Miniaturized Flow Cytometer Using Microfluidic Chip

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Solution Overview

Problem

Conventional flow cytometers are large and bulky, limiting their use to central laboratory environments and preventing remote or field applications, such as early detection of infections in biological warfare scenarios or continuous hematological monitoring.

Innovation Solution

A miniaturized portable flow cytometer with a non-precision fluid driver controlled by a closed-loop feedback system, using manually powered pressure chambers and electrostatically actuated microvalves, along with thermal anemometer flow sensors and optical detection subsystems for scattering and fluorescence analysis, allowing for wearable and field-deployable operation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional flow cytometers are used, then measurement precision is improved, but device size and portability deteriorate

Engineering Contradiction:
Improveflow cytometry measurement accuracyVSAvoidinstrument size
Core Design Contradiction:
Measurement precisionVSVolume of moving object

Solution Approach 1:

The flow cytometer is divided into separate functional modules: a microfluidic chip containing the flow cell and fluid handling, a portable laser unit, and detection components. This segmentation allows each module to be optimized independently and enables compact integration while maintaining measurement precision through controlled microfluidic flow paths.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The microfluidic chip is integrated within a compact housing that contains the laser source, detectors, and control electronics. The flow cell is nested within the microfluidic channel structure, allowing multiple components to occupy the same spatial envelope and dramatically reducing the overall instrument volume while preserving cytometry functionality.

Inventive Principle:
Principle #7Nested doll (Nesting)

2Measurement precision

If bench top flow cytometers are used, then measurement precision is improved, but ease of operation in remote locations deteriorates

Engineering Contradiction:
Improvehematological analysis accuracyVSAvoidportability and field deployability
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The system replaces complex mechanical fluid delivery mechanisms with a microfluidic chip that uses pressure-driven flow and capillary action to transport samples and reagents. This substitution eliminates the need for bulky pumps and complex fluid handling systems, making the instrument portable while maintaining precise control over fluid flow for accurate hematological analysis.

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

Solution Approach 2:

The instrument is designed to operate with simplified parameters suitable for portable use, including automated sample preparation, digital data processing, and user-friendly interfaces. The microfluidic system automatically adjusts flow rates and detection parameters based on input sample characteristics, maintaining measurement precision without requiring skilled operation in remote locations.

Inventive Principle:
Principle #35Parameter changes

3Productivity

If continuous monitoring capability is implemented, then productivity is improved, but device complexity increases

Engineering Contradiction:
Improvecontinuous hematological monitoring capabilityVSAvoidsystem complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The microfluidic chip performs automated sample preparation, including red blood cell lysis and white blood cell isolation, without requiring manual intervention. The system automatically loads reagents, processes samples, and generates results, enabling continuous monitoring while reducing operational complexity through self-contained automated functionality.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The flow cytometer is designed as a multi-functional platform that can perform various hematological analyses using the same microfluidic chip and detection system. The universal design allows the instrument to handle different sample types and analytical protocols without requiring separate specialized equipment, thereby improving productivity through continuous monitoring capability while managing device complexity through software-controlled functionality.

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

Enables early detection of infections by identifying and differentiating between viral and bacterial causes through accurate counting of white blood cells, providing a portable and reliable solution for remote healthcare and biological defense.

Implementation Method 1

The particles are then individually interrogated by a light beam. Each particle scatters the light beam and produces a scatter profile.

Methodology Applied
Scientific EffectLight scattering: Scattering

Implementation Method 2

A laser light source positioned to direct light through the flow channel at particles flowing single file

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS7978329B2Portable scattering and fluorescence cytometer
Publication Date: 2011.07.12 HONEYWELL INTERNATIONAL INC
  • US7978329B2 patent drawing
  • US7978329B2 patent drawing
  • US7978329B2 patent drawing

AI summary

An apparatus having scattering and multi-color fluorescence detecting, analyzing and identification capabilities of blood or other fluids of interest. The sample to be tested may be entered in a disposable microfluidic cartridge which in turn is insertable in a hand-holdable or implantable miniaturized and portable cytometer instrument. This cytometer has significant application in biological warfare agent detection, hematology and other clinical and research fields.