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    • 专利摘要:
    Ozonized oil with antioxidants consisting of the following components: ozonized vegetable oil, preferably olive oil, attenuated aureus staphylococcus, alpha tocopherol and selenium, and its composition is: ozonated vegetable oil 100 ml, staphylococcus aureus 5 to 10 drops, tocopherol alfa 400 mg and selenium 50 to 100 ng/2 ml. The attenuated staphylococcus aureus is obtained by inactivating said bacteria by heat in three cycles of 105ºC for 18 minutes. (Machine-translation by Google Translate, not legally binding)
    公开号:ES2646335A1
    申请号:ES201630796
    申请日:2016-06-10
    公开日:2017-12-13
    发明作者:Nicolás RUBIO GARCÍA
    申请人:Nicolás RUBIO GARCÍA；
    IPC主号:
    专利说明:

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    DESCRIPTION
    Ozonized oil with antioxidants
    Object of the invention
    The object of the present invention is an ozonized vegetable oil to which a series of antioxidant substances suitable for the topical treatment of osteoarthritis are added.
    Background of the invention
    According to a study of the Spanish pain society, in November 2005, 80% of the Spanish population will suffer lumbar or cervical pain at least once in their life. In medical practice this conclusion is accepted, and one is afraid because every time pain and osteoarthritis, which is its fundamental cause, appears in younger and younger people and sport aggravates the problem more, due to the overexertion they suppose for joints The means available for treatment are scarce and ineffective. Osteoarthritis is the most frequent rheumatic pathology, and can not be defined as a disease, but as a group of pathologies that affect the joint and are characterized by the presence of structural, degenerative, regenerative and repair changes of all tissues that form the joint. Until recently the inflammatory factor was not considered of importance, but at present it is considered this of first magnitude. It can be defined in many ways, depending on various points of view: clinical, immunological, biochemical.
    In general, and the most recent epidemiological works on longevity show this, the statistical average of life in the western population today is about 80 years, although we estimate that this figure has been reached some time ago. All this compared to the first published studies on the aforementioned topic, about 1915, in which this figure is around 38-40 years, this figure is currently identical with that existing in sub-Saharan Africa. This substantial change is due to, in general, a series of events, such as the best food, housing, health, working hours,
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    and a long etcetera, all this has meant, that in less than a century and not in all societies, the average life has doubled. All this is enormously positive, but a very important toll is being paid for it, as and according to the statistical studies carried out by the Spanish Society of General Medicine (SEMERGEN), in the environment of 45-50 years, people suffer about three processes of chronic type, among other ophthalmological, hypertension, rhinitis, osteoarthritis, and that logically increase with age. Many people think that this is coincidence, but if you consider that the human organism is not programmed to live an average of 80 years, but if it is for the aforementioned 45-50, and a good example of this is what is happening today in many developing countries, and all for a million years, which is approximately the time of the appearance of man on earth.
    From a certain age the immune response system begins to decline. The thymus gland, which is the brightest star in the entire immunological constellation, begins to atrophy, leaving the entire defensive system in the hands of the ganglionic substitution system, and what to say of the intracellular defensive system, such as molecular biology. Free radicals, which are the result of the activity of the mitochondrial system that continues its function, but which is the neutralizing system that ceases to be effective, said neutralizing system are enzymatic or intracellular antioxidants.
    In general terms and as Richard Epsein of the University of Syracuse says: having good health depends on having the right molecules in the right place and at the right time. Therefore the disease is caused by the appearance of abnormal molecules in cells altered at the wrong time. The biological bases of health and disease have inevitably become molecular in order to understand diseases and treat them etiologically. Therefore, osteoarthrosis can be defined as the clinical consequence of an altered oxidative stress situation at the chondrocyte level.
    It is practically unanimous, that the chondrocyte is the most important cell that we find in the articular cartilage, has a low mitotic activity and a relatively low synthesis capacity and is responsible for maintaining the cartilaginous matrix in a state of equilibrium of low turnover. From the beginning of the joint activity, the chondrocyte is subjected to constant mechanical stimuli and this causes a sequence of immunological events to appear, with the appearance of soluble proteins, called
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    Cytokines, which have specific characteristics and without knowing them, it is not possible to have knowledge of the events that occur. The paracrine action: which shows that it has a very short life, so it has a tendency to act on cells that are in the area adjacent to the place where they are synthesized. Another very important feature is pleiotropism, which consists in the ability to simultaneously activate multiple cell receptors. Finally, the redundancy effect or the faculty that has the same action on different receptors, the cytokines that are produced are: il-1, il-17 and tnf-alpha, and which are responsible for the activation of other cells.
    In general, osteoarthritis is characterized by the degeneration of the articular cartilage and a number of etiological factors have begun to be known, although regardless of the cause and therefore the trigger factor, a series of events are then sequenced at the biochemical, molecular and immunological level. intracellular level The action of mechanical, biological or other risk factors on cartilage chondrocytes are responsible for the loss of balance between synthesis and matrix degradation. This is characterized by an increase in the synthesis and release of pro-inflammatory mediators: cytokines, nitric oxide, prostaglandins, metalloproteases, which clearly favor the development of osteoarthritis, since they are responsible for the breakdown of the state of homeostasis between anabolism and catabolism
    In a normal articulation there is a balance between the degradation and repair processes of the extracellular matrix of the cartilage, and this is carried out in the chondrocyte by means of two processes, the anabolic and the catabolic, and both are manifested by means of cytokines, which activate the specific receptors of cell membranes. These are formed by specific proteins that are capable of transforming an extracellular message into an intracellular message, activating the formerly called 2nd messenger, which is currently called electron transfer by univalent oxygen reduction route, forming incompletely reduced active species by sequential addition of electrons one by one, in the following order: superoxide radical, hydrogen peroxide and hydroxyl radical, all three are free radicals that are currently known to be responsible for oxidative stress in biological systems. A free radical is an atom or a molecule that has a missing electron in its most peripheral orbital or a molecule or molecule fragment that contains one or more missing electrons in its outer orbital, they have a half-life of the order of milliseconds due to their large
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    reactivity. These tremendously reactive molecules or atoms are involved in the onset and development of various diseases. In the biological environment, free radicals are oxygenated compounds and are called reactive oxygen species (ero), which as we have said are responsible for the oxidative damage to biological macromolecules such as DNA, lipids, carbohydrates and proteins. The theory of the toxicity of oxygen by free radicals states that all oxidation, or reduction, can only occur in oxidation steps, or reductions, of a univalent nature. There are also nitrogen free radicals or reactive nitrogen species (ern), whose importance has grown considerably in recent times.
    The univalent oxygen reduction pathway gives rise to three "incompletely reduced" forms, between it and water, the superoxide radical, hydrogen peroxide, which is not a radical, but can generate them, and the hydroxyl radical.
    The superoxide or superoxide anion (O2) radical, contrary to previous views, lacks sufficient reactivity to directly attack the macromolecules, but is potentially toxic, since it can initiate reactions that give rise to other intermediates to its highly reactive. However, in the presence of traces of metal catalysts such as iron and copper, the combination of O2 and H2O2, in the Fenton or Haber-Weiss reaction, gives rise to OH.
    Hydrogen peroxide is a species or state of reduction of two electrons of oxygen, it is a species with great capacity to generate oxidative damage despite not being a free radical and is converted into water by the action of catalase, a process that determines Its half life. Hydrogen peroxide is involved in the regulation of gene expression signal transduction through NFkB and AP-1, both are transcription factors capable of inducing genes such as interleukin-2 (IL-2), TNF or tumor necrosis factor.
    The hydroxyl radical is a state of reduction of three electrons of the oxygen molecule, OH is considered today the main initiator of the attack on all types of macromolecules, although there are other proposed initiators. This substance without net charge is considered as one of the most reactive species present in the body. Its missing electron can react unspecifically with almost any type of molecule in 2-3 molecular diameters from its place of formation. It is the most reactive species, with a
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    estimated half-life around 10-9 seconds, the high reactivity of OH prevents its diffusion over long distances through the cell, a role that corresponds to H2O2, the latter would therefore also be responsible for the propagation of oxidative damage between fractions subcellular, can be generated live as a result of high energy radiation, which can cause hemolytic breakage of body water. Ultraviolet light does not have enough energy to cleave a molecule of water, but it can divide hydrogen peroxide into two molecules of hydroxyl radical. Also and from the hydrogen peroxide and the superoxide radical, the hydroxyl radical can be formed, it is the so-called Fenton reaction, in which both are catalyzed with the presence of traces of elements such as iron and copper.
    Nitric oxide: Nitric oxide has gained great relevance in recent years for the important physiological function it plays, in addition to being considered an important toxic intermediary due to its free radical status. It is a liposoluble and water-soluble gas whose half-life is relatively long, 3-5 seconds. Its formation takes place by an enzymatic reaction in which the enzyme nitric oxide synthase and catalyzes the conversion of L-arginine to L-citrulline, giving as a by-product NO, in numerous cell types. Nitric oxide plays a fundamental role in numerous physiological processes, acts as a regulator of local blood flow, inhibitor of platelet aggregation and producer of activated macrophages, contributing to the immune defense, also acts as a neurotransmitter, the brain being the organ with the highest activity nitric oxide synthase.
    In healthy tissues, the main source of free radicals is mitochondria, this is because these organs are responsible for more than 90% of cellular oxygen consumption since free radicals in biological systems always proceed, in the end, of oxygen metabolism by the univalent route. This generates a series of consequences, which is that among the possible consequences of an accentuated generation of free radicals in the mitochondrial system are diseases such as parkinson's, aging, osteoarthritis, cancer. Quantitatively, the second source of free radicals is the phagocytes of the immune system upon encountering an infectious agent, polymorphonuclear cells and macrophages, which experience a very marked increase in their oxygen consumption, called "respiratory burst." This consumption occurs mainly in plasma membranes where an enzymatic complex, NADPH oxidase, is activated and produces oxygen radicals from basal oxygen and free electrons derived from the pentose pathway. These free radicals contribute sharply to the destruction or
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    inactivation of the infectious agent directly, acting on the DNA of the invading germ, which prevents its replication and therefore the infection spreads.
    The presence of free radicals from oxygen, at the intracellular level, as mentioned, generates by its greed for an electron, an attack on macromolecules, in three plots: at the level of lipids, proteins or DNA.
    The first of these is called lipid peroxidation, which has three perfectly defined phases: initiation, maintenance and termination, which is the best known case and perhaps most important from the point of view of acute toxicity. The initiation consists in the extraction of an electron from a carbon adjacent to a double bond, by an initiator such as OH. Among all the macromolecules present in animal tissues, polyunsaturated fatty acids, are the most sensitive to attack by free radicals due to the possession of double bonds, thus forming an alkyl radical (L) that becomes peroxyl (LOO) , by the addition of oxygen, which can lead to the spread of peroxidation, by generating another alkyl radical in the fatty acid adjoining the membrane. Propagation explains the chain reaction character of lipid peroxidation, whereby a single initiation can damage a large number of molecules. The reaction is terminated by the reaction of adjacent radicals, resulting in cross bridges (L-L) or by fragmentation of fatty acid in a large number of products such as malondialdehyde, which is the most widely used marker. Part of the most recent research is focused on clarifying peroxidation in aggregate systems such as LDL. In these models it is known that both the particle size and the presence of tocopherols can be of paramount importance for the cicetica of autooxidation.
    Oxidative protein damage: Although much more attention has been devoted to lipid peroxidation, it is now known that similar attacks occur to proteins or nucleic acids. The products of these oxidations accumulate in smaller proportions, which has resulted in them having gone unnoticed for a long time, however all these processes are of great importance due to the qualitative nature of the damage or the difficulty of repairing it. Proteins can be attacked, even at the primary structure level, and it has been shown that oxidation in discrete amino acid residues serves as a marker for non-ATP-dependent proteolytic systems, for which names such as macroxyproteinase have been proposed, which would exist been specially designed in the evolution to eliminate oxidized proteins.
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    It has been concluded that H2O2 and the reduced forms of iron and copper interact, at the sites of union of these metals with the proteins, producing free radicals that immediately oxidize the residues of neighboring amino acids. This process is therefore considered specific to the metal binding site, so it can be considered the active center. Among the amino acids sensitive to oxidative damage in proteins, histidine, proline, arginine, lysine and cystem are found and as a consequence carbonyl groups are formed or conversions of some amino acids occur in others, as occurs with the transformation of histidine in asparagine. Carbonyl groups appear in various oxidation systems in vitro, such as those related to cytochrome p450. Carbonyl content increases during aging in rodents and humans. The measurement of oxidative damage to proteins in biological samples is usually carried out by means of the valuation of carbonyl groups by means of spectrophotometric scans or by isotopes, these techniques are extremely sensitive, but are not free from interference.
    Oxidative DNA damage: free radicals react with the components of DNA by addition or abstraction, and the number of products from the attack on DNA exceeds twenty. The low sensitivity of this type of detection has recently led to the evaluation of a large number of products by gas chromatography, mass spectrometry or 8-hydroxideoguanosine (8-ohdg).
    Extracellularly generated free radicals must cross the plasma membrane before reacting with other cellular components and therefore can initiate toxic reactions in it. Unsaturated fatty acids present in the membrane and transmembrane proteins that have oxidizable amino acids are susceptible to being altered by free radicals. These reactions alter the properties of the membranes in such a way that they change their fluidity, increase their permeability, decrease their potential, lose secretory secretions and inhibit cellular metabolic processes, and all this caused by lipid peroxidation. , or to the oxidation of important structural protections.
    The enzyme NADPH-oxidase present in the plasma membrane of phagocytic cells, in an important biological source of free radical production, due to the activation of polymorphonuclear and macrophages that consume a large amount of oxygen, which
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    It will be transformed into a superoxide radical. These oxygen-dependent free radicals can damage the cells that originate them and cells close to the stimulated phagocytes. It has also been seen that NADPH oxidase is an important source of free radicals in arterial smooth muscle cells and endothelium.
    Given the importance of the damage that oxidative stress can produce in cells and in the organism, in recent years we have tried to find indexes that allow us to measure it. Among the proposed indicators, the most relevant are the gssg / gsh ratio, as an indicator of oxidative damage in the cytosol, malondialdhido and hydroxynonenal, as indicators of lipid damage, 8-hydroxy-2-deoxyguanosine, which is an index of oxidative damage in DNA, the carbonyl group and 2-oxohistidine, which is the marker that most interests us in the project.
    Antioxidants: the body has a series of enzymatic and non-enzymatic systems, designed to protect against the action of free radicals by the generated, are called antioxidants. Antioxidants can be defined as any substance that, when present in low concentrations compared to the oxidizable substrate, significantly decreases or inhibits the oxidation of this substrate. In general, talk about antioxidants, such as those molecules in which their consumption is synonymous with health. According to the bibliography, which is very broad in this regard, the levels of vitamin E, catalase and selenium, which is the essential trace element in the thiol group, which are the enzymatic or intracellular antioxidants, are from the very depleted 45 years, by what its supplementation is essential, to avoid the appearance of oxidative stress.
    They can act as follows:
    -preventing the formation of ero.
    -intercepting the attack of ero.
    - kidnapping reactive metabolites and converting them into less reactive molecules.
    - amplifying the resistance of biological targets sensitive to ero attacks. -maintaining a favorable environment for the performance of other antioxidants.
    From the point of view of cell physiology, we can divide them into three types of antioxidants: primary, secondary and tertiary.
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    Primary antioxidants prevent the formation of new species of free radicals. These antioxidants act by converting existing free radicals into less harmful molecules or preventing their formation from other molecules. This group includes superoxide dismutase, glutathione, catalase and metal-binding proteins (ferritin and celluloplasmin), which limit the availability of iron necessary for the formation of the OH radical.
    Secondary antioxidants are non-enzymatic protectors or free radical scavengers that intervene when they are overproduced and the enzymatic systems are overflowed, thus preventing chain reactions. Glutathione, vitamin E, vitamin C, uric acid, bilirubin and albumin are included.
    Tertiary antioxidants repair biomolecules damaged by free radicals. Among them are intracellular proteolytic systems that act by degrading oxidatively damaged proteins, thus preventing their accumulation. We can also highlight the DNA repair enzymes, methionine sulfoxide reductase and phospholipase a2, which cuts the oxidized phospholipids of the membrane.
    Another way to classify the antioxidants widely used in the literature, is from the biochemical point of view: enzymatic and non-enzymatic antioxidants, such as the following:
    Superoxide dismutase.- under this name a family of metalloproteins is included, widely distributed in nature, present in all cells, which use oxygen in their metabolism, and even in some strict and facultative anaerobic bacteria. Superoxide dismutase (SOD) transforms the superoxide radical into hydrogen peroxide, constituting the first natural means of defense (Fridovich, 1989). It should be noted that the superoxide radical is unstable in aqueous medium and spontaneously dismutates forming H2O2. However, the rate of non-enzymatic spontaneous demotion is relatively low. The catalysis of the dismutation reaction carried out by the enzyme superoxide dismutase increases this rate in the order of 10,000 times.
    Four different forms of superoxide dismutase are described, according to the enzyme-linked metal prostate group. Copper and zinc dependent SOD, which appears in most eukaryotic cells, is a soluble protein. There are many isomeric forms and the most abundant of them is located mostly in the cytosol and in
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    smaller amount in the core. These isoforms are found at high concentrations in liver, brain and testicles, to a lesser extent in erythrocytes, lungs and pancreas.
    There are two types of SOD that contain manganese, one of which is found in the mitochondrial matrix, and to a lesser extent in the cytosol. Its presence in the mitochondria is of great importance, since the respiratory chain is one of the most important sources of free radicals in the cells, so that it constitutes one of the barriers against oxidative damage caused by free radicals.
    Glutathione peroxidase: it is also a primary antioxidant, which converts hydrogen peroxide and lipid peroxides into harmless molecules (chance (1979). There are two kinds of glutathione peroxidase, and both require reduced glutathione as a donor of reducing equivalents.
    Glutathione selenium-dependent peroxidase: which is a tetra-American protein, with four selenium atoms, which catalyzes the reduction of hydrogen peroxide and organic peroxides. Its active center contains a cysteine in which sulfur has been replaced by selenium. Its activity is greatly affected by the selenium content that depends on the diet. That is why its supplementation is so important, since it is responsible for being the antioxidant that neutralizes the hydroxyl radical (OH).
    Glutathione peroxidase is not selenium dependent, it only has activity against organic peroxides. Most of its activity is found in the cytosol, but also in the mitochondrial matrix.
    Catalase.- participates in the elimination of hydrogen peroxide, giving rise to water and an oxygen molecule. It is also capable of catalyzing certain peroxidation reactions in the presence of H2O, acting on some alcohols, aldehydes and organic acids as a substrate. Catalase is found mainly in peroxisomes, although in recent years and by several research groups, some catalase activity has also been described at the level of mitochondria and cytosol.
    Glutathione is the most abundant non-protein thiol in mammalian cells and is composed of glutamic acid, cysteine and glycine. Its structure gives it a certain characteristic that makes glutathione have a wide functionality and of great importance inside the cells. Glutathione can be found in two forms.
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    according to its oxidation-reduction state: as GSH or reduced glutathione or as GSSH or oxidized glutathione, which is composed of two molecules of GSH, joined by a disulfide bridge between the cystephanes. GSH performs numerous metabolic functions, one of which is to protect the cell against free radicals, peroxides and other toxic compounds, as well as protect against the harmful effect of radiation. Many of the physiological functions performed by GSH are due to two characteristics of its chemical structure, the first characteristic is that the thiol group of the cysteine that is involved in the redox reactions of glutathione and the second characteristic is that the ganma link -glutamil, which makes it resistant to degradation by cellular peptidases. This bond is only hydrolysable by the enzyme glutamyl transpeptidase, located in the cell membrane.
    Glutathione, thanks to its thiol group, can intervene in redox-like reactions, exchanging electrons to severe cysteine sulfur in its structure, being able to react directly on a free radical. Also the GSH reacts with a free radical forming the GS radical, this radical is stable and persists until it finds another radical and forms a molecule of GSSG.
    Physiological functions of the GSH.- The GSH participates in a large number of physiological processes. and of the most important, it is the role it has against oxidative stress since GSH is one of the main antioxidants in cells, it constitutes an important barrier against oxidative stress, GSH protects the cell membrane against damage oxidative, since it maintains the thiolic status of it. The GSH can also be excreted from the cells and act as an emergency mechanism and act against the damage that an excess of GSSG can cause, since it reacts with the thiol groups of proteins forming mixed disulfides.
    Selenium.- of great relevance, is the regulation in the synthesis of proteins. When GSH oxidizes the processes of initiation and elongation of translation is inhibited. When the GSSG is reduced, the elongation resumes and it seems to be an increase in the concentration of the same, which causes protein synthesis to be inhibited. It also collaborates and in a very effective way in the detoxification of xenobiotics, and is able to perform the uptake of some tissues, also constituting a cysteine reservoir.
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    However, the most important role is to be able to react with free radicals, without any enzymatic intervention and detoxify them, or it can reduce the peroxides formed by glutathione peroxidase. When oxidative aggression occurs, GSH is oxidized to GSSG by means of the reaction catalyzed by glutathione peroxidase, the GSSG formed is immediately reduced to GSH by means of the enzyme glutathione reductase. The latter requires NSDPH as a cofactor, which will be supplied by glucose-6- phosphate dehydrogenase. Both glutathione peroxidase and glution reductase are found predominantly in the cytosol, there is also some activity. Mitochondrial level.
    Vitamin E.- Under this denomination a family of phenolic compounds called toconols is included, of which in the organism there are 4 main types: alpha, beta, gamma and tocopherol delta. These groups of highly lipophilic compounds tend to concentrate on biological membranes and plasma lipoproteins. It is the most potent antioxidant in the body, in terms of its capacity as a blocker of the lipoperoxidation chain or also called lipid peroxidation that begins in the extraction of an electron from a carbon adjacent to a double bond by an initiator, such as the OH. Among all the macromolecules present in animal tissues, polyunsaturated fatty acids are the most sensitive to attack by free radicals, due to the possession of double bonds. Alpha tocopherol is within the group, the most efficient antioxidant of the lipid phase that contains methyl groups adjacent to the hydroxyl groups to the phenolic groups and are optimally positioned in the membranes. Tocopherols also have the ability to capture energy from singlet oxygen.
    Plasma levels of vitamin E in humans are around 22 nanomoles / l, found in tissues such as liver, kidney, adipose or adrenal tissue. The human diet is composed of a multitude of foods that contain this vitamin, such as vegetable oils, such as sunflower, corn, soy, etc., and products made from these oils, such as margarine or mayonnaise. From the studies carried out, the following points can be concluded:
    * the toxicity of vitamin e is very low,
    * Animal studies show that vitamin E is not mutagenic, not carcinogenic or teratogenic.
    * In double-blind studies, oral doses have few side effects, even at doses as high as 3.2 g / dfa.
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    * Doses of up to 1000 mg per day are considered entirely safe and without side effects.
    In general, vitamin E is the main antioxidant of membranes in humans, since the pool of vitamin E is small, the system is only functional, if the rate of the same regenerates at the same rate with which it degrades Therefore, supplementation is absolutely essential in patients suffering from a chronic type of process, such as osteoarthritis, in order to reduce oxidative stress.
    From the data presented above, it is shown that there is always a certain level of oxidative stress, which means that a fraction of the free radicals generated in the body, are able to reach their molecular targets, before they can be eliminated by antioxidant mechanisms . However, most of the free radicals, at least in many parts of the cell, are eliminated with antioxidants, in fact the maintenance of redox homeostasis of the tissue is only possible by means of a balance between the intensity of generation and the intensity of elimination of free radicals. This balance can occur with high levels of generation and destruction and vice versa, as in the different animal species. It can also occur within the same species on different occasions, so when the production of free radicals increases due to exogenous or endogenous causes, such as during exercise or hypermetabolism, compensatory regulation can be given to the rise in antioxidant defenses. When this balance between generation and destruction of free radicals is disturbed, the cell enters a pathological degradative process, hence the enormous importance of the study of the different cellular antioxidant systems.
    Conclusions: since we are talking about a chronic type process, in which episodes of an acute type occur, which must be the doctor who is responsible for their treatment, which we do not mention here because it is not the cause of work, What interests us most is what to do with the patient in the intercrisis. The arthrosic patient and, in general, people from 45-50 years of age, if getting up in the morning, if they do not have any pain, is that they are dead as they say in the jargon of the toilets familiar with this type of pathology. or what is the same is at the beginning of the day when the patient suffering from osteoarthritis has a worse time, because he has to "warm up the joints" and for this he has to spend time, which is different passes each patient. which generates a
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    depleted quality of life, as appropriate. An important medication consumption. frequent work losses, etc ... the interest of this work is prevention.
    That the ozone treatment is effective, it is not questionable and is supported by many published works, but we have to clarify the issue. When we administer ozone, by whatever route (dyscolysis, autohemotherapy, paravertebral), what we inject into the patient is electrons, and what they do is behave like an antioxidant (although it is not), and donate these to the radicals free that are constantly being produced in all cells, and as is known lack an electron in its most peripheral orbit. The problem is that the aforementioned ozone has to be administered much more frequently than weekly, and as proof of this is that the patients at 2-3 days, and after having an important initial improvement, the pains reappear. Obviously you can not administer ozone daily or every two days, among other things because it is expensive and annoying the continuous punctures for it is the administration at small doses is the ideal solution and the idea is in the pure olive oil mixed with ozone, but not The aforementioned ozone is going to be administered throughout life, which is why in the same ozonated oil it is mixed with enzymatic antioxidants, which are those that exist inside the cells and it is the first defensive barrier of all organisms.
    Topical medication administration, that is to say that they access the systemic circulation through the blood capillaries that are under the skin, has the following advantages
    * rapid systemic absorption, without interindividual variability.
    * Avoid the first hepatic step.
    * prevents fluctuations in plasma concentrations.
    * long duration of action.
    * painless, so it increases the acceptance and completion of treatment.
    * decrease in the frequency of administration.
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    Description of the invention
    Ozonized oil with antioxidants, object of the present invention consists of an oil base of vegetable origin to which is added:
    • Attenuated Staphylococcus Aureus that stimulates the defense system without causing diseases and that stimulates the production of the antioxidant catalase inside the cells
    • Tocopherol alfa
    • Selenium
    Attenuated Staphylococcus aureus are heat-inactivated collection bacteria in three cycles of 105 ° C for 18 minutes.
    Preferred embodiment
    A preferred embodiment of the ozonized oil, object of the present description, consists of an oil base of vegetable origin, preferably virgin olive oil, to which the following substances are added per 100 ml:
    • Aureus staphylococcus attenuated from 5 to 10 drops, which stimulates the defense system without causing diseases and stimulates the production of the antioxidant catalase inside the cells.
    • Tocopherol alfa 400 mg
    • Selenium 50 to 100 ng / 2 ml.
    The use of ozonized oil with antioxidants is as follows:
    a) Analysis and determination of the levels of catalase, tocopherol alfa and selenium in blood in the patient.
    b) Determination of the amount of attenuated staphylococcus aureus, tocopherol alfa and selenium to be incorporated within the established limits.
    c) The patient is given daily friction in the areas affected by osteoarthritis with simultaneous application of heat for three months.
    d) New analysis and determination of the levels of catalase, tocopherol alfa and selenium in bleeding in the patient.
    e) Determination of the amount of attenuated staphylococcus aureus, tocopherol alfa and selenium to be incorporated within the established limits and the treatment is repeated.
    权利要求:
    Claims (3)
    [1]

    1. Ozonized oil with antioxidants characterized in that it consists of the following components:
    • Ozonized vegetable oil
    • Aureus staphylococcus attenuated
    • Tocopherol alfa
    • Selenium
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    [2]
    2. Ozonized oil with antioxidants, according to claim 1, characterized in that its composition is:
    • 100 ml ozonized vegetable oil
    • Staphylococcus Aureus attenuated 5 to 10 drops.
    • Tocopherol alfa 400 mg
    • Selenium 50 to 100 ng / 2 ml.
    [3]
    3. Ozonized oil with antioxidants, according to claim 1 or 2, characterized in that the vegetable oil is olive oil.
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    同族专利:
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    ES2646335B1|2018-09-24|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US5183911A|1986-03-01|1993-02-02|Dr. J. Hansler Gmbh|Process for the production of stable ozonized oils from unsaturated vegetable oils|
    WO2001037829A1|1999-11-25|2001-05-31|Gomez Moraleda Manuel Antonio|Composition comprising ozonized oils and/or other ozonized natural and/or synthetic products and their use in pharmaceutical, cosmetic, dietetic or food supplement compositions in human and veterinary medicine|
    WO2007137881A1|2006-06-01|2007-12-06|Sano Medical Bvba|Wound care treatment product|
    WO2012168770A1|2011-06-10|2012-12-13|Universita' Del Salento|Process for ozonization of a vegetable oil|
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