Microfluidic Infrared Spectroscopy for Rapid Microbial Detection

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Solution Overview

Problem

Current methods for detecting microorganisms, such as bacteria, are slow, often requiring over a day to produce results, which delays treatment decisions and is costly, especially in regions lacking well-equipped laboratories, and existing rapid methods are either expensive or not accurate enough for broad pathogen identification.

Innovation Solution

A rapid and integrated detection system using microfluidic separation and infrared spectrometry that identifies microorganisms without culturing, providing results in under an hour, and is portable for use at the point of need, capable of processing small sample volumes from various matrices without the need for nucleotides or antibodies.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional culture-based methods are used to detect microorganisms, then sensitivity and low cost are achieved, but detection time is extended to 1-7 days

Engineering Contradiction:
Improvedetection sensitivityVSAvoiddetection time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent extracts the detection function from the time-consuming culturing process by using direct spectroscopic analysis of intact microorganisms. The system takes out only the essential detection capability while eliminating the 1-7 day culturing wait time, achieving rapid identification within minutes to hours.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent replaces the mechanical/biological culturing system with a spectroscopic measurement system. Instead of allowing microorganisms to grow physically over days, the system uses infrared spectroscopy to directly measure and identify microbial species, substituting a fast physical measurement for a slow biological process.

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

2Loss of time

If rapid detection methods using antibodies or nucleic acid sequences are used, then detection speed is improved, but cost increases and accuracy for broad pathogen identification decreases

Engineering Contradiction:
Improvedetection timeVSAvoidpathogen identification accuracy
Core Design Contradiction:
Loss of timeVSMeasurement precision

Solution Approach 1:

The patent creates a universal detection system that can identify any microorganism based on its spectral fingerprint, rather than requiring specific antibodies or nucleic acid probes for each pathogen. This single system handles diverse pathogens accurately without the cost and complexity of multiple specialized reagents.

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

Solution Approach 2:

The patent changes the detection parameter from specific molecular binding (antibodies/nucleic acids) to global spectral characteristics. By measuring the overall infrared spectrum of intact microorganisms, the system captures unique identifiers for each species, achieving broad and accurate pathogen identification without specialized reagents.

Inventive Principle:
Principle #35Parameter changes

3Quantity of substance

If mass spectrometry based identification is used, then cost per test is reduced, but equipment complexity and operator skill requirements increase significantly

Engineering Contradiction:
Improvecost per testVSAvoidequipment complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The patent employs disposable microfluidic cartridges that contain the complex sample preparation and concentration functions. This allows the main instrument to remain simple and affordable while the disposable cartridges handle the sophisticated tasks, making the system accessible to small and mid-sized organizations without requiring expensive permanent infrastructure.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Solution Approach 2:

The patent introduces microfluidic cartridges as an intermediary between the sample and the spectrometer. These cartridges perform automated sample processing, concentration, and presentation, acting as a mediator that simplifies the main instrument design while maintaining high detection accuracy and reducing operational complexity.

Inventive Principle:
Principle #24Intermediary (Mediator)

4Measurement precision

If samples are shipped to well-equipped laboratories for analysis, then accurate results can be obtained, but logistics costs and time delays increase

Engineering Contradiction:
Improvedetection accuracyVSAvoidsample shipping time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent enables self-service detection by bringing the laboratory capability to the point of need. The portable system allows samples to be analyzed where they are collected, eliminating the need to ship samples to centralized laboratories. This self-contained approach maintains accuracy while removing logistics bottlenecks and time delays.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent segments the centralized laboratory function into a portable, self-contained system that can operate independently at the point of care. By dividing the detection capability from the infrastructure requirements, the system brings accurate analysis to remote locations without requiring sample transport or access to well-equipped central laboratories.

Inventive Principle:
Principle #1Segmentation

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, accurate, and cost-effective identification of microorganisms, reducing morbidity and mortality by allowing timely treatment decisions and minimizing economic losses due to food contamination, while being accessible in diverse environments without the need for specialized equipment or skilled operators.

Implementation Method 1

The sample is processed by a microfluidic separation stage to separate intact microorganisms from the rest of the sample matrix

Methodology Applied
Scientific EffectMicrofluidic separation:

Implementation Method 2

The separated intact microorganisms are then measured using an infrared spectrometer

Methodology Applied
Scientific EffectInfrared spectroscopy: Absorption Spectroscopy

Data Source

PatentUS11859233B2Rapid microbial detection
Publication Date: 2024.01.02 3I DIAGNOSTICS INC
  • US11859233B2 patent drawing
  • US11859233B2 patent drawing

AI summary

Devices and methods are provided to detect the presence of bacteria and small microorganisms, and to identify various microbial attributes rapidly.