This application claims the priority benefit of Taiwan application serial no. 102100461, filed on Jan. 7, 2013. The entirety of the above-mentioned patent application is hereby incorporated by reference herein and made a part of this specification.
1. Technical Field
The technical field relates to an electronic apparatus, an electrical stimulation apparatus and an electrical stimulation method.
2. Related Art
In the field of biomedical sciences, implantable electronic devices such as the implantable neural stimulator (INS) have been widely adopted to monitor internal organs, tissues, neural or cell conditions, and/or restore lost physiological functions. Among the various types of implantable electronic devices, the electrical stimulation apparatus can activate a biological tissue (referred to here as a target tissue) by injecting and accumulating charge in the target tissue. However, the amount of charge (i.e. stimulus resolution) being injected into the target tissue must be accurate.
Generally speaking, the electrical stimulation apparatus can be broadly classified into the voltage-controlled scenario (VCS), the current-controlled scenario (CCS), and the switched capacitor array scenario (SCS). The energy efficiency of the conventional CCS electrical stimulation apparatus is poor, and the energy efficiency of the VCS electrical stimulation apparatus is preferable. A high energy efficiency increases the lifespan of the implantable electronic device.
The disclosure provides an electrical stimulation apparatus, may include an electrode unit, a measurement unit, and a stimulation unit. The electrode unit may be used for contacting a biological tissue (referred to hereafter as a target tissue). The measurement unit may be coupled to the electrode unit. The measurement unit measures a tissue characteristic of the target tissue through the electrode unit. The stimulation unit may be coupled to the electrode unit and the measurement unit. The stimulation unit stimulates the target tissue through the electrode unit by using an electrical stimulation signal, and determines an amount of charge of the electrical stimulation signal according to the tissue characteristic measured by the measurement unit.
The disclosure provides an electrical stimulation method, may include: disposing an electrode unit contacting a target tissue of a biological body; by using a measurement unit, measuring a tissue characteristic of the target tissue through the electrode unit; and by using a stimulation unit, stimulating the target tissue through the electrode unit by using an electrical stimulation signal, wherein an amount of charge of the electrical stimulation signal is determined by the stimulation unit according to the tissue characteristic measured by the measurement unit.
In summary, the disclosure provides an electrical stimulation apparatus and an electrical stimulation method. The measuring unit measures the tissue characteristic of the target tissue, and the tissue characteristic is fed back to the stimulation unit. The stimulation unit can determine the amount of charge of the electrical stimulation signal according to the tissue characteristic measured by the measurement unit, and stimulate the target tissue by using the electrical stimulation signal. Therefore, the electrical stimulation apparatus and electrical stimulation method provided by the disclosure can satisfy the stimulus resolution (charge accuracy) requirements. In some embodiments, the electrical stimulation apparatus provided by the disclosure can use a voltage source to implement the voltage-controlled scenario, to meet both the high energy efficiency and low circuit area requirements.
Several exemplary embodiments accompanied with figures are described in below to further describe the disclosure in details.
The accompanying drawings constituting a part of this specification are incorporated herein to provide a further understanding of the disclosure. Here, the drawings illustrate embodiments of the disclosure and, together with the description, serve to explain the principles of the embodiments.
The terms “connected,” “coupled,” and “mounted” and variations thereof herein (including the claims) are used broadly and encompass direct and indirect connections, couplings, and mountings. For example, if the disclosure describes a first apparatus being coupled to a second apparatus, the first apparatus can be directly connected to the second apparatus, or the first apparatus can be indirectly connected to the second apparatus through other devices or by a certain coupling means.
The stimulation unit 110 is not limited to being implemented in the voltage-controlled scenario (VCS). In other embodiments, the stimulation unit 110 may also be implemented in the current-controlled scenario (CCS) or the switched capacitor array scenario (SCS). The stimulation unit 110 can stimulate the target tissue 10 through the electrode unit 130 by using an electrical stimulation signal having a pulse width, so as to inject charge into the target tissue 10. For example, the stimulation unit 110 can output an electrical stimulation signal having a pulse width of ½ period T to the target tissue 10.
For example,
When the pulse width is fixed, the conventional VCS electrical stimulation apparatus controls an amount of output charge by adjusting a level of the electrical stimulation signal Vo. To accurately control the amount of output charge to suit the different tissue characteristics of different target tissues, the conventional VCS electrical stimulation apparatus requires a user to adjust the level of the electrical stimulation signal Vo.
For example, in some embodiments, the stimulation unit 110 has a plurality of stimulation models. In Step S630, the stimulation models provided by the stimulation unit 110 has different current-time characteristics, such as the stimulation models shown in
For example, in another embodiment, the stimulation unit 110 has a plurality of look-up tables. In Step S630, the look-up tables provided by the stimulation unit 110 respectively correspond to different tissue characteristics. According to the tissue characteristic measured by the measurement unit 120, the stimulation unit 110 can select a target look-up table from the plurality of look-up tables. According to the target look-up table, the stimulation unit 110 can convert the target charge value into the pulse width. Moreover, the stimulation unit 110 can control the pulse width of the electrical stimulation signal according to the pulse width. The implementation details of this embodiment are detailed later in the disclosure.
Therefore, the electrical stimulation apparatus 100 of the present embodiment can satisfy various stimulus resolution (charge accuracy) requirements, and output accurate amounts of charge to the target tissue 10. In the electrical stimulation apparatus 100 of the present embodiment, less voltage levels are needed for the electrical stimulation signal Vo (a single voltage level is possible). The electrical stimulation apparatus 100 of the present embodiment can drastically reduce the circuit area and can be implanted into a biological body.
The measurement unit 120 and the switching unit 131 can be implemented by any methods. For example, in the present embodiment, the switching unit 131 includes a first switch SW1, a second switch SW2, a third switch SW3, and a fourth switch SW4. The measurement unit 120 includes a reference current generator 121, a voltage comparator 122, and an analog-to-digital converter (ADC) 123. The voltage comparator 122 may include an instrumentation amplifier, an operation amplifier, or an error amplifier.
The first switch SW1 has a first terminal coupled to an output terminal of the electrical stimulation signal from the stimulation unit 110, and a second terminal coupled to the first electrode E1. The second switch SW2 has a first terminal coupled to an output terminal of the reference current generator 121 of the measurement unit 120, and a second terminal coupled to the first electrode E1. The third switch SW3 has a first terminal coupled to a first input terminal of the voltage comparator 122 of the measurement unit 120, and a second terminal coupled to the first electrode E1. A fourth switch SW1 has a first terminal coupled to a second input terminal of the voltage comparator 122, and a second terminal coupled to the second electrode E2. In the present embodiment, the second electrode E2 is also coupled to the stimulation unit 110. In other embodiments, the second electrode E2 can be coupled to a ground voltage.
An input terminal of the ADC 123 is coupled to an output terminal of the voltage comparator 122. An output terminal of the ADC 123 is coupled to the stimulation unit 110. The ADC 123 can convert an analog output of the voltage comparator 122 into a digital code. The stimulation unit 110 can measure/compare the potential difference of two sides of the target tissue 10 in the measurement period by using the voltage comparator 122 (Step S622). Therefore, in some embodiments, the stimulation unit 110 in Step S623 can use the potential difference obtained in Step S622 to serve as the tissue characteristic of the target tissue 10. In the present embodiment, since resistance R=V/I (where V is the potential difference of two sides of the target tissue 10, and I is the reference current flowing to the target tissue 10 provided by the reference current generator 121), the stimulation unit 110 can obtain the impedance of the target tissue 10 in Step S623, to serve as the tissue characteristic of the target tissue 10.
In the stimulation period after the measurement period has ended, the first switch SW1 is turned on, and the second switch SW2, the third switch SW3, and the fourth switch SW4 are turned off. The stimulation unit 110 can transmit the electrical stimulation signal Vo with the modulated pulse width to the target tissue 10 through the first switch SW1 and the first electrode E1. Since the stimulation unit 110 has obtained the impedance of the target tissue 10, in the stimulation period, the stimulation unit 110 can determine the pulse width of the electrical stimulation signal Vo according to the impedance of the target tissue 10 (further elaboration later in the disclosure).
However, the implementation methods of the measurement unit 120 and the switching unit 131 are not limited by
In other embodiments for example, when the feedback terminal of the stimulation unit 110 is the analog input terminal, the ADC 123 can be omitted. When the ADC 123 is omitted, the output terminal of the voltage comparator 122 is coupled to the stimulation unit 110.
In another example,
In the measurement period, the switching unit 131 couples the first electrode E1, the third electrode E3, and the fourth electrode E4 to the measurement unit 120. The measurement unit 120 can measure the tissue characteristic of the target tissue 10 in the measurement period through the electrode unit 130. In the stimulation period after the measurement period has ended, the switching unit 131 couples the first electrode E1 to the stimulation unit 110, and couples the second electrode E2 to the ground voltage or the stimulation unit 110. In the stimulation period, the stimulation unit 110 can determine the pulse width of the electrical stimulation signal Vo according to the tissue characteristic measured by the measurement unit 120, and stimulate the target tissue 10 through the electrode unit 130 by using the electrical stimulation signal Vo.
The measurement 120 and the switching unit 131 may be implemented by any methods, such as by reference to the related description of
The controller 112 is coupled to the database 111 and the measurement unit 120. According to the tissue characteristic measured by the measurement unit 120, the controller 112 selects a target look-up table from the plurality of look-up tables of the database 111 (Step S632), and converts a target charge value A to a pulse width C according to the target look-up table (Step S633). Taking Tables 1 and 2 as an example, the target charge value A has 4 bits (recorded as A[3:0]), and the pulse width C has 10 bits (recorded as C[9:0]). The respective bits of the target charge value A[3:0] are A3, A2, A1, and A0, and the respective bits of the pulse width C[9:0] are C9, C8, C7, C6, C5, C4, C3, C2, C1, and C0. For example, assuming the tissue characteristic measured by the measurement unit 120 represents that the impedance of the target tissue 10 plus the impedance of the electrode unit 130 is approximately 10 KΩ, then the controller 112 selects the look-up table of Table 1, for example, as the target look-up table from the plurality of look-up tables in the database 111. After selecting the target look-up table, the controller 112 can convert the target charge value A[3:0] into the pulse width C[9:0] according to the target look-up table. For example, if the target charge value A[3:0] is 9 (i.e. binary 1001), then the controller 112 can correspondingly output 86 (i.e. binary 0001010110) as the pulse width C[9:0].
A control terminal of the DPWM unit 113 is coupled to the controller 112 to receive the pulse width C. According to the pulse width C, the DPWM unit 113 generates a corresponding pulse width modulation (PWM) signal PW. The pulse width of the PWM signal PW corresponds to the pulse width C. For example, if the pulse width C has 10 bits, and the pulse width C[9:0] is 86, then the pulse width of the PWM signal PW is 86/1024 of a period. The DPWM unit 113 can be implemented by any type of digital pulse width modulator, such as a digital counter-based DPWM or a delay-line based DPWM. Since the DPWM is a known device to ones skilled in the art, further elaboration thereof is omitted hereafter.
An input terminal of the stimulation driver circuit 114 is coupled to the output terminal of the DPWM unit 113 to receive the PWM signal PW. An output terminal of the stimulation driver circuit 114 is coupled to the driver unit 130. The stimulation driver circuit 114 outputs the electrical stimulation signal Vo to the target tissue 10 through the electrode unit 130, and the stimulation driver circuit 114 controls the pulse width of the electrical stimulation signal Vo according to the PWM signal PW. The stimulation unit 110 can control the pulse width of the electrical stimulation signal Vo according to the pulse width C (Step S634).
The stimulation period includes a charging period and a discharging period. A control terminal of the driver 1201 is coupled to the output terminal of the DPWM unit 113 to receive the PWM signal PW. The driver 1201 controls the charging switch 1203 according to the PWM signal PW, such that the stimulation voltage VS of the voltage source 1202 is transmitted to the target tissue 10 in the charging period through the first electrode E1 of the electrode unit 130. In the discharging period, the driver 121 controls the charging switch 1203 to turn off. The stimulation unit 110 can control the pulse width of the electrical stimulation signal Vo according to the PWM signal PW, and accumulate charge in the target tissue 10.
The driver 1201 controls the discharging switch 1204 according to the PWM signal PW, such that the ground voltage is transmitted to the target tissue 10 in the discharging period through the second electrode E2 of the electrode unit 130. The stimulation unit 110 can control the discharging switch 1204 according to the PWM signal PW, and discharge/remove the accumulated charge in the target tissue 10. In other words, during the charging period, the stimulation unit 110 couples the electrical stimulation signal Vo to the target tissue 10 through the electrode unit 130. During the discharging period, the stimulation unit 110 couples the ground voltage to the target tissue 10 through the electrode unit 130.
In view of the foregoing embodiments, an electrical stimulation apparatus and an electrical stimulation method are provided. The measuring unit 120 measures the tissue characteristic of the target tissue 10, and the tissue characteristic is fed back to the stimulation unit 110. The stimulation unit 110 can determine the pulse width of the electrical stimulation signal Vo according to the tissue characteristic measured by the measurement unit 120, and stimulate the target tissue 10 by using the electrical stimulation signal Vo with the modulated pulse width. Therefore, by configuring suitable stimulation models or look-up tables in the stimulation unit 110, the electrical stimulation apparatuses and the electrical stimulation methods according to the embodiments can satisfy any stimulus resolution (charge accuracy) requirements by using a small amount of voltage sources (or even a single level voltage source). The electrical stimulation apparatuses provided by some of the embodiments can use a voltage source to implement the voltage-controlled scenario, to meet both the high energy efficiency and low circuit area requirements.
It will be apparent to those skilled in the art that various modifications and variations can be made to the structure of the disclosed embodiments without departing from the scope or spirit of the disclosure. In view of the foregoing, it is intended that the disclosure cover modifications and variations of this disclosure provided they fall within the scope of the following claims and their equivalents.
Number | Date | Country | Kind |
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102100461 | Jan 2013 | TW | national |