Centrifugal Droplet Microfluidic Chip for Stable Microdroplet Generation

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Solution Overview

Problem

Existing microfluidic chips for producing microdroplets suffer from poor stability and reproducibility, complex processes, and high equipment requirements, making them unsuitable for research and mass production.

Innovation Solution

A droplet microfluidic chip design with a centrifugal force-driven mechanism, featuring a dispersion phase chamber, quantitation chamber, capillary nozzle, and continuous phase chamber, which uses centrifugal force to produce microdroplets by forcing dispersion phase liquid into the continuous phase chamber through a capillary nozzle, ensuring uniformity and stability without complex equipment.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional continuous flow microfluidic systems are used, then microdroplets can be produced, but the process becomes complex and equipment requirements increase

Engineering Contradiction:
Improvemicrodroplet production efficiencyVSAvoidprocess complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent replaces complex mechanical pumping and flow control systems with a centrifugal field-driven system. By rotating the chip at controlled speeds, the centrifugal force naturally drives liquid flow through the microchannels and controls droplet formation at the capillary nozzle, eliminating the need for external pumps and complex flow control mechanisms.

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

Solution Approach 2:

The patent uses dynamic rotation speed control to achieve different operational modes. By adjusting the rotation speed, the system can control liquid transport, droplet formation, and even droplet size, providing a simple yet powerful method to optimize microdroplet production without complex mechanical adjustments.

Inventive Principle:
Principle #15Dynamics

2Productivity

If complex droplet-producing processes are used, then microdroplet production is achieved, but stability and reproducibility deteriorate

Engineering Contradiction:
Improvemicrodroplet production capabilityVSAvoidstability and reproducibility
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent changes the operational parameter from complex flow rate control to simple rotation speed control. The centrifugal force, which is a function of rotation speed and radius, provides a stable and easily controllable driving force. This parameter simplification leads to better reproducibility and stability in microdroplet production.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The centrifugal field creates a uniform potential gradient throughout the liquid in the chip. This equipotential distribution ensures consistent flow characteristics and droplet formation across all channels, improving the reproducibility of microdroplet production across multiple parallel channels.

Inventive Principle:
Principle #12Equipotentiality

3Manufacturing precision

If high equipment requirements are imposed, then precise microdroplet control is achieved, but cost and maintenance difficulty increase

Engineering Contradiction:
Improvemicrodroplet control precisionVSAvoidequipment simplicity
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The centrifugal chip system is self-driven by rotation, eliminating the need for external pumps, valves, and flow controllers. The system uses the rotation itself to generate the necessary forces for liquid transport and droplet formation, significantly reducing equipment complexity and maintenance requirements while maintaining precise control.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The rotation mechanism serves multiple functions simultaneously: it drives liquid flow through channels, controls droplet formation at the nozzle, regulates droplet size through centrifugal force, and even facilitates droplet ejection. This multi-functionality reduces the need for separate components, simplifying the overall system.

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

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 chip produces uniform microdroplets efficiently and reliably, reducing equipment complexity, cost, and maintenance difficulty while improving liquid utilization efficiency and throughput, facilitating multi-target detection and reducing detection time.

Implementation Method 1

centrifuging the droplet microfluidic chip with a centrifugal force of 5 g to 100 g to force the dispersion phase liquid into the quantitation chamber from the dispersion phase chamber

Methodology Applied
Scientific EffectCentrifugal force: Centrifugal Force

Implementation Method 2

forcing the dispersion phase liquid into the continuous phase chamber from the quantitation chamber through the capillary nozzle by increasing the centrifugal force to 500 g to 18000 g, thereby producing the microdroplets

Methodology Applied
Scientific EffectCentrifugal force: Centrifugal Force

Data Source

PatentEP4154980B1Droplet microfluidic chip and microdroplet preparation method
Publication Date: 2026.04.01 SHENZHEN YHLO BIOTECH
  • EP4154980B1 patent drawingFigure 1
  • EP4154980B1 patent drawingFigure 2
  • EP4154980B1 patent drawingFigure 3

AI summary

A droplet microfluidic chip and a method for producing microdroplets are disclosed. The droplet microfluidic chip includes at least one droplet-producing unit. The droplet-producing unit includes a dispersion phase chamber, a quantitation chamber, a capillary nozzle, and a continuous phase chamber. The droplet microfluidic chip has a rotation center. The dispersion phase chamber is provided with a loading hole configured to introduce a dispersion phase liquid. The quantitation chamber is in communication with the dispersion phase chamber and further away from the rotation center than the dispersion phase chamber. The capillary nozzle is further away from the rotation center than the quantitation chamber. One end of the capillary nozzle is in communication with the quantitation chamber, and the capillary nozzle is extended from the joining end in a direction away from the rotation center. The continuous phase chamber is in communication with the other end of the capillary nozzle away from the quantitation chamber, and the continuous phase chamber is further away from the rotation center than the capillary nozzle. The continuous phase chamber accommodates a continuous phase liquid.