Sealed Microfluidic Bio Detection With Centrifugal Flow Control

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current biological detection devices suffer from low integration, limited versatility, poor feasibility, compromised detection performance, and high risks of cross-contamination, necessitating manual operations and complex sample handling.

Innovation Solution

A whole-process biological detection device integrating sample-loading, lysis, extraction, amplification, and detection units with controlled fluid flow and reagent storage, utilizing centrifugal force for automated operation and sealed containment to prevent cross-contamination.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If manual operations are used for sample handling and reagent addition, then flexibility in handling different samples is maintained, but the risk of cross-contamination increases and operation complexity increases

Engineering Contradiction:
Improvesample handling flexibilityVSAvoidcross-contamination risk
Core Design Contradiction:
Adaptability or versatilityVSObject-affected harmful factors

Solution Approach 1:

The microfluidic chip is designed with integrated reagent storage chambers and automated fluid control channels that enable the system to perform sample handling, reagent addition, and workflow control autonomously without manual intervention, thereby eliminating cross-contamination risks while maintaining versatility through programmable fluid routing

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The chip integrates multiple functional modules including sample loading, reagent storage, lysis, extraction, amplification, and detection within a single device, allowing it to handle various sample types and perform complete nucleic acid detection workflows automatically, achieving both versatility and contamination prevention

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

2Adaptability or versatility

If nucleic acid extraction and purification modules are added to handle complex samples, then detection sensitivity and versatility improve, but device complexity and manufacturing difficulty increase

Engineering Contradiction:
Improvecomplex sample handling capabilityVSAvoiddevice structure complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The lysis, extraction, and purification functions are merged into a single integrated module within the microfluidic chip, where magnetic bead-based extraction is combined with automated washing and elution channels, achieving complex sample处理能力 without proportionally increasing device complexity through modular integration

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

Multiple functional chambers including sample loading, reagent storage, lysis, magnetic bead extraction, washing, and elution are nested within the compact microfluidic chip structure, allowing complex functionality to be contained in a small integrated device with hierarchical organization of sub-functions

Inventive Principle:
Principle #7Nested doll (Nesting)

3Extent of automation

If integrated whole-process modules are implemented, then automation level and contamination prevention improve, but device complexity and operational reliability requirements increase

Engineering Contradiction:
Improvewhole-process automation levelVSAvoiddevice operational reliability
Core Design Contradiction:
Extent of automationVSReliability

Solution Approach 1:

The automated detection system is segmented into distinct functional modules (sample loading, lysis, extraction, amplification, detection) connected by controlled fluid channels, allowing each module to be independently optimized and tested, which simplifies reliability verification while maintaining high automation and contamination prevention

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

The device achieves high integration, automated operation, and reduced cross-contamination risks, ensuring efficient and reliable biological detection with simplified sample handling and reduced biosafety hazards.

Implementation Method 1

a microfluidic chip device for nucleic acid detection based on centrifugal drive

Methodology Applied
Scientific EffectCentrifugal force: Centrifugal Force

Data Source

PatentEP3895803B1Whole-process biological detection device
Publication Date: 2025.12.10 CAPITALBIO CORP
  • EP3895803B1 patent drawingFigure 1
  • EP3895803B1 patent drawingFigure 2
  • EP3895803B1 patent drawingFigure 3

AI summary

A whole-process biological detection device is provided. The whole-process biological detection device belongs to the technical field of biological detection, and includes at least one reactor (100), where the reactor includes at least one sample-loading unit (1), at least one liquid release-control unit (2), at least one extraction unit (3), at least one liquid switch-control unit (4), at least one liquid collection unit (5), at least one liquid transfer unit (6), at least one liquid flow-control unit (7), at least one liquid quantitative dispersion unit (8) and multiple reaction cells (9). The product of the solution has the characteristics of high integration, no need for additional reagents, simple operation, stable and reliable, etc., thereby achieving the goal of sealing the whole process of biological detection and effectively avoiding cross-contamination between samples and equipment.