Microfluidic Cartridge Metering Stack for Precise Blood Volume Control

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Point-of-care (POC) testing devices face challenges such as inability to precisely control blood sample volume, user-introduced errors due to complex operations, and issues like air bubble formation during sample collection, which affect the accuracy of analyte collection and assay results.

Innovation Solution

A microfluidic device with a cartridge system that includes a metering stack with a porous or mesh material and an assay stack, where the cartridge is compressed to initiate assay reactions, allowing for precise analyte distribution and minimizing user intervention, thereby reducing errors and improving accuracy.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If manual sample collection using plastic pipettes or glass capillaries is used, then users can collect blood samples, but accuracy of sample volume control deteriorates due to user ability limitations and air bubble formation

Engineering Contradiction:
Improvesample collection operationVSAvoidsample volume accuracy
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The microfluidic device performs sample collection, transport, and dispensing automatically without requiring user manipulation of pipettes or capillaries. The system self-regulates sample volume through integrated microfluidic channels and chambers, eliminating user ability limitations and air bubble formation issues.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent replaces manual mechanical operations (filling capillaries, dispensing samples) with an automated microfluidic system that uses integrated channels, chambers, and pressure control to manage sample flow, thereby eliminating user-introduced errors.

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

2Adaptability or versatility

If multiple separated parts (pipettes, test strips) are used for POC testing, then users can perform assays, but device complexity increases and user errors increase due to multiple steps

Engineering Contradiction:
Improveassay capabilityVSAvoidnumber of separated parts
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent combines sample collection, sample preparation, and assay functions into a single integrated microfluidic cartridge. The device merges multiple separated components (pipettes, test strips, preparation chambers) into one unified system with integrated channels and chambers, reducing complexity while maintaining versatility.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The microfluidic device is designed to perform multiple functions within a single cartridge, including sample collection, plasma separation, cell lysis, and various assays, allowing one device to replace multiple specialized tools.

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

3Productivity

If sample preparation steps (plasma separation, cell lysis) are performed manually, then assays can be conducted, but time required increases making it comparable to blood clotting time

Engineering Contradiction:
Improveassay throughputVSAvoidsample preparation time
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The microfluidic device performs sample preparation steps continuously as the sample flows through integrated chambers. Plasma separation and cell lysis occur automatically during sample transport without interruption, eliminating manual transfer times and ensuring continuous processing that completes well before clotting occurs.

Inventive Principle:
Principle #20Continuity of useful action

4Ease of operation

If users manually dispense blood sample from pipette to cartridge, then sample can be transferred, but user-introduced errors increase due to mis-aiming, touching assay pad, or incomplete dispensing

Engineering Contradiction:
Improvesample dispensingVSAvoidassay accuracy
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent replaces manual dispensing operations with an automated microfluidic system that uses integrated channels and pressure control to transport and dispense samples precisely to the assay chamber, eliminating mis-aiming, contamination, and incomplete dispensing errors.

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

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 system enables accurate and efficient multiplexed analysis of fluid analytes with reduced user error, ensuring precise control over sample volume and minimizing unwanted reactions like blood clotting, thus providing reliable point-of-care diagnostic results.

Implementation Method 1

The first channel has a bottom that includes a porous or mesh material and one or more venting holes located along the first channel

Methodology Applied
Scientific EffectPorosity: Porosity

Implementation Method 2

When the cartridge is inserted into the assay reader, the act of inserting the cartridge causes the metering stack to be compressed, which causes at least a portion of the target analyte to flow to the assay components in the assay stack

Methodology Applied
Scientific EffectCompression: Compression

Data Source

PatentUS11857960B2Microfluidic metering and delivery system
Publication Date: 2024.01.02 FITBIT INC
  • US11857960B2 patent drawing
  • US11857960B2 patent drawing
  • US11857960B2 patent drawing

AI summary

This invention provides devices, systems, and methods for performing point-of-care, analysis, including multiplexed analysis, of a biological fluid analyte, such as blood. The invention includes a cartridge for collecting the biological fluid analyte. The cartridge is configured to be inserted into an assay reader, in which one or more assay reactions may be performed. The assay reader is designed to read and report the results of the one or more assay reactions.