Piezoelectric Sensor Antimicrobial Susceptibility Testing

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Solution Overview

Problem

Current antimicrobial susceptibility testing methods require incubation and are time-consuming, lacking flexibility and accuracy, especially for rapidly growing bacteria and fungal organisms, and do not allow for rapid detection of microbial presence without growth.

Innovation Solution

A method using piezoelectric sensors to detect resonance peaks from live microbes, determining the width or standard deviation of these peaks to assess antimicrobial susceptibility and minimal inhibitory concentration (MIC) without the need for incubation, employing software for interpretive categories and database access.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Loss of time

If conventional antimicrobial susceptibility testing methods (broth dilution, disk diffusion, gradient diffusion) are used, then the testing can be performed with simple equipment and materials, but the testing time is long (overnight incubation required) and accuracy is insufficient for rapidly growing bacteria

Engineering Contradiction:
Improvetesting timeVSAvoidaccuracy
Core Design Contradiction:
Loss of timeVSReliability

Solution Approach 1:

The patent replaces the mechanical/biological incubation system with a piezoelectric sensor-based detection system. Instead of relying on microbial growth over time, the system uses piezoelectric sensors to directly detect microbial presence and stress responses, eliminating the need for incubation and enabling rapid testing within minutes while maintaining high accuracy.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent utilizes the piezoelectric effect, where mechanical stress from microbial cells on the sensor surface generates electrical signals. This phase transition from mechanical stress to electrical detection allows real-time monitoring of microbial presence and antimicrobial susceptibility without requiring temporal evolution through incubation.

Inventive Principle:
Principle #36Phase transitions

2Adaptability or versatility

If conventional AST methods are used, then the test can be performed with pre-prepared panels and standardized procedures, but the method lacks flexibility for custom drug selections and cannot detect microbial presence without growth

Engineering Contradiction:
Improveflexibility in drug selectionVSAvoidtesting time
Core Design Contradiction:
Adaptability or versatilityVSLoss of time

Solution Approach 1:

The patent employs an array of multiple piezoelectric sensors, with each sensor capable of detecting different antimicrobial agents. This segmentation allows simultaneous testing of multiple drugs and concentrations across different sensors, providing flexibility in drug selection while maintaining rapid testing capability through parallel processing.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The piezoelectric sensors directly detect microbial presence and stress responses without requiring microbial growth or external reagents. The sensors themselves generate the detection signals through piezoelectric stress generation, eliminating the need for incubation and enabling immediate testing with flexible drug selection.

Inventive Principle:
Principle #25Self-service

3Productivity

If piezoelectric sensors are used to detect resonance peaks from live microbes, then testing time is reduced significantly, but the device complexity increases

Engineering Contradiction:
Improvetesting speedVSAvoidsensor system complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The piezoelectric sensor array serves multiple functions: detecting microbial presence, measuring microbial stress responses, determining antimicrobial susceptibility, and identifying minimum inhibitory concentrations. This multi-functionality consolidates what would otherwise require multiple separate testing systems into a single integrated platform, managing complexity through functional consolidation.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The patent uses an array of identical piezoelectric sensor units, each capable of performing the same detection function. This replication allows parallel testing of multiple samples and drugs while maintaining simplicity in each individual sensor unit, managing overall system complexity through modular duplication rather than complex integration.

Inventive Principle:
Principle #26Copying

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables rapid, reliable detection of antimicrobial susceptibility and MIC determination, reducing testing time and improving accuracy by measuring minute stresses from live microbes, suitable for various microorganisms including bacteria and fungi.

Implementation Method 1

Rapid antimicrobial susceptibility testing using piezoelectric sensor

Methodology Applied
Scientific EffectPiezoelectric effect: Piezoelectric Effect

Implementation Method 2

detecting a resonance peak of a sensor with live microbes on a surface portion of the sensor

Methodology Applied
Scientific EffectResonance: Resonance

Data Source

PatentUS10670566B2Rapid antimicrobial susceptibility testing using piezoelectric sensor
Publication Date: 2020.06.02 DREXEL UNIV
  • US10670566B2 patent drawing
  • US10670566B2 patent drawing
  • US10670566B2 patent drawing

AI summary

A system for and method of antimicrobial susceptibility testing includes detecting a resonance peak of a sensor provided with live microbes on a surface thereof; applying a substance to the live microbes; detecting a resonance peak of said sensor after application of said substance; determining a width of a top of each of said resonance peaks before and after application of the substance from one of: (1) a phase angle versus frequency plot where the phase angle is the phase angle of the electrical impedance of said sensor. (2) a real part of a plot of an electrical impedance versus frequency of said sensor. (3) a plot of a magnitude of electrical impedance versus frequency of said sensor, and (4) a phase angle versus frequency plot where the phase angle is the phase angle between an output voltage and an input voltage of said sensor, and comparing the determined widths of tops of said resonance peaks or standard deviations of the frequency of said resonance peaks to determine antimicrobial susceptibility including the minimum inhibitory concentration (MIC).