Biomedical Instruments Design Biopotential Amplifiers

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Presentation transcript:

Biomedical Instruments Design Biopotential Amplifiers

Amplifier • To increase the amplitude of a weak electric signal Biopotential Amplifiers Basic function • To increase the amplitude of a weak electric signal of biological origin Amplifier Amplified Biopotential Biopotential

• the measured signal should not be distorted Biopotential Amplifiers The basic requirements that a biopotential amplifier has to satisfy are: • the physiological process to be monitored should not be influenced in any way by the amplifier • the measured signal should not be distorted • the amplifier should provide the best possible separation of signal and interferences • the amplifier has to offer protection of the patient from any hazard of electrical shock • the amplifier itself has to be protected against damages that might result from high input voltages as they occur during the application of defibrillators or electrosurgical instrumentation

Biopotential Amplifiers Typical bio-amp requirements • high input impedance - greater than 10 Mohms • safety: protect the organism being studied • careful design to prevent electrical shocks • isolation and protection circuitry to limit the current through the electrode to safe level • output impedance of the amplifier • should be low to drive any external load with minimal distortion • gain greater than 1000 • biopotentials are typically less than a millivolt (1 mV) • most biopotential amplifiers are differential • signals are recorded using a bipolar electrodes • high common mode rejection ratio • biopotentials ride on a large offset signals • rapid calibration of the amplifier in laboratory conditions • adjustable gains

Voltage and Frequency Range for Biopotentials EOG = Electrooculogram ECG = ElectroCardiogram EEG = ElectroEncephalogram ECG = ElectroMyogram

Electrocardiograph (ECG) amplifiers • Beating heart generates electric signal • monitored to understand heart functions • Measurements are functions of • location at which the signal is detected • time-dependence of the signal amplitude • Different pairs of electrodes at different locations yield different measurements • hence placement is standardized • Electrical model of heart • electric dipole located in a partially conducting medium (thorax) • dipole represented as a cardiac vector M • during the cardiac cycle • magnitude and direction of the dipole vector will vary • electric potentials appears throughout the body and on its surface

Electrocardiograph Leads • In clinical electrocardiography • more than one lead must be recorded to describe the heart's electric activity fully • several leads are taken in the frontal plane and the transverse plane • frontal plane: parallel to the back when lying • transverse plane: parallel to the ground when standing • Frontal plane lead placement • called Eindhoven’s triangle • Additional leads • unipolar leads • potential measured at electrodes with a reference: average of 2 or 3 electrodes • Wilson central terminal • three limb electrodes connected through equal-valued resistors to a common node • augmented leads • some nodes disconnected • increase the amplitude of measurement

Functional blocks of electrocardiograph

Problems in ECG Measurement • Frequency distortion • if filter specification does not match the frequency content of biopotential • then the result is high and low frequency distortion • Saturation or cutoff distortion • high electrode offset voltage or improperly calibrated amplifiers can drive the amplifier into saturation • then the peaks of QRS waveforms are cut off • Electric/magnetic field coupling • open lead wires (floating connections) pick up EMI (ElectroMagneticInterference) • long leads produce loop that picks up EMI (induces loop current) • Interference from power lines (common mode interference) • can couple onto ECG signal 60Hz supply noise Coupled to ECG

Interference Reduction Techniques Common-mode voltages can be responsible for much of the interference in biopotential amplifiers. • Solution 1: • amplifier with a very high common-mode rejection • Solution 2: • eliminate the source of interference Ways to eliminate interference • Use shielding techniques • electrostatic shielding: Place a grounded conducting plane between the source of the electric field and the measurement system • very important for EEG measurement • Use twisted cables to reduce magnetic flux, reduce lead loop area

Differential Amplifier • One-amp differential amplifier • gain determination - Vin + • Rule 1: virtual short at op-amp inputs • Rule 2: no current into op-amp gain of differential amplifier • characteristics • no common mode gain, Gc = 1 • input resistance of the diff. amp is lower than ideal op-amp • OK for low resistance sources (like Wheatstone bridge), but not good for many biomedical applications

Differential Amplifier • How do we fix low input resistance of 1-op-amp diff amp? • Option 1: Add voltage follower to each input • Option 2: Add non inverting amp at each input • Provides additional gain

Instrumentation Amplifier • Better option: • connect Ri’s of input amps together • eliminate ground connection • This 3-op-amp circuit is called an instrumentation amplifier • Input stage characteristics • low common-mode gain - rejects common mode voltages (noise) • high input impedance • input stage gain adjusted by R1

Instrumentation Amplifier • Input stage • high input impedance • buffers gain stage • no common mode gaing • can have differential gain • Gain stage • differential gain, low input impedance • Overall amplifier • amplifies only the differential component • high common mode rejection ratio • high input impedance suitable for biopotential electrodes with high output impedance

ECG Amplifier instrumentation amplifier HPF non-inverting amp This ECG amplifier has a gain of 25 in the dc-coupled stages. The high-pass filter feeds a noninverting-amplifier stage that has a gain of 32. The total gain is 25 32 ¼ 800. When mA 776 op amps were used, the circuit was found to have a CMRR of 86 dB at 100 Hz and a noise level of 40 mV peak to peak at the output. The frequency response was 0.05 to 106 Hz for 3 dB and was flat over 4 to 40 Hz. A single op-amp chip, the LM 324, that contains four individual op amps could also be used in this circuit reducing the total parts count.

Driven Right Leg System • Motivation • reduce interference in amplifier • Approach • patient right leg tied to output of an auxiliary amp • common mode voltage on body sensed by averaging resistors, Ra’s & fed back to right leg • provides negative feedback to reduce common mode voltage • if high voltage appears between patient and ground, auxiliary amplifier effectively un-grounds the patient to stop current flow