Porous Microparticle Labeling for Multiplexed Biological Sample Detection
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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
Engineering 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
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.
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.
2Productivity
If multiple samples are processed in parallel using identical instrument resources, then throughput is increased, but device complexity and costs increase
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.
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.
3Measurement precision
If separate analysis processes are performed for each individual sample, then measurement precision is maintained, but productivity decreases
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.
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.
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
Implementation Method 2
separately transferring each subset of porous microparticles from said aqueous environment to a non-aqueous environment
Data Source
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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.