In Situ Hemostatic Foam Implants for Closed-Cavity Bleeding

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Solution Overview

Problem

Existing polymers used for wound treatment often irritate skin and internal tissues, lack suitable mechanical properties, are not biodegradable, and are difficult to deploy within body cavities, making them unsuitable for immediate hemorrhage control in situations where surgical access is limited.

Innovation Solution

A method involving the introduction of a flowable polymer formulation into a body cavity, which foams to form an elastomeric polymer foam, cross-links, and applies pressure to limit bleeding, using mechanisms such as cross-linking condensation polymers, polyol and polyisocyanate mixtures, or two-part formulations to create conformal contact with bleeding injuries.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Object-affected harmful factors

If traditional polymers are used for wound treatment, then they provide basic wound coverage, but they irritate skin and internal tissues

Engineering Contradiction:
Improvetissue irritationVSAvoidbiocompatibility
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

The patent modifies polymer parameters by incorporating hydrophilic groups (such as carboxyl, hydroxyl, or amide groups) into the polymer structure, changing the chemical composition to reduce tissue irritation while maintaining wound coverage functionality

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates composite materials by combining biodegradable polymer matrices with hydrophilic additives or coating layers, resulting in a multi-component system that provides both wound coverage and reduced tissue irritation

Inventive Principle:
Principle #40Composite materials

2Strength

If traditional polymers are used for wound treatment, then they provide structural support, but they lack suitable mechanical properties for internal body use

Engineering Contradiction:
Improvemechanical supportVSAvoidsuitability for internal body use
Core Design Contradiction:
StrengthVSAdaptability or versatility

Solution Approach 1:

The patent adjusts mechanical parameters by controlling polymer molecular weight, cross-linking density, and crystallinity to achieve optimal balance between strength and softness suitable for internal body applications

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates regions with different mechanical properties within the polymer structure, such as a stronger outer layer for structural support and a softer inner layer for tissue compatibility

Inventive Principle:
Principle #3Local quality

3Ease of operation

If traditional polymers are used for wound treatment, then they can be applied to wounds, but they are difficult to place within body cavities

Engineering Contradiction:
Improvewound applicationVSAvoidplacement difficulty in body cavities
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The patent utilizes phase transition by formulating polymers that transition from a flowable state during injection to a gel or solid state after placement in the body cavity, enabling easy delivery through catheters followed by in situ stabilization

Inventive Principle:
Principle #36Phase transitions

Solution Approach 2:

The patent creates dynamically adjustable polymer formulations that change their flow properties in response to environmental conditions such as temperature or pH, allowing for easy injection when cool/liquid and stable placement when warm/gel-like

Inventive Principle:
Principle #15Dynamics

4Reliability

If traditional polymers are used for hemorrhage control, then they can be applied to wounds, but they are not sufficiently biodegradable for internal body cavity use

Engineering Contradiction:
Improvehemorrhage control effectivenessVSAvoidbiodegradability
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent modifies the chemical structure of polymers by incorporating biodegradable linkages (such as ester bonds) and adjusting molecular weight and composition to achieve controlled degradation rates that maintain hemorrhage control effectiveness while enabling safe resorption in the body

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent extracts non-biodegradable components from the polymer formulation and replaces them with biodegradable alternatives, removing the harmful accumulation effect while preserving the hemorrhage control function

Inventive Principle:
Principle #2Taking out (Extraction)

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 polymer foam effectively stabilizes bodily fluids and supports tissues by conformally adhering to wounds, providing mechanical support and limiting fluid movement, even in closed body cavities without requiring knowledge of injury sites, and is biodegradable.

Implementation Method 1

cross-linking a condensation polymer of a polyol and a polyacid within a body cavity

Methodology Applied
Scientific EffectCross-linking: Chemical Bonding

Implementation Method 2

cross-linking a condensation polymer of a polyol and a polyacid within a body cavity

Methodology Applied
Scientific EffectCondensation reaction: Chemical Bonding

Implementation Method 3

applies pressure to limit bleeding

Methodology Applied
Scientific EffectMechanical pressure: Pressure Increase

Data Source

PatentEP3922187B1In situ forming hemostatic foam implants
Publication Date: 2026.01.07 ARSENAL MEDICAL INC
  • EP3922187B1 patent drawingFigure 1A~1C
  • EP3922187B1 patent drawingFigure 2A~2B
  • EP3922187B1 patent drawingFigure 3

AI summary

Systems and methods related to polymer foams are generally described. Some embodiments relate to compositions and methods for the preparation of polymer foams, and methods for using the polymer foams. The polymer foams can be applied to a body cavity and placed in contact with, for example, tissue, injured tissue, internal organs, etc. In some embodiments, the polymer foams can be formed within a body cavity (i.e., in situ foam formation). In addition, the foamed polymers may be capable of exerting a pressure on an internal surface of a body cavity and preventing or limiting movement of a bodily fluid (e.g., blood, etc.).