Microfluidic Impedance Sensor for Label-Free Cell Sorting

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Solution Overview

Problem

Current microfluidic systems for cell sorting and diagnostics require complex and costly fluorescence-activated cell sorting operations, which are not efficient for determining and moving cells without tagging them with fluorescent labels, and often require multiflow control systems.

Innovation Solution

A microfluidic apparatus with a channel and foyer system that uses an impedance sensor to detect and identify cells based on their electrical signature, allowing for controlled movement of cells without fluorescent labels, using a controller to direct cells to different areas for further analysis or dispensing, and an actuator to manage fluid flow.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If fluorescence-activated cell sorting operations are used, then cell sorting and diagnostics can be performed, but the system becomes complex and costly

Engineering Contradiction:
Improvecell sorting accuracyVSAvoidsystem complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent extracts the fluorescent labeling step from the cell sorting process entirely. Instead of requiring fluorescent tags and complex optical detection systems, the invention uses label-free impedance sensing to detect and sort cells based on their intrinsic electrical properties, thereby simplifying the system while maintaining sorting accuracy

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent replaces the optical detection and sorting mechanism (fluorescence-activated cell sorting) with an electrical impedance-based detection and dielectrophoretic sorting mechanism. This substitution eliminates the need for complex optical systems, lasers, and fluorescent reagents, significantly reducing system complexity and cost

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

2Reliability

If fluorescence-activated cell sorting operations are used, then cell sorting can be performed, but the operation becomes costly

Engineering Contradiction:
Improvecell sorting accuracyVSAvoidoperational cost
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent employs inexpensive microfabricated impedance sensors and dielectrophoretic actuators that can be mass-produced using standard semiconductor fabrication techniques. These replace expensive fluorescent reagents, optical components, and specialized equipment, dramatically reducing operational costs while maintaining cell sorting accuracy

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

Solution Approach 2:

The substitution of optical detection with electrical impedance detection eliminates costly fluorescent reagents, lasers, and optical detectors. The dielectrophoretic sorting mechanism uses affordable electrical fields instead of expensive optical sorting systems, reducing both capital equipment costs and per-operation costs

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

3Ease of operation

If multiflow control systems are used, then fluid flow can be controlled, but the device complexity increases

Engineering Contradiction:
Improvefluid flow controlVSAvoidcontrol system complexity
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The patent merges multiple fluid control functions into a single integrated microfluidic channel design. The microfabricated impedance sensor and dielectrophoretic actuator are combined in one device, allowing fluid flow control and cell sorting to be achieved through a unified system rather than separate multiflow control components

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The microfabricated device performs multiple functions (fluid flow control, cell detection, cell sorting) within a single integrated platform. The impedance sensor simultaneously detects cell presence and characteristics, while the dielectrophoretic field provides sorting capability, eliminating the need for separate specialized control systems

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 efficient determination and movement of cells within microliter to picoliter volumes without multiflow control systems, allowing for cost-effective and simpler cell sorting and diagnostics, including health diagnostics for diseases like HIV, Malaria, Tuberculosis, cancer, and cardiac diseases.

Implementation Method 1

A sensor is positioned to detect the passage of a particle of interest, e.g., a cell, through the channel

Methodology Applied
Scientific EffectElectrical impedance: Electrical Impedance Tomography

Implementation Method 2

microfluidic systems and devices such as microfluidic devices or chips

Methodology Applied
Scientific EffectMicrofluidics:

Data Source

PatentEP3436799B1Microfluidic apparatuses for fluid movement control
Publication Date: 2023.08.30 HEWLETT PACKARD DEVELOPMENT COMPANY LP
  • EP3436799B1 patent drawingFigure 1A~1B
  • EP3436799B1 patent drawingFigure 1C~2
  • EP3436799B1 patent drawingFigure 3~4

AI summary

According to an example, a microfluidic apparatus may include a fluid slot and a foyer that is in fluid communication with the fluid slot via a channel having a relatively smaller width than the foyer. The microfluidic apparatus may also include an electrical sensor to measure a change in an electrical field caused by a particle of interest in a fluid passing through the channel from the fluid slot to the foyer, an actuator to apply pressure onto fluid contained in the foyer, and a controller to receive the measured change in the electrical field from the electrical sensor, determine, from the received change in the electrical field, an electrical signature of the particle of interest, and control the actuator to control movement of the particle of interest based upon the determined electrical signature of the particle of interest.