Agitated Liquid Sample Detection Device for Rapid Analyte Binding

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Solution Overview

Problem

Current methods for detecting Mycoplasma species in liquid samples are inadequate due to the absence of a cell wall, making traditional antibiotics ineffective, and existing detection technologies are not suited for rapid and concurrent detection of multiple analytes.

Innovation Solution

A device with an elongate chamber and a carrier or agitator that agitates the liquid sample, coupled with antibodies immobilized on the carrier or chamber walls, facilitating the binding of analytes to their respective antibodies, allowing for quantitative or qualitative detection using various techniques such as microscopy or immunoassays.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional detection methods are used, then detection can be performed, but detection speed is slow and multiple analytes cannot be detected concurrently

Engineering Contradiction:
Improvedetection speedVSAvoiddetection system complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The detection device is segmented into multiple functional zones within a single chip, with each zone containing specific antibodies for different analytes. This allows concurrent detection of multiple analytes through spatial segmentation, improving productivity without requiring multiple separate detection systems.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A single detection device integrates multiple antibody-specific detection functions into one universal platform. The chip can simultaneously detect multiple different analytes (Mycoplasma species, bacteria, viruses) using a unified detection mechanism, eliminating the need for multiple specialized detection systems.

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

2Reliability

If diffusion-based binding is used, then antibody-analyte binding occurs, but binding efficiency is low for low-concentration analytes

Engineering Contradiction:
Improvedetection sensitivityVSAvoidbinding time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The device incorporates vibration or agitation mechanisms that actively mix the liquid sample, forcing analytes into close proximity with immobilized antibodies. This mechanical agitation replaces passive diffusion, significantly improving binding efficiency and detection sensitivity for low-concentration analytes while reducing binding time.

Inventive Principle:
Principle #18Mechanical vibration

Solution Approach 2:

The patent introduces an intermediary carrier or agitator that facilitates contact between analytes and antibodies. This intermediary element actively mediates the binding process by bringing reactants together, overcoming the limitations of diffusion-only mechanisms and enhancing detection sensitivity.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Adaptability or versatility

If beta-lactam antibiotics are used, then cell wall synthesis is inhibited, but they are ineffective against Mycoplasma due to absence of cell wall

Engineering Contradiction:
Improveantibiotic effectivenessVSAvoidtreatment failure
Core Design Contradiction:
Adaptability or versatilityVSObject-affected harmful factors

Solution Approach 1:

The detection device enables preliminary identification of Mycoplasma infections before treatment is initiated. By detecting the presence of Mycoplasma species (which lack cell walls) through antibody binding, clinicians can select appropriate antibiotics that do not rely on cell wall synthesis inhibition, preventing treatment failure beforehand.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The detection system provides feedback information about the presence and type of pathogen (including cell wall-less Mycoplasma) to guide antibiotic selection. This feedback loop enables clinicians to adjust treatment strategies based on actual pathogen characteristics, ensuring effective therapy despite the limitations of beta-lactam antibiotics against Mycoplasma.

Inventive Principle:
Principle #23Feedback

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 efficient detection of Mycoplasma species and other analytes in liquid samples, including those present in low concentrations, without relying on diffusion, thus overcoming the limitations of traditional detection methods.

Implementation Method 1

a carrier or agitator in said elongate chamber, said carrier or agitator having opposite end portions and a side portion, the carrier or agitator dimensioned to travel in said chamber along said length axis and/or permit said liquid sample to flow in the chamber therearound, thereby agitating the liquid sample

Methodology Applied
Scientific EffectAgitation: Stirring

Implementation Method 2

at least one anti-analyte antibody coupled to either the carrier and/or the chamber side wall... bring analytes into sufficiently close physical proximity with their corresponding antibody to cause binding of the antibody to its corresponding analyte

Methodology Applied
Scientific EffectAntigen-antibody binding: Absorption (physical)

Data Source

PatentUS9482670B2Rapid detection of analytes in liquid samples
Publication Date: 2016.11.01 ADVANCED ANIMAL DIAGNOSTICS
  • US9482670B2 patent drawing
  • US9482670B2 patent drawing
  • US9482670B2 patent drawing

AI summary

A device for detecting at least one analyte (and in some embodiments two, three, or four or more different analytes) in a liquid sample generally comprises (i) a support having a chamber for receiving a biological fluid therein, wherein said chamber is an elongate chamber having a length axis; (ii) a carrier or agitator in said elongate chamber, said carrier or agitator having opposite end portions and a side portion, the carrier or agitator dimensioned to travel in said chamber along said length axis and/or permit said liquid sample to flow in the chamber therearound, either (or both) thereby agitating the liquid sample; and (iii) at least one anti-analyte antibody coupled to either the carrier and/or the chamber side wall.