Nonwoven Filter for Rapid Microorganism Detection

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Solution Overview

Problem

Current methods for detecting microorganisms in clinical samples are often slow, costly, and limited by sensitivity, particularly in clinical settings, and face challenges with interference from treatment chemicals and the need for large sample volumes.

Innovation Solution

A device and method utilizing a nonwoven article with a filter holder and adaptor to concentrate microorganisms from fluid samples, allowing for rapid detection using a detection reagent and luminometer, enabling the detection of microorganisms in small volumes within 15 minutes.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Speed

If ATP bioluminescence assays are used for rapid detection, then detection speed is improved, but detection sensitivity deteriorates due to requiring at least 1×10^5 cfu/ml

Engineering Contradiction:
Improvedetection speedVSAvoiddetection sensitivity
Core Design Contradiction:
SpeedVSMeasurement precision

Solution Approach 1:

The nonwoven article performs preliminary concentration of microorganisms from the fluid sample before detection. By filtering and concentrating the sample through the nonwoven matrix, the method prepares the sample in advance to achieve sufficient concentration for sensitive detection, resolving the contradiction between rapid detection and detection sensitivity

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The nonwoven article acts as an intermediary between the fluid sample and the detection reagent. It concentrates microorganisms from large volumes of fluid and presents them in a concentrated form to the detection system, enabling both rapid and sensitive detection without requiring large sample volumes

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If large sample volumes are used to increase detection sensitivity, then detection sensitivity is improved, but device complexity and ease of operation worsen

Engineering Contradiction:
Improvedetection sensitivityVSAvoiddevice complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The nonwoven article provides localized concentration capability within a compact device structure. Rather than requiring complex large-volume handling systems, the concentration function is localized to the nonwoven matrix where microorganisms are trapped and concentrated from passing fluid, maintaining simplicity while achieving high sensitivity

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The nonwoven article utilizes its porous structure to concentrate microorganisms from fluid samples. The porous matrix allows fluid to pass through while trapping and concentrating microorganisms, enabling sensitive detection in a simple, compact device without complex mechanisms

Inventive Principle:
Principle #31Porous materials

3Measurement precision

If antibody-coated particles are used for specific bacterial concentration, then detection sensitivity is improved, but cost increases

Engineering Contradiction:
Improvedetection sensitivityVSAvoidcost
Core Design Contradiction:
Measurement precisionVSQuantity of substance

Solution Approach 1:

The nonwoven article serves as a disposable, cost-effective alternative to expensive antibody-coated particles. While it may provide non-specific or less specific concentration compared to antibody-based methods, it achieves sufficient sensitivity for clinical applications at a much lower cost, making the testing process economically viable

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

Solution Approach 2:

The method changes the concentration parameter by using physical filtration through nonwoven materials rather than specific biological binding. This parameter change allows concentration of microorganisms based on physical properties (size, shape) rather than specific antigen-antibody interactions, reducing cost while maintaining adequate sensitivity for detection

Inventive Principle:
Principle #35Parameter changes

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

The solution enables rapid and sensitive detection of microorganisms in fluid samples, reducing the need for large sample volumes and minimizing interference, making it suitable for clinical applications.

Implementation Method 1

passing a fluid sample suspected of containing at least one microorganism strain or target cellular analyte from the lumened or cannulated device through the device and contacting the nonwoven article

Methodology Applied
Scientific EffectFiltration: Filter (physical)

Implementation Method 2

contacting the nonwoven article with at least one detection reagent and detecting the presence of the at least one microorganism strain or target cellular analyte concentrated by the nonwoven article

Methodology Applied
Scientific EffectAdsorption: Adsorption

Implementation Method 3

Rapid detection methods based on ATP bioluminescence assays have been used to determine microbial contamination in fluids such as water

Methodology Applied
Scientific EffectBioluminescence: Bioluminescence

Data Source

PatentUS11525154B2Devices, methods, kits, and systems for detecting microorganism strains or target cellular analytes in a fluid sample
Publication Date: 2022.12.13 3M INNOVATIVE PROPERTIES CO
  • US11525154B2 patent drawing
  • US11525154B2 patent drawing
  • US11525154B2 patent drawing

AI summary

Devices for detecting microorganism strains or target cellular analytes are provided. The device includes a filter holder, the filter holder comprising a tip portion; a nonwoven article disposed on the tip portion of the filter holder; and an adaptor attacked to the filter holder, the adaptor defining an aperture. Methods of detecting microorganisms and/or cellular analytes in a fluid sample using the devices are also provided. The method includes obtaining the device; placing a lumened or cannulated device in fluid communication with the device; and passing a fluid sample suspected of containing at least one microorganism strain or target cellular analyte from the lumened or cannulated device through the device and contacting the nonwoven article. The method further includes contacting the nonwoven article with at least one detection reagent and detecting the presence of the at least one microorganism strain or target cellular analyte concentrated by the nonwoven article. Kits and systems including the devices are also provided.