Microfluidic Flow Velocity Estimation Using Optical Path Changes

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Solution Overview

Problem

Existing microfluidic systems face challenges in accurately measuring flow velocity in narrow microchannels due to clogging and the difficulty in using conventional methods, making it difficult to maintain a consistent flow velocity for cell culture and drug testing applications.

Innovation Solution

A microfluidic device equipped with a first container, channel, controller, light sources, and an arithmetic processor that estimates flow velocity by detecting changes in optical path length using light intensity, allowing for easy measurement in narrow channels.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional flow velocity measurement methods are used, then measurement can be performed in wide channels, but measurement becomes difficult in narrow microchannels (1 mm or less)

Engineering Contradiction:
Improveflow velocity measurementVSAvoidmeasurement ease in narrow channels
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent replaces conventional mechanical flow velocity measurement methods with an optical measurement system. A light source irradiates the culture solution in the container, and a light detector measures the intensity of transmitted light. The arithmetic processor calculates flow velocity based on changes in optical density over time, eliminating the need for physical probes in the narrow microchannel.

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

Solution Approach 2:

The patent introduces an intermediary measurement approach by measuring flow velocity indirectly through optical properties of the culture solution in the container rather than directly in the microchannel. The change in optical density of the culture solution, caused by flow through the microchannel, serves as an intermediary parameter to calculate flow velocity.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If continuous monitoring of flow velocity is implemented, then clogging can be detected early, but device complexity increases

Engineering Contradiction:
Improveclogging detection capabilityVSAvoidmonitoring system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent makes the optical measurement system multi-functional. The same light source and light detector used for measuring culture solution concentration or other parameters can also monitor flow velocity by detecting changes in optical density over time. This eliminates the need for separate monitoring equipment, reducing overall device complexity while maintaining reliability.

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

Solution Approach 2:

The culture solution itself serves as the measurement medium. The optical properties of the culture solution (absorption, scattering) provide the signal for flow velocity measurement, eliminating the need for external tracers, dyes, or additional sensors. The system uses the inherent properties of the culture solution to enable self-monitoring.

Inventive Principle:
Principle #25Self-service

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 accurate and easy measurement of flow velocity in narrow channels, detects clogging early, and supports continuous monitoring of flow velocity, enhancing cell culture and drug testing processes.

Implementation Method 1

a first light intensity that is an intensity of the first light that has passed through the culture solution in the first container is detected

Methodology Applied
Scientific EffectAbsorption (EM radiation): Absorption (EM radiation)

Data Source

PatentUS20250332588A1Microfluidic device and flow velocity estimation method
Publication Date: 2025.10.30 HAMAMATSU PHOTONICS KK
  • US20250332588A1 patent drawing
  • US20250332588A1 patent drawing
  • US20250332588A1 patent drawing

AI summary

In a microfluidic device, a channel is connected to a first container, a culture solution flows through the channel, and a biological sample is disposed in the culture solution. The controller moves the culture solution in the channel to change a liquid amount of the culture solution in the first container. A first light source irradiates the culture solution with a first light passing through a liquid surface of the culture solution. A first light detector detects a first light intensity that is an intensity of the first light that has passed through the culture solution in the first container at a first timing, and a second light intensity that is an intensity of the first light that has passed through the culture solution in the first container at a second timing.