in lungs of the white mice affected by the experimental influenza infection under the normal conditions and in case of regular application of "ORVI-Biofon" device showed a decrease in concentration of influenza virus in lungs of the irradiated mice, as compared with the control group, 3...6 times on the third day; and 2.....5 times on the seventh day. Authors of said reference conclude that application of "ORVI-Biofon" device allows reduce lethality of white mice at least 10 times and decrease concentration of the virus in lungs of white mice 2...5 times, preventing subsequent complications and lethality. Thus, the possibility to record the polarized electromagnetic radiation emitted from inactivated strains" viruses (at least those of influenza) of biological cells onto a means for recording and reproducing, and the possibility to radiate the polarized electromagnetic waves by said means, and also the possibility to suppress activity of an experimental virus, similar to the recorded one, can be considered as proved. Examples 1, 2, 3, 4 cite actual instances of capability of means for recording and reproducing (substances-carriers of information) to record the polarized electromagnetic waves of inactivated microorganisms and to emit similar polarized electromagnetic waves in the course of a change of physical state of a means for recording and reproducing. In terms of physics, the capability of means for recording and reproducing to record and reproduce the polarized electromagnetic waves is described in sufficient detail in; Zhvirblis V.E. Asymmetry versus Chaos, or What the Biofield Is. This physical phenomenon in said reference is substantiated as follows, verbatim: "The right- and left-polarized electromagnetic waves interact with the right- and left- structure substances differently. For example, when asymmetric is a crystal lattice (as that of quartz crystal), or asymmetric is a structure of molecules (similarly to molecules of natural aminoacids). But interaction of a asymmetric electromagnetic field with an asymmetric substance is of the mutual nature. This results not only in purely optical effects, but also in those of quite a material property, for example the interaction allows obtain these or other organic compound mirror isomers in abundance. Reference is made to Fig 10; Fig. 10 shows an alteration of symmetry of the mirror isomers of organic molecules under the action of any asymmetric (right- or left- polarized) field. Regular tetrahedrons ABCD, having various substitutes on their apexes bonded with carbon atom in centre O, transform into tetrahedrons A"B"C"D" and A"B"C"D", which tetrahedrons are not the exact mirror twins anymore; further the relative arrangement of all atoms changes (r" is not equal to r")- This effect cannot depend on spatial orientation of a molecule, and is to be defined only by sign and amount of chiral energy dE* absorbed by a molecule; this effect may be4 characterized by a value of de=±dE*/E, where E is energy of the molecule bonds in the non-deformed state. As the thermal motion is spherically symmetrical, then- at any temperature, chiral influence being absent - de=0. In other words, under the action of the electromagnetic radiation, polarized circularly, properties of the asymmetrical molecules inevitably change; and , in general case, properties of the mirror isomers are capable of being changed under the action of any asymmetrical fields, inclusive of the static ones. But what is the use of such effect as it is far too small? And the use is that any, even the most negligible, asymmetric influence on a substance cannot be smoothed by the spherically symmetric thermal motion: their symmetry is principally different. No matter how an asymmetric molecule, disposed in asymmetric field, would be handled, its properties in a comparison with properties existing in the unperturbed state, will not be the same, and said field cannot be influenced by thermal noise-these molecules respond to asymmetric influence in the manner as if they were at the absolute zero temperature. This is the circumstance that may have the decisive influence on the result of action exerted by weak fields on biological objects. Thus the last-mentioned reference rather exhaustively explains the physical principles of recording of the polarized electromagnetic radiation on crystals. In light of the matters discussed above, it can be asserted both in terms of practice and physics that the physical phenomenon consisting in capability of a means for recording and reproducing to emit the polarized electromagnetic waves recorded thereon, which waves are similar to the polarized electromagnetic waves of an inactivated strain, is well known in science and is widely employed in practical medicine. Regarding how the polarized electromagnetic radiation emitted by an inactivated strain is recorded , first follows a more detailed review as to generation of the polarized electromagnetic radiation of an inactivated strain of a pathogenic microorganism. The cell shell of most pathogenic and conditionally pathogenic microorganisms represents a plasma membrane having protein molecules embedded therein as shown in Fig. 10: See Alberts et al,Molecular Biology of Cell. Reference is made to Fig. 9. Schematic 3-D imaging of a small section of a cell membrane. The plasmatic membrane serves as an highly selective filter, and is responsible for inputting the nutritive substances into a cell and for outputting the discharge therefrom. Owing to the presence of a membrane, a difference of ion concentrations within a cell and in the extra-cellular space is maintained. All biological membranes, inclusive of the plasma one, represent ensembles of the lipid and protein molecules. The lipid molecules [ibid] arrange a continuous double layer having thickness 5 about 5nm. Reference "Alberts et al, Molecular Biology of Cell" notes that every plasmal membrane has an electrical field gradient. And the inner side of a membrane has the negative charge with respect to the outer side. The mean difference of electric potentials between the inner and outer shells of a lipid membrane being U5 = 50 ...100 mV [ibid], strength of its electrical field is determined by the following expression: Hence, the membrane proteins abide in a very strong electric field, and their structure in said field is subjected to transformation. According to Werth, Ch., R. Tomson, Solid Body Physics", the molecules in he static electrical field are the polarized ones, a value of complete polarization P being defined by the following expression: The membrane proteins (Fig. 10) in the external electric field E5 are polarized and will emit the polarized electromagnetic waves. According to "Basharienov A. et a/, Measurement of radiothermal and plasma radiations in UHF range", the radiation polarization may have the regular or chaotic nature. The regular polarization of radiation has the linear, elliptic or circular nature. Radiation from the membrane proteins in the external electric field E5 will be predominantly the left-polarized, or right-polarized, depending on a direction the electric field E5 has on the pathogenic strain"s plasma membrane. Addition of two such left- and right-polarized waves of one frequency and one amplitude produces the plane-polarized radiation (e.g. E5 = 0). Addition of plurality of the plane-polarized waves, having no predominant orientation in any direction, produces, in sum, the non-polarized radiation (e.g. when E5 = 0). Therewith, the presence of electrostatic field E5 on the plasma membrane of a pathogenic strain causes the right- or left-polarized electromagnetic radiation to emerge. For the purpose of establishing the blocking field d Inact on the plasma membrane of a pathogenic microorganism"s deposited strain, and of rendering a pathogenic microorganism from its active state into the inactive one, the membrane function of receiving the external signals and of quickly responding to environmental changes can be employed: See Alberts et al, Molecular Biology of Cell. The invention at issue provides for rendering a pathogenic microorganizm"s deposited strain from its active state into the inactive one with the use of an extreme agent selected from the group consisting of toxic substances, e.g. antibiotics of the bacteriostatic action or viruses, UF-radiation having wavelength of 0.1 - 0.3 mcm for a period of 10-300s. According to "Kaznacheyev V.P., Mikhaylova L.P. Bionformational function of natural electromagnetic fields": for rendering a pathogenic microorganism"s deposited strain from its active state into the inactive one, the following substances were used: mercury dichloride having concentration of 5 mg/1, UF-radiation (exposure for 40-45 s, lamp SYB-30, distance -0.5 m), virus of classic bird plague and adenovirus of type 5 in titre of 103....10"4 s; and the action exerted by the group of cells exposed to an extreme agent (A-cells), using the electromagnetic waves emitted by said cells, upon a similar group of the cells that were not affected by the extreme agents (B-cells) was investigated. In the course of the work, 12 thousands trials were done which gave the following findings: 1. Intensity of electromagnetic radiation sharply rises when A-cells are subjected to the action exerted by an extreme agent. 2. Under the most favourable conditions of the electromagnetic action exerted by A-cells upon B-cells, the latter perished in 70-80% of all cases. 3. Duration of exertion of A-cells" electromagnetic radiation upon B-cells was 4-72 hours. 4. Intensity of A-cell" electromagnetic radiation was 10...1000 quantums/sq.cm. 5. Interaction of the A- and B-cells is effected by electromagnetic waves in the UF, visible and IR-ranges. Reference "Wiener N., Cybernetics" notes that IR-radiation by A-cells in the molecular spectra frequencies influences the self-assembling process of complex molecules on genetic arrays. According to "Biscar G.P., Kollia S. Resolved pseudoraman band of PGA", its authors believe that the electromagnetic transfer of information may take place owing to the electronic-molecular resonance. Reference "Bauer E.S., Theoretical Biology" describes a possibility of the polarized ray emission, and mentions significance of the polarized light for some biological processes. Apart from the aforementioned techniques, there are other known methods of both inactivation of pathogenic microorganisms and recoding of their electromagnetic radiation onto various information carriers, for example-nosodes (nosodes are the preparations made according to certain homeopathic techniques of the pathologically altered members (or parts of members) of human and animals, as well as the sacrificed cultures of microorganisms, products of decomposition of members and fluids containing causative agents of diseases, or products thereof). For example, "Heel" company produces Grippe-Nosode-lnjeel preparation for treatment and prevention of influenza [Official Web-site of Heel company]; wherein as the basic substance used are thermally inactivated strains of influenza viruses: Type-A (H1N1), corresponding to Singapore/6/86; Type-A(h3N3) corresponding to Beijing/32/92; Type-B Panama/45/90. "Heel" company also produces the preparations made on the basis of inactivated bacteria (Bases of informational antimicrobial therapy (part 1), e.g: Staphylococcus-lnjeel - for furunculosis cases Pertussis-Nosode-lnjeel - for whooping cough cases A possibility to record information from a tested object onto an information carrier presently is universally doubtless and is widely used in homeopathy. Industry produces a broad variety of reprinters [Official Web-site "Scientific-practical laboratory "Resonance". Active reprinter having an operator protection unit] intended for energo- informational transfer (re-recording) of the medicinal properties of various preparations (homeopathic preparations, nosodes, toxins, etc.) from ampules and homeopathic grist onto various carriers (water, alcohol, homeopathic grist, etc.). The object at the base of the instant invention is to create a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms. Another object at the base of the instant invention is to create a device for changing the activity of a strain of pathogenic microorganisms, radiation of biological cells. The stated object is achieved in that a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms comprising a working cell disposed in a vessel with a strain of inactivated pathogenic microorganisms and haying a least one means for recording and reproducing a spectrum of radiation of biological cells, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, a control unit connected to the means for changing temperature, in accordance with the invention comprises at least one auxiliary cell for restoring the level of polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms in the working cell, also disposed in the vessel with the strain of inactivated pathogenic microorganisms, said at least one auxiliary cell having at least one means for recording and reproducing a spectrum of radiation of biological cells , and means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and the auxiliary cell being connected via its inputs to respectively an output of the control unit and to outputs of subsequent auxiliary cells, and via its output to an input of the working cell, wherein the working and auxiliary cells are electrically coupled by means of a wire to each other and to the strain of inactivated pathogenic microorganisms. It is advisable that the device comprise at least one standard cell disposed in the vessel with the strain of inactivated pathogen microorganisms, serving for restoration of the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell and in the auxiliary cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and being connected respectively via its inputs to an output of the control unit and to outputs of subsequent standard cells, and via its output to an input of the working cell and to inputs of the auxiliary cells, wherein the standard cell is electrically coupled to the working cell, to the auxiliary cell and to the strain of inactivated pathogenic microorganisms by means of an electrical link. It is useful that the device comprise a generator of electromagnetic oscillations which is mounted directly adjacent to the vessel containing the strain of inactivated pathogenic microorganisms. It is advantageous that a chip containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction be used as the means for recording and reproducing a spectrum of radiation of biological cells. It is useful that at least one crystal selected from the group consisting of silicon, germanium, diamond, gallium arsenide be used as the means for recording and reproducing a spectrum of radiation of biological cells. The indicated object is also achieved in a device for changing the activity of a strain of pathogenic microorganisms comprising a working cell having a least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, a control unit connected to the means for changing temperature, in accordance with the invention comprises at least one auxiliary cell for restoring the level of polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms in the working cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, the auxiliary cell being connected via its inputs to respectively an output of the control unit and to outputs of subsequent auxiliary cells, and via its output to an input of the working cell. It is advisable that the device comprise at least one standard cell serving for restoration of the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell and in the auxiliary cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and being connected respectively via its inputs to an output of the control unit and to outputs of subsequent standard cells, and via its output to an input of the working cell and to inputs of the auxiliary cells, a unit for deleting polarized electromagnetic radiation, an input of which is connected to an output of the control unit, an output to an input of the working cell and to an input of at least one auxiliary cell, serving to delete polarized electromagnetic radiation from strains of microorganisms which are in an active state and in an inactivated state from the working cell and at least from one auxiliary cell. It is useful that the working cell, at least one auxiliary cell and at least one standard cell be positioned directly adjacent to each other and be coupled to each other by means of an electromagnetic link. It is advisable that a chip containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction be used as the means for recording and reproducing a spectrum of radiation of biological cells. Further the invention will be explained by a description of the best embodiments with reference to accompanying drawings, in which: Fig. 1 shows a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms, in accordance with the invention; Fig. 2 shows a variant of execution of the means for recording and reproducing a spectrum of radiation of biological cells, used in a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms, in accordance with the invention; Figs. 3 a,b,c show diagrams of a change of the temperature of the means for recording and reproducing during the recording and reproducing of polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms, in accordance with the invention; Fig. 4 shows a device for changing the activity of a strain of pathogenic microorganisms, in accordance with the invention; Fig. 5 shows a variant of embodiment of the means for recording and reproducing a spectrum of radiation of biological cells, which is used in the device for changing the activity of a strain of pathogenic microorganisms, in accordance with the invention; Fig. 6 shows a diagram of a change of the value of the cutoff voltage E on the plasmatic membrane of a strain of pathogenic microorganisms in relation to the number n of test tubes, in accordance with the invention; Figs. 7 a - 7 j show diagrams of control pulses which are fed from the control unit to the working, auxiliary and standard cells and to the generator for deleting, diagrams of changes of the level of polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms on the working, auxiliary and standard cells and diagrams of changes of parasitic polarized electromagnetic radiation on the working and auxiliary cells, in accordance with the invention; Figs. 8 a, b show diagrams of sequences of control pulses which are fed from the control unit to the working cell and a diagram of a change of the activity of a strain of pathogenic microorganisms during their elimination from a human organism, in accordance with the invention. Fig. 9 is a schematic 3-D imaging of a small section of a cell membrane. Fig. 10 shows an alteration of symmetry of the mirror isomers of organic isomers of organic molecules under the action of any symmetric field. A device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms comprises a working cell 1 (Fig. 1), disposed in a vessel 2 with a strain of inactivated pathogenic microorganisms. The working cell 1 has at least one means 3 for recording and reproducing a spectrum of radiation of biological cells and a means 4 for changing the temperature which is coupled to a means 3 for recording and reproducing a spectrum of radiation of biological cells. The device also comprises a control unit 5 which is connected via its output 6 to an input 7 of the means 4 for changing temperature. In accordance with the invention the device comprises at least one auxiliary cell 8 which serves for restoration of the level of polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms in the working cell and is also disposed in the vessel 2 with the strain of inactivated pathogenic microorganisms. The auxiliary cell 8 has at least one means 9 for recording and reproducing a spectrum of radiation of biological cells and a means 10 for changing temperature which is electrically connected to the means 9 for recording and reproducing a spectrum of radiation of biological cells. The means 10 for changing temperature is connected via its input 11 to an output 12 of the control unit 5. Wherein the means 9 for recording and reproducing a spectrum of radiation of biological cells is connected via output 13 to an input 14 of the means 3. Fig. 1 shows a device comprising one working cell 1 and two auxiliary cells 8, 8". Wherein an output 13" is connected to an input 14" of the means 9 and to the input 14 of the means 3. A means 10" of the second auxiliary cell 8" is connected via input 11" to output 12" of the control unit 5. The working cell 1 is electrically coupled by means of a wire 15 to a strain 16 of inactivated pathogenic microorganisms disposed in the vessel 2. The device contains a generator 17 of electromagnetic oscillations, which is mounted directly adjacent the vessel 2 containing the strain 16 of inactivated pathogenic microorganisms and serves to generate a wide spectrum of electromagnetic oscillations. The control unit 5 works in accordance with a predetermined algorithm which determines the sequence of connecting the cells. An example of the algorithm is provided below. The device also contains at least one standard cell 18 disposed in the vessel 2. The purpose of this cell is to restore the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell 1 and in the auxiliary cells 8, 8". In the embodiment being described the device contains three standard cells 18, 18" and 18" and means 19, 19", 19", 20, 20", 20". The standard cell 18 has at least one means 19 for recording and reproducing a spectrum of radiation of biological cells, to which a means 20 for changing temperature is connected. An input 21 of the means 20 is connected to an output 22 of the control unit 5. Wherein an output 23 of the means 19, which serves as an output of the standard cell 18, is connected to the input 14 of the means 3 serving as an input of the working cell 1, to an input 14" of the means 9 of the auxiliary cell 8 and to an input 24 of a means 9". In the aforesaid device the means 19 of the standard cell 18 is coupled via the wire 15 to the means 9 of the auxiliary cell 8, to the means 9" of the auxiliary cell 8", to the means 3 of the working cell 1 and the strain 16 of inactivated pathogenic microorganisms, and also to the means 19", 19" of the standard cells 18", 18". In the embodiment being described an output 25 of the means 19" for recording and reproducing a spectrum of radiation of biological cells of the standard cell 18" is connected to an input 26 of the means 19 for recording and reproducing a spectrum of radiation of biological cells of the standard cell 18, to the input 14 of the means 3 for recording and reproducing a spectrum of radiation of biological cells of the working cell 1. An output 27 of the means 19" is connected to an input 26" of the means 19". Inputs 21" and 21" of the means are connected to outputs 22" and 22" of the control unit 5. In the aforesaid device a chip 28, containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction, is used as the means 3 or 9 or 19 (Fig. 2) for recording and reproducing a spectrum of radiation of biological cells. In the embodiment being described, the chip 28 contains three crystalline semiconductors 29, 30, 31, wherein the crystalline semiconductor 29 serves as a collector, the crystalline semiconductor 30 as a base and the crystalline semiconductor 31 as an emitter. Wherein the base semiconductor 30 with respect to the collector semiconductor 29 and to the emitter semiconductor 31 has different types of conductance. In the aforesaid device, collector junction 32 and emitter junction 33, which are positioned respectively between the collector and base semiconductors 29, 30 and between the base and emitter semiconductors 30, 31, are used as the means 4 or 10 or 20 for changing temperature. These semiconductors are connected to a source 34 via a switch 35. The temperature T to which the crystalline semiconductors 29, 30, 31 are heated is determined by the power P which is dissipated on the semiconductor junctions 32, 33 when current flows, and is determined by the equation where: Ii is the emitter current, I2 is the base current, U is the voltage between the collector and emitter, (3 is a transfer constant of the base current. Using a current setting element 36 connected to the base semiconductor 30, it is possible to adjust the value of the current I2 flowing through the base semiconductor 30, and consequently the temperature T to which the chip 28 is heated. Execution of the means 3 on the base of a transistor chip is more preferable than the execution of that means on the base of a diode chip, since the former makes it possible to use the source 34 with a wider range of change of the supply voltage and to use its energy with maximum efficiency. Crystals of silicon, germanium, diamond and gallium arsenide may be used as the crystalline semiconductor. A chip 28 (Fig. 2) is used as the means 3, 9, 9", 19, 19", 19" for recording reproducing a spectrum of radiation of biological cells. Simultaneously with recording polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms on the means for recording and reproducing a spectrum of radiation of biological cells, action is effected on the strain of pathogenic microorganisms with electromagnetic radiation from the generator 17 of electromagnetic oscillations, which is in the range of from 10 Hz to 1014 Hz in order to increase the intensity of radiation of the strain 16 of inactivated pathogenic microorganisms. The block diagram of the device for changing the activity of a strain of pathogenic microorganisms is on the whole similar to the block diagram of the device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms. The device for changing the activity of a strain of pathogenic microorganisms contains a working cell 37 (Fig. 4) disposed in a body 38. The working cell 37 has at least one means 39 for recording and reproducing a spectrum of radiation of biological cells and a means 40 for changing temperature which is coupled to the means 39 for recording and reproducing a spectrum of radiation of biological cells. The device also contains a control unit 41 which is connected at its output 42 to an input 43 of the means 40 for changing the temperature of a crystal. In accordance with the invention the device contains at least one auxiliary cell 44 which serves for restoration of the level of polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms in a working cell and is also disposed in the body 38. The auxiliary cell 44 has at least one means 45 for recording and reproducing a spectrum of radiation of biological cells and a means 46 for changing temperature which is electrically coupled to the means 45 for recording and reproducing a spectrum of radiation of biological cells. The means 46 for changing temperature is connected at its input 47 to an output 48 of the control unit 41, while the output 49 of the means 45 is connected to an input 50 of the means 39 of the working cell 37. A device is shown in Fig. 4 which contains one working cell 37 and two auxiliary cells 44 and 44". The auxiliary cell 44" contains a means 45" for recording and reproducing a spectrum of radiation of biological cells which is electrically coupled to a means 46" for changing temperature, an input 47" of which is connected to an output 48" of the control unit 41. An output 51 of the means 45" is connected to an input 52 of the means 45 and to the input 50 of the means 39. The device contains at least one standard cell 53 also disposed in the body 38, the cell 53 serving to restore the level of polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms in the working cell 37 and in the auxiliary cells 44 and 44". The standard cell 53 has at least one means 54 for recording and reproducing a spectrum of radiation of biological cells to which a means 55 for changing temperature is connected. An input 56 of the means 55 of the standard cell 53 is connected to an output 57 of the control unit 41. Wherein an output 58 of the means 54 of the standard cell 53 is connected to the input 50 of the means 39 of the working cell 37, to the input 52 of the means 45 of the auxiliary cell 44 and to an input 59 of the means 45" of the auxiliary cell 44". In the variant being described, the device contains three standard cells 53, 53", 53", containing means 54, 54", 54" for recording and reproducing a spectrum of radiation of biological cells, to which the means 55, 55", 55" for changing temperature are respectively connected. Wherein, inputs 56", 56" of the means 55", 55" are connected to outputs 57", 57" of the control unit 41. An output 60 of the means 54" is connected to an input 61 of the means 54, and also to the input 50 of the means 39, to the input 52 of the means 45, and to the input 59 of the means 45". An output 62 of the means 54" is connected to an input 63 of the means 54", to the input 61 of the means 54, and also to the input 50 of the means 39, to the input 52 of the means 45, to the input 59 of the means 45". The device also contains a unit 64 for deleting polarized electromagnetic radiation, an input 65 of which is connected to an output 66 of the control unit 41, while an output 67 is connected to an input 68 of the means 39 of the working cell 37, an output 69 - to an input 70 of the means 45 of the auxiliary cell 44, an output 71 to an input 71" of the means 45" of the auxiliary cell 44". In this device the means 39, 45, 45", 54, 54", 54" are made similar to means 3, 9, 19. In the aforesaid device a chip 28, containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction, is used as the means 39 (Fig. 5) or 45 or 54 for recording and reproducing a spectrum of radiation of biological cells. In the embodiment being described, the chip 28 contains three crystalline semiconductors 29, 30, 31, wherein the crystalline semiconductor 29 serves as a collector, the crystalline semiconductor 30 as a base and the crystalline semiconductor 31 as an emitter. Wherein the base semiconductor 30 with respect to the collector semiconductor 29 and to the emitter semiconductor 31 has different types of conductance. In the aforesaid device, collector junction 32 and emitter junction 33, which are respectively between the collector and base semiconductors 29, 30 and between the base and emitter semiconductors 30, 31, are used as the means 40 or 46 or 55 for changing temperature. These semiconductors are connected to a source 34 via a switch 35. The temperature T to which the crystalline semiconductors 29, 30, 31 are heated is determined by the power P which is dissipated on the semiconductor junctions 32, 33 when current flows, and is determined by the equation Using a current setting element 36 connected to the base semiconductor 30, it is possible to adjust the value of the current flowing through the base semiconductor 30, and consequently the temperature T to which the chip 28 is heated. Crystals of silicon, germanium, diamond and gallium arsenide may be used as the crystalline semiconductor. Diagrams are shown in Fig. 6 which are diagrams of a change of the value of the cutoff voltage E on the plasmatic membrane in relation to the number n of test tubes 72 with the strains 73 of pathogenic microorganisms therein which are sequentially inactivated with the device. In Fig. 6 are shown the moments 6.1, 6.2 and 6.3 of switching on the auxiliary cell 44, which makes it possible to increase the value of the cutoff voltage E and to inactivate a number of test tubes with strains 73 which is ten times greater than when only one working cell is used. In order to ensure effective inactivation of the strain 73 of pathogenic microorganisms and to exclude the recording of information from that strain onto the means 39, 45 and 44" of the working cell 37 and the auxiliary cells 44 and 44" in the process of the cycle of changing their temperature, it is necessary that the cutoff potential E16 on the plasmatic membrane of the inactivated strain 16 of pathogenic microorganisms by module exceeds the potential E73 on the plasmatic membrane of the strain 73 of pathogenic microorganisms which is being inactivated. In order to ensure the successive effective inactivation of a large number n of test tubes 72 with strains 73 of pathogenic microorganisms therein, it is necessary that the cutoff potential E16 on the plasmatic membrane of the strain 16 of pathogenic microorganisms by module would substantially exceed the potential E73 on the plasmatic membrane of the strain 16 of pathogenic microorganisms which is being inactivated Fig. 7 shows time diagrams of the operation of the device for one working cell, one auxiliary cell and two standard cells. Figs. 7a and 7b show respectively a sequence of control pulses applied to the input of the working cell 37 and to the input of the auxiliary cell 44. Fig. 7c shows a deletion pulse formed by the generator 64 of deletion and applied to the inputs of the working cell 37 and the auxiliary cells 44, 44". Figs. 7d and 7e show pulses applied to the inputs of the first and second standard cells respectively. Fig. 7f shows a diagram of a change of the level of polarized electromagnetic radiation of the working cell 37. Fig. 7g shows a diagram of a change of the level of polarized electromagnetic radiation of the auxiliary cell 44. Fig. 7h shows a diagram of a change of the level of polarized electromagnetic radiation of the standard cell 53. Fig. 7i shows a diagram of a change of the parasitic polarized radiation of the working cell 37. , Fig. 7j shows a diagram of a change of the parasitic polarized radiation of the auxiliary cell 44. It is evident from the presented diagrams that connection of the working cell 37 takes place during each session of inactivation of a strain of pathogenic microorganisms, connection of the auxiliary cell 44 - at each fifth session of inactivation, connection of the generator 64 for deletion - at each 20th session, connection of the standard cell 53 at each 21st session, connection of the second standard cell 53" - at each 101st session. Such an algorithm of operation makes it possible to ensure a high level of inactivation of a strain of pathogenic microorganisms with a large number of sessions of inactivation. Now consideration will be given to the operation of the device with a concrete example of a change of the activity of bacterial cells Staphylococcus aureus in a human organism. At first a culture of deposited Staphylococcus aureus cells is taken and by any known method they are put into a lowly active state, which is characterized by a high positive potential on their plasmatic membrane, for example, by subjecting them to ultraviolet radiation which has bacteriostatic action. Then the spectrum of radiation of inactivated Staphylococcus aureus cells is received and recorded. When there is a change of the temperature of the crystalline semiconductors of the means for recording and reproducing of the working, auxiliary and standard cells in the process of their intensive absorption of polarized photons radiated by conformed membrane and transmembrane molecules of the plasmatic membrane of inactivated Staphylococcus aureus cells, stable energetic states are created in the crystalline semiconductors, which are capable of radiating similar photons during repeated cycles of a change of temperature. Then the device is positioned directly adjacent to a patient 74, in the organism of which here are identical Staphylococcus aureus biological cells which are in an active state. The algorithm of operation of the device may be any and, for example, correspond to the algorithm shown in Fig. 7, wherein the period T (Fig. 8) between sessions of action is set on the basis of the time of restoration i3 of the activity of pathogenic microbes in a patient"s organism. Maintaining the Staphylococcus aureus cells in an inactivated state for a lengthy period of time t4 makes it possible to completely free the patient"s organism from this pathogenic Staphylococcus aureus microorganism by eliminating them with the immune system of a human and pushing them out with other microorganisms included in the makeup of the patient"s microflora. For example, to completely free the patient"s organism from Staphylococcus aureus during an acute inflammatory process, it is necessary to carry out 6 - 24 sessions a day for 10 - 14 days, in the case of a chronic process it is necessary to carry out 3-6 sessions a day for 8-30 days. It is possible to successively or simultaneously record several strains of pathogenic microorganisms into the device for recording polarized electromagnetic radiation. For example, all the known pathogenic strains of the Staphylococcus genus may be recorded in the device for recording polarized electromagnetic radiation. Then use of the device for changing the activity of a strain of pathogenic microorganisms, in which polarized electromagnetic radiation of all known inactivated strains of the Staphylococcus genus are recorded, makes it possible to inactivate and then eliminate any pathogenic strain of the Staphylococcus genus, which is in the organism of a human or animal. The proposed device may implement the inactivation in the organism of a human or animal of not only bacteria, but also viruses, fungi, mycoplasma, prions, single-celled simples and their toxins, wherein the device and method for their inactivation and elimination are similar to that described above. WE CLAIM : 1. A device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms comprising: a working cell disposed in a vessel with a strain of inactivated pathogenic microorganisms and having a least one means for recording and reproducing a spectrum of radiation of biological cells and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells; a control unit connected to the means for changing temperature; characterized in that it comprises at least one auxiliary cell for restoring the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell, also disposed in the vessel with the strain of inactivated pathogenic microorganisms, said at least one auxiliary cell having at least one means for recording and reproducing a spectrum of radiation of biological cells, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and the auxiliary cell being connected via inputs to respectively an output of the control unit and to outputs of subsequent auxiliary cells, and via its output to an input of the working cell, wherein the working and auxiliary cells are electrically coupled by means of a wire to each other and to the strain of inactivated pathogenic microorganisms. 2. A device as claimed in claim 1, wherein there is provided: at least one standard cell disposed in the vessel with the strain of inactivated pathogen microorganisms, serving for restoration of the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell and in the auxiliary cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and connected respectively via its inputs to an output of the control unit and to outputs of subsequent standard cells, and via its output to an input of the working cell and to inputs of the auxiliary cells, the standard cell being electrically coupled to the working cell, to the auxiliary cell and to the strain of inactivated pathogenic microorganisms by means of an electrical link. 3. A device as claimed in claim 1, wherein there is provided: a generator of electromagnetic oscillations which is mounted directly adjacent to the vessel containing the strain of inactivated pathogenic microorganisms. 4. A device as claimed in claim 1, wherein a chip containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction are used as the means for recording and reproducing a spectrum of radiation of biological cells. 5. A device as claimed in claim 1, wherein at least one crystal selected from the group consisting of silicon, germanium, diamond, gallium arsenide is used as the means for recording and reproducing a spectrum of radiation of biological cells. 6. A device for changing the activity of a strain of pathogenic microorganisms comprising: a working cell having a least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of a strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells; a control unit connected to the means for changing temperature; characterized in that it comprises: at least one auxiliary cell for restoring the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, the auxiliary cell being connected via its inputs to respectively an output of the control unit and to outputs of subsequent auxiliary cells, and via an output to an input of the working cell. 7. A device as claimed in claim 6, wherein there are provided: at least one standard cell serving for restoration of the level of polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms in the working cell and in the auxiliary cell, having at least one means for recording and reproducing a spectrum of radiation of biological cells on which polarized electromagnetic radiation of the strain of inactivated pathogenic microorganisms is recorded, and a means for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and connected respectively via its inputs to an output of the control unit and to outputs of subsequent standard cells, and via its output to an input of the working cell and to inputs of the auxiliary cells; a unit for deleting polarized electromagnetic radiation, an input of which is connected to an output of the control unit, an output to an input of the working cell and to inputs of the auxiliary cells, and serving to delete polarized electromagnetic radiation from the working cell and the auxiliary cells. 8. A device as claimed in claim 6 or claim 7, wherein the working cell, at least one auxiliary cell and at least one standard cell are positioned directly adjacent to each other and are coupled to each other by means of an electromagnetic link. 9. A device as claimed in claim 6, wherein a chip containing at least two crystalline semiconductors having different types of conductance and at least one semiconductor junction are used as the means for recording and reproducing a spectrum of radiation of biological cells. 10. A device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms, substantially as herein described, particularly with reference to the accompanying drawings. 11. Device for changing the activity of a strain of pathogenic microorganisms, substantially as herein described, particularly with reference to the accompanying drawings. The present invention discloses a device for recording polarized electromagnetic radiation of an inactivated strain of pathogenic microorganisms onto a crystal and a device for changing the activity of a strain of pathogenic microorganisms. Said devices comprise a working cell (1) having at least one means (3) for recording and reproducing a spectrum of radiation of biological cells, a means (4) for changing temperature which is coupled to the means for recording and reproducing a spectrum of radiation of biological cells, and a control unit (5) connected to the means for changing temperature. The invention may be used for inactivation and subsequent elimination of pathogenic and conditionally pathogenic microorganisms in a human or animal organism. |
---|
243-CAL-2001-(11-10-2011)-CORRESPONDENCE.pdf
243-CAL-2001-(11-10-2011)-PA.pdf
243-CAL-2001-CORRESPONDENCE.pdf
243-cal-2001-granted-abstract.pdf
243-cal-2001-granted-claims.pdf
243-cal-2001-granted-correspondence.pdf
243-cal-2001-granted-description (complete).pdf
243-cal-2001-granted-drawings.pdf
243-cal-2001-granted-form 1.pdf
243-cal-2001-granted-form 18.pdf
243-cal-2001-granted-form 2.pdf
243-cal-2001-granted-form 3.pdf
243-cal-2001-granted-form 5.pdf
243-cal-2001-granted-letter patent.pdf
243-cal-2001-granted-priority document.pdf
243-cal-2001-granted-reply to examination report.pdf
243-cal-2001-granted-specification.pdf
243-cal-2001-granted-translated copy of priority document.pdf
Patent Number | 218693 | ||||||||
---|---|---|---|---|---|---|---|---|---|
Indian Patent Application Number | 243/CAL/2001 | ||||||||
PG Journal Number | 15/2008 | ||||||||
Publication Date | 11-Apr-2008 | ||||||||
Grant Date | 09-Apr-2008 | ||||||||
Date of Filing | 24-Apr-2001 | ||||||||
Name of Patentee | PETRENKO SERGEI IVANOVICH | ||||||||
Applicant Address | 603137,NIZHNY NOVAGOROD, ULITSA ZHUKOVA, D.16, KV.50, RUSSIAN FEDERATION. | ||||||||
Inventors:
|
|||||||||
PCT International Classification Number | A01K67/00.A61N5/00 | ||||||||
PCT International Application Number | N/A | ||||||||
PCT International Filing date | |||||||||
PCT Conventions:
|