Multi-Well Legionella Tray With Breathable Lid for Faster Quantification

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Solution Overview

Problem

Existing methods for quantifying biological material in liquid samples, such as bacterial concentration in water, are inefficient and lack the ability to optimize growth conditions for accurate detection and quantification.

Innovation Solution

A multi-well sample testing apparatus with a permeable, transparent, and non-toxic tray and lid member configuration that includes breathable film layers and adhesive layers, allowing for air bubble capture and even distribution of liquid samples, along with dissolvable films or capsules to enhance bacterial growth conditions.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional membrane filtration methods are used to quantify bacterial concentration, then detection capability is achieved, but the process is time-consuming and requires complex equipment

Engineering Contradiction:
Improvebacterial concentration detectionVSAvoidtesting time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The apparatus divides the sample testing process into multiple independent wells (e.g., 20 wells in a tray), allowing parallel processing of multiple samples or dilutions simultaneously. This segmentation enables batch testing rather than sequential testing, significantly reducing total testing time while maintaining detection precision for each individual well.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent introduces an intermediary medium (nutrient broth or agar) that facilitates bacterial growth and detection. Instead of directly filtering and counting bacteria, the method uses this intermediary medium to culture bacteria, making them visible through color changes or colony formation, thereby simplifying the detection process and reducing time requirements.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If MPN method with multiple tubes is used for quantification, then bacterial concentration can be determined, but device complexity and material usage increase

Engineering Contradiction:
Improvebacterial concentration quantificationVSAvoidnumber of tubes and materials
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent merges multiple individual tube tests into a single integrated multi-well tray apparatus. Instead of using separate tubes for each sample or dilution, all samples are processed in one tray with multiple wells, reducing the number of separate components, materials, and handling steps while maintaining the statistical accuracy of MPN quantification.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The multi-well tray apparatus serves multiple functions simultaneously: it holds multiple samples, provides individual containment for each well, allows parallel incubation, and enables systematic enumeration of positive wells. This universal design replaces the need for multiple specialized tubes and accessories, simplifying the overall testing system while preserving quantification accuracy.

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

3Reliability

If sample distribution is not optimized, then testing can proceed, but bacterial growth conditions are not maximized affecting detection accuracy

Engineering Contradiction:
Improvedetection accuracyVSAvoidsample distribution process
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The apparatus design ensures that each well receives an optimized local environment for bacterial growth, including appropriate volume of sample and medium, proper aeration, and suitable nutrient conditions. The uniform well geometry and standardized dimensions guarantee consistent local quality across all wells, maximizing detection reliability without requiring complex manual adjustment for each well.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The tray and lid are pre-configured with alignment features, ventilation holes, and well positioning that facilitate automatic or semi-automatic sample distribution. The preliminary design of the apparatus structure enables efficient and accurate sample allocation to each well, reducing the operational complexity while ensuring optimal growth conditions are established before incubation begins.

Inventive Principle:
Principle #10Preliminary action

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 apparatus optimizes bacterial growth conditions, enabling accurate detection and quantification of biological materials by maximizing permeability and maintaining sample integrity during incubation, thereby improving detection accuracy and efficiency.

Implementation Method 1

a breathable film layer disposed about the adhesive layer

Methodology Applied
Scientific EffectPermeation: Permeation

Implementation Method 2

The lid member includes an adhesive layer configured to be sealed to the planar surface of the sample tray

Methodology Applied
Scientific EffectAdhesion: Adhesive

Data Source

PatentUS20260043062A1Multi-well sample testing apparatus and methods of sample testing using the same
Publication Date: 2026.02.12 IDEXX LABORATORIES INC
  • US20260043062A1 patent drawing
  • US20260043062A1 patent drawing
  • US20260043062A1 patent drawing

AI summary

A testing apparatus for the detection of Legionella bacteria in a liquid sample includes a sample tray and a lid member. The sample tray defines a planar surface and a plurality of wells recessed relative to the planar surface and is formed from a permeable, transparent material that is non-toxic to Legionella bacteria. The lid member includes an adhesive layer configured to be sealed to the planar surface of the sample tray and formed from a first permeable material, a breathable film layer disposed directly about the adhesive layer and formed from a second, different permeable material, and a backing layer disposed directly about the breathable film layer.