The present application relates to the field of surgery, in particular to an electric field generating device, a control method for the electric field generating device, and a computer-readable storage medium.
Electric field therapy is a therapy implemented through a portable, non-invasive medical device, and its principle is to use a low-intensity, medium-frequency designed electric field to apply to such target biological tissue as microtubules having proliferation and diseased cells, interfere with the mitosis of diseased cells, and cause affected diseased cells to undergo apoptosis and inhibit the growth of the diseased cells.
Currently, in the existing devices used to destroy diseased cells or inhibit the division of diseased cells, an electrical signal generator applies a series of electrical signals to an electrode pair. Since two electrodes in the electrode pair are directly facing each other, a vertical electric field is generated between the two directly facing electrodes of the electrode pair, and the vertical electric field is applied to a target biological tissue region containing target biological tissue.
It has been found through research that a pair of electrodes is located at the periphery of a target biological tissue region, and target biological tissue (such as diseased cells) in the target biological tissue region is not guaranteed to be within the vertical electric field range of the pair of electrodes in the prior art, or is not located entirely within the vertical electric field range of the pair of electrodes in the prior art. That is, the coverage of the vertical electric field in the prior art is too fixed and small, so the coverage of the target biological tissue is limited, and thereby the intensity of the electric field covering a target biological tissue region is limited, and it is ineffective in inhibiting the division of such target biological tissue as diseased cells.
In a first aspect, the present application provides an electric field generating device, including:
In a second aspect, the present application provides a control method for the electric field generating device in the first aspect, including:
In a third aspect, the present application provides a computer-readable storage medium having a computer program stored thereon, the computer program implementing, when executed by a processor, following steps of a control method for an electric field generating device:
The additional aspects and advantages of the present disclosure will be given or may become apparent in the following description, or may be understood through the implementation of the present application.
The above and/or additional aspects as well as advantages of the present application will become apparent and are easily understood in the following description with reference to the following drawings. In these drawings:
The present application provides an electric field generating device, a control method for the electric field generating device and a computer-readable storage medium, so as to solve the technical problem in the prior art that, it is ineffective in inhibiting the division of such target biological tissue as diseased cells due to the limited intensity of the electric field covering a target biological tissue region, and thereby the intensity of the electric field covering the target biological tissue is limited.
The present application will be described hereinafter in conjunction with the embodiments and the drawings. Identical or similar reference numbers in the drawings represent an identical or similar element or elements having an identical or similar function. In addition, the detailed description about any known technology will be omitted when it is unnecessary to the features in the present application. The following embodiments are for illustrative purposes only, but shall not be used to limit the scope of the present application.
As can be appreciated by a person skilled in the art, unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the present application is a part. Terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and will not be interpreted in an idealized or overly formal sense, unless expressly so defined herein.
As used herein, the singular forms, “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. Moreover, the terms “comprises,” “comprising,” “includes,” and/or “including,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, components, and/or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. In the case that one element is connected or coupled to another element, it may be directly connected or coupled to the other element, or an intermediate element may be arranged therebetween. At this time, the element may be connected or coupled to the other element in a wireless or wired manner. In addition, the expression “and/or” is used to indicate the existence of all or any one of one or more of listed items, or combinations thereof.
It has been found through research that a pair of electrodes is located at the periphery of a target biological tissue region, and target biological tissue (such as diseased cells) in the target biological tissue region is not guaranteed to be within the vertical electric field range of the pair of electrodes in the prior art, or is not located entirely within the vertical electric field range of the pair of electrodes in the prior art. That is, the coverage of the vertical electric field in the prior art is too fixed and small, so the coverage of the target biological tissue is limited, and thereby the intensity of the electric field covering a target biological tissue region is limited, and it is ineffective in inhibiting the division of such target biological tissue as diseased cells.
The present application provides a target electric field generating device and a control method for the electric field generating device, so as to solve the above technical problems in the prior art.
The technical solution of the present application and how to solve the above technical problems by using the technical solution of the present application will be described in detail hereinafter in conjunction with specific embodiments. The following specific embodiments can be combined with each other, and same or similar concepts or processes may not be reiterated in some embodiments. The embodiments of the present application will be described hereinafter with reference to the accompanying drawings.
The electric field generating device in the embodiments of the present application is for surgical use and is applicable for surgical medical instruments.
The present application provides a target electric field generating device, as shown in
The electrical signal generator 25 is electrically connected to the n electrodes 10.
The control signal generator 40 is electrically connected to the electrical signal generator 25, and configured to control the electrical signal generator 25 to apply a first electrical signal to m electrodes of the n electrodes 10, and apply a second electrical signal to at least two electrodes of n-m electrodes, to generate an electric field between the electrodes with the first electrical signal and the electrodes with the second electrical signal, where a voltage of the second electrical signal is less than a voltage of the first electrical signal, 1≤m<n, and m is an integer.
Optionally, the first electrical signal and the second electrical signal may be outputted by one electrical signal generator, or may be outputted by two electrical signal generators respectively.
Optionally, the n electrodes 10 may be attached to a target part of a human body or an animal body according to the set manner.
Optionally, there is at least one electrode with the first electrical signal and at least two electrodes with the second electrical signal, and the quantity of electrodes with the first electrical signal is smaller than the quantity of electrodes with the second electrical signal.
Optionally, the control signal generator 40 may be a central processing unit (Central Processing Unit, CPU), a general-purpose processor, a data signal processor (Digital Signal Processor, DSP), an application specific integrated circuit (Application Specific Integrated Circuit, ASIC), or a field-programmable gate array (Field-Programmable Gate Array, FPGA) or other programmable logic devices, transistor logic devices, hardware members or any combination thereof. It may implement or execute various illustrative logical blocks, modules and circuits described in connection with the content of the present application. The control signal generator 40 may also be a combination that implements computing functions, such as a combination of one or more microprocessors, a combination of a DSP and a microprocessor, etc.
In the embodiments of the present application, it is able to flexibly select the quantity of electrodes surrounding the target biological tissue region according to a position of the target biological tissue in the target biological tissue region, and control which electrodes to be applied to the second electrical signal, so that a coverage area of the electric field generated between the electrode with the first electrical signal and the electrodes with the second electrical signal best matches the position of the target biological tissue. Therefore, it is able to improve a matching degree between the coverage area of the electric field and the position of the target biological tissue, a coverage, and flexibility or adaptability of the electric field on the target biological tissue, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Moreover, multiple electric fields can be generated between the electrode with the first electrical signal and at least two electrodes with the second electrical signal, and can be superimposed so as to enhance the intensity of an electric field at a superimposed region. When at least two electrodes with the second electrical signal are selected reasonably, it is able to improve the coverage of the electric field on the target biological tissue, thereby to improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In some embodiments, as shown in
In some embodiments, as shown in
In some embodiments, as shown in
Optionally, the n first switch units include a first one of the first switch units to an nth one of the first switch units, the n second switch units include a first one of the second switch units to an nth one of the second switch units, and the n electrodes include a first electrode to an nth electrode.
The first one to the nth one of the first switch units and the first one to the nth one of the second switch units are electrically connected to n electrodes respectively, i.e., the first one of the first switch units and the first one of the second switch units are electrically connected to the first electrode, a second one of the first switch units and a second one of the second switch units are electrically connected to the second electrode, . . . , the nth one of the first switch units and the nth one of the second switch units are electrically connected to the nth electrode.
Optionally, as shown in
In some embodiments, the electric field generating device further includes at least one of the following:
The constant voltage signal means that a size of the voltage is maintained, the fluctuating voltage signal means that the sum of absolute values of positive and negative deviations of the voltage does not exceed 10% of a rated value.
Optionally, the first electrical signal generating circuit 20 includes an alternating current signal generating circuit, a pulse electrical signal generating circuit or a square wave electrical signal generating circuit, the alternating current signal generating circuit is used to output an AC voltage signal, the pulse electrical signal generating circuit is used to output a pulse voltage signal, and the square wave electrical signal generating circuit is used to output a square wave voltage signal.
In some embodiments, the absolute value of the voltage amplitude of the second electrical signal is 0V, 1V or 5V.
As shown in
Specifically, the first electrical signal generating circuit 20 is electrically connected to six electrodes and used to apply the first electrical signal to the six electrodes. The second electrical signal generating circuit 30 is electrically connected to the six electrodes and used to apply the second electrical signal to the six electrodes.
Optionally, the control signal generator 40 controls one of the first switch units 501 to transmit the first electrical signal to the electrode 101, and controls the remaining first switch units 501 to be turned off. At the same time, the control signal generator 40 controls one of second switch units 601 that is electrically connected to the electrode 101 to be turned off, and controls the remaining second switch units 601 to transmit the second electrical signal to the electrodes 102-106.
For example, the electrode 101 is controlled to have the first electrical signal, and the electrodes 102-106 are controlled to have the second electrical signal, so a first electric field is generated between the electrode 101 and the electrode 102, a second electric field is generated between the electrode 101 and the electrode 103, a third electric field is generated between the electrode 101 and the electrode 104, a fourth electric field is generated between the electrode 101 and the electrode 105, and a fifth electric field is generated between the electrode 101 and the electrode 106. The first electrical signal applied to the electrode 101 is controlled to be a high voltage signal (for example, between 0 and 500V), and the second electrical signal applied to the electrodes 102-106 is controlled to be a low voltage signal (for example, 0 to 10V), that is, there are multiple potential differences between the electrode 101 and the electrodes 102-106, and multiple electric fields are generated between the electrodes 101 and the electrodes 102-106, so it is able to increase the coverage area of the electric field on the patient's target region, and thereby increase the intensity of the electric field covering the patient's target region, increase the intensity of the electric field covering the target biological tissue, where the target biological tissue region includes the target biological tissue and the normal biological tissue, and improve the effect of inhibiting the division of such target biological tissue as diseased cells.
As can be appreciated, it is able to control the electrode 101 and the electrode 102 to have the first electrical signal, and the electrodes 103-106 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 103 and the electrode 105 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 102, the electrode 104 and the electrode 106 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 103, the electrode 104 and the electrode 105 to have the second electrical signal, which is not particularly defined in the present application.
In the embodiments of the present application, it is able to flexibly select the quantity of electrodes surrounding the target biological tissue region according to a position of the target biological tissue in the target biological tissue region, and control which electrodes to be applied to the second electrical signal, so that a coverage area of the electric field generated between the electrode with the first electrical signal and the electrodes with the second electrical signal best matches the position of the target biological tissue. Therefore, it is able to improve a matching degree between the coverage area of the electric field and the position of the target biological tissue, a coverage, and flexibility or adaptability of the electric field on the target biological tissue, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Moreover, multiple electric fields can be generated between the electrode with the first electrical signal and at least two electrodes with the second electrical signal, and can be superimposed so as to enhance the intensity of an electric field at a superimposed region. When at least two electrodes with the second electrical signal are selected reasonably, it is able to improve the coverage of the electric field on the target biological tissue, thereby to improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Optionally, still referring to
Optionally, the set order includes: a clockwise order, a counterclockwise order, an n-pointed star shape order, or any other hop or non-continuous orders.
Optionally, a time interval for the second switch units 601 to be turned on or off sequentially according to the set order is not less than 20 ms and not greater than 500 ms.
Optionally, the electrode 101 is controlled to be applied with the first electrical signal within a first time period, the electrode 102 is controlled to be applied with the second electrical signal within a second time period, the electrode 103 is controlled to be applied with the second electrical signal within a third time period, the electrode 104 is controlled to be applied with the second electrical signal within a fourth time period, the electrode 105 is controlled to be applied with the second electrical signal within the fifth time period, and the electrode 106 is controlled to be applied with the second electrical signal within the sixth time period. The first time period, the second time period, the third time period, the fourth time period, the fifth time period and the sixth time period may be all the same, all different, or partially the same, and may be set according to actual situations, which is not particularly defined in the present application.
In the above-mentioned embodiment, the electrode 101 is controlled to be applied with the first electrical signal continuously, and the remaining electrodes 102-106 are controlled to be applied with the second electrical signal sequentially according to the set order, where the voltage of the second electrical signal applied to the remaining electrodes 102-106 is smaller than the voltage of the first electrical signal. As compared with applying the first electrical signal to all electrodes and switching the first electrical signal among all electrodes, in the embodiment of the present application, one electrode is applied with the first electrical signal, the remaining electrodes are applied with the second electrical signal, and the second electrical signal is switched among the remaining electrodes, so the power consumption is reduced, thereby reducing the power consumption of the electric field generating device and extending the standby duration of the battery used for power supply of the electric field generating device.
The electric field generated by the electric field generating device is used to destroy diseased cells or inhibit the division of diseased cells, and the electric field is referred as a tumor treating field (Tumor Treating Field, TTF) in the present application. TTF can inhibit the proliferation of rapidly dividing active cells, such as cancer cells, and disrupt these active cells.
Optionally, still referring to
Optionally, the set order includes: a clockwise order, a counterclockwise order, an n-pointed star shape order, or any other hop or non-continuous orders.
Optionally, a time interval for the second switch units 601 to be turned on or off sequentially according to the set order is not less than 20 ms and not greater than 500 ms.
Optionally, the time at which each electrode has the first electrical signal or the second electrical signal may be set according to actual situations, which is not particularly defined in the present application.
Thus, the electrodes 101-106 are applied with the first electrical signal and the second electrical signal sequentially according to the set order, which further reduces the power consumption of the electric field generating device, thereby preventing the electric field generating device from overheating.
Based on the same inventive concept, the present application provides in some embodiments a control method for the above-mentioned electric field generating device, including:
In the control method for the electric field generating device of the embodiments of the present application, n electrodes surround the target biological tissue region in a set manner, and the electrical signal generator is controlled to apply the first electrical signal to m electrodes of the n electrodes, and apply the second electrical signal to at least two electrodes of the n-m electrodes, where n is an integer not less than 3, 1≤m<n, and m is an integer. In the embodiments of the present application, it is able to flexibly select the quantity of electrodes surrounding the target biological tissue region according to a position of the target biological tissue in the target biological tissue region, and control which electrodes to be applied to the second electrical signal, so that a coverage area of the electric field generated between the electrode with the first electrical signal and the electrodes with the second electrical signal best matches the position of the target biological tissue. Therefore, it is able to improve a matching degree between the coverage area of the electric field and the position of the target biological tissue, a coverage, and flexibility or adaptability of the electric field on the target biological tissue, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In addition, multiple electric fields can be generated between the electrode with the first electrical signal and at least two electrodes with the second electrical signal, and can be superimposed so as to enhance the intensity of an electric field at a superimposed region. When at least two electrodes with the second electrical signal are selected reasonably, it is able to improve the coverage of the electric field on the target biological tissue, thereby to improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In some embodiments, controlling the electrical signal generator to apply the first electrical signal to m electrodes of the n electrodes, and apply the second electrical signal to at least two electrodes of the n-m electrodes, to generate the electric field between the electrodes with the first electrical signal and the electrodes with the second electrical signal includes:
In some embodiments, controlling the first switch assembly to transmit the first electrical signal to m electrodes of the n electrodes, and controlling the second switch assembly to transmit the second electrical signal to at least two electrodes of the n-m electrodes, to generate the electric field between the electrodes with the first electrical signal and the electrodes with the second electrical signal includes:
The first switch assembly includes n first switch units, and the second switch assembly includes n second switch units. The n first switch units include the first one of the first switch units to the nth one of the first switch units, the n second switch units include the first one of the second switch units to the nth one of the second switch units, and the n electrodes include the first electrode to an nth electrode.
The first one to the nth one of the first switch units and the first one to the nth one of the second switch units are electrically connected to n electrodes respectively, i.e., the first one of the first switch units and the first one of the second switch units are electrically connected to the first electrode, a second one of the first switch units and a second one of the second switch units are electrically connected to the second electrode, . . . , the nth one of the first switch units and the nth one of the second switch units are electrically connected to the nth electrode.
As shown in
Specifically, the first electrical signal generating circuit 20 is electrically connected to six electrodes and used to apply the first electrical signal to the six electrodes. The second electrical signal generating circuit 30 is electrically connected to the six electrodes and used to apply the second electrical signal to the six electrodes.
Optionally, the control signal generator 40 controls one of the first switch units 501 to transmit the first electrical signal to the electrode 101, and controls the remaining first switch units 501 to be turned off. At the same time, the control signal generator 40 controls one of second switch units 601 that is electrically connected to the electrode 101 to be turned off, and controls the remaining second switch units 601 to transmit the second electrical signal to the electrodes 102-106.
For example, the electrode 101 is controlled to have the first electrical signal, and the control electrodes 102-106 are controlled to have the second electrical signal, so a first electric field is generated between the electrode 101 and the electrode 102, a second electric field is generated between the electrode 101 and the electrode 103, a third electric field is generated between the electrode 101 and the electrode 104, a fourth electric field is generated between the electrode 101 and the electrode 105, and a fifth electric field is generated between the electrode 101 and the electrode 106.
The first electrical signal applied to the electrode 101 is controlled to be a high voltage signal (for example, between 0 and 500V), and the second electrical signal applied to the electrodes 102-106 is controlled to be a low voltage signal (for example, 0 to 10V), that is, there are multiple potential differences between the electrode 101 and the electrodes 102-106, multiple electric fields are generated between the electrodes 101 and the electrodes 102-106, and multiple electric fields can be superimposed so as to enhance the intensity of an electric field at a superimposed region. When at least two electrodes with the second electrical signal are selected reasonably, it is able to improve the coverage of the electric field on the target biological tissue, thereby to improve the effect of inhibiting the division of such target biological tissue as diseased cells.
As can be appreciated, it is also able to control the electrode 101 and the electrode 102 to have the first electrical signal, and the electrodes 103-106 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 103 and the electrode 105 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 102, the electrode 104 and the electrode 106 to have the second electrical signal, or control the electrode 101 to have the first electrical signal, and the electrode 103, the electrode 104 and the electrode 105 to have the second electrical signal, which is not particularly defined in the present application.
In the embodiments of the present application, it is able to flexibly select the quantity of electrodes surrounding the target biological tissue region according to a position of the target biological tissue in the target biological tissue region, and control which electrodes to be applied to the second electrical signal, so that a coverage area of the electric field generated between the electrode with the first electrical signal and the electrodes with the second electrical signal best matches the position of the target biological tissue. Therefore, it is able to improve a matching degree between the coverage area of the electric field and the position of the target biological tissue, a coverage, and flexibility or adaptability of the electric field on the target biological tissue, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In some embodiments, controlling the first switch assembly to transmit the first electrical signal to m electrodes of the n electrodes, and controlling the second switch assembly to transmit the second electrical signal to at least two electrodes of the n-m electrodes, to generate the electric field between the electrodes with the first electrical signal and the electrodes with the second electrical signal includes: controlling a first one of first switch units to transmit the first electrical signal to a first electrode of n electrodes, and controlling a second one of the first switch units to an nth one of the first switch units to be turned off; simultaneously controlling a first one of second switch units that is electrically connected to the first electrode to be turned off, and synchronously controlling at least two second switch units among a second one of the second switch units to an nth one of the second switch units to be turned on sequentially according to a set order, to transmit the second electrical signal to at least two electrodes of n electrodes except the first electrode according to the set order.
The first switch assembly includes n first switch units, and the second switch assembly includes n second switch units. The n first switch units include the first one of the first switch units to the nth one of the first switch units, the n second switch units include the first one of the second switch units to the nth one of the second switch units, and the n electrodes include the first electrode to an nth electrode.
The first one to the nth one of the first switch units and the first one to the nth one of the second switch units are electrically connected to n electrodes respectively, i.e., the first one of the first switch units and the first one of the second switch units are electrically connected to the first electrode, a second one of the first switch units and a second one of the second switch units are electrically connected to the second electrode, . . . , the nth one of the first switch units and the nth one of the second switch units are electrically connected to the nth electrode.
In the above-mentioned embodiment, one of n electrodes is controlled to be applied with the first electrical signal continuously, and the remaining electrodes 102-106 are controlled to be applied with the second electrical signal sequentially according to the set order, where the voltage of the second electrical signal applied to the remaining electrodes 102-106 is smaller than the voltage of the first electrical signal. As compared with applying the first electrical signal to all electrodes and switching the first electrical signal among all electrodes, in the embodiment of the present application, one electrode is applied with the first electrical signal, the remaining electrodes are applied with the second electrical signal, and the second electrical signal is switched among the remaining electrodes, so the power consumption is reduced, thereby reducing the power consumption of the electric field generating device.
By way of example, still referring to
Optionally, the set order includes: a clockwise order, a counterclockwise order, an n-pointed star shape order, or any other hop or non-continuous orders.
Optionally, a time interval for the second switch units 601 to be turned on or off sequentially according to the set order is not less than 20 ms and not greater than 500 ms.
Optionally, the electrode 101 is controlled to be applied with the first electrical signal within a first time period, the electrode 102 is controlled to be applied with the second electrical signal within a second time period, the electrode 103 is controlled to be applied with the second electrical signal within a third time period, the electrode 104 is controlled to be applied with the second electrical signal within a fourth time period, the electrode 105 is controlled to be applied with the second electrical signal within the fifth time period, and the electrode 106 is controlled to be applied with the second electrical signal within the sixth time period. The first time period, the second time period, the third time period, the fourth time period, the fifth time period and the sixth time period may be all the same, all different, or partially the same, and may be set according to actual situations, which is not particularly defined in the present application.
In the above-mentioned embodiment, the electrode 101 is controlled to be applied with the first electrical signal continuously, and the remaining electrodes 102-106 are controlled to be applied with the second electrical signal sequentially according to the set order, where the voltage of the second electrical signal applied to the remaining electrodes 102-106 is smaller than the voltage of the first electrical signal. As compared with applying the first electrical signal to all electrodes and switching the first electrical signal among all electrodes, in the embodiment of the present application, one electrode is applied with the first electrical signal, the remaining electrodes are applied with the second electrical signal, and the second electrical signal is switched among the remaining electrodes, so the power consumption is reduced, thereby reducing the power consumption of the electric field generating device and extending the standby duration of the battery used for power supply of the electric field generating device.
In some embodiments, m is 1, and controlling the first switch assembly to transmit the first electrical signal to m electrodes of the n electrodes, and controlling the second switch assembly to transmit the second electrical signal to at least two electrodes of the n-m electrodes, to generate the electric field between the electrodes with the first electrical signal and the electrodes with the second electrical signal includes:
The first switch assembly includes the n first switch units, and the second switch assembly includes the n second switch units.
In the above-mentioned embodiment, n electrodes are controlled to have the first electrical signal (high voltage signal) and the second electrical signal (low voltage signal) sequentially according to the set order, which further reduces the power consumption of the electric field generating device, thereby preventing the electric field generating device from overheating.
Optionally, still referring to
Optionally, the set order includes: a clockwise order, a counterclockwise order, an n-pointed star shape order, or any other hop or non-continuous orders.
Optionally, a time interval for the second switch units 601 to be turned on or off sequentially according to the set order is not less than 20 ms and not greater than 500 ms.
Optionally, the time at which each electrode has the first electrical signal or the second electrical signal may be set according to actual situations, which is not particularly defined in the present application.
Thus, the electrodes 101-106 are applied with the first electrical signal and the second electrical signal sequentially according to the set order, which further reduces the power consumption of the electric field generating device, thereby preventing the electric field generating device from overheating.
Optionally, a time interval for the second switch units 601 to be turned on or off sequentially according to the set order is not less than 20 ms and not greater than 500 ms.
Note that the target biological tissue region includes the target biological tissue and a normal biological tissue, and the target biological tissue includes diseased cells, a tumor or a lesion, etc.
In order to further verify the technical effect of the present application, a case where the target biological tissue is a tumor is taken as an example, a two-dimensional model is performed on the target biological tissue and n electrodes surrounding the target biological tissue region, and a three-dimensional model is performed on a human thorax and a tumor in the human thorax.
A finite element modeling process is as follows.
A geometric model is constructed in COMSOL. Next, a circle with a diameter of 40 mm (millimeters) is constructed as the tumor (i.e., the target biological tissue 81), a square with a side length of 200 mm is constructed as the target biological tissue region 80, where a center of the square coincides with a center of the circle of the tumor, and a region of the square outside the circle represents the normal biological tissue 82 outside of the tumor. Straight lines with a length of 80 mm (h1 is 80 mm in
Material electrical parameter settings. The conductivity of a tumor region (i.e., the target biological tissue 81) is set to 0.245/m and the dielectric constant thereof is set to 2000. The conductivity of a surrounding normal biological tissue 82 is set to 0.11 S/m and the dielectric constant thereof is set to 1980.
Applied voltage waveform. In this embodiment, a continuous sine wave with a frequency of 150 kHz (kilohertz) and a peak-to-peak value of 120V (volts) is applied, that is, the first electrical signal generating circuit is an AC signal generating circuit and outputs an AC voltage signal with a frequency of 150 kHz (kilohertz) and a peak-to-peak value of 120V (volts).
Note that the first electrical signal outputted by the first electrical signal generating circuit is a high voltage signal, and the second electrical signal outputted by the second electrical signal generating circuit is a low voltage signal.
The electrode 107 is set as a power source receiving end, and configured to receive the first electrical signal outputted by the first electrical signal generating circuit, and the electrodes 108 to 110 are set as ground ends, and configured to receive the second electrical signal outputted by the second electrical signal generating circuit.
According to the above settings, following three cases are shown.
1. In a case where a single electrode is grounded, the electrode 107 is set to receive the first electrical signal (the high voltage signal) outputted by the first electrical signal generating circuit, and the electrode 108 is set to receive the second electrical signal (the low voltage signal) outputted by the second electrical signal generating circuit, that is, the electrode 107 receives a power source voltage, and the electrode 108 is grounded.
2. In a first case where two electrodes are grounded, the electrode 107 is set to receive the first electrical signal (the high voltage signal) outputted by the first electrical signal generating circuit, and the electrode 108 as well as the electrode 109 are set to receive the second electrical signal (the low voltage signal) outputted by the second electrical signal generating circuit, that is, the electrode 107 receives a power source voltage, and the electrode 108 as well as the electrode 109 are grounded.
3. In a second case where two electrodes are grounded, the electrode 107 is set to receive the first electrical signal (the high voltage signal) outputted by the first electrical signal generating circuit, and the electrode 108 as well as the electrode 110 are set to receive the second electrical signal (the low voltage signal) outputted by the second electrical signal generating circuit, that is, the electrode 107 receives a power source voltage, and the electrode 108 as well as the electrode 110 are grounded.
Average field strengths on the tumor in different cases are shown in Table 1.
Based on the above, when the quantity of electrodes with the high-voltage signal is maintained, the greater the quantity of electrodes with the low-voltage signal, the greater the average field strength in the tumor region.
In the embodiments of the present application, it is able to increase the coverage area of the electric field on the target biological tissue, increase the intensity of the electric field covering the target biological tissue region, and thereby increase the intensity of the electric field covering the target biological tissue, and improve the effect of inhibiting the division of such target biological tissue as diseased cells.
A finite element modeling process is as follows.
Construction of a human thorax. Approximate shapes of actual tissues are constructed in Rhino3D NURBS 7, and compared with multiple (Computed Tomography, CT) scanning, slices, so as to modify boundary contours, thereby ultimately restoring a realistic human body model. The modeling content includes skin, fat, muscles, bones, lungs, heart and liver. Some over-detailed tissues (such as connective tissues, pleurae) that have similar electrical parameters and are difficult to model are merged into muscle tissues. A final model is shown in
Construction of a single electrode. Each electrode is modeled as a double-layer structure as shown in
Construction of an electrode array. The electrode array is composed of multiple electrodes. For example, 5 electrodes, 10 electrodes, 15 electrodes, and other quantities of electrodes may form multiple different electrode arrays.
As shown in
Construction of Tumor Models. A total of four virtual tumor models are created, as shown in
After the model has been constructed, separate meshes for various tissues including electrodes, gels, skin, fat, bones, muscles, lungs, heart, liver and tumors are generated through mesh generation by using HyperMesh14.0, and then imported into COMSOL Multiphysics 5.5 one by one, so as to solve electrical quasi-static equations of Maxwell's equations by using a current module.
Material electrical parameter settings. As shown in Table 2, the conductivity and dielectric constant of each tissue are set to corresponding values.
Simulation power source settings: Frequency domain simulation is used, a frequency thereof is set to 150 kHz, and a normal current density on each electrode is set to 100 mA/cm2 (milliamps per square centimeter).
Field strength evaluation method: COMSOL is used to calculate a curve diagram between the electric field strength-volume (EVH) at the tumor, as shown in
Note that the first electrical signal outputted by the first electrical signal generating circuit is a high voltage signal, and the second electrical signal outputted by the second electrical signal generating circuit is a low voltage signal.
The front electrode array is set as a power source receiving end, and configured to receive the first electric signal outputted by the first signal generation circuit, and the back electrode array, the left side electrode array and the right side electrode array are set as ground ends, and configured to receive the second electric signal outputted by the second signal generation circuit.
In the case of Tumor T1 and Tumor T2, simulation results are shown in Table 3, where EAUC values are compared. Two cases presented in Table 3 are as follows.
1. In a case where a single electrode array is grounded, the front electrode array (e.g., the first electrode array 201 in
2. In a first case where two electrode arrays are grounded, the front electrode array (e.g., the first electrode array 201 in
As the results in Table 3 indicate, the EAUC value in the case where two electrode arrays are grounded is higher than the EAUC value in the case where the single electrode array is grounded, i.e., the EAUC value is increased. It can be observed from Table 3 that, for Tumor T1, the EAUC value in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded, is increased by 1.22%. For Tumor T2, the EAUC value in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded, is increased by 1.23%.
The distribution of the electric field in a horizontal plane of the thorax including Tumor T1 is shown in
The distribution of the electric field in a horizontal plane of the thorax including Tumor T2 is shown in
In the case of Tumor T3 and Tumor T4, simulation results are shown in Table 4, where EAUC values are compared. Two cases presented in Table 4 are as follows.
1. In a case where a single electrode array is grounded, the front electrode array (e.g., the first electrode array 201 in
2. In a case where two electrode arrays are grounded, the front electrode array (e.g., the first electrode array 201 in
As shown in Table 4, the EAUC value in the case where two electrode arrays are grounded is higher than the EAUC value in the case where the single electrode array is grounded, i.e., the EAUC value is increased. It can be observed from Table 3 that, for Tumor T3, the EAUC value in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded, is increased by 16.20%. For Tumor T4, the EAUC value in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded, is increased by 15.79%.
The distribution of the electric field in a horizontal plane of the thorax including Tumor T3 is shown in
The distribution of the electric field in a horizontal plane of the thorax including Tumor T4 is shown in
From the above results, it may be found that when the case where the electrode array on the side close to the tumor and the back electrode array are grounded is used, as compared with the case where only the back electrode array is grounded, it is able to increase the field strength in the tumor region, increase the field strength coverage of the electric field generated between the electrode arrays, thereby to further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In addition, as shown in
1. In a case where a single electrode array is grounded, the front electrode array (e.g., the first electrode array 201 in
2. In a case where two electrode arrays are grounded, the front electrode array (e.g., the first electrode array 201 in
It is observed that two second electrode arrays 202 with the low-voltage signal are arranged on the back, as compared with a case where only one second electrode array 202 with the low-voltage signal is arranged on the back, it is also able to increase the field strength at the tumor. Table 5 shows the comparison of EAUC values at the four aforementioned tumor models between the case where one second electrode array 202 is arranged on the back and the case where two second electrode arrays 202 are arranged on the back.
From Table 5, it may be derived that, for Tumor T1, the EAUC value is increased by 4.12% in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded. For Tumor T2, the EAUC value is increased by 4.49% in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded. For Tumor T3, the EAUC value is increased by 15.08% in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded. For Tumor T4, the EAUC value is increased by 9.57% in the case where two electrode arrays are grounded, as compared with the case where the single electrode array is grounded.
The distribution of the electric field in a horizontal plane of the thorax including Tumor T1 is shown in
The distribution of the electric field in a horizontal plane of the thorax including Tumor T2 is shown in
The distribution of the electric field in a horizontal plane of the thorax including Tumor T3 is shown in
The distribution of the electric field in a horizontal plane of the thorax including Tumor T4 is shown in
Based on the above, when the quantity of electrodes with the high-voltage signal is maintained, as the quantity of electrodes with the low-voltage signal increases, the field strength coverage of the electric field generated between the electrode arrays is increased, thereby to further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
In the embodiments of the present application, when the quantity of electrodes with the first electrical signal (high voltage signal) is maintained, the more the quantity of electrodes with the second electrical signal (low voltage signal), the more the electric fields generated between the electrodes with the first electrical signal and the electrodes with the second electrical signal, the larger the coverage area of the electric fields on the target biological tissue region, so as to increase the intensity of the electric field covering the target biological tissue region, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Based on the same inventive concept, the embodiments of the present application provide a computer-readable storage medium having a computer program stored thereon, the computer program implements, when executed by a processor, the control method for the electric field generating device in any of the above optional embodiments of the present application.
The computer-readable storage medium in the embodiments of the present application is applicable for various optional embodiments of the control method for the electric field generating device. The computer-readable storage medium may be a non-volatile readable storage medium or a volatile readable storage medium, which is not particularly defined herein.
When the embodiments of the present application are implemented, at least the following beneficial effects can be achieved.
Firstly, in the electric field generating device of the embodiments of the present application, n electrodes surround the target biological tissue region in a set manner, and the electrical signal generator is controlled to apply the first electrical signal to m electrodes of the n electrodes, and apply the second electrical signal to at least two electrodes of the n-m electrodes, where n is an integer not less than 3, 1≤m<n, and m is an integer. In the embodiments of the present application, it is able to flexibly select the quantity of electrodes surrounding the target biological tissue region according to a position of the target biological tissue in the target biological tissue region, and control which electrodes to be applied to the second electrical signal, so that a coverage area of the electric field generated between the electrode with the first electrical signal and the electrodes with the second electrical signal best matches the position of the target biological tissue. Therefore, it is able to improve a matching degree between the coverage area of the electric field and the position of the target biological tissue, a coverage, and flexibility or adaptability of the electric field on the target biological tissue, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Moreover, multiple electric fields can be generated between the electrode with the first electrical signal and at least two electrodes with the second electrical signal, and can be superimposed so as to enhance the intensity of an electric field at a superimposed region. When at least two electrodes with the second electrical signal are selected reasonably, it is able to improve the coverage of the electric field on the target biological tissue, thereby to improve the effect of inhibiting the division of such target biological tissue as diseased cells.
Secondly, in the above-mentioned embodiments of the present application, one of n electrodes is controlled to be applied with the first electrical signal continuously, and the remaining electrodes 102-106 are controlled to be applied with the second electrical signal sequentially according to the set order, where the voltage of the second electrical signal applied to the remaining electrodes 102-106 is smaller than the voltage of the first electrical signal. As compared with applying the first electrical signal to all electrodes and switching the first electrical signal among all electrodes, in the embodiment of the present application, one electrode is applied with the first electrical signal, the remaining electrodes are applied with the second electrical signal, and the second electrical signal is switched among the remaining electrodes, so the power consumption is reduced, thereby reducing the power consumption of the electric field generating device.
Thirdly, in the above-mentioned embodiments of the present application, n electrodes are controlled to have the first electrical signal (high voltage signal) and the second electrical signal (low voltage signal) sequentially according to the set order, which further reduces the power consumption of the electric field generating device, thereby preventing the electric field generating device from overheating.
Lastly, when the quantity of electrodes with the first electrical signal (high voltage signal) is maintained, the more the quantity of electrodes with the second electrical signal (low voltage signal), the more the electric fields generated between the electrodes with the first electrical signal and the electrodes with the second electrical signal, the larger the coverage area of the electric fields on the target biological tissue region, so as to increase the intensity of the electric field covering the target biological tissue region, thereby to increase the intensity of the electric field covering the target biological tissue, and further improve the effect of inhibiting the division of such target biological tissue as diseased cells.
As can be appreciated by a person skilled in the art, steps, measures and schemes in various operations, methods and processes that have already been discussed in the embodiments of the present application may be replaced, modified, combined or deleted. In a possible embodiment of the present disclosure, the other steps, measures and schemes in various operations, methods and processes that have already been discussed in the embodiments of the present application may also be replaced, modified, rearranged, decomposed, combined or deleted. In another possible embodiment of the present application, steps, measures and schemes in various operations, methods and processes that are known in the related art and have already been discussed in the embodiments of the present application may also be replaced, modified, rearranged, decomposed, combined or deleted.
Such words as “first” and “second” are merely for illustrative purposes, rather than to implicitly or explicitly indicate the number of the defined technical features. In this regard, the technical features defined with such words as “first” and “second” may implicitly or explicitly include one or more technical features. Further, such a phrase as “a plurality of” is used to indicate that there are at least two, e.g., two or three, components, unless otherwise specified.
It should be further appreciated that, although with arrows, the steps in the flow charts may not be necessarily performed in an order indicated by the arrows. Unless otherwise defined, the order of the steps may not be strictly defined, i.e., the steps may also be performed in another order. In addition, each of at least parts of the steps in the flow charts may include a plurality of sub-steps or stages, and these sub-steps or stages may not be necessarily performed at the same time, i.e., they may also be performed at different times. Furthermore, these sub-steps or stages may not be necessarily performed sequentially, and instead, they may be performed alternately with the other steps or at least parts of sub-steps or stages of the other steps.
The above embodiments are partial embodiments of the present application, it should be appreciated that those skilled in the art may make various improvements and modifications without departing from the principle of the present disclosure, and theses improvement and modifications shall fall within the scope of the present disclosure.
Number | Date | Country | Kind |
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202111231292.6 | Oct 2021 | CN | national |
This application is a continuation of PCT Application No. PCT/CN2022/124124, filed on Oct. 9, 2022, which claims priority to Chinese Patent Application No. 202111231292.6, filed on Oct. 22, 2021. All of the aforementioned applications are incorporated herein by reference in their entireties.
Number | Date | Country | |
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Parent | PCT/CN2022/124124 | Oct 2022 | WO |
Child | 18592976 | US |