Multi-Chamber Blood Separation Container for Mononuclear Cell Purity

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Solution Overview

Problem

Conventional biological sample isolation devices fail to isolate white blood cells effectively for cancer diagnosis, as they often mix white blood cells with a large quantity of specific gravity adjusters, reducing cell bioavailability.

Innovation Solution

A biological sample isolation container with an isolation chamber, collection chamber, waste liquid chamber, and siphon flow paths that utilize centrifugal force and siphoning to separate and collect specific components like mononuclear cells without mixing them with the adjuster, maintaining cell bioavailability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If conventional centrifugal isolation is used to separate white blood cells, then separation is achieved, but white blood cells are mixed with large quantity of specific gravity adjuster reducing cell bioavailability

Engineering Contradiction:
Improvepurity of isolated cellsVSAvoidcell bioavailability
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The container is divided into multiple functional chambers: isolation chamber for initial centrifugal separation, collection chamber for receiving and re-centrifuging the isolated component, and waste liquid chamber for disposal. This segmentation allows the specific component to be isolated and then re-processed to remove the specific gravity adjuster, thereby improving cell bioavailability while maintaining separation purity

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent extracts the specific component (white blood cells) from the mixture of blood and specific gravity adjuster through centrifugal separation. The isolated component is then transferred to the collection chamber where it is re-centrifuged to separate the cells from the specific gravity adjuster, effectively extracting the harmful substance while preserving the valuable cells

Inventive Principle:
Principle #2Taking out (Extraction)

2Ease of operation

If manual collection of isolated components is performed, then flexibility is maintained, but labor intensity and potential contamination increase

Engineering Contradiction:
Improveautomation of collection processVSAvoidcontamination risk
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The system performs automatic collection through the integrated multi-chamber container design with siphon flow paths that enable automated transfer of liquids between chambers. The container itself provides the collection function through its structured chambers, eliminating the need for manual intervention and reducing contamination risk while maintaining operational ease

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

The device efficiently isolates and collects mononuclear cells without reducing their bioavailability, ensuring high-quality samples for diagnostic purposes.

Implementation Method 1

The siphon flow path connects the isolation chamber and the collection chamber, and uses siphoning to send the liquid, which contains a specific component that has been isolated for each component by centrifuging of the biological sample and reagent, from the isolation chamber to the collection chamber

Methodology Applied
Scientific EffectSiphoning: Syphon

Implementation Method 2

biological sample isolation container that is placed in a rotating device and rotates around a specific rotation center to apply centrifugal force, thereby collecting a specific component contained in a biological sample that has been isolated for each component

Methodology Applied
Scientific EffectCentrifugal force: Centrifugal Force

Implementation Method 3

The collection chamber holds the specific component centrifuged in the isolation chamber, some of the reagent, and a first component contained in the biological sample, which have been sent from the isolation chamber, and after these are suspended, causes only the specific component to settle outward in the radial direction in which centrifugal force is applied

Methodology Applied
Scientific EffectCentrifugal separation: Centrifugal Separation

Implementation Method 4

The second siphon flow path connects the collection chamber and the waste liquid chamber, and uses siphoning to send the waste liquid from the collection chamber to the waste liquid chamber, out of the liquid stored in the collection chamber

Methodology Applied
Scientific EffectSiphoning: Syphon

Data Source

PatentEP4675249A1Biological sample separation container, biological sample separation control device, biological sample separation control method, and biological sample separation control program
Publication Date: 2026.01.07 PHC HLDG CORP
  • EP4675249A1 patent drawingFigure 1
  • EP4675249A1 patent drawingFigure 2
  • EP4675249A1 patent drawingFigure 3

AI summary

A container (30) is provided with an isolation chamber (33), a collection chamber (34), a waste liquid chamber (35), a siphon flow path (33a), and a siphon flow path (34a). The isolation chamber (33) holds a specific gravity adjusting agent (L2) and blood (L1), which have been layered. The collection chamber (34) holds a centrifuged mononuclear cell layer (L4), some of the specific gravity adjusting agent (L2), and plasma (L5), and allows the mononuclear cell layer (L4) to settle in a liquid after being suspended. The waste liquid chamber (35) holds the supernatant liquid of the suspension as waste liquid. The siphon flow path (33a) connects the isolation chamber (33) and the collection chamber (34), and uses siphoning to send a liquid containing the mononuclear cell layer (L4). The siphon flow path (34a) connects the collection chamber (34) and the waste liquid chamber (35), and uses siphoning to send the waste liquid.