Microfluidic Vapor Bubble Shear for Immunoassay Precision

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Micro, nano, and pico-liter scale immunoassays face challenges with non-specific binding (NSB) due to viscosity and surface tension forces in biological fluids, leading to reduced signal-to-noise ratios and assay imprecision, which current solutions like lateral flow and lab-on-a-chip devices fail to adequately address.

Innovation Solution

A device that generates fluid motion using a heating element to transform a fluid volume from a liquid to a vaporized state, creating shear forces and reducing NSB by enhancing the interaction between analytes and antibodies through controlled fluid displacement within a molecular binding site.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If diffusion is used as the primary mechanism for target and sensor collisions in laminar flow, then the device structure is simple, but the assay precision and signal-to-noise ratio are reduced due to non-specific binding

Engineering Contradiction:
Improveassay precisionVSAvoiddevice structure
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent introduces dynamic fluid motion through acoustic waves or magnetic fields to replace static diffusion-based mixing. This dynamic approach enhances target-sensor collision efficiency and reduces non-specific binding, thereby improving assay precision without requiring complex mechanical mixing components

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The patent replaces mechanical mixing systems with acoustic or magnetic field-based fluid manipulation. This substitution eliminates the need for mechanical moving parts while achieving enhanced mixing and reduced non-specific binding, resolving the contradiction between measurement precision and device complexity

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

2Measurement precision

If sample size is reduced to micro, nano, and pico-liter scales, then the sensitivity of detection is improved, but non-specific binding increases due to viscosity and surface tension forces

Engineering Contradiction:
Improvedetection sensitivityVSAvoidnon-specific binding
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The patent applies dynamic acoustic or magnetic fields to create fluid motion at micro, nano, and pico-liter scales. This dynamic manipulation overcomes the detrimental effects of viscosity and surface tension, reducing non-specific binding while maintaining high detection sensitivity through enhanced target-sensor interactions

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The patent changes the physical state and motion parameters of the fluid at micro-scale volumes by introducing acoustic waves or magnetic fields. This parameter change transforms the fluid from static diffusion-dominated flow to dynamic motion, reducing surface tension effects and non-specific binding while preserving detection sensitivity

Inventive Principle:
Principle #35Parameter changes

3Productivity

If static fluid conditions are maintained in laminar flow, then the device operation is simple, but the interaction efficiency between analytes and antibodies is reduced

Engineering Contradiction:
Improveinteraction efficiencyVSAvoidfluid motion control
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent replaces mechanical fluid motion systems with acoustic or magnetic field-based manipulation. This substitution achieves enhanced analyte-antibody interaction efficiency through field-induced fluid motion without introducing complex mechanical components, thereby improving productivity while maintaining operational simplicity

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 device significantly reduces non-specific binding and increases the efficiency of target and sensor collisions, improving the sensitivity and precision of immunoassays by actively managing fluid motion and shear forces at micro, nano, and pico-liter scales.

Implementation Method 1

heat the fluid volume interfaced with the heating element. The fluid volume may be heated in response to a voltage being applied to the heating element, with the heat transforming the fluid volume from a liquid state into a vaporized state

Methodology Applied
Scientific EffectPhase change (liquid to vapor): Phase Change

Implementation Method 2

The heating element may be a thermal ink-jetting (TIJ) resistor

Methodology Applied
Scientific EffectJoule heating: Joule Heating

Implementation Method 3

The vaporized state of the fluid volume may expand in a direction away from the heating element to encompass the heating element and at least a majority of the target fluid within the molecular binding site

Methodology Applied
Scientific EffectThermal expansion: Thermal Expansion

Data Source

PatentUS11318466B2Microfluidic fluid flow in a target fluid
Publication Date: 2022.05.03 HEWLETT PACKARD DEVELOPMENT COMPANY LP
  • US11318466B2 patent drawing
  • US11318466B2 patent drawing
  • US11318466B2 patent drawing

AI summary

One example includes a device that may include a heating element and a molecular binding site. The heating element may heat a fluid volume, interfaced with the heating element, in response to a voltage being applied to the heating element, the heat transforming the fluid volume from a liquid state into a vaporized state to generate fluid motion within the fluid volume. The molecular binding site may be disposed proximate to the heating element, in which a portion of the fluid volume expands when the fluid volume transforms from the liquid state into the vaporized state, the vaporized state of the fluid volume generating the fluid motion within a target fluid that is disposed within the molecular binding site.