DE2456932A1 - Magnetic field oxygenation enclosure - for gas exchange between blood and a gas atmosphere in a magnetic field - Google Patents

Abstract

Several devices are incorporated into a system in which they have direct contact with one another. In these devices, blood or its constituents, culture material for bacteria or viruses, body organs or parts thereof, synthetic blood or even animals can be influenced, cultivated or modified using a wide variety of medical and physical media. A magnetic-field oxygenator encompassed by the above definition is anti-statically and moveably mounted in a moveable housing. Several oxygenators may be so enclosed in an airtight housing having rubber-sealed doors and a heating device. Gives wide range of conditions which can be brought into use in a single appts.

Description

The invention relates to a novel magnetic field oxygellator system to enrich the blood and its components with oxygen and other various Gases with simultaneous use of drugs and physical oil methods.

According to the state of the art, there are many devices for upgrading of the blood known, but none in which the individual blood components such as blood plasma - erythrocytes - leukocytes - lymphocytes - platelets - and arophaen separated are treated in the individual oxygen systems.

The process of the invention is optionally blood exchange in the same way as with heart-lung machines or dialysis machines from all is.

The blood exchange can also-as an exchange transfusion at the same time Infusion of group-matched or artificial canned blood which had previously been Oxygenator system has gone through, take place.

The blood drawn from the patient is placed in a blood collection container, which is used via the oxygenator system with direct blood flow from the same into the oxygen system.

The blood passes through it for the purpose of detoxification and absorption of harmful substances a kidney dialyzer and, after fractionation, is passed through the entire oxygenator system pumped through it with their various apparatuses. From the blood collection container it is finally reintroduced to the patient.

The present invention accordingly includes a metabolic detoxification of the whole blood and body cells as well as an elimination of bacteria and Viruses, blasmoids and oncogenic anoxic metabolites or a retransfusion of the same to normal cells with oxidative, normal processes.

Accordingly, the invention includes means of fibrinolytic-glucolytic - photolytic - biomagnetic - physico-chemical effects on the cell membrane or the cell nucleus and its genetic molecular structures (ll'TS) a disinhibition the immunoparalysis in the sense of a reverse transmutation of the blood and tissue cells with normal metabolic processes, with the exchange transfusion at intervals must be repeated.

In a further embodiment of the invention, the same is at many serious infectious diseases, intermediate metabolic disorders and blood diseases effective, as well as with tumor incidence in humans, ornaments and plants.

In the Iilagnetfeld-Oxygenatoranlagen can also preferably so human and animal organs - organ cells - stem cells, brain cells - tissues of all kinds, as well as bacteria - viruses - yeasts - plasmids, up to artificial blood will. The systems can and can be used for antibody production serve for research in animal and plant experiments of all kinds.

This versatility of this invention is in the oxygenators described does not exist and is a novel magnetic field oxygenator system according to the state of the art.

In terms of the solution according to the invention, the following are recorded called media, which alternatively or alternately in different concentrations and variable current intensities within the magnetic field oxygenator system Use: Enzymes - lytic coenzyme Sp '; # ren (citric acid cycles - ascobic acids - L + lactic acid lipoic acids - amino acids - asparagine - apple fumaric acid - active acetic acid - gluthione - glucuronic acid - cysteine etc.) Growth-inhibiting hormones different types of biocatalysts - metals - minerals - trace elements - magnetic Suspensions - proteolytic ferines e cytostatic antibiotic solutions polyglucoses - Globulins - Peptides Glycolysis-lowering substances Polychemothereme Roborants Tissue extracts electrolytes - anticoagulants - colloids - lxucleoside - aquabidest, sterile water plasma expanders - crystalline solutions - heparin human serums aytochrome, halone 3romeline - redox dyes - amygadlin - endotoxins - flavonoids animal poisons of various kinds - interferon - flocarbon + glycerin - erythropoietin - Polonine - RF factor -BCG vaccine- nutrient solutions and soils ijosoden - homeopathic and herbal ingredients Highly active drugs in microbead form For example, gases and gas mixtures with different temperatures are listed: Pure oxygen, carbonic acid, ozone, helium, neon and other known noble gases, nitrous oxide and others The invention includes effective types of radiation that can be produced in seconds Fractions with variable intensities, optionally in combinations with each other Influence blood or its components during the foaming process. It are named for example: Ultraviolet light orange -Ultravio? L; ett with replaceable Filter ultrasound - microwaves - millimeter waves X-ray telecobalt photons Ultra-high frequency flash light effects laser According to the invention, further physical Applications in the oxygenators effective with the media mentioned under 5-15 can optionally come into action at the same time: Hyperthermia Hypothermia Overpressure Negative pressure magnetic fields by means of dynamo sheet or ferrite magnets Galvanization - Direct currents and other stimulation currents of a known type As additional equipment within the invention are mentioned: kidney dialyzer blood fractionation apparatus Blood centrifuges - Ultracentrifuges Central gas supply systems Ozone devices Drug container systems Sterilization system - hot water boiler - turbine overpressure- vacuum unit Cooling - heating units Blood containers Blood pumps - Exchange infusion pumps Suspension and insertion devices for organs - tissues - blood cells - bacteria - viruses - Culture media and for animals in the form of bowls, cages, etc.

Electronics Photometers Blood Gas Concentration Meters Coagulometers - pil measuring apparatus - thromboelastiogram apparatus.

Filter systems (membrane blood filter - silicone rubber filter - microbeads - and charcoal granule filter - nuclear filter - molecular virus ultrafilter - bacterial filter - Nylonfi lt er.) Hsrmosowlden - measuring cells - control and alarm systems ultrasonic air traps White blood cell infusion supply bottles with supply lines with agitator blades, spray tube valve system, electric vacuum pumps or water jet pumps Membrane with diffuser and eyector moistened and nebulizer glands Additionally are also to be mentioned: Electrical supply and discharge lines Hose supply and discharge lines with multiple cannula attachments and electric valve-electric motors of different types Type duplex pumps - nebulizer for oxygen and medication add.

In addition, apparatus for determining the plasma tolerance to Heparin - prothrombin - index determinations - ffln # brinogenspiegel - determinations the antithroinbin time determination apparatus - oxyhemometry, become the same called to prevent fibrinolysis and also the hyperthermic syndrome.

Sterile disposable syringes to remove from the blood suction valve on the oxygenators the appropriate media can be obtained for intratumoral or intramuscular use to administer.

Pulse generator The description of the invention includes that all media and concentrations mentioned under 5-30 are optionally in the apparatus in combinations with variable currents with each other or one after the other simultaneous work processes and reaction processes within the oxygenators It is used without the blood coagulating or hemolyzing or being allergic reacts and dissolves the mucoprotein envelope of oncogenic cells, neutralizing hydroxylamines and rendering the cell membrane of the Ca cell permeable to said media and the matrix the same retransformed The description according to the invention of the overall arrangement therefore consists of: 1. Steel frame construction with synthetic glass or stainless steel cladding outside, and the inside part with sliding outer walls and movable medicine container doors. The interiors can be heated or subcooled. The apparatus can be mobile.

2. Plastic, glass, metal container or heatable porcelain with Approx. 6 liters of blood capacity with a carboxylated inner layer, can be hung or screwable to the frame construction. At the top of the container is a hanging thermostat with a stirrer blade. The container can optionally also have a double wall have for the purpose of flowing through hot air of 37 degrees Cels.

The container, like the oxygenators, can also be in the frame construction can be hung and driven to pivot horizontally or vertically with the help of small gates will. A high frequency irradiation system can be attached to the container, to keep the blood at 37 degrees cels. keep constant.

3. Kidney dialyser $ -: t of known type electronically controlled with Anticoagulants and electrolyte supplements, etc.

3a. Active charcoal granule filter 4. Ultra-centrifuge arrangement in order to Separation of the blood into plasma and solid components, whereby'd the plasma and the solid Add ingredients to individual oxygenators.

5. Blood fractionation device to separate the individual solid components such as brythro, leukocytes, lymphocytes or thrombocytes to be separated and separated from the plasma to distribute in the oxygenators in solutions of known type.

6-9. For example, 4 smaller oxygenators are shown above, arranged next to or one behind the other in the frame structure to the work cycle to expire.

10. Main and collective oxygenator Ln all of which are described under 6-9 Blood elements flow together so that the secured work cycle repeats in the same can be. The magnet and galvanization systems are used in all oxygenators electronically controlled.

11. E-cut magnet system with windings adjustable in height in the central shaft of the oxygenator inserted, with hand lever lock, fixed to the oxygenator and magnet. (Also screwed to steel frame) The magnet system has power rectifier osscilator and Amplifier for variable alternating or direct currents and consists of dynamo sheet IV or ferrite cores. The middle E-bar of the magnet is shortened.

12. Electroplating system in the inner walls on the bottom and the top Inner wall of the oxygenators running from left to right of the chamber up to V2A steel contacts, which are attached to the outer part of the oxygenator to provide variable field strengths to be made.

13. Positive-negative pressure units with powerful electric air pumps or turbines, to increase and decrease pressure in the oxygenators during the entire foaming process to create. The overpressure and underpressure units have connections to the medication containers.

14. Hyperthermia, within the double walls of the oxygenators, especially the right chamber, in which heating coils are built, or overheating by means of hot, liquid or gaseous elements, which are set to approx. 42 degrees Cels. heated or cooled to 37 degrees Cels, normal temperature.

15. Hypothermia, also effective in the double wall of the left oxygenator chamber for the purpose of subcooling the blood foam to 4 degrees Cels.

Glycerine - water mixtures - liquid are mentioned as cooling elements Nitrogen cooling coils or other known types.

16. Medication container system, the same as those described under 5 Contains media, consisting of synthetic glass walls and doors in which the containers hung, screwed or held magnetically. The chambers are sealed to include the temperature differentiated in the form of warmth and cold the arrangements the container can come in 3 forms. They are located at the oxygenators themselves, are superordinate or the drugs are poured out. Appropriate Hose supply and discharge lines to the oxygenators are attached to the containers, and leave the sealed chambers to also enter the spray tube or valve system to be passed into the defoaming spray rod.

17. Hanging frame for the oxygenators; the same are on the frame inserted, mounted swiveling by means of electric motors, in # form- the oxygenators along with Anchoring pin or

Discs. The oxygenators are operated by means of hand lever locks on the Hanging frame fixed. The shape and the materials can be different, z. B. steel frame construction or aluminum or synthetic glass.

18. Electric hot water boiler with powerful circulation pumps and turbines for the purpose of flushing the entire system with disinfectants. The entire system can also be sterilized with ozone and oxygen.

19. Pressurized gas cylinders contain all types of electron.

Call-up valves, seal control valves, pressure reducers, hose feed lines flexible type to all oxygenators, which are electronically controlled. Water heater odet coolant arrangements can be attached to the gas supply lines to the oxygenators will.

20. The electronics for fully automatic regulation and control of the Invention 1-30, the flow diagram of which is similar to that described Directs work processes; the entire apparatus can also be connected to a clearly arranged control panel for automatic control with self-service.

21. Blood membrane filters on the outlet port are attached to clot To filter blood.

21a. Active charcoal filter 22. Silicone rubber filter for the purpose of filtering radioactive substances.

23. Approaches to the tube end piece in front of the blood pump for the purpose of supply of highly sensitized leukocytes and T + B lymphocytes from infusion bottles.

24. Ultrasonic air traps and other guard systems are mentioned for the purpose of monitoring the flowing blood for air bubbles in the form of two alarm relays, 25. Infusion pumps of known type, e.g. B. the Insomat from Braun, Melsungen.

26. Hose supply and drainage systems for the entire invention from 1 - 30, which are made of metal, flexible plastic PVC., rubber, or compressed gas hoses exist. They have to be acid, gas, heat and cold resistant and are optional provided with electromagnetic probes, connections or valves of all kinds Multiple branch lines and taps, pressure reducers, couplings, adapters, pumps and electr.

Inlets and outlets for the entire apparatus, etc. All of the above Parts can optionally be connected to one another, inserted or attached.

27. Microbead requests for the purpose of supplying highly active drugs in the form of pearls, attached anywhere on the oxygenators and electronically retrievable.

28. The defoaming spray stick inserted into the oxygenators or screwed in, includes all media described under 5-10-20 can be sprayed or misted. The same is done with a small electric motor turned and screwed into the outer wall of the oxygenator in an airtight, rubber-sealed manner.

29. Heat and Kltesonde-Bühler, which as contact parameters as critical monitors are coupled and do not exceed the prescribed limit values and, if necessary, triggers an alarm and causes the equipment to stop.

30. Spray tube valve systems with agitator blades are as described under 29 used and operated and all media described under 5-10 and 20 sprayed.

31. Put a cap between the left oxygenator and the middle bar so that the blood bubbles no longer occur during the defoaming process can be driven into these chambers. The same is operated electrically.

31 a + b contain a mechanism attached to the oxygenator attached outside, in which there is an inflatable balloon, which by means of Compressed air is inflated and the interior of the oxygenator is compressed to foam the blood becomes liquid.

31a shows the container with balloon and valve opening 31b shows FIG Cover inserted into the upper dome of the right Gxygenator, which is inflatable is.

32. Quartz glass window, on both sides in the oxygenator walls themselves or on the hinged lock of the oxygenator gates.

32a. A photon valve with connection to a photon aggregate.

33. Represents the flashlight system with internal opening, or the unisoll lamp.

34. Is the ozone generating device with magnetic valve connections on the supply lines.

35. Are the feed lines from the fractionation apparatus in the Oxygenator6 and from the oxygenators 7-10 via reusable connections using duplex pumps.

36. Selectively operated blood outlet valve into the filter systems.

37. Pressure relief valve, electronically controlled 38. "I1 39. V2A steel connections for galvanization 40. Inlet and outlet valve for Hypothermia and hyperthermia by means of hot or cold gases or liquids 41. Are the gas connections for the named gases, also in mixed form, cooled or heated.

42. Electronic drug chamber retrieval valves, optional left or right oxygenator chamber, attached or potted.

43. Gas pressure manometer with suction valve and bacterial filter 44. Suction valve for gas analytical measurements with the blood gas concentration meter and bacteria filter.

45. E-contact connection for the entire apparatus.

46. Hand lever locks on the magnets, lock them also the oxygenator door or the two-shell oxygenator, as well as on the anchorage the oxygenators on the steel frame.

47. Oxygenator doors, rubber-sealed, on the various figures shown.

48. Insert basin or steel net for organs shown in Figure II -, tissue, blood cell and bacterial cultures.

49. Are the oxygenator diaphragms of a known type with diffuser and Eyektor.

50. Humidifier / nebulizer nozzle for water 51. Rubber piercing inserts in the oxygenator wall.

52. Iris diaphragm or filter closure flap 53. Oxygen bag Clear Description of the individual numbers on the oxygenator No 1 is steel frame construction with sheet steel walls and synthetic glass doors (antistatic), mobile on castors, 2 blood collection containers - high frequency irradiated 3 lier dialyzer 3a active charcoal filter 4 ultracentrifuge 5 - Blood fractionation device 6-9 oxygenators, small, optionally in number of 10 main or collective oxygenator 11 B-section magnet system 12 Electroplating system 13 Hyper-hypo-printing Units with automat. Pressure control 14 hyperthermia units 15 hypothermia units 16 Medication container system 17 Hanging frame for the oxygenators 18 Ice water boiler with circulating turbines 19 compressed gas cylinders of various types 20 electronics 21 blood coagulator filters 21a Active charcoal filter 22 Silicone rubber filter for radioactive substances 23 Leuko-lymphocyte supply 24 Ultra-air trap 25 Blood infusion pump 26 Hose-supply and drainage systems of various types 27 microbead system 28 defoaming spray stick 29 Cold and heat probes 30 Spray tube valve system 31 Closing cap, right oxygenator chamber 31a compressed air balloon with housing and valve 31b plastic-plastic skin 32 quartz glass window at various points 32a photon valve 33 flashing system with internal opening 34 Ozone generating device 35 Feed lines from fractionation app. to oxygen.

36 P. blood outflow valve and inflow valve 37 pressure relief valve 38 vacuum valve 39 V-2A steel contacts for galvanic.

40 outlet and inlet valve, (hyper-hypothermia) 41 gas connections (mixed gas hoses) 42 Medication retrieval valves or nozzles 43 Gas pressure manometers with suction valve and Bacterial filter on the suction device -44 valve for gas analysis measurements 45 E-contact connection for the entire apparatus. 46 Hand lever locks on a magnet - Oxygenator halves 47 doors for the oxygenator, rubber-sealed 48 suspension devices for organ and / or bacterial cultivation.

49 Oxygenator membrane with diffuser and eyector 50 humidifier / nebulizer nozzle for water 51 piercing rubber cast into the oxygenator wall or airtight screwed in 52 iris diaphragm or filter flap 53 oxygen bag In The method of operation of the invention will be briefly discussed below.

Figure I shows the overall view (1), the housing with steel frame construction, mobile on wheels and includes all equipment and oxygenator systems. The housing can also be made of sheet steel with synthetic glass walls and doors, and is rubber-sealed so that the entire interior system is at 40 degrees cels. constant can be held.

In Figure I is a blood container (2), radiofrequency irradiated and a stirrer insert for approx. 6 str. whole blood with inlet and outlet valves (3) the kidney dialysis machine of known type, from which the dialyzed blood is transferred Roller pumps over the activated carbon filter from (Da) to (4) into the ultracentrifuge is pumped. This is done using plastic pipes. In the ultracentrifuge that will Blood is centrifuged into plasma and solids, with the plasma in the oxygenator (6) flows and the amount of solid components into the blood fractionator (5) to 'the separation between erythrocytes, white blood components and platelets each separately in the oxy-genatoreK '; - 9) or more connected oxygenators initiate, with the simultaneous addition of solutions.

The oxygenators (6-9) start immediately after being filled from the blood fractionation apparatus with the hanging frame (17) in a slow rhythm, alternating vertically and horizontally to move to mix the blood components, also as in oxygenator (10) all media and equipment described from 5-25 via a gas system (19) (34) to be mixed with the cell components and foamed.

During these work processes in the oxygenators (6-9), the magnet systems (11) active to by means of a variable alternating magnetic field and with additional alternating Switching on the electroplating system to influence the oxygenated foam (12).

Through the quartz glass window (32) are at the same time UV rays or Lightning effects (33), or the other types of radiation mentioned, transmitted through, the reverse transmutation of the oncogenic cell or its defective genetic molecular The structure can be changed electro-magnetically to the normal cell.

In order to achieve this, there are further effective agents according to the invention possibly necessary and result from the current state of research. Thought are highly effective Medicines in bead form, which are attached to each oxygenator in a container (27) and can be accessed electronically.

It is known that tumor cells can be treated with positive or negative pressure (13-14) become unstable and vulnerable to the various drugs and types of radiation, and they are effectively used within the oxygenators.

The application of hyper or hypothermic effects to the Cell membrane or the cell nucleus via heating and cooling units (14-15) is advantageous. These media are let into the double wall of the oxygenator and have an effect in the left ventricle an overheating of the blood components to approx. 40 degrees Csls, in the case of foamed oxygenated blood foam; the same then becomes through the middle Chamber driven into the right oxygenator chamber to be there after it has been closed via the anti-foaming spray rod with simultaneous action of the refrigeration units to + 4 degrees ces. to be cooled down.

The liquefied blood is then reduced to approx. +37 Graa Cels.

heats up and passes through the outlet valve (36) to until reinfusion to go through the filter systems listed below.

The medication containers are on the oxygenators, or in the same, or shown cast-in and depending on the need are constantly set to approx. +37 degrees Cels. # Kept supercooled.

The spray tube valve system includes the drugs and all introduced under 5-10-15 media through the same into the oxygenator chambers can be. The same can be in both chambers and rubber cuffs sealed from above are introduced into the chambers and driven by small E. motors.

Photons can affect the cell nucleus via the cell membrane and are entered via the valve (32a).

A further embodiment of the invention includes that the material from the oxygenators via lines or direct connection valves according to the figures flows together so that all of the blood components come together in the collective oxygenator (10). In the same the processes can take place again, as in the oxygenators (6-9) described.

The necessary membranes (49) that hold the blood and the aforementioned Gases in a heated or supercooled state pearl up the blood, are well known Tried and tested in other oxygenator systems and used in the oxygenators (6-10).

The vertical and horizontal rotations are made within the The suspension frame of the oxygenator is mounted on an axle on the tubular steel frame and powered by electric motors.

The hanging frames (17) have the exact fit for the oxygenators. The vertical and horizontal rotary movements can optionally also be omitted and the operations take place with fixed oxygenates.

The liquefied material flows through the electronically controlled outlet valve (36) Blood after overpressure generation in the oxygenators in the blood membrane filter (21), to filter coagulated blood.

From here it seeps through the activated charcoal filter (21a), which consists of small grains of charcoal that chem.

clean. According to the flow principle, it then flows from stopped into the Silicone rubber filter (22) to eliminate or increase radioactive components filter. In (23) highly active lymphocytes, leukocytes, or macrophages etc. which are specially grown in the oxygenators (7-9) and lytically eliminate the oncogenic cells.

The last stage is the ultrasonic trap system (24) with Guard devices against air bubbles. The reinfusion is then carried out via the Blood pumps (25) of a known type made in the arterial circulation.

The measuring probes or feelers and gasanalyciscben p? Ratu: ^ er as well as photometric Apparatus and coagulometers including pH measuring devices can be connected to the oxygenators themselves be attached, or poured and fully automatically the blood constant in regulate these measuring ranges via injection nozzles by the electronics.

The invention is also applicable to the cultivation of bacteria, viruses, Yeasts, artificial blood, organs, or tissue parts, or cells, so-called cell fusion of all kinds.

The production of antibodies for research, therapeutic purposes and for the study of metabolic processes in the same and their therapies thought.

In addition, animal experiments can be carried out in the same via insert containers (48) take place depending on the size of the oxygenator.

In Figure 14, a multiple magnetic field oxygenator system is shown, in which in succession under the same conditions as in detail above described, the individual media can be tested for blood compatibility, until reinfusion into the arterial circulation.

The various embodiments of the invention are illustrated with the aid of the figures and illustrations with partial numbering, for example, where the individual oxygenators basically work in the same way. All include the parts mentioned in Figures I and II in chambers 1-53.

Figure I shows the overall view of the invention within the steel frame structure with all representations mentioned 1-51, whereby the additional equipment, systems, and the electrical supply and discharge lines and the hose systems not for the sake of clarity are shown, not even in the other figures of the magnetic field OM'y'genators.

Fig. II shows an overall view in cross section with the items 1-51 connections and electrical call valves described. The oxygenator itself is made of plastic or stainless steel, double-walled, with a medicine container attachment and a magnet system installed in the central shaft. Inside the oxygenator run galvanization system, spray tube valve system with defoaming spray stick, X-feed blades with the respective feed connections.

The oxygenators can be in a steel frame or in a Hanging frame stored and fixed by means of hand lever locks or else rotatable about an axis and arranged to be pivotable or rotatable by means of an electric motor be. Height-adjustable screws on the magnet and axle allow adjustment of the magnet.

The materials of the oxygenators can be plastics such as PVC Artificial glass, Lexan, polycarbotnates, polymers, mixed polymers, silicone rubber, Collagens, poly carbonate glass, metals, stainless steel, or heatable porcelain.

The shape of the oxygenators is round and consists of two mirror images, self-supporting, equal parts as bowls with a size of approx. 15 cm to 2 m in diameter. The inner walls are carboxylated against hemolysis of blood components. Both spherical shapes are connected by a shaft-like central web, seamlessly cast or drawn, can optionally have hand lever lock or magnetic tape lock, or hinge-mounted be. The oxygenators have openings for the valves described and for the Magnetic core insert facing the interior. The openings are rubber-sealed.

The oxygenators have rubber-sealed caps of various types Kind that include quartz glass window inserts and valve fittings.

There are also openings for the anti-foaming spray stick and the valve tube system in place.

The oxygenators have double walls, in which the heating or Cooling gases ~ circulate. Inlet and outlet openings for the same are in the outer one Double wall pierced and rubber-sealed.

Liquid cooling media, heating or cooling coils can also be fed into the Double wall are fed.

The medicine containers can be poured into plastic glass oxygenators otherwise they are put on, like the various blood analysis tests described Control apparatus.

The materials of the oxygenators are heat and cold resistant and must be acid and bacteria resistant. They also have to be able to withstand strong pressure.

In the middle hatch is a molded fit for the purpose of receiving the E-cut magnets.

Fig. III shows a synthetic glass oxygenator in cross section, consisting made of two mirror-inverted parts, which are anchored on the hinge and have rubber magnetic closures or hand lever locks are sealed. One half is shown with pouring depressions the hollow spherical shape, the central shaft for the magnet system, the cast-in electroplating system and all connections described in 1-51.

Fig. IV shows a cylinder oxygenator as an overall view, pivotable with built-in equipment and connections 1-51.

Fig. V shows the front view of a double centrifuge oxygenator with a hinged cover made of synthetic glass, the magnet and electroplating system and the cast-in or screwed-in connections 1-51 described.

VI shows the top view of an oxygenator system based on the flow principle with the purpose of making shorter arrangements for oxygenator 10 without larger hose lines to reach.

Fig. VII shows a hollow ball oxygenator made of two plastic hollow balls, the one with the intermediate insulating ring in which the electroplating system runs, placed one on top of the other are. Create rib-shaped magnetic cores built into the plastic mold a large variable magnetic field. The measuring containers are in place. It also includes that all systems and connections described in 1-51 'in the hollow sphere oxygenator are appropriate.

Figure VIII shows the front view of a horseshoe oxygenator from a Plastic frame in which the magnets are inserted; inside runs the Electroplating plant. Two base trays for foaming with a membrane and one for liquefied blood are shown. The representation includes all connections 1-51.

Fig. IX shows the E-section magnetic core in the transverse # hnit # with a shortened E-cut in the middle part, height adjustment screws and hand lever locks.

Fig. X shows the cross section of a single chamber oxygenator with sideways arranged magnetic cores and galvanization running inside and the cover housing with spray tube valve system with agitator blades. The drug chambers are next to the Magnetic cores arranged. Other connections and devices described under 1-51 are partially shown.

Fig. XI shows the defoaming spray rod made of plastic with channel system and drainage groove, inserted in the oxygenator wall, with electric motor and supply lines Mistake. The media 5-15 are sprayed in the same.

Fig. XII shows a pivotably mounted, movable by means of an electric motor Oxygenator system, with the oxygenator (10 #, and the attached oxygenators (6 - 9), without hose lines and attached drug chambers. The same can also be cast from synthetic glass, with a hinged half and cast-in supply lines from 1-51.

Fig. XIII shows the cross section of a magnetic field Oxy enatorenanlage with housing, the oxygenators 6 - 9) with direct connections to the oxygenator (10) are shown above. The oxygenators (6 - 9) can be swiveled on rollers mounted, extendable or rotatable in a circle with direct connections to the oxygenator (10). The magnets, galvanization and medication chamber can be seen. The end plate is made of plastic glass through which the spray tube valve system or the defoaming spray wand can be passed through. Otherwise all connections 1-51.

XIV shows a magnetic field oxygenator system mounted in a frame with any number of small oxygenators, each as a so-called test oxygenator system are superior. All media and equipment described under 3 - 30 are included Additional equipment and connections, especially the drugs described under 5 and gases can be tested in sequence while they are up to the oxygenator (10), as well through the filter system (21-25), the blood pump or the blood container. Otherwise all connections 1-51.

XV shows the front view of a magnetic field oxygenator system, with surrounding magnet systems, internal galvanization, attached drug chambers, three openings with three quartz glass windows and blood drain connections into the filter systems.

The smaller oxygenators (6 - 9) can optionally be placed on the oxygenator (10) are put on and are not shown; however, all with the 1-51 affected parts.

XVI shows a schematic representation of the tanking process within the overall system up to the infusion pump (25) in plan view. All other additional systems described are not shown.

The electronics are active according to the functional sequence.

FIG. XVII shows two magnetic field oxygenators arranged in the same direction with side-mounted magnet systems and medication chamber and inside Galvanization. The blood supply can be seen, as well as the gas connections for the purpose of frothing blood, whereby the blood has to pass through two membranes. The first known type is said to be oxygen mix with blood and the second should reduce the blood vesicles minimally, before they run over the ascent tube filled with medicine beads, to the top via a deflector, which contains a UV emitter, via the galvanic one Grid to the collecting basin and from there via the filter systems to (255 of the blood infusion pump to get. A metal grid structure is attached to the upper end of the ascent tube, to fix the pearls.

thirty. XVIII shows a disposable silicone rubber magnetic field oxygenator with arboxilized inner surface and cast-in connections for the higher-level Medicines Chamber and those from 1-51. The blood foam is galvanized in the lower part over the galvanization grid. The quartz glass window is shown. The system consists of a steel frame that can be folded apart. Inflatable Silicone rubber sleeves seal the closures. The silicone rubber is double-walled inflatable.

Fig. XIX shows a cylindrical magnetic field oxygenator with all Connections 1-53, whereby the entire inner wall consists of a single ferrite core or copper inner wall, through which a pulse generator and a Treatment coil, which are connected to one another with a cable, inside the Magnetic field oxygenator generates a pulsating magnetic field. The one inside running galvanization system, the galvanic metal mesh and the foaming membranes can be seen. Half of the cylinder wall itself can be made of synthetic polymers exist, in which the magnet jacket is cast.

The figure can consist of three parts: lid, base and cylinder can be screwed into each other and are locked against each other with hand lever locks fixed, or by means of a clamp at the upper and lower end against each other sealed, fitted and screwed, with four locking screws on each cylinder are attached, and the drug containers are in direct contact with the injection valves The upper cover plate consists of quartz glass inside.

Fig. XIX shows a cylinder oxygenator consisting of five parts with all connections and equipment from (1-53).

The upper end pouch (47) consists of a hinged circular one Plastic plate with inserted medicament chambers (16), which are distributed in a circular manner are, a round quartz glass insert (32), the supply valves from the oxygenators (6 - 9) and an inlet valve (36 @) in the oxygenator bag (53) Blood liquefaction through the hyperpressure valve (13), which is a branch valve, once in the magnet chamber and once in the oxygen bag, compressed inwards.

The same is seamless and consists of two parts made of synthetic fibers or plastics and has a mounting strip in the upper part into which the valves from (16) are used. The listed valves of electromagnetic structure are built into the medication plate and optionally have a connection in the magnet chamber or in the oxygen bag (53).

The material of the oxygen bag must consist of PVC or polymers and must be magnetic field permeable and can be used as a single use.

The oxygen bag can also optionally be omitted. The blood foam is then foamed directly into the magnet chamber (11), flow through the above-mentioned Media and physical methods-affects the whole facility and is about the Filter (21-24) re-incorporated as arterial blood by the blood pump.

Take in the magnetic coil (11) surrounding the upper part of the cylinder the blood components by means of magnetic energies under changing magnetic fields a pulse generator via a treatment coil with network connections. The cylinder part is on the outer plastic base with hand lever locks on the lower part inserted knobs or fixed to the bar. The spool has a rubber piercing opening (51) for the purpose of taking blood samples from the chamber coil wall or from the oxygen bag, which for this purpose has a magnetic mounting knob to adhere to the bobbin to be able to.

The cast base, in which the above-mentioned parts are placed, is made of plastic and consists of a round disc with two side walls and a hollow inner wall and is provided with openings, valves or other connections for (36, 44,18, 20, 29, 28, 35, 57, 38, 39, 40, 41, 46,51).

The lower cover is ball-bearing and mobile and comes with -Help of an electric motor moves. So the entire cylinder oxygenator is over once an axis inserted in the middle rotated and a second time with gears bottom Oxygenators (6 - 9) on a table directly behind the cylinder oxygenator are arranged or screwed to the wall, moved sideways. About magnetic Direct connections of their media are taken over one after the other by the valve (-36).

The insert grids in the metal grid are filled with highly active microbead drugs, against which the oxygen-saturated blood bubbles rub. Through at every grille arranged inlet valves for oxygen are taking the blood bladders again Oxygen uptake during the friction again saturated and fine-bubble through the several different types of drug bead additives attached to the top are pressed through (27) to be cooled to +4 degrees Celsius in the defoaming chamber, # with it they liquefy. All processes of saturation and reduction in size of blood bubbles are done under magnetic fields.

The insert grids have a tube with openings on the bottom for oxygen. The top insert grid also has a fine-meshed sletz so that the Pearls cannot be pressed upwards. At the lower end of the insert grid a plastic or metal grid is arranged to reduce the size of the blood blisters and stored in the base. To reverse blood liquefaction in the left ventricle To avoid this, a compressed air balloon (31a) is inserted into the central base wall is applied, which drives the blood blisters upwards.

The shape of the insert grids can be different. To the full The volume of the cylinder can also be filled on a kidney-shaped insert grid thought, with the drug grid and the defoaming cylinder shown are. The amount of the stakes can be arbitrary, but always so that a large one Aufeprührraum is available in the cylinder.

After the blood bubbles or liquid blood has passed through the Defoaming cylinder, the blood enters the blood collection chamber, which is from the outside via ultra-high frequency radiators to approx.

60 degrees Celsius is heated so that the blood inside is also heated to approx.

37 degrees Celsius is heated.

The illustrated diffuser, eyektor and oxygenator membrane, as well as the galvanization system in the form of an inserted grid which operates under direct current and the superordinate drug bead grid up to the finest bead filter that wears off with iris diaphragm or filter cover: closing flap (52) can all be inserted into the base wall, which groove guides has to be used, or the entire representation is inserted in a stainless steel or plastic container, internally carboxylated. All Parts can be taken apart and sterilized individually.

The purpose of the iris diaphragm or filter shutter (52) is that the blood foam is not pressed back in the case of excess pressure treatment by closing the same will. The bezel can be made of metal or plastic and is electronic made.

The oxygenator bags are visibly flanged to the attachment nozzle.

The central cast base wall can be dismantled in two parts and has valve inserts in the wall, so that tempered gas (19) in the parts of the left Medication grid inserts and over (50) in the magnet chamber or the oxygenator bag comes.

In the right chamber, a heater system is shown, around the Blood foam, which was previously heated to 40 degrees Celsius in the left chamber, to cool down to +4 degrees Celsius in the magnetic chamber and again in the heating system temperature to 37 degrees Celsius by means of ultra-high frequency or infrared radiation.

The insert on the right is a cylindrical hollow body made of metal or plastic, in whose tubes the heat media circulate, in each of them The tube shown by itself contains the corresponding temperature.

In the metal insert there is a plastic fiber cylinder with a spiral shape Arrangements made of non-wettable plastic material through which the blood foam liquefied flows through 'and flows into the filter systems (21-29 in order to be called arterial Blood mixed with all blood components from the oxygenators (6 - 9) via the shown oxygenator (10) to be incorporated.

The oxygenator (10) is movably mounted on rollers on a slide rail. He drives the oxygenators arranged opposite him (6 - one after the other, will stopped via sensor probes, and takes the liquid media via solenoid valve openings from the oxygenators (6 - 9) into the blood frothing chamber as a collecting container.

The oxygenators (6 - 9) are on roller bearings all around directly on the oxygenator (10) are driven by electric motors and have direct magnetic contact with oxygenate # 'r (1Q at the level of the blood frothing chamber. With a slight overpressure they release the media away.

The oxygenators (6-9) correspond exactly to the same in the invention Construction with all connections to equipment and additional equipment.

The oxygenator system is controlled fully electrically or fully electronically.

The top cover is made of quartz or synthetic glass with quartz glass inserts to be radiolucent according to the figure.

All media valves etc. described are cast in or screwed in arranged.

The top lid is cast in one piece, or two of the same Parts provided with hinges, can be opened, with the hinges attached at the rear and the sealing channel is rubber-sealed. The top cap is completely removable due to the insert parts. The drug chambers :: can also open be screwed in the same and are accessed via magnet tile. So it is either the chamber or a spray bottle with the various drugs screwed the cover onto a valve attachment with different openings.

The blood foam or its components can be in each individual Oxygenator - no specific number is required - to be tested. she are arranged next to or one above the other, so that the blood foam or its components can continuously flow into the next oxygenator.

The rising blood foam etc. from the drug bead grid comes in a collecting container. In an elastic oxygenator bag, which is double-walled, internally carboxylated and permeable to magnetic fields, becomes the blood foam compressed.

As the pressure increases, it liquefies and then becomes emptied into the fiber cylinder. Before the pressure is applied in the oxygenator bag the iris diaphragm closed.

Another Irish representation of a magnetic field oxygenator is a Syl-onde resygenator whose cylinder walls run continuously from (47) down to (475, with attached Medicament chambers (16), a quartz glass window (32) ', the gas pressure manometer (43), Hand lever locks (46) and all connections (1- 51).

The interior of the solenoid is completely empty, so that all Media can be sprayed via the connections (1-51).

then it goes through #the filters (21-25) and then becomes again incorpated.

All of the components shown and described in Figures I to XIX are optionally interchangeable and combinable and can be arranged in size to be different.

Optionally, individual parts can also be left out. In Figure XIX The diffuser, eyector and galvanization remain permanently in the left chamber, the fiber cylinder always in the right ventricle to protect the blood from hemolysis. The remaining parts are interchangeable.

Claims (1)

Claims I. 1. Device characterized in that in the same menrere Äpparate are arranged so that they are in direct contact with each other and that in same apparatus blood or its components, breeding ground for bacteria or Viruses, organs or organ components, artificial blood or even animals influenced or ignited the various physical and medicinal media or can be changed. 2. Magnetic field oxygenator according to claim 1, characterized in that the same in a mobile housing (1) is antistatic and mobile. Magnetic field oxygenators (6-10) according to Claim 1, characterized in that that the same are built into a mobile, antistatic housing (1), and that the housing itself is heatable and air-tight with rubber-sealed doors is. 5. Magnetic field oxygenator system according to claim 1, 2, characterized in that that in (1) the blood collection container (2), which has a heated double wall, with an agitator is provided and irradiated from the outside with high frequency, and that after opening the solenoid valve, the blood flows into the kidney dialyzer (3) to cleaned by an activated charcoal filter (3a) after opening the solenoid valves Roller or hose pumps to be pumped into the ultra centrifuge (4). Brook the separation of solid and liquid blood components, the plasma flows into the Oxygenator (6) and the solid components in the blood fractionation device (5) magnetic exhaust valves. Flow into the blood fractionation device via a magnet Wentil also from the medication container (16) after electronic retrieval of solutions different types for the erythrocytes, leukocytes and limphocytes; become the same then also pumped into the oxygenators (7 - 9) or through direct contact headed into this. 4. Magnetic field oxygenator system according to claims 1-3, characterized in that that the oxygenators (6-10) consist of two hollow spheres with double walls, in which heating coils or cooling coils are installed. In the same can also Hot or cold gases, or liquids such as glycerine-water mixtures or liquids Nitrogen are filled to be heated via the heating and cooling units (14 - 15) or to be cooled and thereby via thermostats, sensors or probes (29) of the electronics (20) to be controlled. An electronically controlled pressure relief valve (40) regulates the thermal Operations. The hollow spherical shells are self-supporting with two identical mirror images Parts are hinged and have turned-out edges into which the electromagnetically Controlled magnetic tapes are potted or screwed in to ensure a safe To achieve closure by means of the airtight hand lever closures. The two hollow spherical soaps of the respective oxygenators (6-10) are with a cast-in or with a plastic central duct made of fixed connector. In the middle shaft there is also a shaft running upwards poured in, which lets in the magnet system (11). ~ This is where the inserted magnet parts become by means of an opening in the middle shaft directly opposite each other after switching on of the magnetic field effective when the blood foam is driven past by means of oxygen, etc. will. 5. Magnetic field oxygenator system according to claim 1 - 4, characterized in that that the materials of the same are made of stainless steel, plastics, Lexan, PVC, polymers, Mixed polymers, plomeres, polycarbonates, collagens, synthetic glass, or according to American Patent 161 7441, glass-heated porcelain or any combination that Orders of magnitude between 10 cm and two meters can succumb to the interior wall coating is carboxylated. Also silicone gum oxygenators, which are thrown away after use, are shown. In addition, all oxygenators are acid, bacteria, cold and heat resistant. The oxygenators themselves have round doors (47) that are rubber or magnetic tape sealed are. Quartz glass windows (32) are provided in the double wall of the oxygenators to allow radiation to pass through and the flash devices inserted. The flash light influences the Foam of blood, which is driven from the left ventricle into the right ventricle. 6. MagnetSeld-Oxygenatorellanlage according to claim 1 - 3 characterized in that that the oxygenators in a hanging frame 17), which is made of metal or plastic is cast, over the storage knobs (51) and hand lever locks firmly in the frame (1) are fixed and stored. If necessary, the oxygenators become electronic solved in order to be able to rotate about an axis by means of an electric motor. 7. Magnetic field oxygenator system according to claim 1 - 5, characterized in that that in the oxygenator double walls recesses for the valves, contacts, and Stakes of the numbers (5, 11, 12, - 16, 18, 19, 27 - 31, 31a, 32a, 33 - 44, 49 - 51) are available, which are controlled via the electronics (20) the, and connection have with all electrical supply and discharge lines, as well as with the hose connection (26). 8. Magnetic field oxygenator system according to claim 1 2 5, 8 characterized in that that the galvanization system t125 within the blood fragments via the V2A steel contacts 39) becomes effective and runs in the bottom or ceiling inner walls of the oxygenator. It can also be in the form of a metal grid that is placed in or over the blood, be used inside the oxygenator and is used during the blood-oxygen frothing switched on. The electroplating system (12) consists of an ammeter, rectifier, and potentiometer and is subject to variable currents. 9, magnetic field oxygenator system according to claim 1, 8, characterized in that that the magnet system (11 consists of two different sizes of the E-cut magnet cores and the central core is shorter than the two outer ones. The magnets exist made of dynamo sheet or ferrite cores and are wound with a coil on the mains current connected and contain a power rectifier, osscilator, pulse generator and amplifiers for variable frequencies and field strengths according to the heart rate. The magnets are fixed by means of hand lever locks (46) or screwed to the walls. (45) is the E-contact for the solenoid and the Oxygenator system. 10. Magnetic field oxygenator system according to claim 18 8, characterized in that that the sterilization of the entire system in an autoclave in the water for 25 minutes is kept at 125 degrees Celsius for a long time. The same thing happens in all oxygenatoron and valves with the help of the circulation turbines with hot water boiler (18)., The water is then sucked off through the blood outflow valve (36) and then the same process is repeated with hot air or ozone, with the hyper and hypothermia aggregates (14, 15) are switched on and the gases are then switched on with the help of the hypothermia unit (15) discharged via the blood outflow valve (36) and the gas pressure manometer (43) will; in the process, bacteria are released and eliminated. 11. Magnetic field oxygenator system according to claim 1 - 5, 8 characterized in that that the drug container (16), spray tube valve system (30) and defoaming spray stick (28) screwed or cast directly onto the oxygenators (6 - 10) are, with direct contacts to the valves (42). The medication containers are influenced by heat and cold via (14 and 15) and then as pressurized gas via (13) through the valves or Nozzles pressed into the oxygenators. Compressed gas bottles are inserted into the drug chambers, which are electronically controlled by means of solenoid valves in the oxygenator chambers Portioning systems at time intervals including the media described of microbeads, inject. 12. Magnetic field oxygenator system according to claim 1 ~ 2,4,5,8,10 thereby characterized in that a compressed air valve is attached to each of the oxygenators (6-10) is, in the housing of a silicone rubber balloon or a simple rubber balloon through the valve (31a) is inflated directly until the right oxygenator chamber is filled, around the blood through compression and additional thermal gas influence to defoam. 13. Magnetic field oxygenator system according to claim 1, 2, 5, 7, characterized in that that the defoamed blood or its components from the oxygenators (6-10) the e tromagnetic opening of the blood outlet valve (36) in the blood coagulation filter (21) flow in; from here they flow through the active charcoal filter (21a) and then the silicone rubber filter (22) for the purpose of filtering radioactive substances. The infusions (23) etc. are fed into the connecting tube (22 - 27). and are made up of white blood cells or platelets. A final check of the whole blood is carried out in the ultra-air trap (24), which responds immediately with an electronic stop when an error occurs and an alarm relay triggers. 14. Magnetic field oxygenator system according to claim 1,3,5, characterized in that that after the whole blood has passed through with all blood components, the same either is introduced into a blood collection container (2) to repeat the oxygenic process, is fed directly into the blood infusion pumps (25), or from the blood collection container flows directly into the blood pump. 15. Magnetic field oxygenator system according to claim 1, 2, 7, characterized in that that on the oxygenator 6-10) a gas pressure manometer (43) with overpressure and underpressure valve and built-in bacterial filter is attached, as well as a valve for gasanabjtiache. Measurements (44), as well as piercing openings for rubber inserts in the oxygenator wall (ski) for the purpose of blood foam removal, and blood foam removal, finally a valve membrane for photon action (32a) on the blood foam and its components. 16. Magnetic field oxygenator system according to claim 1,2,4,5,7,8,10,11 characterized,. that in the inset dishes, chambers or grids (48) bacteria, Viruses, yeasts, plasmoids, parasites etc for organs or organ components, tissue, Plants or animals are bred or influenced, which also occurs in nutrient media can go. 17. Magnetic field oxygenator system according to claim 1, 2, characterized in that that claim a humidifier-nebulizer nozzle (50) on each oxygenator in the double wall is built in and made electronically (20). 18. Magnetic field oxygenator system according to claim 1 -17, characterized in that that same out. two mirror-inverted shaped pieces made of synthetic glass, hollow spherical It is cast with recesses for the magnet system and with a carboxylated inner wall coating. The electroplating system (12) is included, as are all connections and valves t-51) poured. The two cast blocks are hinged and rubber-sealed and have magnetic and hand lever locks (46). They are stored on an axis and are vertical with an e-notor and adjusted horizontally. 19. Magnetic field oxygenator system according to claim 1-17, characterized in that that the cylinder oxygenator is mobile, the built-in apparatus can be swiveled are stored with all connections, valves and nozzles (1-51). 20. Magnetic field oxygenator system according to claim 1-17, characterized in that that the same is arranged as a centrifuge oxygenator system with a lid lock, through which all connections, valves and nozzles (1-51) are cast or screwed in are. All media are sprayed through this by means of (27), (28) and (30). 21. Magnetic field oxygenator system according to claim 1 - 1 7 characterized in that that the same is arranged as a flow-through oxygenator system, without larger hose lines and other supply and discharge lines but with all connections (1-51). 22. Magnetic field oxygenator system according to claim 1 -17, characterized in that that the same is arranged as a two-part spherical oxygenator system in a plastic rib arrangement, in which the magnet inserts are installed. In an all-round insulating ring is the galvanization (12). The spherical oxygenator includes all connections from (1-51.). 23. Magnetfeld-Oxygenatorenanlgge according to claim 1-17, characterized in that that a F1-shoe-Ma # netoxygenator is shown that all connections (1-51) contains. The magnets (~ 11, and the galvanization (12) are in the plastic ribs used. 24. Magnetic field oxygenator system according to claims 1 -17, characterized in that that the two ferrite magnets (E-shaped and the oxygenators (10) with surround all connections (1-51). The windings and the land lever locks, which hold the magnets together (46) can be seen. 25 MagFnetSeld oxygenator system according to claims 1 - 17 characterized by p-: e, that a single-chamber oxygenator is shown with magnets arranged on the side (1i) ,. internal galvanization with grid (12) and drug chambers (16) and all connections, valves and nozzles (1-51). 26. Magnetic field oxygenator system according to claim 1-17, characterized in that that a defoaming spray rod (28) is provided which is electrically rotatable and through which the media can be sprayed in an internal channel system Spray openings and valves as well as a drainage channel for liquefied blood. Of the The spray wand is rubber-sealed and built into the oxygenator wall and included all connections (1-51). 27. Magnetic field oxygenator system according to claim 1-17, characterized in that that a synthetic glass oxygenator with direct connections to the oxygenators (6-9) is shown is, which consists of two hinged parts that can be opened and hinged Plastic or synthetic glass is cast. It rests on an axle and rotates with the aid an electric motor and is inserted in the steel frame and with all connections connected by (1-51). 28. Magnetic field oxygenator system according to claim 1-17, characterized in that that an oxygenator system with the oxygenators (6-10) is shown with galvanization (12), drug chambers (16) and magnet system (11). The oxygenators (6 - 9) are Mounted on studs, can be swiveled through 360 degrees and have outflow openings to the oxygenator 10 and contain all connections from (1-510-29. Magnetic field oxygenator system according to claims 1 - 17, characterized in that a test oxygenator system is shown is with any number of small oxygenators z. B. 6 to 30 through which all Media can be tested sequentially until the blood components pass to oxygenator 10, to the filter systems (21 - 24) and finally to the blood infusion pump (25) arrive. The system stands in a steel frame and is per oxygenator a magnet system, an electroplating system and a drug container system available. The oxygenators are pivotably mounted on an axis in the hanging frame, have continuous contact valves from oxygenator to oxygenator and are with all Connections from (1-51). 30 .. Magnetic field Ox, - generator system according to claim 1 - 1'1 thereby characterized in that an oxygenator system is shown obliquely downwards running center shaft from the left to the right oxygenator chamber and inside running galvanization system and magnets running outside. The plant has three oxygenator doors, an externally mounted drug container system (16) and includes all connections from (1-51). 31. Magnetic field oxygenator system according to claim 1-17, characterized in that that a scheme according to the flow principle of the systems 1 - 25 with all connections is shown by (1-51. 32. Magnetic field oxygenator system according to claim 1-17, characterized in that that a two-part oxygenator system is shown with microbead-filled Tubes and rising blood foam, which previously through the membranes (49) to Very fine beading of the foam is oxygenated and pressed through, also with an externally arranged Magnet system (11) and internal galvanization (12) on both oxygenators, which the blood foam towards through a galvanic grid in the collecting space to the filters (21-25). Otherwise all connections from (1-51), 33. Magnetic field oxygenator system according to Claims 1 to 17, characterized in that the same consists of a double-walled silicone rubber tube oxygenator and as a so-called Disposable oxygenator is used with all connections (1-51) The magnet system (11) is hand-lever locked in (1), a hinged tubular steel frame rack, t with externally arranged medicament chambers 16). The frothing kettle is located in (1) with the membrane (49) together with connections and the galvanization grid (12), wherein the disposable oxygenator by means of a magnetic lock with the foaming kettle is connected or screwed in. 34 '. Magnetic field oxygenator system according to Claims 1 - 18, characterized in that that the same from a cylinder oxygenator made up of five disassemblable parts consists, 47,16,11, 10,47, all of which are rubber-fixed with hand lever locks (46) are mounted on the tubular steel frame (1), all of (1-53) described Equipment and connections include and by means of electric motors as a complete system an axis in the bottom cover or on the side wall can be moved via a gear drive. 35. Magnetic field oxygenator system according to claim 1-18, characterized in that that in (16), the medicament lid, which is made of synthetic glass, plastics, or stainless steel consists and is internally carboxylated, the magnetic treatment coil, which is cylindrical is attached and fixed under the drug system in a rubber-sealed manner. Of the The lid also contains the quartz glass insert (32), the photon valve (32a), the Flash light system (33), as well as the valve connections for (35-44,13-15,18,20,26, 29,30). 38. Magnetic field oxygenator system according to claim 1-18, characterized in that that the solenoid is cylindrical, made of ferrite or copper metal, on the outside is plastic-coated, and that the same via a network connection with a pulse generator is connected so that a constant and alternating magnetic field of variable intensity is created, which influences and changes the blood components during the foaming process, and that blood samples are taken through a piercing membrane in the solenoid wall and that the magnetic cylinder can be inserted into the socket via pins can. 37. Magnetic field oxygenator system according to claim 1-18, characterized in that that the solenoid wall can also be spherical with valve inserts inside the wall and screw-in base on which parts (49, 12, 16, 27, 28) are mounted, and with all additional equipment and connections (1 -5 # 38. Magnetic field oxygenator system according to claim 1 - 18, characterized in that the oxygen bag consists of a semi-rigid Plastic compound or an elastic balloon, with a stiff metal bracket for the drug spray valves under a recess for the quartz glass window is pressed in, but is replaceable. In this metal rail are those Valve connections cast or screwed in, so that the oxygen bag with the Drug cap has direct connection. In the center of the bracket is the 'quartz glass inserted circularly. The edges thereof can be magnetically adhered to the medicament lid be sucked tight. The oxygen bag is temporarily squeezed together by means of a pressure relief valve (37). The blood blisters are thus tempered via a chemical defoaming agent Aquabidestl or other solutions additionally influenced by bursting liquefied and then run into the fiber cylinder. 39. Magnetic field oxygenator system according to claim 1-18, characterized in that that the oxygen bag is flanged to the outlet or inlet port and is disposable is, a new oxygen bag can be used and that the plastic compound or the fabric is permeable to magnets. 49. Magnetic field oxygenator system according to claim 1-18, characterized in that that the base is round, has a bottom plate and that the outer wall until about halfway up around the solenoid (11) so that the same in the The base can be inserted and fixed to the mounting knobs with hand lever locks can. The base has openings and valve inserts for (18,20,28,29,35,37,38,39,40, 41, 51a) or the other media mentioned from 1-53. The middle wall extends up to the level of the magnetic coil and consists of two side panels that can be folded apart. The inner walls have valve connections for Oxygen, other gases or media or drugs that enter the frothing chamber, the metal or artificial grille via perforated tubes with valve connections in the left or right chamber can be sprayed. The supply lines come from (19) through the base and through the end plate (47). ~ 41. Magnetic field oxygenator system according to Claims 1 - 18, characterized in that that poured into the inner walls of the base and within the central wall mares are used as a guide rail for the medication grid arrangements and filter inserts as well as for the heating system in the right chamber. 42. Magnetic field oxygenator system according to claim 1-18, characterized in that that in the inner wall of the pedestal valve connections electromagnetic Art are for taking blood samples, probes, cold and heat connection openings for heated gases. These flow through the right pipe system to the liquefied Blood components of +4 degrees Celsius, which are from the magnet chamber or the oxygen bag comes, to be gradually heated to 10, 20, 30, to 37 degrees Celsius for each circulation tube. The round, cylindrical heating insert is exchangeable and is inserted into the base of the base screwed in and has blood outflow openings (36) through the bottom and end plate wall in (21). A cylindrical, non-wettable synthetic fiber insert with an incline downward turns is inserted into the heating insert and has Contact with the same. The temperature is transferred to the blood or per tube its components. The warmed blood then flows through an outflow duct in (21). Magnetic field oxygenator system according to Claims 1 - 18, characterized in that that in the end plate (47) is a rubber-sealed opening into which the Diffuser and eyektor (49) or a frothing nozzle is fitted. Pour into it Gases and blood components mix in, are foamed up to 40 degrees Celsius and again flow through a plastic membrane (49), whereby the blood components from (2) through (25) via (36) into (49) and foamed into the chamber flow in. 44. Magnetic field oxygenator system according to -llsp7uch 1 -18 characterized in that that in the foaming chamber a metal lattice network completely filling the volume of the same is used and has external contact via the electroplating system. The blood foam, oxygenated to approx. 40 degrees, is galvanized Mesh pressed through and the internal cell structure galvanic influences more variable Intensities reduced by means of the amplifier osscilator. 45. Magnetic field oxygenator system according to claims 1 - 18 thereby characterized that optionally the hedikamenten bead lattice with fine bead filter as well as oxygen bags, heating pipe systems or synthetic fiber cylinders can be omitted can and the entire chemical-physical processes according to claim without this Lens sets can be made. 46. Magnetic field oxygenator system according to claim 1-18, characterized in that that the flowing out liquid blood elements from (36) in (21,21a, 22,23,24,29,) in (25) reach the blood pump and incorpate the patient intraarterially from there be made with the exchange transfusion being made fluid continuous or artificial Blood or canned blood + the treatment of the withdrawn blood is incorporated into the body will (+ while). 47. wiagnetfeld oxygenator system according to claim 1-18, characterized in that that the magnetic field oxygenators including additional equipment in a tubular steel frame, is built on metal or plastic plates inside a mobile stainless steel box. This is heated inside to around 40 degrees Celsius and has a mobile connection to the outlet valves (36) of the oxygenators (6 - #, to the individual blood elements collectively absorb. The oxygenators (6 - 9 to -fO) can be attached to a mounting rail be mounted on a wall and the main oxygenator is electronic on one Driving carriage steered past while he was by each individual oxygenator or test oxygenator absorbs substances through the inlet valves. 48 magnetic field oxygenator system according to claims 1 - 18, characterized in that that the drug pearls are highly active substances that the blood blisters adhere to rub the same, absorb the substances under oxygenation and that saturation of gases by means of these friction effects and the surface enlargement of the Blowing increases the effect significantly. 49. Magnetic field oxygenator system according to claim 1 - 47, characterized in that that in them bacteria, viruses, yeast, artificial blood, organs or tissue parts, or cells called cell fusion, can be cultured. Also is to the Generation of antibody production for research, therapeutic purposes and for Study of metabolic processes in the same and their'therapies.