Noninvasive Bio-impedance Measurement Using Voltage Current Pulse Technique

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  • 7/29/2019 Noninvasive Bio-impedance Measurement Using Voltage Current Pulse Technique

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    International Conference on Electrical, Electronics and Biomedical Engineering (ICEEBE'2012) Penang (Malaysia) May 19-20, 2012

    AbstractNoninvasive detection is a fundamental prerequisite

    for pervasive healthcare system and biosensing. Along with different

    noninvasive techniques such as ultrasound, X-ray, magnetic

    resonance and optical imaging, electrical impedance spectroscopy is

    emerging as more suitable technique for tissue level diagnosis. This

    paper presents a noninvasive technique for bioelectrical impedance

    estimation by means of impedance spectroscopy applying voltage-

    current pulse technique and least square curve fitting method. Simple

    circuit for current injection and voltage detection is presented with

    common mode noise suppression circuit requires only two electrodes

    would reduce problems due to electrode polarization. The currentsource is presented with constant output current as low as 100 A,

    about 1M load variation and 10 MHz mid-range bandwidth.

    Voltage detection and impedance estimation is done with Data

    Acquisition (DAQ) tool box of Matlab R2008a and curve fitting

    technique. Successful simulation results in bioelectrical impedance

    estimation are found with 1.5% maximum error; suggest impedance

    measurement below 100 kHz because of higher response of

    permittivity and conductivity of biological tissues in this band than

    the high frequency band (MHz band).

    Keywordsbioelectrical impedance, impedance spectroscopy,curve fitting, data acquisition tool box, non-invasive biosensing.

    I. INTRODUCTIONERVASIVE healthcare system automatically calls for

    intermittent, continuous or even contactless (wearable and

    wireless) and distant biomedical sensing [1]. Such systems

    not involve pathological patients only but also the healthy

    people that for the sake of preventive measurement. Therefore,

    an invasive sensor is not certainly going to be popular among

    the healthy people. Besides, invasive sensing precludes

    continuous monitoring and it is sometimes not possible for

    specific cases (e.g. blood glucose monitoring) which inevitably

    calls for noninvasive sensors. There are different popular

    noninvasive techniques for bio-sensing like optical

    spectroscopy, ultrasound, X-ray and magnetic resonance

    imaging which typically measure the effect of absorption,reflection or transmittance of non-ionizing radiation that

    illuminates a portion of the subject. Such techniques offer

    basic information on mass or proton density distribution. On

    the other hand, one more technique that provides information

    Sagar K. Dhar is with the Premier University, 1/A, O.R. Nizam Road,

    Prabartak Circle, Panchlaish, Chittagong, Bangladesh (phone:

    8801818837084; e-mail: [email protected]).

    Quazi D. Hossain is with Chittagong University of Engineering and

    Technology, 163 Kaptai Road, Chittagong, Bangladesh (e-mail:

    [email protected]).

    related to tissue structures and their physiological states and

    functions is bioelectrical impedance, has been of significant

    interest because of its several advantages such as

    noninvasiveness, low cost, ease of application and capability

    for online monitoring [2], [3] which measures the conductivity

    and permittivity of bio-logical tissues changed directly or

    indirectly by the measuring variable.

    The original bio-impedance technique was involved with

    bioelectrical impedance analysis. Within a decade, this

    technique is evolved into Bioelectrical Impedance

    Spectroscopy (BIS) which is also called multiple frequencybioelectrical impedance analysis. It enables to have an overall

    figure of impedance which is of significant interest in

    biomedical sensing for example, the tissue impedance at zero

    frequency corresponding to extra-cellular resistance is useful

    for the evaluation of mammary and lung cancers and fatty

    tissues. BIS applies multiple frequency stimulation to measure

    body impedance and study shows its viability for the

    applications of body fluid measurement [4], [5] which

    estimates extracellular fluid, intracellular fluid, and total body

    water; also applicable for tissue volume change and tissue

    characterization with impedance plethysmography [6]. It is

    well known that the electrical properties of biological tissues

    differ significantly depending on their structure andcharacteristics [7]. Depending on such variation it is possible

    to detect benign tissues with Electrical Impedance

    Tomography (EIT). This has been reported by investigators

    that electrical properties of tumors get changed significantly

    and according to Fricke and Morse [8], tumor tissues show

    higher permeability at 20 kHz compared to that of normal or

    non-malignant tissues. Study shows that extracellular

    resistance and intracellular resistance of cancer tissues are

    significantly higher and plasma membrane capacitance is

    significantly lower than normal tissues [9]. Similar results also

    found by other investigations based on microwave bio-sensing.

    Again, impedance measurement of bodily fluid such as saliva

    and blood provides much fundamental information onphysiological state like glucose level and electrolyte

    concentration. Study shows significant change in blood

    conductivity and permittivity due to different level of glucose

    [10]. Besides, any significant change in tissue characteristics

    would be detectable with electrical impedance spectroscopy

    and study shows its viability for visceral fat measurement [11],

    prostate and lung cancer detection and bone fracture [12].

    Biomedical sensing which directly or indirectly related to

    change in biological tissues, diagnosis based on bioelectrical

    Non-invasive Bio-impedance Measurement

    Using Voltage-Current Pulse Technique

    Sagar K. Dhar and Quazi D. Hossain

    P

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    mailto:[email protected]:[email protected]:[email protected]:[email protected]
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    International Conference on Electrical, Electronics and Biomedical Engineering (ICEEBE'2012) Penang (Malaysia) May 19-20, 2012

    impedance spectroscopy is emerging with greater prospects for

    noninvasive bio-sensing than any other noninvasive

    techniques. This paper presents bioelectrical impedance

    measurement by means of voltage current pulse technique.

    Bio-impedance parameters Re, Ri and Cm of electrical

    equivalent circuit shown in Fig. 1 are estimated with least

    square curve fitting method in Matlab 2008a. A current source

    is designed with the option of setting any constant current

    value as less as 100 A, mid-range bandwidth of 10 MHz andload variation up to 1 M . Voltage detection is designed with

    an instrumentation amplifier to provide good noise

    performance and necessary signal gain along with parallel port

    interfacing through Data Acquisition Toolbox of Matlab

    R2008a.

    II.METHODS

    The electrical equivalent circuit of biological cells is usually

    represented with similar circuit shown in Fig. 1 which is

    comprised of extra-cellular medium resistance, intra-cellular

    medium resistance and cell membrane capacitance [13]. In

    every case, subjected electrical current will flow through

    biological cells or extra-cellular medium. Again, the currentthrough the cells may be classified as the current across the

    trans-membrane ionic channel (shown as the path with Rm) or

    across the plasma membrane. The cell membrane shows

    dielectric property where the intra-cellular medium and

    extracellular medium shows resistive behavior represented

    with Re and Ri which consequently provides the capacitance

    effect to plasma membrane represented with Cm. Due to the

    very high trans-membrane channel resistance, it may be

    ignored and the circuit is simplified with single extra-cellular

    medium resistance Re, intra-cellular medium resistance Ri and

    cell membrane capacitance Cm.

    Fig 1. Electrical equivalent circuit of biological cells.

    Bioelectrical impedance in this paper is measured with

    electrical impedance spectroscopy by means of voltage-current

    pulse technique. Since, a discrete pulse contains all frequency

    components, injection of a short duration current pulse would

    provide complete frequency response of biological tissues. The

    frequency behavior is detected by the distortion in voltage

    pulse which is solely defined by the electrical behavior of

    biological tissues and it is important to last the current pulse

    duration until the resulting voltage is stable which practicallymeans that Cm has to be completely charged. The transfer

    function of bioelectrical equivalent circuit is provided by (1)

    and the change in pulse shape is shown in Fig. 2.

    (1)

    When a current pulse is injected, the voltage across the

    tissue would be V(t) = I(t)*h(t) where I(t)*h(t) represents the

    convolution sum of time domain current, I(t) and the impulse

    response of the bioelectrical equivalent circuit, h(t).

    Consequently, the Fourier transform of V(t) will provide the

    voltage transform V(s). So, once the time domain voltage V(t)

    and current I(t) are acquired and are transformed to V(s) and

    I(s), the impedance spectroscopy Z(s) is recovered by (2)

    which represents both magnitude and phase of impedance

    represented by (3) and (4).

    ( ) ( ) ( )Z s V s I s= (2)

    (3)

    (4)

    ( ) ( )( )0 max eZ w Z w R= = = (5)

    Once impedance data is retrieved from frequency transform of

    voltage and current pulse, it is enough either to work with

    magnitude or phase to estimate Re, Ri and Cm. In this paper,

    magnitude data of impedance is fitted with (2) by means of

    least square method with iterated value of Ri and Cm where the

    value of Re is directly calculated with (5).

    Fig 2. Pulse response of bioelectrical circuit.

    2 2 2 2 2 2( ( ) ) ( )

    ( )2 2 2

    1 ( )

    R R R R R w C w C R Re e i e i m m e iZ w

    R R w Ce i m

    + + +=

    + +

    ( )( )

    ( )

    ( )

    2 221

    2 22 2 2 2tan

    1 1

    e e i e im e

    e i m e i m

    R R R R R w CwC Rw

    R R w C R R w C

    + + = + + + +

    ( ) ( ) ( )( )R R R C 1 R R Ce e i m e i mH s jw s s= = + + +

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    International Conference on Electrical, Electronics and Biomedical Engineering (ICEEBE'2012) Penang (Malaysia) May 19-20, 2012

    III. BIOIMPEDANCE MEASUREMENT SYSTEM

    Impedance measurement is accomplished in two sections

    comprising of current injection & voltage detection and

    impedance estimation as shown in Fig. 3. The first section

    involves two major hardware parts of impedance measurement

    system: 1) current source and 2) voltage sensor. The second

    section involves the software to transform the voltage and

    current in frequency domain to estimate impedance

    spectroscopy and impedance parameters Re, Ri and Cmsubsequently.

    A. Current Pulse Generation

    Current source is the most important part of bioelectrical

    impedance measurement system and should have very good

    stability in providing current irrespective to the load variation

    and current value should be in 700 A to 1mA [2]. Moreover,

    the current source should have tuning option of both amplitude

    and pulse width and invariable operation in low and high

    frequencies simultaneously.

    The constant current pulse in this paper is developed by

    means of conversion of a voltage pulse which is generated

    with the mono-stable operation of a 555 timer. Since, thevoltage pulse width is easily tunable in such operation; it in

    other words provides the tuning of current pulse width. The

    voltage pulse is then converted to constant current pulse

    according to the circuit shown in Fig. 4. The current to load is

    solely depended on RS, I = VIN/RS, and tunable as low as 100

    A. To meet up the stability as a current source against a wide

    load variation, operational amplifier AD380JH is selected with

    very high differential and common mode input impedance of

    100 G which makes the circuit applicable for constant

    current source up to 1 M as shown in Fig. 5. The frequency

    response of the source in Fig. 6 reveals its mid-range

    bandwidth as large as 10 MHz.

    Fig 3. Block diagram of bio-impedance measurement system.

    Fig 4. Current pulse generation circuit.

    Fig 5. Variation of source current with Load.

    Fig 6. Frequency response of current source.

    B. Voltage Detection

    Pulse based impedance measurement systems generally use

    four electrodes [14]: two for current injection and two for

    voltage detection. This paper presents only two electrode

    arrangement for both current injection and voltage detection

    shown in Fig. 7 which would reduce tissue irritation due to

    polarization. Here, current is injected by the electrodes B and

    A where the voltage is detected across electrode A and ground

    which would be equivalent to voltage across A and B

    according to the virtual ground phenomenon and makes

    possible two electrode setup for voltage detection.

    Fig 7. Voltage detection with two electrodes.

    U1

    4

    3

    5

    10

    9

    82

    11

    RS

    Rlimit

    AD380JH

    AB

    Re

    RiCm

    Voltage

    Pulse1

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    International Conference on Electrical, Electronics and Biomedical Engineering (ICEEBE'2012) Penang (Malaysia) May 19-20, 2012

    Biomedical sensors usually suffer from common mode noise

    and to implement and manipulate bio-medical electrical signal

    information, it is very important to deploy the front amplifier

    with high common mode rejection ratio (CMRR) and high

    differential gain. This paper presents the instrumentation

    amplifier setup shown in Fig. 8 with the common mode

    rejection performance shown in Fig. 9 where the gain ACL is

    set at desired value according to (6). Finally, the voltage is

    acquired with an ADC and parallel port interfacing by theDAQ of Matlab R2008a for processing and estimation of

    bioelectrical impedance parameters Re, Ri and Cm.

    1 2CL GA R R= + (6)

    C. Impedance Estimation

    Once the potential across bio-logical tissues is fetched,

    voltage spectrum is found using FFT in Matlab. By the same

    procedure current spectrum is also found from known pulse

    information and together with voltage and current spectrum,

    impedance spectroscopy is found by (2). At this final point, the

    magnitude of impedance spectrum data are calculated and

    fitted to (3) to find impedance parameters Ri and Cm applying

    least square method as shown in Fig. 10 and Re is directly

    found by (5).

    Fig 8. Common mode noise suppression circuit.

    Fig 9. Noise rejection with suppression circuit.

    Fig 10. Curve fitting method.

    IV. RESULT AND DISCUSSION

    Electrical impedance is successfully estimated with around

    1.5% maximum tolerance. The program of the impedance

    parameter estimation is run in Matlab R2008a according to the

    flow chart shown in Fig. 10. To test the accuracy of the curve

    fitting algorithm, some predetermined value of Re, Ri and Cmare set to create known impedance data and the outcome of the

    program for Re, R i and Cm are checked with predefined value.

    Table I shows some instances of impedance parameter output

    by the curve fitting program with error percentage. It is found

    only 1.5% error in curve fitting method.

    TABLE IESTIMATED IMPEDANCE PARAMETERS

    Re ( ) Err.

    % Re

    Ri ( ) Err. %

    Ri

    Cm (F) Err. %

    Cm

    3.0000e+3 0 1000 0 8.005e-6 0.0625

    5.0000e+3 0 2000 0 7.005e-6 0.0714

    6.9999e+3 1.43 3000 0 5.985e-6 0.2500

    8.9999e+3 0.01 4000 0 5.005e-6 0.1000

    1.1000e+4 0 5010 0 4.005e-6 0.1250

    1.3000e+4 0 6000 0 3.005e-6 0.1667

    1.5000e+5 0.050 7000 0 2.007e-6 0.3500

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    International Conference on Electrical, Electronics and Biomedical Engineering (ICEEBE'2012) Penang (Malaysia) May 19-20, 2012

    101

    102

    103

    104

    105

    250

    300

    350

    400

    450

    500Variation of Cm

    Frequency

    (b)

    Impedance

    Fig 11. Variation of impdance (a) with Re and (b) with Cm.

    After successful estimation of impedance components Re, Riand Cm from current and voltage pulse, different impedance

    spectroscopy curves shown in Fig. 11 are plotted for the

    variation of Re and Cm. Result shows that the variation of

    electrical impedance for Re is more in lower frequencies

    (below 1 kHz) although has good variation in higher

    frequencies too. On the other hand, impedance variation for

    Cm is strictly within 10 kHz and almost no change thereafter.

    But it is also found that the bio-impedance change due to Ri(intracellular medium change) is reflected in high frequencies

    (MHz band). Research shows much more close relation of bio-

    information with Re and Cm than Ri and according to the result

    found, it is suggested to design bio-medical sensors below 100

    kHz rather than MHz band for better sensitivity.

    V.CONCLUSION

    In the present work, stable current source and voltage

    detection circuit with common mode noise suppression for

    bioelectrical impedance measurement is presented.

    Appropriate signal processing for impedance estimation from

    impedance spectroscopy is modeled based on least square

    curve fitting technique. Moreover, it is investigated that the

    variation of bioelectrical impedance is higher in frequencies

    less than 100 kHz for extra-cellular medium and plasmamembrane capacitance variation. Such findings along with

    presented impedance measurement system would be applicable

    for noninvasive bio-sensing based on bioelectrical impedance

    spectroscopy.

    ACKNOWLEDGMENT

    The authors wish to acknowledge the invaluable

    suggestions, support and resources by Dr. Sabuj Baran Dhar,

    Assistant professor, Coxs Bazar Medical College Hospital

    and Mr. Tanzilur Rahman, Research Assistant, University of

    Tokyo.

    REFERENCES

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    [3] M. E. Valentinuzzi, Bioelectrical impdeance techniques in medicine.Part I: Bioimpedance measurement. First section: General concepts,Crit. Rev. Biomed. Eng., vol. 24, no. 4-6, pp. 223-255, 1996.

    [4] S. F. Siconolfi, R. J. Gretebeck, W. W. Wong, R. A. Pietrzyk, and S. S.Suire, Assessing total body water from bioelectrical responsespectroscopy, J. Appl. Physiol., vol. 82, pp. 704-710, Feb. 1997.

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