Electrode Insert for Rapid Microorganism Detection in Standard Bottles

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Solution Overview

Problem

Existing blood culture methods for diagnosing bloodstream infections are time-consuming, often requiring transport to automated systems that can lead to false negatives and delay the initiation of appropriate antibiotic therapy, especially due to the need for specific and costly non-standard containers.

Innovation Solution

An instrumented device adaptable to standard containers, equipped with measuring and reference electrodes, allowing for rapid on-site detection of microorganisms in liquid samples using electrochemical methods, compatible with existing collection bottles and minimizing time from sample collection to analysis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If automated blood culture systems are used, then detection accuracy is improved, but analysis time and device complexity increase

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

Solution Approach 1:

The invention separates the detection function from the incubation function. The portable device performs rapid electrochemical detection of bacterial metabolites (acid production) directly from the blood culture bottle, while the incubation continues in standard conditions. This segmentation allows independent optimization of each function and eliminates the need for complex automated systems.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention uses an intermediary measurement approach by detecting bacterial metabolites (carbonic acid) rather than the bacteria themselves. The pH-sensitive chromophore or fluorophore acts as an intermediary that converts bacterial metabolic activity into a measurable electrochemical signal, enabling rapid detection without direct bacterial observation.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If automated blood culture systems are used, then detection accuracy is improved, but device complexity and cost increase

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

Solution Approach 1:

The portable device can be adapted to work with standard blood culture bottles from different manufacturers, making the system universally compatible. The device performs multiple functions: it measures pH changes, detects bacterial growth, and provides rapid results without requiring specialized incubation equipment, thereby reducing overall system complexity.

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

Solution Approach 2:

The invention replaces complex mechanical automated systems with a simpler electrochemical sensing approach. Instead of using large automated incubators with multiple sensors and moving parts, the portable device uses electrochemical detection of pH changes, significantly reducing mechanical complexity while maintaining detection accuracy.

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

3Loss of time

If rapid on-site detection is implemented, then analysis time is reduced, but electrode degradation occurs

Engineering Contradiction:
Improveanalysis timeVSAvoidelectrode durability
Core Design Contradiction:
Loss of timeVSReliability

Solution Approach 1:

The invention extracts the detection function from the incubation process. The portable device is inserted into the blood culture bottle only for brief measurement periods (a few seconds to minutes) to capture pH changes, then removed. This allows rapid detection without prolonged exposure of electrodes to the harsh biological environment, preserving electrode durability.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The blood sample is pre-incubated in the culture bottle under optimal conditions before measurement. When the portable device is inserted, the bacterial metabolism has already produced measurable pH changes, allowing rapid detection without prolonged electrode exposure. The preliminary incubation prepares the sample for quick measurement.

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

Enables rapid and accurate detection of microorganisms in liquid samples, reducing the time to initiate appropriate antibiotic therapy by integrating with standard containers, avoiding electrode degradation, and ensuring compatibility with existing systems.

Implementation Method 1

The detection of microorganisms is achieved, in particular, by electrochemistry

Methodology Applied
Scientific EffectElectrochemical detection:

Data Source

PatentEP4332572B1Instrumented device used for detecting the presence of microorganisms in a liquid sample
Publication Date: 2026.01.14 COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES
  • EP4332572B1 patent drawingFigure 1A~1C
  • EP4332572B1 patent drawingFigure 2A~2B
  • EP4332572B1 patent drawingFigure 3A~3B

AI summary

The invention relates to an instrumented device adaptable to a container (1) comprising a casing for receiving a liquid sample (LSE), the device comprising at least two electrodes, referred to as a measuring electrode (E1) and a reference electrode (E2). The instrumented device includes at least one measuring element (2) made of an electrically insulating material. This measuring element (2) has means for removably cooperating with the casing of the container. The measuring element (2) has a first surface intended to come into contact with an internal volume of the container when the measuring element (2) is adapted to the container (1), and a second, opposing surface accessible from the outside, the first surface of the measuring element (2) carrying the measuring electrode (E1) and the reference electrode (E2).