Biomimetic Fetal Chamber With Sterile Amniotic Fluid Recirculation

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing extracorporeal systems for premature fetal development outside the womb face challenges in maintaining asepsis, facilitating fetal movement, protecting the umbilical cord connection, and preventing skin ulcers, while replicating the natural amniotic fluid environment in an environmentally friendly and biomimetic manner.

Innovation Solution

A fetal chamber system with a biomimetic design comprising a first and second section with sealing means, an amniotic fluid circuit, and umbilical cord protection, along with features to prevent pressure ulcers, allows for easy fetal transfer and maintains a sterile, movable environment.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If artificial amniotic fluid is continuously replaced to prevent bacterial and viral development, then asepsis is maintained, but cost increases and environmental damage occurs

Engineering Contradiction:
ImproveasepsisVSAvoidamniotic fluid
Core Design Contradiction:
ReliabilityVSLoss of substance

Solution Approach 1:

The system recycles amniotic fluid by filtering it through a membrane filter and UV sterilization unit, then returning the purified fluid to the fetal chamber. This eliminates continuous fluid replacement while maintaining asepsis, reducing both cost and environmental impact.

Inventive Principle:
Principle #34Discarding and recovering

Solution Approach 2:

The amniotic fluid circulation system operates continuously, constantly filtering and sterilizing fluid to maintain aseptic conditions without interruption. This continuous action replaces the need for periodic complete fluid replacement.

Inventive Principle:
Principle #20Continuity of useful action

2Strength

If the fetal chamber is designed as a single integrated unit, then structural integrity is maintained, but ease of fetal transfer is reduced

Engineering Contradiction:
Improvestructural integrityVSAvoidfetal transfer
Core Design Contradiction:
StrengthVSEase of operation

Solution Approach 1:

The fetal chamber is divided into a first section containing the fetal bed and a second section, connected by a connection area. This segmentation allows the fetal bed to be accessed and manipulated independently for easy fetal transfer while maintaining the overall structural integrity of the complete chamber system.

Inventive Principle:
Principle #1Segmentation

3Strength

If the fetal bed is made completely rigid to ensure containment, then structural support is provided, but fetal movement is restricted and skin ulcers occur

Engineering Contradiction:
ImprovecontainmentVSAvoidskin ulcers
Core Design Contradiction:
StrengthVSObject-affected harmful factors

Solution Approach 1:

The fetal bed combines rigid and elastic materials in different regions. The rigid portions provide structural support and containment, while the elastic portions allow fetal movement and prevent pressure points. This local differentiation of material properties prevents skin ulcers while maintaining containment.

Inventive Principle:
Principle #3Local quality

4Ease of operation

If the umbilical cord connection is exposed to allow access, then ease of connection is maintained, but risk of cord accidents increases

Engineering Contradiction:
Improveconnection accessVSAvoidcord safety
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The system includes a protection means positioned in the connection area that shields the umbilical cord connection point from accidental damage. This protective barrier is in place before any potential harm can occur, allowing cord access to be maintained while preventing accidents.

Inventive Principle:
Principle #11Beforehand cushioning (Prior cushioning)

5Reliability

If the fetal chamber is kept closed to maintain sterile environment, then asepsis is preserved, but fetal movement freedom is reduced

Engineering Contradiction:
ImproveasepsisVSAvoidfetal movement
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The fetal chamber incorporates an elastic film that provides a flexible, sealed enclosure. This flexible membrane maintains the sterile closed environment while allowing fetal movements to occur freely within the confined space, accommodating both asepsis requirements and movement needs.

Inventive Principle:
Principle #30Flexible shells and thin films

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 system provides a biomimetic environment for premature fetal development, reducing infection risk, minimizing umbilical cord accidents, and preventing ulcers, while efficiently recycling and sterilizing amniotic fluid, thus improving survival rates of extremely premature fetuses.

Implementation Method 1

an amniotic fluid unit configured to sterilise the amniotic fluid

Methodology Applied
Scientific EffectSterilization:

Implementation Method 2

a pump configured to pump the amniotic fluid from the at least one fluid outlet port into the amniotic fluid unit and out from the amniotic fluid unit into the at least one fluid inlet port

Methodology Applied
Scientific EffectPumping: Pump

Implementation Method 3

an elastic film comprising at least one fluid inlet port

Methodology Applied
Scientific EffectElasticity: Elasticity

Data Source

PatentEP4663177A1Chamber system for mammalian fetal development and maturation
Publication Date: 2025.12.17 HOSPITAL SANT JOAN DE DEU
  • EP4663177A1 patent drawingFigure 1
  • EP4663177A1 patent drawingFigure 2
  • EP4663177A1 patent drawingFigure 3~4

AI summary

The present invention refers to a system for maturing a premature mammalian fetus. The system comprises a fetal chamber and an amniotic fluid circuit. The fetal chamber comprises a first section, a second section and a connection area. The first section comprises a first rigid frame, an elastic film comprising at least one fluid inlet port; and a first sealing means. The second section comprises a second rigid frame, a fetal bed comprising at least one fluid outlet port and a second sealing means. The connection area comprises at least one opening. The first and second sections have an open position and a closed position. The amniotic fluid circuit is configured to provide an amniotic fluid to and from the fetal chamber and to sterilise the amniotic fluid. The system maintains asepsis, facilitates transfer from the mother's uterus, allows a certain degree of movements and prevents skin damage and ulcers.