Porous Microparticle Labeling for Multiplexed Biological Sample Detection

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current diagnostic methods face limitations in achieving high throughput while minimizing waste and costs, particularly in cartridge-based testing, where processing multiple samples efficiently and accurately is challenging due to the constraints of existing cartridge designs and reagent resource utilization.

Innovation Solution

A method involving a sample-specific subprocess and a generic subprocess, where biological liquid samples are separately labeled with differently labeled porous microparticles, allowing for individual identification and mixing in a non-aqueous environment for detection, enabling efficient detection and quantitation of analytes without cross-contamination.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Loss of substance

If sample pooling strategies are used to reduce costs, then testing cost is reduced, but sensitivity of the test decreases and complex logistics are required

Engineering Contradiction:
Improvetesting costVSAvoidsensitivity of the test
Core Design Contradiction:
Loss of substanceVSMeasurement precision

Solution Approach 1:

The invention divides the testing process into two distinct phases: a pooled screening phase where multiple samples are tested together, and an individual reflex phase where only positive samples from the pool are tested separately. This segmentation allows cost reduction through pooling while maintaining sensitivity by ensuring individual testing of positive samples, thus resolving the contradiction between cost reduction and sensitivity preservation.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The method performs preliminary pooled testing before individual sample testing. By first identifying positive pools through combined testing, the system pre-screens samples efficiently and then applies individual testing only where necessary. This preliminary action reduces overall testing costs while maintaining accuracy by targeting reflex testing only to samples that actually require it.

Inventive Principle:
Principle #10Preliminary action

2Productivity

If multiple samples are processed in parallel using identical instrument resources, then throughput is increased, but device complexity and costs increase

Engineering Contradiction:
ImprovethroughputVSAvoidcartridge design complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The invention designs a universal cartridge system where a single cartridge type can process multiple samples through pooled testing. The cartridge includes features like multiple sample receptacles, a common reaction chamber, and integrated mixing mechanisms that enable parallel processing of multiple samples without requiring separate specialized cartridges for each sample, thus increasing throughput while controlling complexity.

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

Solution Approach 2:

The method merges multiple individual sample processing workflows into a single pooled processing workflow. By combining samples from multiple receptacles into a single reaction chamber for simultaneous testing, the system achieves parallel processing capability without proportionally increasing device complexity, as the same basic cartridge structure handles multiple samples.

Inventive Principle:
Principle #5Merging (Combining)

3Measurement precision

If separate analysis processes are performed for each individual sample, then measurement precision is maintained, but productivity decreases

Engineering Contradiction:
Improvedetection accuracyVSAvoidthroughput
Core Design Contradiction:
Measurement precisionVSProductivity

Solution Approach 1:

The testing process is segmented into pooled screening and individual reflex testing phases. During the pooled phase, multiple samples are processed together in a single reaction chamber, maintaining detection accuracy through the pooling methodology while significantly increasing throughput. The segmentation allows parallel processing without sacrificing the precision that would come from individual testing, as the pooled result triggers targeted individual testing only when necessary.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The system maintains continuous useful action by keeping the reaction chamber occupied with pooled samples throughout the screening phase, rather than processing samples sequentially. The chemical reactions proceed continuously in the shared reaction chamber, maximizing instrument utilization and throughput while maintaining detection precision through the validated pooled testing approach.

Inventive Principle:
Principle #20Continuity of useful 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

This approach enhances throughput, reduces waste, and optimizes reagent use by allowing multiple samples to be processed in a single system, ensuring accurate identification and quantitation of analytes with minimal cross-talk between samples.

Implementation Method 1

separately exposing each of said separate subsets of microparticles to one biological liquid sample each, thus allowing each sample to be absorbed by one specifically labelled subset of porous microparticles

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 2

separately transferring each subset of porous microparticles from said aqueous environment to a non-aqueous environment

Methodology Applied
Scientific EffectPhase separation: Phase Change

Data Source

PatentEP4078181B1A method of detecting and/or quantitating an analyte of interest in a plurality of biological liquid samples
Publication Date: 2024.03.20 BLINK AG
  • EP4078181B1 patent drawingFigure 1A
  • EP4078181B1 patent drawingFigure 1B
  • EP4078181B1 patent drawingFigure 2

AI summary

The present invention relates to a method of detecting and/or quantitating an analyte of interest in a plurality of biological liquid samples. Furthermore, the present invention relates to a kit and a cartridge for performing a method for detecting and/or quantitating an analyte of interest in a plurality of samples.