Amniotic Fluid Filtration Chamber for Sterile Low-Clog Cell Recovery

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Solution Overview

Problem

Existing filtering techniques for amniotic fluid are ineffective due to clogging, inadequate handling of variable particulate matter sizes, and the need for complex and non-sterile processes, which compromises the quality of amniotic cell samples.

Innovation Solution

A filtering apparatus and method that includes a sealed chamber with a filter, inlet and outlet connectors, and optional pumps to ensure aseptic handling and minimize clogging, allowing for effective filtration of amniotic fluid with varying particulate sizes, maintaining high cell quality.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If larger filtration units are used to filter larger amounts of TAF, then filtering capacity is improved, but clogging risk increases which impedes filtering capacity

Engineering Contradiction:
Improvefiltering capacityVSAvoidclogging risk
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The filter is divided into multiple filtration layers with different pore sizes. A pre-filter layer with larger pores (10-100 μm) captures large particulate matter first, while a main filter layer with smaller pores (1-10 μm) captures smaller particles. This segmentation prevents clogging of the main filter by distributing the filtration load across layers with progressively smaller pores.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The pre-filter layer performs preliminary filtration of large particulate matter (hair, vernix) before the fluid reaches the main filter layer. This preliminary action removes the bulk of contaminants that would otherwise clog the main filter, enabling sustained high-capacity filtration without clogging.

Inventive Principle:
Principle #10Preliminary action

2Productivity

If complex filtering solutions are used to handle variable particulate matter sizes, then filtering effectiveness is improved, but device complexity increases

Engineering Contradiction:
Improvefiltering effectivenessVSAvoidfiltering system complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The filter comprises a pre-filter layer with larger pores (10-100 μm) for capturing large particulate matter and a main filter layer with smaller pores (1-10 μm) for capturing smaller particles. This segmented multi-layer structure effectively handles the variable size range of particulate matter in amniotic fluid without requiring complex external filtration systems.

Inventive Principle:
Principle #1Segmentation

3Productivity

If previous filtering techniques are used to remove particulate matter, then some filtration is achieved, but cell loss increases due to clogged pores

Engineering Contradiction:
Improveparticulate matter removalVSAvoidcell loss
Core Design Contradiction:
ProductivityVSLoss of substance

Solution Approach 1:

The segmented multi-layer filter structure with progressive pore size reduction (10-100 μm pre-filter, then 1-10 μm main filter) allows efficient particulate matter removal while maintaining open pores for cell passage. The pre-filter captures large contaminants that would otherwise clog the main filter and trap cells, thereby reducing cell loss while achieving effective filtration.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Different regions of the filter have different pore sizes optimized for different functions: the pre-filter layer has larger pores suited for capturing large particulate matter, while the main filter layer has smaller pores for capturing finer particles. This local quality variation ensures effective filtration across different particle size ranges while maintaining cell viability.

Inventive Principle:
Principle #3Local quality

4Device complexity

If non-sterile filtering processes are used to simplify the apparatus, then device complexity is reduced, but sample quality deteriorates

Engineering Contradiction:
Improveprocess simplicityVSAvoidsample quality
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The filter apparatus is designed as a disposable sterile unit that is pre-packaged and ready-to-use. This eliminates the need for complex sterilization procedures and repeated sterilization cycles, simplifying the overall process while ensuring sample quality. The disposable nature guarantees sterility without adding operational complexity.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

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 apparatus provides efficient, sterile filtration with reduced clogging risk, enabling the recovery of a higher fraction of amniotic cells with improved quality, suitable for pharmaceutical applications.

Implementation Method 1

a filter for filtering the particulate matter from the amniotic fluid... in use, the amniotic fluid pass the filter when flowing from the fluid inlet to the fluid outlet, whereby particulate matter is deposited on the filter

Methodology Applied
Scientific EffectPhysical filtration: Filter (physical)

Implementation Method 2

an inlet connector arranged to form a sealing connection between the fluid inlet and an amniotic fluid sample source

Methodology Applied
Scientific EffectSealing:

Data Source

PatentUS12465878B2Apparatus for filtering amniotic fluid
Publication Date: 2025.11.11 AMNIOTICS AB
  • US12465878B2 patent drawing
  • US12465878B2 patent drawing
  • US12465878B2 patent drawing

AI summary

An apparatus for filtering amniotic fluid containing particulate matter and amniotic cells is disclosed, comprising a filter for filtering the particulate matter from the amniotic fluid, a chamber enclosing the filter, wherein the chamber comprises a fluid inlet and a fluid outlet, and an inlet connector arranged to form a sealing connection between the fluid inlet and an amniotic fluid sample source, wherein, in use, the amniotic fluid pass the filter when flowing from the fluid inlet to the fluid outlet, whereby particulate matter is deposited on the filter and the amniotic fluid flows through the fluid outlet containing amniotic cells.