Flow Cell Immobilization Using Density and Magnetic Positioning

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Solution Overview

Problem

Existing flow cell technologies face challenges in achieving balanced immobilization of target materials across opposed sequencing surfaces, leading to uneven distribution and migration of sequencing-ready nucleic acid fragments and other target materials, which affects sequencing efficiency and readability of spatial clouds.

Innovation Solution

The method involves using fluids with different densities or a combination of magnetic forces and magnetically responsive target materials to immobilize target materials on both sequencing surfaces, ensuring even distribution by applying conditions that cause materials to migrate to respective surfaces based on their properties such as density, charge, or magnetism.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional flow cell technologies are used, then sequencing reactions can be performed, but the target materials become unevenly distributed and migrate during the process

Engineering Contradiction:
Improvedistribution uniformityVSAvoidspatial distribution stability
Core Design Contradiction:
Manufacturing precisionVSStability of the object's composition

Solution Approach 1:

The patent applies magnetic forces as a counteracting mechanism to balance the gravitational settling of magnetic bead-target material complexes. By introducing a magnetic field through a magnet positioned near the flow cell, the magnetic attraction force counterweights the gravitational force, preventing migration and achieving uniform distribution of target materials across the flow cell surface.

Inventive Principle:
Principle #8Anti-weight (Counterweight)

Solution Approach 2:

The patent changes the physical state and distribution characteristics of target materials by adjusting magnetic field parameters. By varying the strength and configuration of the magnetic field, the patent controls the positioning and distribution of magnetic bead complexes, transforming them from a gravitationally-driven settled state to a magnetically-controlled uniform distribution state.

Inventive Principle:
Principle #35Parameter changes

2Quantity of substance

If target materials are introduced into the flow cell, then sequencing-ready nucleic acid fragments become available, but they migrate and fail to maintain even distribution

Engineering Contradiction:
Improvetarget material availabilityVSAvoidspatial distribution uniformity
Core Design Contradiction:
Quantity of substanceVSManufacturing precision

Solution Approach 1:

The magnetic force generated by the external magnet counterweights the gravitational force acting on the magnetic bead-target material complexes. This balance prevents the complexes from settling and migrating, maintaining their uniform spatial distribution throughout the flow cell while preserving the quantity of available target materials for sequencing.

Inventive Principle:
Principle #8Anti-weight (Counterweight)

Solution Approach 2:

The patent introduces a magnetic field as an intermediary force field between the external magnet and the magnetic bead-target material complexes. This intermediary magnetic field mediates the interaction, providing controlled attraction that maintains uniform distribution without requiring direct physical contact or mechanical manipulation of the target materials.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Reliability

If conventional immobilization methods are used, then target materials can be attached to surfaces, but sequencing efficiency and readability are reduced due to uneven distribution

Engineering Contradiction:
Improveimmobilization effectivenessVSAvoidsequencing efficiency
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

By balancing gravitational and magnetic forces, the patent achieves reliable immobilization of target materials in a uniform distribution pattern. This prevents the clustering and migration that occur with conventional methods, thereby improving sequencing efficiency and the readability of spatial clouds without compromising immobilization effectiveness.

Inventive Principle:
Principle #8Anti-weight (Counterweight)

Solution Approach 2:

The patent creates a magnetically-controlled equipotential environment within the flow cell where magnetic bead-target material complexes experience balanced forces. This equipotential state ensures uniform distribution and stable immobilization across the entire flow cell surface, maximizing the effective area for sequencing reactions and improving overall productivity.

Inventive Principle:
Principle #12Equipotentiality

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

This approach results in a more uniform distribution of target materials across sequencing surfaces, improving sequencing metrics and readability of spatial clouds, thereby enhancing the overall utilization and efficiency of the flow cell.

Implementation Method 1

applying a magnetic force to another of the two opposed sequencing surfaces, thereby pulling some other of the target material to the other of the two opposed sequencing surfaces

Methodology Applied
Scientific EffectMagnetic force: Magnetic Field

Implementation Method 2

one of: the first fluid has a density less than a density of the target material and the second fluid has a density greater than the density of the target material

Methodology Applied
Scientific EffectDensity gradient: Density Gradient

Data Source

PatentUS20250361557A1Immobilization in flow cells
Publication Date: 2025.11.27 ILLUMINA INC
  • US20250361557A1 patent drawing
  • US20250361557A1 patent drawing
  • US20250361557A1 patent drawing

AI summary

In an example, a target material is immobilized on two opposed sequencing surfaces of a flow cell using first and second fluids. The first fluid has a density less than a target material density and the second fluid has a density greater than the target material density; or the second fluid has a density less than the target material density and the first fluid has a density greater than the target material density. The first fluid (including the target material) is introduced into the flow cell, whereby at least some of the target material becomes immobilized by capture sites on one of the sequencing surfaces. The first fluid and non-immobilized target material are removed. The second fluid (including target material) is introduced into the flow cell, whereby at least some of the target material becomes immobilized by capture sites on another of the sequencing surfaces.