Microfluidic Card Serpentine Channel for Rapid PCR Thermal Cycling

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Solution Overview

Problem

Conventional PCR technology has not kept pace with the need for higher throughput and speed, as it is limited by the time required for temperature-dependent steps in thermal cycling.

Innovation Solution

A microfluidic device with a heating assembly that forms differential temperature zones on a microfluidic card, allowing the reaction mixture to pass repeatedly through these zones via a serpentine channel array for rapid thermal cycling, enhancing PCR speed and throughput.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional PCR thermal cycling is used, then DNA amplification can be achieved, but the cycle time is too long and throughput is limited

Engineering Contradiction:
ImprovePCR throughputVSAvoidcycle time
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The heating assembly is divided into multiple independent heating zones (first heating zone, second heating zone, third heating zone) that can be independently controlled to create distinct temperature zones. This segmentation allows simultaneous performance of different PCR steps (denaturation, annealing, extension) at different locations, enabling parallel processing and reducing overall cycle time while maintaining amplification efficiency

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention transitions from conventional single-dimension thermal cycling (heating and cooling the entire reaction volume uniformly) to multi-dimensional temperature control with spatially distributed heating zones. The microfluidic card with serpentine channel allows the reaction mixture to flow through different temperature zones in sequence, creating a spatial dimension for thermal cycling that dramatically reduces cycle time while maintaining DNA amplification efficiency

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Speed

If rapid thermal cycling is implemented, then PCR speed increases, but temperature uniformity and amplification efficiency may deteriorate

Engineering Contradiction:
ImprovePCR speedVSAvoidamplification efficiency
Core Design Contradiction:
SpeedVSReliability

Solution Approach 1:

Each heating zone is optimized for its specific function with localized temperature control. The first heating zone maintains higher temperature for denaturation, while the second and third zones are optimized for annealing and extension respectively. This local quality optimization ensures that each PCR step occurs at the ideal temperature, maintaining amplification efficiency even during rapid cycling

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The serpentine channel design ensures continuous flow of the reaction mixture through all heating zones without dead volumes or stagnant regions. The microfluidic system maintains continuous thermal cycling action throughout the reaction mixture, eliminating idle time between cycles and ensuring that every portion of the sample undergoes complete thermal processing, thereby maintaining reliable amplification efficiency at high speeds

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

The device achieves rapid PCR cycle times of less than 2 seconds per cycle, maintaining effective DNA amplification efficiency and temperature uniformity, thereby addressing the limitations of conventional PCR methods.

Implementation Method 1

the heating assembly provides differential heat to different sections of the card such that a plurality of different temperature zones are formed on the card

Methodology Applied
Scientific EffectDifferential heating: Heating

Implementation Method 2

The internal channel extends in a serpentine pattern to form a plurality of lateral sections that are oriented transverse to the longitudinal axis such that a fluid passing through the channel array passes through the lateral sections as it moves downstream of the inlet

Methodology Applied
Scientific EffectFluid flow through temperature zones: Convection

Implementation Method 3

The device achieves rapid PCR cycle times of less than 2 seconds per cycle, maintaining effective DNA amplification efficiency and temperature uniformity

Methodology Applied
Scientific EffectRapid heat transfer: Conduction (thermal)

Data Source

PatentUS11192103B2Micro-fluidic device for rapid PCR
Publication Date: 2021.12.07 UNIV OF UTAH RES FOUND
  • US11192103B2 patent drawing
  • US11192103B2 patent drawing
  • US11192103B2 patent drawing

AI summary

The present disclosure describes systems and devices capable of providing rapid polymerase chain reaction processes. A microfluidic card is insertable into a heating assembly. The heating assembly provides separate temperature zones to the card. The card includes a channel array that traverses repeatedly through the separate temperature zones so that a reaction mixture passing through the channel is subjected to thermal cycling.