Microfluidic Chip Waveform Profiling for Genomic DNA Identification

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Solution Overview

Problem

Current molecular diagnostic devices are limited in their ability to rapidly and accurately characterize genomic material from samples, particularly in identifying organisms like bacteria and viruses, due to imprecise standard microbiological methods and the need for known primers in PCR, which restricts analysis to known organisms, and lack automation in waveform profiling.

Innovation Solution

A molecular diagnostic device comprising a cartridge with a binding and release substrate for genomic material and a microfluidic chip for amplification and detection, enabling automated isolation, amplification, and mapping of genomic material, allowing for simultaneous processing of multiple samples without cross-contamination and portable use.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If standard microbiological methods (culturing and Gram-staining) are used for organism identification, then the process is simple and accessible, but the identification precision is insufficient and cannot differentiate among different organisms or strains

Engineering Contradiction:
Improveidentification precisionVSAvoidmethod complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces mechanical microbiological methods (culturing, staining) with molecular biological methods (PCR, waveform profiling) that use chemical and biochemical processes to achieve precise genomic DNA analysis for organism identification

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

Solution Approach 2:

The patent changes the identification approach from phenotypic parameters (morphology, staining characteristics) to genotypic parameters (genomic DNA sequences, melting temperature profiles), enabling differentiation at the strain level

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If PCR is used for organism detection, then small amounts of genomic material can be detected, but the method is limited to known organisms requiring specific primers and cannot provide mapping information

Engineering Contradiction:
Improvedetection sensitivityVSAvoidorganism identification range
Core Design Contradiction:
Measurement precisionVSAdaptability or versatility

Solution Approach 1:

The patent combines PCR (for sensitive detection of known organisms) with waveform profiling (for broad-spectrum detection and mapping of any genomic DNA) into a single integrated system, enabling both specific detection and exploratory analysis

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

Solution Approach 2:

The patent segments the analysis into two complementary approaches: PCR targeting specific known sequences for sensitive detection, and waveform profiling analyzing overall genomic structure for broader identification and mapping capabilities

Inventive Principle:
Principle #1Segmentation

3Productivity

If automated inline PCR platforms are used, then throughput and automation are increased, but the ability to further analyze and map genomic material after PCR is lacking

Engineering Contradiction:
ImprovethroughputVSAvoidpost-PCR analysis capability
Core Design Contradiction:
ProductivityVSAdaptability or versatility

Solution Approach 1:

The patent merges automated PCR amplification with waveform profiling analysis in a single integrated platform, allowing genomic material to be both amplified for sensitivity and subsequently analyzed for mapping and identification purposes

Inventive Principle:
Principle #5Merging (Combining)

4Adaptability or versatility

If waveform profiling is used for organism identification, then detection can be performed without knowing the organism identity, but the method does not provide mapping or sequence information of the genomic material

Engineering Contradiction:
Improveunknown organism detectionVSAvoidsequence information
Core Design Contradiction:
Adaptability or versatilityVSLoss of information

Solution Approach 1:

The patent uses PCR amplification as an intermediary step that preserves and enriches the genomic material, enabling subsequent waveform profiling analysis to generate both identification data and mapping information from the amplified products

Inventive Principle:
Principle #24Intermediary (Mediator)

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

Facilitates rapid and accurate characterization of genomic material, enabling on-site genetic testing within an hour of sample procurement, overcoming limitations of existing technologies by automating the process and allowing for simultaneous processing and mapping of genomic material.

Implementation Method 1

the solid substrate capable of binding and releasing genomic material (i.e., binding and release substrate) comprises charge switch material

Methodology Applied
Scientific EffectCharge switching: Electrostatics

Data Source

PatentUS10814321B2Method and molecular diagnostic device for detection, analysis and identification of genomic DNA
Publication Date: 2020.10.27 CANON USA INC
  • US10814321B2 patent drawing
  • US10814321B2 patent drawing
  • US10814321B2 patent drawing

AI summary

At least one exemplary embodiment of the invention is directed to a molecular diagnostic device that comprises a cartridge configured to eject samples comprising genomic material into a microfluidic chip that comprises an amplification area, a detection area, and a matrix analysis area.