The invention addressed herein relates to a method of exciting a mechanical resonance in a structural component of a microorganism and to a method of selecting effective operating parameters to perform the invention. Under further aspects, the invention relates to applications of the method in various technical fields and to a coil arrangement for performing the method.
In various technical fields, activity of microorganisms needs to be reduced or avoided. A well-known approach is to use chemicals, in particular antibiotics, to achieve this goal. This approach has numerous undesired side-effects, such as polluting the environment with toxic substances or creating multi-resistant germs.
The object of the present invention is to provide an alternative method for reducing the activity of a microorganism. In particular, it is a goal to achieve this effect based on physical means.
This object is achieved by a method according to claim 1.
The method according to the invention is a method of exciting a mechanical resonance in a structural component of a microorganism. The method comprises exposing said microorganism to an oscillating magnetic field, which oscillates at least at a first frequency. The first frequency corresponds to a frequency of a mechanical resonance of said structural component.
Within the present patent application, the term microorganism is meant to include single-celled organisms, such as bacteria and archaea, as well as viruses. A structural component may e.g. be a bacterial membrane, a cell organelle of a bacterium or a virus capsid. A cell organelle is e.g. a flagellum or a mitochondrion or the germs membrane itself.
The idea of the inventor is to excite a resonance frequency, which may be estimated from observed movements of the specific microorganism. This resonance may be excited to a degree that leads to a damage of the respective structural component. In consequence, the activity of the microorganism may be reduced, or the microorganism may be destroyed.
The waveform of the oscillating magnetic field may be purely sinusoidal, i.e. being defined by a single frequency being said first frequency. The waveform may be more complex, e.g. involving higher order harmonics of the first frequency. The waveform may e.g. have a saw tooth form or the form of rectangular pulses with a repetition frequency according to said first frequency. Various kinds of modulation are possible.
Variants of the method result from the features defined in claims 2 to 9.
In one embodiment of the method according to the invention, the first frequency is in the range up to 30 Megahertz, in particular in the range 0.01 Hertz to 400 KHz.
As an example, the applied magnetic field may oscillate at a frequency adapted to the rotational movements of the flagellae of a specific type of bacteria.
In one embodiment of the method according to the invention, the oscillating magnetic field is generated by driving an alternating current of the first frequency through a coil arrangement comprising at least one coil. The dimension of the coil may be adapted to the specific situation, e.g. to the size of a container in which the microorganism is held when performing the method. Such a container may e.g. be a microscope slide, a petri dish or an artificial vessel. In context of various technical field, such a container may also be a tube filled with water, an ingredient for preparing a nutrition product or any medium susceptible to microbial activity. The coil may e.g. be a circular coil with several hundred windings.
In one variant of the method using a coil arrangement, the coil arrangement comprises a pair of coils. The coils of the pair of coils are arranged on a common axis and spaced apart in direction of the axis. The microorganism is placed in a space between said coils of the pair of coils. Using pair of coils for generate the magnetic field has the advantage that access to the microorganism is possible from different sides in the space between the coils. The coil arrangement may form a so-called Helmholtz-coil.
In one variant of the method, the direction of said alternating current is either parallel in said coils of the pair of coils or is opposite in said coils of the pair of coils (gradient).
With parallel current direction, a region with a homogenous magnetic field can be created in the space between the coils and close to the axis. With current running in the first coils opposite to the direction of the second coil, a magnetic field gradient of the field component parallel to the axis is created. Homogenous field and field gradient may have different effects on different species of microorganisms. The relative current directions in the coils of the pair of coils is an operating parameter, which may be selected according to the needs.
In one embodiment of the method according to the invention, alternating current of said first frequency is driven through a first coil of said pair of coils and wherein alternating current of a second frequency is driven through a second coil of said pair of coils.
In this embodiment, separate current sources for the two coils are applied. Due to the difference between first and second frequency, there are periods of time during which the currents in both coils run in parallel, such that a homogenous field is created, and there are periods of time, during which a field gradient is created.
In one embodiment of the method according to the invention, a combination of duration of said exposing and of field strength of said oscillating magnetic field is selected such that a microbial activity is reduced, in particular such that said structural component of said microorganism is damaged.
The peptidoglycan architecture (contains N-Acetyl-glucosamin and N-Acetylmuroaminacetat) or/and the cytoplasma membrane may be destroyed by applying the method. The pressure inside bacteria is approx. 2 atmospheres. A little damage in the peptidoglycan membrane will lead to a blow-out.
In a variant of the method, which may be combined with any of the above-mentioned variants, the microorganism is brought in contact with magnetic nanoparticles at least while exposing the microorganism to the oscillating magnetic field.
Nanoparticles have a size between 1 and 100 nanometers in diameter. The nanoparticles may be brought in contact with the microorganism already before exposing the microorganism to the oscillating magnetic field. The magnetic nanoparticles may be permanently magnetized, they may e.g., comprise hard-magnetic material. As another example, the magnetic nanoparticles may be magnetized by a magnetic field, to which they are exposed, such as the oscillating magnetic field applied in the method according to the present invention. The magnetic nanoparticles may comprise iron or cobalt, in particular, the magnetic nanoparticle may comprise ferrite oxide or iron sulfate. The nanoparticles may comprise other magnetizing molecules.
The magnetic particles may consist only of substances, which have no poisonous effect to living cells. The magnetic particles may comprise a core of magnetic material and a coating, which coating need not to be magnetic and which prevents contact between the core and a surrounding, such as for example with a bodily fluid. For example, the magnetic particles may comprise ferromagnetic material or superparamagnetic material. The latter has the advantage that no magnetization of the particles is present once an external magnetic field is switched off and sticking together of the particles due to their magnetism is avoided.
In a specific embodiment of the above variant, the nanoparticles are designed to attach themselves to said structural component of said microorganism.
They may for example attach themselves to the outer surface of the cell membrane of the microorganism. They may be designed to be able to enter into the microorganism and then attach themselves to a cell organelle. Designing the nanoparticles to have this attaching property may involve applying a specific coating to the nanoparticles. The coating may be selected to attach to specific surfaces defined by their chemical properties.
An attachment to the surface of the bacterial membrane is conceivable. Magnetic nanoparticles inside the germs or on their surface could cause an amplified resonance and increase the damage potential to the membrane of the bacteria or other germs.
With this embodiment, the effect of the oscillating field onto the structural component is much stronger and the mechanical resonance of the structural component is more efficiently excited. Microbial activity is reduced more efficiently when this embodiment of the invention is applied.
The inventor has observed that the oscillating magnetic fields affect the germs also without using magnetic nanoparticles according to the above discussed embodiment.
On the one hand, the germinal membranes peptidoglycans are affected by the generation of a specific resonance. The peptidoglycan architecture (contains N-Acetyl-glucosamin and N-Acetylmuroaminacetat) or/and the cytoplasma membrane may be destroyed by applying the method. The pressure inside bacteria is approx. 2 atmospheres. A little damage in the peptidoglycan membrane will lead to a blow-out.
Static magnetic fields interact with moving charges via the Lorentz-force:
F=q[v×B],
where q is the charge and v the velocity-vector. Since the force on opposite charges acts in opposite directions, electric dipoles show the tendency to align orthogonal to the velocity. This might slow down the vital coherent motion.
Alternating magnetic fields induce rotating electrical fields according to Maxwell's first field equation:
rot E=−∂B/∂t.
In a conducting non-magnetic medium this rotating field induces eddy-currents. The strength of these eddy-currents is proportional to the conductivity of the electrolyte and to the frequency and strength of the magnetic field oscillations. These eddy currents may disturb the coherent intra-cellular flow, too. Furthermore, these effects may induce strong enough oscillations for the cellular wall to break open when a cellular resonance frequency is met.
Further in the scope of the invention lies a method according to claim 10.
It is a method of rating a first frequency regarding efficacity.
The method comprises the steps
The microorganisms of a pure bacterial culture may undergo the rating according to this method. To evaluate the effectiveness of the above-described frequency application, high tech fluorescence microscopy, quantitative smears, counting chambers and comparison cultures after incubation can be used. The rating of efficacity may be a killing rate specific for the first frequency. Identically prepared bacterial cultures may be used to determine and comparing the efficacity of different choices for the first frequency.
The rating of efficacity may in addition include the aspect, that another type of bacteria, virus or other cells undergoing the same treatment is not affected or damaged. For compatibility in the experimental field, human HEKs cells or lymphocytes can be seeded with the sample germs and thus the same application can be performed to kill or damage the germs. No damage of the inoculated cells in culture is shown by the electromagnetic therapy application described above.
In one embodiment of the method of rating a first frequency regarding efficacity, the rating of efficacity applies to a set of values of operating parameters of the method according to the invention. The set comprises at least the first frequency.
Together with rating the effect of the first frequency, other operating parameters may be selected appropriately to achieve a high efficiency.
In one embodiment of the method of rating a first frequency regarding efficacity, the set of values of operating parameters is defined as
The relative direction of the current may be selected to be parallel or opposite in a pair of coils, e.g. in a Helmholtz-pair as discussed in more detail below.
Further in the scope of the invention lies a method according to claim 13.
It is a method of determining a species-specific frequency of the method according to the invention. The method comprises repeatedly performing the method according to the invention with various values of said first frequency. In each repetition of the method of rating a first frequency regarding efficacity is applied to a microorganism of a first species. A table of ratings of efficacity in dependency of said first frequency is established, wherein the frequency with the highest rating of efficacity is selected as the species-specific frequency for said first species.
This method can be repeated for a second species, a third species and so on. A table or a database of species-specific frequencies may be established based on the method.
In one embodiment of the method, a frequency range for the first frequency is estimated based on observed movements of the first species of microorganisms. Various values of the first frequency are selected from the frequency range, which is estimated based on observed movements.
This embodiment of the method has the effect that a species-specific frequency may be found in a short time. Testing a huge list of possible frequencies for their effect on a certain species of microorganism can be avoided. A concentration of the tests to an interesting region of frequencies is possible. As an example, species-specific flagella movements may be systematically observed and screened for characteristic frequencies. These results may be collected in a database, which in turn is the basis for setting up tests for identifying the most effective frequency of an oscillating magnetic field.
The invention is further directed to a use of the method according to any one of claims 1 to 9 for reduction of microbial activity in the technical fields of water treatment, nutrition industry, cell culture industry or paper industry as well as in the general reduction or limitation of the reproduction of specific germs in all areas, as well as in human and animal tissue cultures, external treatment of blood preparations.
The invention is further directed to a coil arrangement according to claim 16. This coil arrangement is adapted for performing the method according to the invention. The coil arrangement is formed of a number of mutually isolated loops of flexible wire, in particular of stranded wire. The loops surround a free space into which said microorganism can be placed. E.g., the free space has a diameter large enough to receive a container containing said microorganism when performing the method according to the invention. This container may be a petri dish, as an example. It may as well be a part of a human or animal body infected by said microorganism. The loops are connected in series through a multiple connector pair, allowing for connecting and disconnecting several of said loops simultaneously.
The multiple connector may be a DSUB-15 connector pair consisting of a male and a female connector, having 15 corresponding connector pins or connector sockets, respectively. As an example, an inlet wire and 15 wires connected to pins of the male part of the multiple connector may be grouped in one tube. The wires may be connected to transposed positions of the sockets of the female part, wherein the inlet wire is connected to the first socket, wherein the first pin is connected to the second socket, and so on, such that last pin (pin 15 in this example) ends as outlet wire on the side of the tube where the female part of the connector is attached. The individual wires inside the tube are mutually isolated from each other. The whole tube may be arranged as one circular loop, which in this case results in a coil arrangement having 16 loops. The whole tube may be arranged in multiple windings, too, such that each winding of the tube produces 16 loops of the coil arrangement. E.g. 16 windings of the tube result in a coil arrangement having 256 loops in total. This coil arrangement allows arranging a large number of loops in a flexible and efficient way. The flexibility of the coils in the arrangement makes the whole arrangement suitable for local application of magnetic fields.
Such a coil arrangement may e.g. be formed by approximately circular loops, having an average diameter of 90 mm and surrounding a cylindrical free space of diameter 77-80 mm. The wires may consist of copper strands having a total cross section of 0.3 mm2. In this case, with 256 loops and 16 windings of the tube, a tube length of approximately 4.5 meters results, which length can be handled relatively easy while producing the windings of the tube. By connecting the male and female parts of the multiple connector, the full number of loops are connected in series in one step.
The coil arrangement may be designed to produce in the center of the coil arrangement a magnetic field in the milli Tesla (mT) range, when a current of 1-4 Ampère (A) flows through the coil arrangement. The coil arrangement may be connected to a power supply in a way that a capacitor is connected in series to the coil. To be select an appropriate size for the capacitor, a capacitor decade consisting of several capacitors connected in parallel to each other may be used, wherein the individual capacitors may be activated by closing a switch in the respective one of parallel branches. E.g. the combination of 100 pico Farad (pF), 1 nano Farad (nF), 10 nF, 100 nF and 1 micro Farad (mF) covers a range suitable for the coil dimensions as discussed in the above example.
According to a further example, the coil arrangement has a larger average diameter of 200 mm and has the double number of windings of the tube, compared to the above embodiment. This further embodiment has 32 windings of the tube and thus comprises 512 coil loops in total. This leads to a tube length of approximately 10 meters.
Under the rough assumption, that only half of the magnetic field energy is situated within the coil, an approximation of the magnetic field strength achievable with a coil arrangement fed with current I can be calculated according to the following formula:
B(t)≈√{square root over (μ0L/2V)}*I(t)
where β0 is the induction constant and V the mean volume of the coil, B(t) the time dependent magnetic field and I(t) the time dependent current in Ampere. Example:
The invention shall now be further exemplified with the help of figures. The figures show:
Coil-arrangements as shown in
Number | Date | Country | Kind |
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PCT/EP2020/084421 | Dec 2020 | WO | international |
00472/21 | Apr 2021 | CH | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2021/083802 | 12/1/2021 | WO |