Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3876373 A
Publication typeGrant
Publication dateApr 8, 1975
Filing dateMar 8, 1971
Priority dateMar 18, 1968
Publication numberUS 3876373 A, US 3876373A, US-A-3876373, US3876373 A, US3876373A
InventorsGlyptis Nicholas D
Original AssigneeGlyptis Nicholas D
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method and apparatus for modifying the reproductive mechanism of organisms
US 3876373 A
Abstract  available in
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent [1 1 Glyptis 1 1 Apr. 8, 1975 METHOD AND APPARATUS FOR MODIFYING THE REPRODUCTIVE MECHANISM OF ORGANISMS [76] Inventor: Nicholas D. Glyptis, 756 E.

Northwest l-lwy., Elmhurst, 111. 60067 [22] Filed: Mar. 8, 1971 [21] Appl. No.: 122,159

' Related U.S. Application Data [63] Continuation of Scr. No. 713,912. March 18. 1968,


[52] US. Cl 21/54 R; 21/102 R; 195/1; 250/531; 426/235; 426/237; 426/238 [51] Int. Cl. A611 1/00; A611 3/00 [58] Field of Search ..250/49.5 R, 49.5 TE,

250/495 GC,49.5 TC, 531; 21/54 R, 102 R; 195/78, 1; 99/217, 221, 233, 253; 426/235,

[56] References Cited UNITED STATES PATENTS 2.553.289 5/1951 Alexander et a1 21/54 R UX 2.729.748 1/1956 Robinson 250/495 TE 2.824.969 2/ 1958 Crowley-Milling 250/495 TE 2,887,583 5/1959 Emanuelson 21/102 R X 2,891,838 6/1959 Kaye 21/58 3.013.154 12/1961 Trump 250/495 R 3.057.792 10/1962 Frohlich... 250/495 R X 3.057.795 10/1962 Frohlich... 250/495 TC UX 3.095,359 6/1963 Heller 21/54 R UX 3,383,163 5/1968 Menashi... 21/54 R 3,600,126 8/1971 He1lund.... 21/54 R Primary E.\'aminerBarry S. Richman Attorney, Agent, or FirmWegner, Stellman, McCord, Wiles & Wood [5 7 ABSTRACT A method and apparatus for sterilizing matter by inhibiting the reproduction of organisms therein. The matter is treated at low energy levels, as by the use of a plasma discharge or by electromagnetic excitation to destroy or disrupt the functioning of the DNA molecule of the organisms.


A major aspect of this invention is concerned with a method for modifying the reproductive mechanism of organisms and with apparatus for practicing the method. More particularly, one aspect of the invention is concerned with the sterilization of matter by inhibiting the reproduction of organisms therein.

A principal feature of the invention is that organism reproduction is inhibited by subjecting the organism to a low energy excitation which, it is presently believed, alters the DNA (deoxyribonucleic) macromolecule of the cells of the organism by one or a combination of three effects:

1. circulating electric currents;

2. disruption by ionized particles;

3. hot chemical reactions.

These effects result from or are enhanced by exposure of the matter to an ionized atmosphere or plasma.

Prior sterilization methods in common use have been of three types heat, gas or radiation. Heat sterilization generally involves exposure to steam under pressu:e (often superheated) for several hours. Kills have betn achieved in shorter time under extreme conditions of temperature and pressure which are not suit able for general use. Gas sterilization, as with ethylene oxide, kills by alkylation of the organism and requires a long period of gas immersion, sometimes as much as 24 hours, depending on the nature of the article being sterilized. With high moisture levels, the time can sometimes be reduced to 3 hours. It is suitable only for a batch-type operation; and the long time required makes it quite expensive. Radiation sterilization, as with radio-active cobalt 60 (gamma rays), electron beam penetration or the like, is carried out at very high energy levels. Potentials of the order of 0.5 to million electron volts (MEV) and currents from 0.5 to milli amperes are common. Such energies require extensive shielding to protect the operator. It is not unusual to carry out the work within a concrete enclosure having walls 6 to 8 feet thick. The equipment used is expensive. The high energy levels used often alter the material being sterilized, as by changing taste or color, for example. The capability of sterilizing at low energy levels eliminates the expense and inconvenience of shielding, and side effects on the matter being treated.

A feature of one form of the invention is that the matter to be treated is exposed to a plasma, i.e., an ionized gaseous environment, in which the particles making up the environment are charged at a low energy level. More particularly, the plasma is established by exciting a rearfied atmosphere, generally by an electric field. One or a om bination of the following effects contribute to the prevention of organism reproduction:

l. the establishment of circulating alternating currents within the DNA molecule of the organism, resulting in destructive heating or disruption of its electrochemical molecular communication system;

2. disruption of the DNA molecule by the impact of a charge particle of the plasma;

3. a chemical reaction between a constituent of the atmosphere and organism which takes place very rapidly as a result of the high energy level of the plasma.

Another feature is that the atmosphere which is ionized includes gas particles which penetrate the matter and the organism therein to a greater extent than ionized air particles.

A further feature is that the plasma is excited by electric, magnetic or electromagnetic fields at one or more discrete frequencies for selective kill of undesirable organisms. By exciting the plasma with one or more specific frequencies, the energy may be concentrated in narrow portions of the specturm where it is most effective, and the total energy minimized, avoiding modification of other organisms. This selectivity permits use of the process in curing certain illnesses.

Still another feature of the invention is that the molecular structures of the organisms are oriented to enchance the selectively of the action of the discrete frequency excitation.

Yet a further feature is that the low energy charged particles of the plasma have a mean-free path substantially greater than the diameter of the DNA molecule of the organism. This characteristics of the method contributes to the efficiency of the sterilization operation.

An apparatus for practicing one form of the method includes means defining a chamber, a pair of spaced electrodes in the chamber, means for evacuating the chamber, a source of electrical energy connected with the electrodes and means within the chamber for supporting the matter to be subjected to the low energy plasma.

Another feature of the apparatus of the invention is that is includes a means for establishing plural electric and magnetic fields at plural frequencies. For example, with an electrostatically excited apparatus, a plurality of pairs of spaced electrodes are provided, having electric shields between adjacent electrodes, with different pairs of the electrodes connected with different sources of electric energy.

Further features and advantages of the invention will readily be apparent from the following specification and from the drawings, in which:

FIG. 1 is a diagrammatic illustration of an apparatus for practicing the invention;

FIG. 2 is a schematic diagram of a spark gap power pp y FIG. 3 is a schematic diagram of a fixed frequency alternating current power supply;

FIG. 4 is a schematic diagram of a variable frequency alternating current power supply;

FIG. 5 is a plot of voltage as a function of time for the spark gap power supply;

FIG. 6 is a plot of current as a function of time corresponding with the voltage of FIG. 5;

FIG. 7 is a plot of the percentage of kill curve as a function of the dosage factor;

FIG. 8 is a diagrammatic illustration of the path of a charged particle showing several organism cells;

FIG. 9 is a simplified, diagrammatic illustration of an organism cell;

FIG. 10 is a diagrammatic illustration of the circulating currents in a DNA molecule;

FIG. 11 is an outline drawing of a modified apparatus;

FIG. 12 is a diagrammatic illustration of another modified apparatus;

FIG. 13 is a diagrammatic illustration of another modified apparatus;

FIG. 14 is an elevation of an apparatus for continuous processing of articles;

FIG. 15 is a plan view of a continuous processing apparatus;

FIG. 16 is a diagrammatic illustration of another apparatus useful in practicing the invention;

FIG. 17 is a plan view of the apparatus of FIG. 16;

FIG. 18 is a diagrammatic plan view of a processing apparatus for practicing the invention as a part of a continuous operation; and

FIG. 19 is a fragmentary elevation taken along line 19-19 of FIG. 18.

As a part of the following description of the invention of the invention, there will be given specific information regarding a preferred mode of performing the process. This specific information represents details of a method which has been found to be effective. However, several variations in the specific steps are discussed herein and others will be apparent.

In FIG. 1 an article 20 is shown in a chamber 21 in which an environment is established for promoting sterilization of the article. The article 20 may be a foodstuff which is sterilized in order to permit storage for an extended period without spoilage, or may be a product which should be utilized in a sterile state.

Chamber 21 is formed by a cylindrical wall member 22, as of glass, with upper and lower plates 23, 24, respectively, sealed to the ends of the cylinder by gaskets 25. The end plates 23, 24, are secured together by tie rod 27 and nut 28. In practice, several tie rods are used, although only one is illustrated in the drawing for simplicity. End plates 23 and 24 are conductive and are connected with an electrical source which establishes an electric field within the chamber 21. The plates are preferably of metal as is tie rod 27. A sleeve 31, of insulating material, surrounds tie rod 27 where it passes through plate 23, electrically isolating the plates. The interior of chamber 21 is connected through a passage 24a in plate 24 with a vacuum pump 33, through a valve 34 with a source 35 of additive gas and through valve 36 with an air inlet.

Inside chamber 21 a platform 40 is mounted on legs 41 above passage 24a. Article 20 is supported above platform 40 on an openwork frame 42, of insulating material, which holds the article without masking the contents.

Briefly, the sterilization operation is carried on in the following manner. Chamber 21 is evacuated by operation of vacuum pump 33 and then a plasma is formed within the chamber by establishing an electric field between plates 23, 24, which serve as electrodes. The term plasma as used herein means an environment in which the molecules are ionized. The ionized molecules of the atmosphere penetrate the package of article 20 and reach any living organisms therein.

If alternating energy is present in the treatment zone within chamber 21 at an appropriate frequency, as in the field exciting the plasma, or in an auxiliary field, electrical currents are induced in the nucleus of the organism cells, and more particularly in the DNA molecule thereof, which alter or destroy the DNA molecule and prevent reproduction of the cell. With the capability of cell reproduction lost, the organism dies. The cells of different organisms respond to currents at different frequencies, permitting selective treatment. The ionized environment provides coupling between the field and the organism.

Ionized (charged) particles of the plasma have sufficient energy to penetrate the protein shell of the organism cells. When the charged particles strike the DNA molecules, cross linkages in the molecule are broken or modified, impairing the reproductive capacity of the organism. The ionized particles are equivalent to the secondary electrons and ions generated by high intensity electron beam sterilization, but are excited directly at a low energy level.

The constituents of the plasma (primarily oxygen and nitrogen with an air environment) react chemically with the organism. Under ordinary conditions, the reactions occur slowly and may have no adverse effect on the organism. With a plasma in which the molecules have an elevated energy level, the reactions are greatly speeded up.

It is important to the process that charged particles of the plasma reach the cells of the organism. Several gases have molecules with'greater mobility or a higher molecular coupling coefficient than the constituents of air. Such an additive gas may be introduced into chamber 21 by opening valve 34 after the chamber has been evacuated.

The plasma within chamber 21 may be established by different types of electrical excitation. The spark gap power supply of FIG. 2 has input terminals 45 connected with a suitable electrical source, as I20 volt, 60 cycle AC. A step-up auto transformer 46 is connected with a tuned circuit including capacitor 47 and inductor 48, which is the primary winding of an output transformer 49. Vibrator switch contacts 50, connected in series with inductor 48, are magnetically actuated to close and open 120 times per second by coil 51, connected through on-off switch 52 across the line. When the contact is closed, current flows from capacitor 47 and transformer 46 to inductor 48 and oscillation occurs at a rate determined by the values of capacitor 47 and inductor 48. The output, a burst of oscillatory energy recurring at a 120 cycle rate, is connected from secondary winding 53 to the electrode plates 23 and 24 of chamber 21.

In FIG. 3 a simple 60 cycle AC power supply is shown having an adjustable auto transformer 55 with a primary winding 56 connected through input leads 57 and an on-off switch 58 with a 60-cyc1e source. The output of the autotransformer is derived from secondary winding 59 through an adjustable tap 60 and is connected with a primary winding 61 of a step-up transformer 62. The secondary winding 63 of the step-up transformer is in turn connected with electrode plates 23 and 24.

A third power supply is illustrated in FIG. 4. A variable frequency driving signal from generator 65 is connected with a higher voltage amplifier 66. A voltage control 67 permits the operator to set the operating conditions of the amplifier and thus the output voltage. In a representative embodiment, the variable frequency generator has a range of I-lz to IOOKHz and the peak voltage output'of the amplifier is of the order of 50,000 volts.

The selection of one or a combination of the exciting signals depends on the nature of the organism to be treated. Specific examples will be given below.

FIGS. 5 and 6 are curves illustrating the nature of the ionizing voltage and current, respectively, with the spark gap power supply of FIG. 2. The ionizing voltage comprises a series of energy bursts at a cycle rate (determined by the closure of contacts 50) with each burst containing several cycles of energy at a fundamental frequency determined by the inductance 48 and capacitance 47 of the tuned circuit. In this case the oscillatory frequency is of the order of 1 kilohertz, but has an irregular pulse shape which results in the presence of many harmonics. Accordingly, the exciting energy covers a wide range of frequencies. The waveshapes occurring on alternate half-cycles of the 60- cycle energizing voltage are similar in shape but opposite in polarity. The current curve of FIG. 6 shows the major portion of the current flows during the initial half cycle of the energizing voltage establishing the plasma within the chamber. With a chamber having 15 inches spacing between the upper and lowerelectrodes 23,24 and a diameter of 10 inches, the voltage waveform of FIG. 5 has a peak-to-peak value of 70 kilovolts and the current waveform has a peak-to-peak value of O. 14 ampere. This gives a peak power rating of the order of 10 KVA. The duty cycle is of the order of 10 per cent, however, so that the average power required is low as compared with the peak power.

The effectiveness of the plasma discharge in killing microorganisms is illustrated in FIG. 7 where the per cent kill is plotted logarithmically as a function of the dosage factor. The dosage factor is a composite term which combines the time duration and the intensity of the plasma discharge. The curve shows that for a particular microorganism a dosage factor can be selected which will reliably effect a 100 per cent kill. Different dosage factors may be necessary for different types of organisms. The plasma discharge does not appreciably raise the temperature of the matter treated. However, it has been found that efficiency of the process may be improved by operating at an elevated temperature, but below a temperature at which the matter is modified.

It is my theory that several different factors contribute to the sterilizing effect of the processes described herein. First, the alternating fields coupled through the plasma to the organisms set up disruptive currents which alter the DNA molecules to an extent sufficient to prevent reproduction. I believe these currents are complex functions of electron and ion mobilities and concentrations, in the nature of currents in semiconductors. Complex resonant current conditions have been observed in effecting a complete kill. Although circulating electric currents are believed to be a major factor in disrupting the ability of the DNA molecule to control reproduction of the organism, more complex effects also take place, including electron spin resonance and multiple nuclear magnetic resonance, both of which modify the characteristics of the organism. All these effects are believed to be caused, at least to some extent, by subjection of the organisms to an alternating field, electric, magnetic or electromagnetic, at an appropriate frequency or combination of frequencies.

The plasma improves the energy transfer from the fields to the organism.

Second, charged particles of the plasma penetrate the microorganisms and, upon striking a cell, give up energy which breaks bonds within the DNA molecules. If, for example, the phosphate-sugar bond is broken, reproduction is inhibited. The effectiveness of this aspect of the process depends on the relation between the mean-free path of the particles (i.e., the distance they travel before striking an organism or another particle) and the organism size. Preferably, the mean-free path is greater than 5 or even 10 organism diameters. This characteristic is related to the level of vacuum in which the plasma is established, the mean-free path being an inverse function of the pressure. The significance of this characteristic is illustrated in FIG. 8 where charged particles follow paths 75, 76 and 77 through organism cells 78. The charged particles which follow paths 76 and 77 are shown striking cells 78a and 7812 while the particle which follows path passes between the organism cells and strikes another particle at X. If the particle population is large (high pressure), most of the charged particles strike other particles when they have traveled a distance which is short with respect to the organism size, and very few particles will strike an organism. Accordingly, it is important that the pressure be reduced to increase the mean-free path of the charged particles.

Third, a chemical reaction between the plasma constituents and the organism destroys the organism. This is analogous to the alkylation of gas sterilization, but much faster. The energy of the particles resulting from the excited condition of the plasma speeds up the chemical reaction so that even oxygen or nitrogen from the atmosphere are effective sterilizing agents. More common sterilizerrs, as ethylene oxide, may be used, with a further time saving.

It is estimated that approximately 50 per cent of the energy of the charged particles is dissipated in penetrating the cell while the other 50 per cent is utilized in destroying the capacity of the organism to reproduce. The diagrammatic representation of a typical cell in FIG. 9 shows that the nucleus 80 is surrounded by a shell 81 which in turn is surrounded by a protein layer '82. The gaseous constituents of atmosphere, principally oxygen and nitrogen, are not particularly efficient in penetrating the protein layer and shell of an organism. The treatment can be improved by utilizing a gas which is more effective in this respect. Examples are ethylene oxide and CCl F one of the gases sold as a refrigerant under the trademark FREON. When ethylene oxide is used, the chemical action of the process is also enhanced.

A catalyst (as cesium) may be used to modify the characteristics of the plasma, permitting an increase of power without the use of excessive voltages. Above 30KV some shielding may be desirable to limit the radiation of soft X-rays. Such shielding is much simpler than that used for present high intensity radiation.

The DNA molecule has a spiral chain link configuration illustrated in FIG. 9 with a variety of chemical links between the longitudinal members 84, illustrated by the dashed lines 83. This cross-linked construction permits the establishment of a variety of circulatory currents in different paths, indicated by the arrows. The various paths have different resonant characteristics and permit selective modification in the DNA molecule by subjecting it to excitation at a frequency or frequencies which establish currents in some paths but not in others.

A control over the sterilization'process is commonly made by including in one or more of the articles treated a spore strip of an organism which is particularly difficult to kill. One such organism is bacillus subtillus var. globigii. In a typical test, a strip having 10 organisms thereon is placed in the article to be treated. Following treatment, the strip, or a sample from the strip, is incubated to determine whether the organisms are capable of multiplication.

With the apparatus of FIG. 1 and the power supplies of FIGS. 2 and 3, consistent kills have been achieved using the following procedure:

I. Evacuate chamber 21 to a pressure of 300 microns;

2. Energize with the spark gap power supply of FIG.

2 for a period of 3 minutes;

3. Open air inlet valve 36 to return the chamber to atmospheric pressure;

4. Evacuate again to a pressure of 300 microns;

5. Add a gas (as CCl F to a pressure of 5,000 microns, permitting thorough penetration of the article by the gas;

6. Evacuate to 1,500 microns;

7. Energize from the spark gap source for 3 minutes.

At this point in the treatment, consistent 99 per cent kills have been achieved. It is believed that losses in the spark gap power supply have reduced the treatment efficiency so that the kill is not 100 per cent effective. The following additional steps insure complete kill:

8. Admit air to atmospheric pressure;

9. Evacuate to 500 microns;

l0. Energize from the power supply source of FIG. 3 with a voltage of 1,500 volts, RMS (and a current of the order of 0.5-0.9 amps);

l l. Admit air to atmospheric pressure;

12. Evacuate to 500 microns;

13. Add CCI F to 5,000 microns;

l4. Evacuate to 1,500 microns;

15. Apply 3 minutes power from the power supply of FIG. 3.

With the power supply of FIG. 4, the following procedure has been found effective for the vacillus subtillus:

1. Evacuate to 300 microns;

2. Energize for 3 minutes, varying the frequency from 2,00OH to 20,000I-I at each of three peak-to-peak voltage settings, IZOKV, 160KV and 200KV;

3. Evacuate to 300 microns;

4. Add CCl F- to 4,500 microns;

5. Energize for 2 minutes, 20 seconds, as in (2) above.

Salmonella paraphi have been killed with this treat ment:

1. Evacuate to 300 microns;

2. Energize for 5 minutes (100 seconds each) 2,0001-12 at 120KV 5,000 Hz at 150KV 10,0001-12 at I70KV;

3. Evacuate to 300 microns;

4. Add CCI F to 4,500 microns;

5. Evacuate to 500 microns;

6. Energize for 5 minutes (100 seconds each) 2,000H at 140KV 5,0001'1 at 150KV 10,00011 at I90KV;

7. Add CClgF- at 1,000 microns;

8. Energize for 6 minutes 40 seconds (100 seconds each) 2,000H at 300KV 5,000H at 220KV 10,000H at 200KV 20,0O0I-I at 160KV.

Sterilization has been effected within a tin coated steel can. An ordinary can of tuna fish from a grocers shelf was opened and a globigii spore strip placed inside. The cover of the can was resealed with solder. The can was then subjected to the following treatment:

1. Evacuate to 500 microns;

2. Energize for 3 minutes at 160001-1 40KV;

3. Evacuated to 500 microns;

4. Energized for 3 minutes at 1,400H and 55KV. The spore strip was incubated. At the end of 12 hours, there was an indication that the globigii had grown. The rate of growth then diminished and at the end of 72 hours no globigii remained alive. A globigii control strip incubated with the test strip showed continued growth throughout the 72 hour period.

An apparatus is illustrated in FIG. 11 for exciting a plasma with different types of energy. An elongated cylindrical body 90, as of glass, defines the space within which the plasma may be formed, and has transverse extensions 91, 92 and 93, 94 forming crosses therewith adjacent either end. The ends of the cylindrical body and of each of the cross extensions are closed by plates 95 through which connections may be made to the interior of the body. Extending outwardly from the cover members for extensions 91 and 92 are supporting tubes 96 for electrode plates as 97, 98, 99 and 100, within the extensions. In the specific structure of the drawing, electrode 97 cooperates with electrode 100 while electrode 98 cooperates with electrode 99, so that electric fields are established therebetween when the elec trodes are energized as by power supplies of the character shown in FIGS. 2 and 3. Focusing electrodes 103 may be associated with each of the field establishing electrodes. Adjacent electrode assemblies (i.e., electrode 97 and its associated focusing electrode 103) are isolated from the adjacent electrode assemblies by shields 104. The article 105 to be treated is supported in the treatment zone on a platform 106 at the intersection of the main body and the transverse extensions 91, 92.

The apparatus is evacuated by a pump 108 connected through valve 109 with extension 94. Test probes as Langmuir or Faraday probes may be introduced into the interior of the chamber through axial extensions 110, at either end. Gauges, as for pressure level and temperature, may be introduced into extension 93 at 1111.

Magnetic coils 112, 113, 114, placed around the cylindrical housing and extensions 91, 92, surrounding the position of the article being sterilized, provide excitation the exciatation of the plasma magnetically at one or several frequencies. Furthermore, suitable energization of the coils with direct current sets up a magnetic bottle or magnetic well effect which concentrates and contains the plasma.

FIG. 12 illustrates schematically another apparatus for electrically stimulating a plasma discharge at a plurality of frequencies. Here a cylindrical chamber has therein three sets of opposed electrodes 121, 121 122, 122', and 123, 123. Each pair of electrode is connected with the corresponding signal generator, 121a, 122a and 123a. The signal generators may be operated at the same or at different frequencies depending on the nature of the organism (not shown) to be treated. Shield members (shown diagrammatically at 124) are interposed between adjacent electrodes.

FIG. 13 illustrates a specific structural arrangement in which adjacent electrodes 127 are isolated by portions 128 of the wall of chamber 129 which extend inwardly beyond the location of the electrodes.

In FIG. 14 an apparatus is shown for thecontinuous processing of articles 135 carried through a treatment zone on conveyor belt 136. A plasma is formed in the atmosphere and the organisms within the articles are excited by electromagnetic radiation from a horn radiator 137 connected through waveguide 138 with a suitable source, as a signal generator, not shown. A second horn radiator 139 is connected with another source of power through waveguide 140 and is located below conveyor 136, directing radiated energy upwardly toward articles 135. If treatment at additional frequencies is desirable, further radiators may be placed at other points along the length of conveyor 136. Alternatively, as shown in FIG. 15, the articles on conveyor 136 may also be subjected to a magnetic field (or a piurality of them) established by currents flowing through coils 142. The pole pieces 143 associated with each coil serve to concentrate the flux in the path of the articles.

FIGS. 16 and 17 illustrate an apparatus for applying a unidirectional magnetic orienting field to the matter being treated. The chamber 150 defining the treatment zone is again provided by cylinder 151 closed by conductive end plates 152, 153. Details of the connections with the electrical circuit, the vacuum pump and the source of additive gas are not shown, but may be generally the same as that illustrated in FIG. 1. Article 154, to be treated, is located within chamber 150. A magnetic structure 155 has a pair of tapered poles 156 diametrically located on either side of chamber 150 and intermediate the ends thereof. A pair of coils 157 on core 155 are energized by direct current to establish a high intensity unidirectional magnetic field within the chamber 150. The unidirectional field may be of the order of at least one kilogauss and may be as high as 20 kilogauss, depending on the nature of the organisms treated. The intense magnetic field serves to orient the molecular structure of the organism to be treated in a plane generally at right angles to the axis of the plasma. In addition to the electrical field established between the plates 152 and 153, the plasma may be excited magnetically by coils 160, 161 wound around the cylinder 151. The alternating plasma fields from coils 160, I61 are also at right angles to the unidirectional magnetic orienting field. The orienting field coils need be energized only when the plasma is excited.

The establishment of a uniform orientation for the structure of the organism improves the frequency selective characteristics of the process so that the organisms may be treated with a lesser dosage factor than is required when they are not oriented. Coils 163, 164, 165 and 166 extend generally the length of cylinder 151 and have their axes parallel therewith. They are energized with direct current, the polarity of diametrically opposed coils being the same, as indicated in FIG. 17. These coils focus and concentrate the plasma in the center of chamber 150, for maximum effectiveness in treatment of organisms located at the center of the treatment zone.

In FIGS. 18 and 19 an apparatus is shown for performing the process as a part of a continuous production line. A plurality of enclosures 170 are mounted on a conveyor 171 for travel in a closed loop 172. Each container has a top 173 and a bottom 174 which may be opened by a suitable mechanism (not shown); and is attached by a flexible connector 176 with a distributor 177 mounted at the center of the conveyor loop.

Each container is airtight when closed and may be evacuated. Energizing electrodes and coils, as those illustrated in FIGS. 1, l1 and 16, and otherwise disclosed herein, are provided for the container, though they are not illustrated in detail. Flexible connector 176 includes multiple passages and electrical conductors for establishment of a desired environment in the treatment zone of the associated containers 170 and for the excitation of a plasma therein.

Distributor 177 has a fixed portion 177a to which are connected suitable conduits and electrical cables 178, 179, 180 from vacuum pump 182, gas source 183 and electrical source 184, respectively. The upper portion 177b of rotary distributor 177 turns with respect to the fixed base 177a in synchronism with movement of containers 170 around loop 172, and suitable porting and switching (not shown) controls the connection of each container with the vacuum pump, gas or electrical source at proper times.

At loading station 186 the cover 173 of container 170 is opened and an article 187 deposited therein as from a belt conveyor 188. Cover 173 then closes and the sterilization process commences. After the container 170 has traveled around the conveyor loop 172, container bottom 174 is opened at a discharge station 190 and article 187 is deposited on a conveyor belt 191 which moves it on for further handling.

It has been found that the sterilization process may sometimes be more efficient at an elevated temperature. Accordingly, a portion of conveyor loop 172 may extend through a heating tunnel, the entrance and exit of which are indicated by broken lines 192, 193.

While I have shown and described certain embodiments of my invention, it is to be understood that it is capable of many modifications. Changes, therefore, in the construction and arrangement may be made without departing from the spirit and scope of the invention as without in the appended claims.

I claim:

1. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma by exciting said rarefied atmosphere with alternating energy comprising a plurality of discrete frequencies, said energy including electromagnetic radiation and alternating magnetic fields at different frequencies, and exposing the organism to the plasma.

2. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma by exciting the rarefied atmosphere with an electric field including a wide range of frequencies, having a basic frequency of the order of 10 kilohertz, established periodically at a repetition rate of 120 Hertz and exposing the organism to the plasma.

3. The method of claim 2 in which the ratio of average power to peak power in establishing said field is of the order of O.l.

4. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma having an axis by excitation of said rarefied atmosphere and aligning the molecular structure of the organism with respect to the plasma by the application of a unidirectional magnetic field at right angles to the plasma axis.

5. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma by exciting said rarefied atmosphere with alternating energy covering a wide range of frequencies applied sequentially and exposing the organism to the plasma.

6. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma by exciting said rarefied atmosphere with alternating energy at a first frequency pulsed at a lower frequency, said pulsation at said lower frequency creating a wide range of excitation frequencies, and exposing the organism to the plasma.

7. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere, establishing a low energy plasma by exciting said rarefied atmoshere with alternating energy comprising a plurality of discrete frequencies applied sequentially and exposing the organism to the plasma.

8. A method of modifying the reproductive mechanism of an organism which comprises establishing a rarefied atmosphere in a medium selected from a group comprising ethylene oxide, and a paraffin hydrocarbon with one or more fluorine atoms, establishing a low energy plasma by excitation of said rarefied atmosphere and exposing the organism to the plasma.

9. An apparatus for creating a low energy plasma, comprising;

means defining a treatment zone;

field establishing means operatively associated with said zone and including a plurality of pairs of spaced electrodes;

means providing an electric shield between adjacent electrodes;

a plurality of sources of alternating energy at different frequencies connected with different pairs of said electrodes to create a plasma in said zone; and

means within said zone for supporting matter to be subjected to the plasma.

10. An apparatus for sterilizing matter, comprising:

a plurality of chambers traveling in a closed path between a loading and a discharging station, each chamber having field establishing means operably associated therewith;

means operable during travel of each chamber from the loading station to the discharge station for establishing a treatment zone therein, including means for maintaining a rarefied atmosphere in the chamber and a source of electrical energy connected with said field establishing means to create a low energy plasma in the chamber;

means within each chamber for supporting matter to be subjected to the plasma; and

conveyor means for delivering matter to be sterilized to said loading zone and for removing sterilized matter from the discharge zone.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2553289 *Mar 12, 1947May 15, 1951Bausch & LombMethod for depositing thin films
US2729748 *Jul 13, 1951Jan 3, 1956High Voltage Engineering CorpApparatus for sterilizing foods, drugs and other substances by scanning action of high-energy electrons
US2824969 *Jan 17, 1955Feb 25, 1958Vickers Electrical Co LtdTreatment of materials by electronic bombardment
US2887583 *Oct 8, 1956May 19, 1959High Voltage Engineering CorpElectron accelerator for irradiation
US2891838 *Apr 10, 1957Jun 23, 1959Ben Venue Lab IncNon-inflammable ethylene oxide sterilant
US3013154 *Nov 14, 1958Dec 12, 1961High Voltage Engineering CorpMethod of and apparatus for irradiating matter with high energy electrons
US3057792 *Dec 22, 1958Oct 9, 1962Siemens AgMethod for improving the imprintability of synthetic material
US3057795 *Feb 12, 1960Oct 9, 1962Siemens AgMethod and device for improving the coatability of synthetic plastics
US3095359 *Nov 16, 1959Jun 25, 1963New England Inst For Medical RHigh-frequency treatment of matter
US3383163 *Jan 24, 1964May 14, 1968Little Inc ATreatment of surfaces
US3600126 *Feb 5, 1968Aug 17, 1971Hellund Emil JAsepsis process and apparatus
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4007007 *Feb 22, 1974Feb 8, 1977Hans Otto Ernst GazdaApparatus for decontaminating liquids of bacteria
US4042325 *Jun 21, 1976Aug 16, 1977Eli Lilly And CompanyMethod of killing microorganisms in the inside of a container utilizing a plasma initiated by a focused laser beam and sustained by an electromagnetic field
US4066544 *Sep 3, 1976Jan 3, 1978Multorgan S.A.Method and apparatus for electro shock degermination of water
US4207286 *Mar 16, 1978Jun 10, 1980Biophysics Research & Consulting CorporationSeeded gas plasma sterilization method
US4348357 *Dec 12, 1980Sep 7, 1982Motorola, Inc.Plasma pressure pulse sterilization
US4524079 *Nov 10, 1983Jun 18, 1985Maxwell Laboratories, Inc.Deactivation of microorganisms by an oscillating magnetic field
US4524080 *Jun 14, 1983Jun 18, 1985House Food Industrial Company LimitedMethod of improving quality of wheat flour
US4539068 *Aug 27, 1982Sep 3, 1985Fujitsu LimitedVapor phase growth method
US4557939 *Oct 12, 1983Dec 10, 1985House Food Industrial Co. Ltd.Method for improving a hardly soluble gelling agent
US4727029 *Apr 10, 1984Feb 23, 1988Hitachi Koki Company, LimitedApparatus and method for the pretreatment of biological specimens for use in scanning electron microscopes
US4801427 *Feb 25, 1987Jan 31, 1989Adir JacobProcess and apparatus for dry sterilization of medical devices and materials
US4880512 *Oct 14, 1988Nov 14, 1989Kollmorgen CorporationPulsed light selective photolysis process for treatment of biological media and products made thereby
US4917586 *Nov 22, 1988Apr 17, 1990Adir JacobProcess for dry sterilization of medical devices and materials
US4943417 *Nov 22, 1988Jul 24, 1990Adir JacobApparatus for dry sterilization of medical devices and materials
US4976920 *Mar 31, 1989Dec 11, 1990Adir JacobProcess for dry sterilization of medical devices and materials
US5048404 *Nov 2, 1990Sep 17, 1991Foodco CorporationHigh pulsed voltage systems for extending the shelf life of pumpable food products
US5087418 *Aug 31, 1990Feb 11, 1992Adir JacobProcess for dry sterilization of medical devices and materials
US5200158 *Sep 19, 1991Apr 6, 1993Adir JacobProcess and apparatus for dry sterilization of medical devices and materials
US5366746 *Oct 4, 1993Nov 22, 1994Utah State University FoundationUltra-high temperature pasteurization and electron beam technology for sterilization of meat and meat products
US5470597 *Sep 30, 1994Nov 28, 1995Utah State UniversityUltra-high temperature pasteurization of meat products
US5603972 *May 8, 1995Feb 18, 1997Mcfarland; Archie R.Irradiation method and apparatus
US5690978 *Sep 30, 1996Nov 25, 1997Ohio State UniversityHigh voltage pulsed electric field treatment chambers for the preservation of liquid food products
US5750072 *Jan 27, 1997May 12, 1998Sangster; BruceSterilization by magnetic field stimulation of a mist or vapor
US5944919 *Oct 6, 1997Aug 31, 1999Ethicon, Inc.Process for blackening surgical needles
US6083544 *Jun 19, 1998Jul 4, 2000Karen M. AddeoProcess for the use of pulsed electric fields coupled with rotational retorting in processing meals ready to eat (MRE)
US6214297Mar 24, 1999Apr 10, 2001The Ohio State UniversityHigh voltage pulse generator
US6247395 *Mar 3, 1999Jun 19, 2001Yamamoto Vinita Co., Ltd.High-frequency thawing apparatus
US6393975 *Jan 31, 2001May 28, 2002Stork Food And Dairy Systems B.V.Treatment apparatus and method for preserving pumpable food products in a pulsed electric field
US6429608Feb 20, 2001Aug 6, 2002Mitec IncorporatedDirect injection accelerator method and system
US6447719 *Oct 2, 2000Sep 10, 2002Johnson & JohnsonPower system for sterilization systems employing low frequency plasma
US6458321Oct 2, 2000Oct 1, 2002Ethicon, Inc.Sterilization system employing low frequency plasma
US6653641Feb 26, 2001Nov 25, 2003Mitec IncorporatedBulk material irradiation system and method
US6683319Jul 16, 2002Jan 27, 2004Mitec IncorporatedSystem and method for irradiation with improved dosage uniformity
US6707049Mar 21, 2001Mar 16, 2004Mitec IncorporatedIrradiation system with compact shield
US6713773Oct 10, 2000Mar 30, 2004Mitec, Inc.Irradiation system and method
US6781330Jul 18, 2002Aug 24, 2004Mitec IncorporatedDirect injection accelerator method and system
US6841124Oct 7, 2002Jan 11, 2005Ethicon, Inc.Sterilization system with a plasma generator controlled by a digital signal processor
US6852277Mar 19, 2001Feb 8, 2005Ethicon, Inc.Sterilization system employing a switching module adapted to pulsate the low frequency power applied to a plasma
US6885011Apr 2, 2002Apr 26, 2005Mitec IncorporatedIrradiation system and method
US6931095Mar 19, 2003Aug 16, 2005Mitec IncorporatedSystem and method for irradiating large articles
US6939519Jun 27, 2002Sep 6, 2005Advanced Sterilization ProductsPower system for sterilization systems employing low frequency plasma
US7067822Nov 21, 2003Jun 27, 2006Mitec IncorporatedBulk material irradiation system and method
US7154103Jul 22, 2003Dec 26, 2006Mitec IncorporatedMethod of providing extended shelf life fresh meat products
US7244459 *Nov 18, 2003Jul 17, 2007Hydrodyne IncorporatedShock wave treatment of meat
US7280874Feb 9, 2001Oct 9, 2007Boehm Charlene AMethods for determining therapeutic resonant frequencies
US7696488 *Jul 17, 2007Apr 13, 2010Nuctech Company LimitedIrradiating device and method for controlling the same
US8642655Mar 9, 2011Feb 4, 2014Benjamin JohnsonSystems and methods for preventing cancer and treating skin lesions
US20020068012 *Mar 19, 2001Jun 6, 2002Platt Robert C.Sterilization system employing a switching module adapted to pulsate the low frequency power applied to a plasma
US20040093049 *Nov 10, 2003May 13, 2004Akinori ItoMethod and equipment for treating electrostatic field and electrode used therein
US20040097180 *Nov 18, 2003May 20, 2004Hydrodyne IncorporatedShock wave treatment of meat
US20040113094 *Nov 21, 2003Jun 17, 2004Mitec IncorporatedBulk material irradiation system and method
US20040126466 *Jul 22, 2003Jul 1, 2004Mitec IncorporatedMethod of providing extended shelf life fresh meat products
US20040262146 *Jun 30, 2004Dec 30, 2004Platt Robert C.Sterilization system plasma generation control
US20050178977 *Apr 15, 2005Aug 18, 2005Mitec IncorporatedIrradiation system and method
EP0163693A1 *Nov 5, 1984Dec 11, 1985Maxwell LabDeactivation of microorganisms by an oscillating magnetic field.
EP1192953A2 *Oct 1, 2001Apr 3, 2002Ethicon, Inc.Power system for sterilization systems employing low frequency plasma
EP1201254A2 *Oct 1, 2001May 2, 2002Ethicon Inc.Sterilization power system employing low frequency plasma
WO1981002809A1 *Jan 23, 1981Oct 1, 1981Tegal CorpPackage and sterilizing process for same
WO1982001996A1 *Nov 19, 1981Jun 24, 1982Corp TegalPlasma pressure pulse sterilization
WO1985002094A1 *Nov 5, 1984May 23, 1985Maxwell LabDeactivation of microorganisms by an oscillating magnetic field
WO1995009544A1 *Oct 3, 1994Apr 13, 1995Univ Utah StateMethod of producing pasteurized raw meat products
WO1999058163A1 *May 11, 1998Nov 18, 1999James D BondSterilization by magnetic field stimulation of a mist or vapor
U.S. Classification422/23, 426/238, 435/270, 422/22, 426/237, 426/235, 435/173.1, 422/186.5
International ClassificationH05H1/46, A61L2/14, A61L2/02, A23L3/26
Cooperative ClassificationH05H1/46, A61L2/14, A23L3/26
European ClassificationA23L3/26, H05H1/46, A61L2/14
Legal Events
Jul 1, 1983AS14Letters of administration
Jul 1, 1983ASAssignment
Effective date: 19830620