Trapezoidal Microchamber for Stable 3D Cell Rotation

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Solution Overview

Problem

Conventional systems face challenges in performing 3D hydrodynamic microvortical rotation of live single cells or cell clusters for 3D microscopy, particularly in maintaining stable rotation axes perpendicular to the optical axis, which is crucial for high-resolution volumetric imaging.

Innovation Solution

A microfluidic device with a trapezoidal microchamber is used, where fluid communication is established between the microchamber and a main flow channel, enabling recirculating flow and optical trapping to rotate cells around a stable axis perpendicular to the optical axis, facilitating 3D imaging.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If conventional microfluidic systems are used for cell rotation, then 2D rotation about an axis parallel to the optical axis is achieved, but 3D rotation about an axis perpendicular to the optical axis cannot be realized

Engineering Contradiction:
Improverotation capabilityVSAvoiddevice structure
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent transitions from 2D rotation (parallel to optical axis) to 3D rotation (perpendicular to optical axis) by introducing a new spatial dimension for the rotation axis. This is achieved through a microvortex chamber with a specific geometric configuration that generates rotational flow perpendicular to the optical detection axis, enabling true three-dimensional cell imaging.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Solution Approach 2:

The device is divided into functionally distinct segments: a microvortex chamber for generating rotational flow, an optical trapping region for positioning cells, and an imaging region for detection. This segmentation allows each component to be optimized independently while working together to achieve 3D rotation capability.

Inventive Principle:
Principle #1Segmentation

2Reliability

If optical trapping is used to position cells at the center of microvortex, then rotation control is improved, but system complexity and cost increase

Engineering Contradiction:
Improverotation stabilityVSAvoidsystem components
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The microvortex chamber geometry is designed to automatically generate stable rotational flow patterns that inherently trap and rotate cells without requiring external optical trapping systems. The recirculating flow field itself provides the positioning and rotation function, making the system self-sufficient and eliminating complex optical trapping apparatus.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent replaces the optical trapping mechanism (which requires complex laser systems and optical components) with a hydrodynamic trapping mechanism based on microvortex flow. This mechanical/fluid-based approach achieves the same cell positioning and rotation function with simpler, more robust equipment.

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

3Ease of operation

If diamond shaped side chambers are used for microvortex formation, then cell rotation is achieved, but vortex stability is insufficient

Engineering Contradiction:
Improverotation functionVSAvoidmicrovortex stability
Core Design Contradiction:
Ease of operationVSStability of the object's composition

Solution Approach 1:

The patent optimizes the geometric parameters of the microvortex chamber, specifically using a trapezoidal cross-section with carefully selected angles and aspect ratios. This geometric parameter optimization creates flow conditions that enhance vortex stability and maintain consistent rotational characteristics over time, addressing the instability issue of conventional diamond-shaped chambers.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The microvortex chamber employs an asymmetric trapezoidal geometry rather than a symmetric diamond shape. This asymmetry in the chamber design creates a more stable recirculating flow pattern that maintains consistent vortex formation and rotation, improving upon the symmetry-based designs that suffer from stability issues.

Inventive Principle:
Principle #4Asymmetry

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 allows for precise and stable 3D rotation of cells, enabling high-resolution volumetric imaging with minimal perturbation, providing comprehensive views of cells beyond traditional 2D imaging.

Implementation Method 1

3D hydrodynamic microvortical rotation of at least one live single cell or cell cluster

Methodology Applied
Scientific EffectHydrodynamic microvortex: Vortex Ring

Implementation Method 2

recirculating flow profile

Methodology Applied
Scientific EffectRecirculating flow: Convection

Implementation Method 3

an optical trap may be used to position the cell at the center of the microvortex

Methodology Applied
Scientific EffectOptical trapping: Optical Tweezers

Data Source

PatentUS10162162B2Microfluidic systems and methods for hydrodynamic microvortical cell rotation in live-cell computed tomography
Publication Date: 2018.12.25 THE ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIV OF ARIZONA
  • US10162162B2 patent drawing
  • US10162162B2 patent drawing
  • US10162162B2 patent drawing

AI summary

Microfluidic devices for 3D hydrodynamic microvortical rotation of at least one live single cell or cell cluster, systems incorporating the devices, and methods of fabricating and using the devices and systems, are provided. A microfluidic chip rotates at least one live single cell or cell cluster in a microvortex about a stable rotation axis perpendicular to an optical axis within a chamber having a trapezoidal cross-sectional shape located below a flow channel. An optical trap may be used to position the cell or cells with the microvortex, and the cell or cells may be subject to live-cell or cell cluster computer tomography imaging.