Disposable Microfluidic PCR Chips with Glass Substrates

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Solution Overview

Problem

Current microfluidic diagnostic devices face challenges in cost-effectiveness and sample preparation, with reusable chips risking cross-contamination and being made from materials that are not chemically inert, thermally stable, or optically transparent enough for diagnostic applications.

Innovation Solution

A microfluidic device with parallel processing channels, compatible with qPCR processes, featuring wells arranged like industry standard multiwell plates for easy integration with liquid handling equipment, and using conductive polymer electrodes for electrical control, allowing for independent reactions and efficient PCR amplification.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If reusable microfluidic chips are used to reduce cost, then manufacturing cost decreases, but cross-contamination risk increases and reliability deteriorates

Engineering Contradiction:
Improvemanufacturing costVSAvoidcross-contamination risk
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent employs disposable microfluidic chips that are discarded after a single use, eliminating cross-contamination risks associated with reusable chips while maintaining cost-effectiveness through inexpensive single-use design. The chip is intended for one-time use only and is disposed of after the assay is complete.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

2Ease of manufacture

If conventional microfluidic materials are used, then ease of manufacture improves, but chemical inertness and thermal stability deteriorate

Engineering Contradiction:
Improveease of manufactureVSAvoidchemical inertness and thermal stability
Core Design Contradiction:
Ease of manufactureVSStability of the object's composition

Solution Approach 1:

The patent employs a composite structure consisting of a polymeric microfluidic chip body combined with a separate glass slide substrate. The glass slide provides the required chemical inertness and thermal stability for PCR applications, while the polymeric chip enables ease of manufacture and integration of microfluidic features. This composite approach allows the device to meet both manufacturing and performance requirements.

Inventive Principle:
Principle #40Composite materials

3Adaptability or versatility

If complex channel networks are used to perform complete analyses, then functionality increases, but device complexity increases

Engineering Contradiction:
ImprovefunctionalityVSAvoiddevice complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent divides the microfluidic chip into distinct functional zones including separate reaction chambers, heating elements, and detection regions. The chip is designed with modular functional segments that can be independently controlled and optimized, allowing complex analyses to be performed through coordinated operation of simpler subsystems rather than requiring a single complex integrated structure.

Inventive Principle:
Principle #1Segmentation

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 cost-effective, efficient PCR amplification and analyte detection with reduced risk of cross-contamination, using materials that are chemically inert and thermally stable, and compatible with automated processing systems.

Implementation Method 1

The heating element is formed on the plate and heats that portion of the microfluidic PCR circuit

Methodology Applied
Scientific EffectHeating: Heating

Implementation Method 2

using conductive polymer electrodes for electrical control

Methodology Applied
Scientific EffectElectrical conduction: Conduction (electrical)

Data Source

PatentUS11235333B2Method and apparatus for use in temperature controlled processing of microfluidic samples
Publication Date: 2022.02.01 CALIPER LIFE SCIENCES INC
  • US11235333B2 patent drawing
  • US11235333B2 patent drawing
  • US11235333B2 patent drawing

AI summary

Embodiments of the invention comprise microfluidic devices, instrumentation interfacing with those devices, processes for fabricating that device, and methods of employing that device to perform PCR amplification. Embodiments of the invention are also compatible with quantitative Polymerase Chain Reaction (“qPCR”) processes. Microfluidic devices in accordance with the invention may contain a plurality of parallel processing channels. Fully independent reactions can take place in each of the plurality of parallel processing channels. The availability of independent processing channels allows a microfluidic device in accordance with the invention to be used in a number of ways. For example, separate samples could be processed in each of the independent processing channels. Alternatively, different loci on a single sample could be processed in multiple processing channels.