Aptamer-Graphene Oxide Spore Detection System

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for detecting Clostridium difficile spores are inadequate, leading to challenges in rapid identification and control of infections, particularly in healthcare settings where antibiotic resistance and mortality rates are high.

Innovation Solution

Development of aptamers with specific nucleic acid sequences that selectively bind to surface proteins of Clostridium difficile spores, combined with graphene oxide nanoparticles, for enhanced detection and visualization of spores.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional detection methods are used for Clostridium difficile spores, then the detection process is simple, but the detection sensitivity and specificity are insufficient

Engineering Contradiction:
Improvedetection sensitivity and specificityVSAvoiddetection system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent uses a composite detection system combining aptamers (nucleic acid molecules) with fluorescent labels and graphene oxide nanoparticles. This composite structure enhances detection sensitivity and specificity through the synergistic effects of high-affinity aptamer binding, fluorescent signal amplification, and graphene oxide's electron transfer properties, while maintaining a relatively simple overall detection workflow.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent employs fluorescent labels with specific emission wavelengths and graphene oxide nanoparticles with controlled concentrations to optimize detection parameters. By adjusting the fluorescent label-to-aptamer ratio and graphene oxide concentration, the system achieves enhanced signal-to-noise ratio and improved detection limits without significantly complicating the detection protocol.

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If aptamers with high binding affinity are developed, then detection specificity improves, but the complexity of aptamer design and selection increases

Engineering Contradiction:
Improvedetection specificityVSAvoidaptamer design complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent utilizes in vitro selection methods (SELEX - Systematic Evolution of Ligands by EXponential enrichment) where the aptamer sequence is self-selected through iterative binding and amplification cycles. The aptamer automatically evolves high binding affinity and specificity for the target spore surface proteins through this self-service selection process, reducing the need for manual design intervention while achieving high detection specificity.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The aptamer design incorporates universal structural elements (stem-loop configurations) that can be adapted to different target sequences. This modular approach allows the same aptamer framework to be used for detecting various C. difficile spore surface proteins, reducing overall design complexity while maintaining high specificity for each target through sequence-specific binding regions.

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

3Illumination intensity

If graphene oxide nanoparticles are incorporated into the composition, then visualization capability is enhanced, but the complexity of composition preparation increases

Engineering Contradiction:
Improvevisualization capabilityVSAvoidcomposition preparation ease
Core Design Contradiction:
Illumination intensityVSEase of manufacture

Solution Approach 1:

The patent uses fluorescent labels as intermediaries between the aptamer-spore complex and the detection system. The fluorescent labels absorb light at specific wavelengths and emit at longer wavelengths, providing signal amplification and enhanced visualization capability. This intermediary approach allows simple UV-Vis or fluorescence microscopy to detect the spores effectively without requiring complex imaging equipment, thus enhancing visualization while keeping preparation relatively simple.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The fluorescent labels and graphene oxide nanoparticles create an optical copy or signal representation of the spore presence. Instead of directly imaging the spores themselves, the system generates a fluorescent signal that copies the spatial distribution and concentration of spores, making them visible under fluorescence microscopy with enhanced sensitivity and easier preparation compared to direct imaging methods.

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

The aptamer-graphene oxide composition enables effective visualization and detection of Clostridium difficile spores, facilitating rapid identification and potentially reducing the spread of infections by enhancing detection sensitivity and specificity.

Implementation Method 1

the at least one aptamer comprises a fluorophore, wherein fluorescence is visible when the at least one aptamer is bound to the surface protein of Clostridium difficile spores

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Implementation Method 2

graphene oxide, wherein fluorophore is quenched by the association with the graphene oxide

Methodology Applied
Scientific EffectFluorescence quenching: Absorption (EM radiation)

Data Source

PatentUS11898146B2Aptamers against <i>Clostridium difficile</i>, compositions comprising aptamers against <i>Clostridium difficile </i>and methods of using the same
Publication Date: 2024.02.13 LIV PROCESS INC
  • US11898146B2 patent drawing
  • US11898146B2 patent drawing
  • US11898146B2 patent drawing

AI summary

Compositions comprising optimized aptamers capable of specifically binding to a surface protein of Clostridium difficile spore are provided. A method for detecting, enriching, separating, and/or isolating Clostridium difficile spores is provided.