First class
First class
of Biosignals
MEBiom, 1st year, 3rd Period (P3)
(ECTS: 6.0), 2024/2025
Department of Bioengineering
Instituto Superior Técnico / University of Lisbon
perceivable, the previous scheme was added for a better understanding.
Summary
Instrumentation and Acquisition of Biosignals, DBE/Técnico, 2024/2025 Figure 11 - Actual prototype aspect
Presentation
Main Objectives
• Principles of sensors and transducers and of acquisition and processing of biomedical signals
• Design and implementation of (biomedical) signal acquisition systems with embedded systems
• Understand simple electronic circuits involving linear passive (RLC) and active (OpAmp) components for signal
amplification, conditioning and filtering (Chapter 2).
• Understand the basic blocks and tools for acquisition and digital conversation of analog signals (using the
Arduino embedded system) (Chapter 3).
• Design, implement and test simple circuits to measure and control directly or indirectly physical or biological
variables.
Teaching Assistants
• BSc Mariana Nunes (IST)
2. Four (4) laboratory sessions are guided works exploring basic circuits of signal acquisition, amplification, and conditioning .
These sessions are important for the project.
3. The grade for each lab is Pass/Fail. Each attendance and participation in session activities is worth 5% (1 point) of the final
grade.
4. Two (2) laboratory sessions are dedicated to support the implementation of a project of signal acquisition and processing, ba sed
on the circuits tested in the first sessions. The project (50%) will be delivered in the beginning of the last week.
5. The grading of the Project will be obtained based on the evaluation of a report (max. 10 pages in IEEE Transactions format), an
oral presentation, and a functional prototype.
• Prototype System
• Video Demonstration
• Presentation
Report 8 pp max
Format/Graphical issues Quality of the format, of the figures and tables of the document 5%
Title, authors and Abstract Title, authors and short abstract 5% 0.5
Introduction and problem statement Motivation and relevance of the problem 5% 1.0
Background Summary of the problem fundamentals and context 10% 1.0
Implementation details Technical description of the proposed system 20% 2.0
Experimental results Description of the validation and testing procedures used in the work 15% 2.0
Discussion and Conclusions Summary description and discussion of the main findings 5% 1.0
References List of the state-of-the-art references 5% 0.5
Presentation 5 minutes presentation and questions in a total of 15 minutes 30%
Metrology Principles
• Quantity (or Measurand): “Property of a phenomenon, body, or substance, where the property
has a magnitude that can be expressed as a number and a reference”
• Measurement: “Process of experimentally obtaining one or more quantity values that can
reasonably be attributed to a quantity”
• Measuring Instrument: “Device used for making measurements, alone or in conjunction with
one or more supplementary devices”
• Measuring System: “Set of one or more measuring instruments and often other devices,
including any reagent and supply, assembled and adapted to give information used to generate
measured quantity values within specified intervals for quantities of specified kinds”
(*)
Bio-chemical and
electrical signaling
• Piezoelectric (force)
Peltier
• Photovoltaic (light)
• Thermoelectric (temperature)
Instrumentation and Acquisition of Biosignals, DBE/Técnico, 2024/2025
Transducers
Capacitive
• Property conversion
(aka non generating – require external energy)
• Capacitive
• Inductive
• Resistive
• Photoconductive
• Deformation
– X-ray
– Radioactivity
https://www.physoc.org/explore-physiology/what-is-physiology/
• PNS
• Electromyograph y (EMG)
• Electrooculogr aphy ( EOG)
• ANS
• Electrocardiog raphy (ECG)
• Electroder ma l Activity (E DA)
Indirect
Instrumentation and Acquisition of Biosignals, DBE/Técnico, 2024/2025
Physiological Phenomena
• Bioelectrical: Because living cells, tissues and organs produce electrical or
electromagnetic fields (e.g. cellular action potentials)
• Biomechanical: Because living cells, tissues and organs produce and are
subjected to forces or displacement (e.g. respiratory cycles)
• Biochemical: Because living cells, tissues and organs produce, react and
abundantly use chemical compounds (e.g. neurotransmitters)
• Biophysical: Because living cells, tissues and organs are composed by organised
arrangements of molecules (e.g. DNA)
PHOTOPLETHYSMOGRAPHY (PPG)
This sensor presented several limitations that led to its substitution. Firstly, it
ked mechanical stability, since the position of the LEDs was changed when the
gertip was placed between them, compromising their alignment and, therefore, the
signal acquisition. The analog signal had a greater amplitude and a more defined PHOTOPLETHYSMOGRAPHY (PPG)
veform if the two LEDs were compressed against the fingertipPHOTOPLETHYSMOGRAPHY
during the acquisition. (PPG)
wever, this compression induced other problems, not only because it affected the
gnment of the LEDs, but also because the contact with the LEDs Figure 21. Themotion
induced montageandof the circuit on the bread board and the output connection to Arduino board. Afterwards, a
green led was placed in order to blink everything the heart rate was between a favorable range of values (60-100 Hz).
ysiological artifacts (namely due to the presence of another biosignal when the LEDs
re compressed using the fingertips of the other hand). In addition, the need to compress
LEDs would make the sensor user-dependent and unable accurate comparisons of the
ults obtained for different individuals. Finally, our group verified that theThe datasignal
analog from the analog input was sent serially to the PC and was plotted using
the Arduino tool
ained with this sensor was significantly affected by the interference of the 50Hz power Serial Plotter. To guarantee that the same analog signal was correctly
visualized in Arduino,
e. This artifact was intensified by the illumination of the laboratory, whose light was the oscilloscope was used as a control (Fig.12).
o received by the LED.
8
Figure 13 shows the signal from the analog circuit, represented in blue, and the Lisbon, June 2017
output of the Lisbon,
filteringJune
step2017
with a fourth order Butterworth low-pass filter with a cut-off
Instrumentation and Acquisition of Biosignals, DBE/Técnico,
frequency2024/2025
of 25Hz, represented in red. Even though the filtered signal had a lower
amplitude, almost all the noise associated with the power line (f=50 Hz) was successful
Signal Acquisition Instrumentation in
Bioengineering
hes – IST
io – FMUL INSTRUMENTATION AND SIGNAL ACQUISITION IN BIOENGINEERING
FINAL PROJECT
Fig. 1 – Heart chambers and tissues associated to electrical heart LISBON, PORTUGAL, JUNE 17, 2017
activity. [2]
The aim of this project was to build a simple analog circuit capableof non-invasively
recording the ECG of healthy subjects and analyze its output with a micro-processor.
1
For that, an experimental protocol was designed to illustrate the system working and GONÇALO FRAZÃO
Figure 11 & LUÍS
- Actual prototype RITA2
aspect
9
some tests were performed in order to validate it.
1
78136, [email protected]
Fig. 16 and
Instrumentation – Oscilloscope
Acquisitionscreenofdisplaying the measured
Biosignals, signal. 2024/2025
DBE/Técnico,
2
78680, [email protected]
Characterization of Gait Analysis
Figure 7: Sensor mount ed on t he body during t he gait analysis and t he reference axis considered.