We have developed a precise off-diagonal magnetoimpedance (MI) gradiometer that can operate in an unshielded environment and at room temperature with 200 pT root-mean-square noise in a 100 Hz bandwidth. The MI sensor probe is compact and easy to handle. The achieved noise level corresponds approximately to the maximum magnetocardiography (MCG) signal reported so far. We have performed MCG measurements using the developed gradiometer system in an unshielded environment, and a real-time signal like MCG can be identified by the MI gradiometer when the distance between the sensor head and chest surface is less than 3 mm. However, the signal seems to be affected by the movement of the chest surface caused by the heartbeat. A peak magnetic signal of 100 pT (corresponding to conventional MCG) was observed when the sensor head was set 10 mm apart from the chest surface to avoid the influence of the chest movement. Under such conditions, the signal needed to be averaged over more than 50 cycles to identify the peak magnetic signal.

Magnetocardiography (MCG) is a noninvasive, noncontact tool for the diagnosis of heart diseases. MCG measurements do not affect the electrophysiological properties of the heart. However, existing experimental and clinical data show that MCG is more sensitive (in comparison with methods based on the measurement of electric potentials) to local currents that are generated at the interfaces of myocardium fragments with different electrophysiological properties.1 

Superconducting interferential devices (SQUIDs) have previously been used to measure biomagnetic signals from humans. Recently, atomic vapor laser magnetometers, which have the ability to measure very clear MCG signals, have started to be used for mapping the MCG signal above the chest. The possibility of MCG measurement using a room-temperature flux gate sensor has also been reported.2 A flux gate sensor with a probe a few centimeters in length can achieve a picotesla per square-root hertz noise level.

Other developments include a linear magnetic sensor based on the off-diagonal giant magnetoimpedance GMI effect.3,4 Furthermore, arrays of flexible GMI sensors have been developed to measure magnetic brain signals.5 Compared with other sensors used for MCG measurements, the MI sensor has the advantage of being compact and easy to handle. Using a highly sensitive off-diagonal MI sensor, we have successfully measured biomagnetic fields in living cell-tissue preparations as small 5 mm2 in size.6 In this study, we developed a precise first-order off-diagonal MI gradiometer for the purpose of future medical use as an MCG device.

The noise level of the MI gradiometer, which can operate in an unshielded environment and at room temperature, is 200 pT root-mean-square (rms) in a 100 Hz bandwidth. The achieved noise value corresponds approximately with the peak value of the MCG signal in the literature. Each sensor probe in the head pair of the gradiometer was 10 mm in length. The peak magnetic signal intensity of 100 pT (a value which corresponds to a conventional MCG) was observed when the front edge of the sensor head was set 10 mm apart from the chest surface. Under these conditions, the signal needed to be averaged over more than 50 cycles to identify the peak magnetic signal.

Figure 1 shows the MI characteristics of the amorphous wire element of length 1 cm and diameter 30 μm used in this study. When the high-frequency ac current passes through the amorphous wire MI sensor element, the skin effect is induced, and the impedance of the amorphous wire depends on the skin depth. In general, the skin depth is related to the circumferential permeability of the soft magnetic material, and therefore, the impedance depends on the magnetic field through the change in permeability.7 The change in impedance with applied magnetic field Z(Hex)/Z(Hex = 0) is more than 100% when the ac current is higher than 40 MHz. In this study, we used the MI element in combination with a pick-up coil for the magnetic-field detector, which utilizes the off-diagonal MI effect. The sensitivity of the off-diagonal MI effect, which can achieve a linear response for an external magnetic-field intensity that is less than the anisotropy field of the element, is higher than that of the original GMI effect under the condition of no magnetic-field bias.

FIG. 1.

MI characteristics of the CoFeSiB amorphous wire, 10 mm in length and 30 μm in diameter, used for the sensing element.

FIG. 1.

MI characteristics of the CoFeSiB amorphous wire, 10 mm in length and 30 μm in diameter, used for the sensing element.

Close modal

It is necessary to develop a precise gradiometer to detect very weak magnetic fields such as biomagnetic fields in an unshielded environment. The basic circuit of the pulse-excitation-type complementary metal–oxide–semiconductor (CMOS) MI gradiometer is shown in Figure 2. The sharp pulse current having a short rising time tr (10 ns or less) is supplied by the CMOS inverter to the amorphous wire of the MI element. The equivalent ac frequency for the skin effect is roughly estimated by feq = 1/2tr = 50 MHz. The pick-up coil is used in combination with the amorphous wire 30 μm in diameter). The signal detection circuit consists of an analog switch, hold condenser, and timing circuit to control the analog switch. The output voltage of the MI sensor (Eout) is therefore proportional to the applied external magnetic field (Hex). The linearity and hysteresis of the sensor is less than 2% over a ±10 μT full-scale range. To cancel out the effect of uniform magnetic-field noise, the amorphous wire has two coils: a sensing coil and a reference coil. The distance between the two pick-up coils is set to 3 cm. The difference in the sensitivities of the sensing and reference elements can be adjusted to within 1.5% by the use of a variable resistance.

FIG. 2.

Circuit diagram of the first-order gradiometer.

FIG. 2.

Circuit diagram of the first-order gradiometer.

Close modal

Figure 3 shows the magnetic-field noise spectral density of the gradiometer in an unshielded environment compared with the environmental magnetic-field spectral density measured by commercial flux gate sensor. The environmental magnetic noise is 1 nT/Hz1/2 at 1 Hz, while the gradiometer noise is 20 pT/Hz1/2 at 1 Hz. The cancelling ratio of the environmental magnetic field is calculated to be 34 dB. The rms noise of 200 pT in a 100 Hz bandwidth (1–100 Hz) can be estimated by operating the gradiometer in an unshielded environment.

FIG. 3.

Magnetic-field spectral density of the environmental magnetic field Bn and equivalent magnetic noise of the MI gradiometer output ΔB.

FIG. 3.

Magnetic-field spectral density of the environmental magnetic field Bn and equivalent magnetic noise of the MI gradiometer output ΔB.

Close modal

MCG measurements using the MI gradiometer were carried out on a male subject (aged 54) in the sitting position. We measured the MCG at a point on the chest surface 25 mm to the left of the pit of the stomach. Figure 4(a) illustrates the experimental setup. The MI gradiometer was placed on a wooden table, and we measured the magnetic-field component (Bz) perpendicular to the chest surface. The distance D is that from the chest surface to the front edge of the MI gradiometer. Figure 4(b) and (c) represent the simultaneous measurement of the electrocardiography (ECG) and MCG signals when D is less than 3 mm. In spite of superposing noise with an amplitude 300 pT, we can identify a sharp magnetic peak that corresponds to the R wave of the ECG. However, a negative magnetic peak is observed following the T wave of the ECG. The magnetic signal averaged over ten cycles is shown in Figure 5(b). The peak magnetic field is about 400 pT, which is much higher than the maximum MCG value (100 pT) reported so far. The signal seems to be affected by the movement of the chest surface caused by the heartbeat. To avoid this effect, the sensor head was placed 10 mm apart from the chest surface. The peak magnetic signal following the ECG T wave is not observed, but in this case, we were able to identify a peak magnetic signal intensity of 100 pT after averaging over 50 cycles as shown in Figure 5(c).

FIG. 4.

(a) Setup for the MCG measurement. Simultaneous measurement of the (b) ECG and (c) MCG at a point on the chest surface 25 mm to the left of the pit of the subject’s stomach. The distance D between the sensing element and the chest surface is less than 3 mm.

FIG. 4.

(a) Setup for the MCG measurement. Simultaneous measurement of the (b) ECG and (c) MCG at a point on the chest surface 25 mm to the left of the pit of the subject’s stomach. The distance D between the sensing element and the chest surface is less than 3 mm.

Close modal
FIG. 5.

(a) ECG wave form, (b) MCG wave averaged over ten cycles for D < 3 mm, and (c) MCG wave averaged over 50 cycles for D = 10 mm, where D is the distance from the chest surface to the sensing element.

FIG. 5.

(a) ECG wave form, (b) MCG wave averaged over ten cycles for D < 3 mm, and (c) MCG wave averaged over 50 cycles for D = 10 mm, where D is the distance from the chest surface to the sensing element.

Close modal

We have developed a precise first-order off-diagonal MI gradiometer for MCG measurements in an unshielded environment and at room temperature. We achieved an rms noise level of 200 pT in a 100 Hz bandwidth in an unshielded environment. We successfully measured the MCG signal perpendicular to the chest surface at a point 25 mm to the left of the pit of the subject’s stomach. The peak magnetic signal of 100 pT (a value which corresponds to a conventional MCG) was observed when the front edge of the sensor head was set 10 mm apart from the chest surface to eliminate the effect of the chest surface movement. Under these conditions, the signal needed to be averaged over more than 50 cycles to identify the peak magnetic signal.

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