Automated Fluidic Disc for Cell Isolation
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Solution Overview
Problem
Current methods for isolating specific cells from blood or bone marrow are inefficient and unreliable, posing challenges for regenerative medicine and fetal gene diagnosis, particularly in ensuring the quality and safety of immune cells, T-cells, and fetal nucleated red blood cells.
Innovation Solution
An automated system utilizing a fluidic disc mounted on a centrifuge rotor, which manipulates cells through centrifugal forces and fluid channeling, enables the reliable isolation of immune cells, T-cells, and fetal nucleated red blood cells by separating blood components based on density and size, using computer-controlled actuators and sensors to manage the process.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If manual cell isolation methods are used, then operational flexibility is maintained, but reliability and consistency of cell isolation quality deteriorates
Solution Approach 1:
The system uses automated feedback control where sensors detect cell concentration and composition in real-time, and the control system automatically adjusts centrifugal force and fluid flow parameters to maintain optimal isolation conditions without continuous manual intervention
Solution Approach 2:
The patent replaces manual mechanical operations with an automated control system that uses sensors, computers, and algorithms to control centrifugal separation and fluid manipulation, ensuring consistent and reliable cell isolation
2Productivity
If automated processing is implemented, then productivity and consistency are improved, but device complexity increases
Solution Approach 1:
The fluidic disc integrates multiple functions including sample loading, centrifugal separation, cell concentration, and harvest into a single rotating component, allowing automated processing while reducing the number of separate devices needed
Solution Approach 2:
The system nests the fluidic disc within the centrifuge rotor, with the disc containing multiple chambers and channels that perform sequential processing steps, enabling complex automated operations within a compact structure
3Speed
If centrifugal force is increased to separate cells faster, then separation speed improves, but cell damage risk increases
Solution Approach 1:
The system dynamically adjusts centrifugal force parameters during different stages of processing, using lower speeds for initial separation and higher speeds for final concentration, optimizing both speed and cell integrity
Solution Approach 2:
Sensors monitor cell separation progress in real-time and provide feedback to the control system, which automatically adjusts centrifugal force to achieve optimal separation while preventing excessive force that could damage cells
4Productivity
If fluid manipulation is used to concentrate cells, then cell concentration efficiency improves, but system complexity increases
Solution Approach 1:
The system uses pneumatic actuators and fluid pressure control to manipulate cell-containing fluids through channels and chambers in the rotating disc, enabling automated cell concentration without complex mechanical manipulation
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 system allows for precise and safe isolation of targeted cells for patient treatment and fetal gene diagnosis, reducing the risk of miscarriage and ensuring high-quality cell samples for medical applications.
Implementation Method 1
The fluidic disc is mounted to a spinning rotor and it is used to manipulate cells by channeling fluids while subjected to centrifugal forces
Implementation Method 2
separating blood components based on density and size
Data Source
AI summary
The present invention provides an automated system and method to isolate nucleated blood cells from whole blood or bone marrow. A disc mounted to a centrifuge system with spinning rotor is used to manipulate cells by channeling fluids while subjected to high gravitational field. The disc embodies at least two axisymmetric processing stations connected by a circular channel. Each station contains multiple chambers connected by fluidic channels to controllably transfer fluids. First stage separation allows for the isolation of the buffy coat layer while the second stage separation utilizes gradient density fluids to isolate the targeted nucleated cells from the buffy coat layer in the spinning disc.


