Peptone-Based Pharmaceutical Foam for Stable Medical Applications

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing pharmaceutical foams prepared from full-length proteins lack sufficient strength and durability, which is crucial for medical and surgical applications, as they often require higher molecular mass for stability but result in foams that are not strong enough for extended use or repeated applications.

Innovation Solution

The development of a pharmaceutical foam composition using peptones, which are short peptide lengths obtained by enzymatic hydrolysis of full-length proteins, creating a stable foam with superior compression strength and durability, free from the full-length protein, and optionally including fibrin, fibrinogen, and thrombin for enhanced properties.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Stability of the object's composition

If full-length proteins are used as surfactants to form foam, then the foam can be formed with higher molecular mass providing stability, but the compression strength and durability of the foam are insufficient for extended medical use

Engineering Contradiction:
Improvefoam stabilityVSAvoidcompression strength
Core Design Contradiction:
Stability of the object's compositionVSStrength

Solution Approach 1:

The full-length protein is segmented into smaller peptide fragments through enzymatic hydrolysis. These peptide fragments (e.g., 90 or fewer amino acids) maintain the ability to form stable micelles and foam structures while providing superior compression strength and durability compared to full-length proteins.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The molecular mass parameter of the surfactant is changed from full-length protein (high molecular mass) to peptone/peptide fragments (lower molecular mass). This parameter change resolves the contradiction by showing that lower molecular mass peptides can achieve both foam stability and enhanced compression strength.

Inventive Principle:
Principle #35Parameter changes

2Stability of the object's composition

If full-length proteins are used to prepare foam, then the foam structure can be maintained, but the immunogenicity remains high which limits medical application safety

Engineering Contradiction:
Improvefoam structureVSAvoidimmunogenicity
Core Design Contradiction:
Stability of the object's compositionVSObject-affected harmful factors

Solution Approach 1:

Segmenting the full-length protein into smaller peptide fragments through enzymatic hydrolysis reduces the immunogenicity while preserving the foam-forming capability. The peptide fragments maintain structural integrity for foam formation but present fewer immunogenic epitopes.

Inventive Principle:
Principle #1Segmentation

3Duration of action of stationary object

If full-length proteins are used as foam basis, then the foam can be formed, but the degradation rate in vivo is slow which delays wound healing

Engineering Contradiction:
Improvefoam durabilityVSAvoiddegradation time
Core Design Contradiction:
Duration of action of stationary objectVSDuration of action of moving object

Solution Approach 1:

Changing the molecular size parameter from full-length protein to peptone/peptide fragments creates a foam that degrades faster in vivo. The smaller peptide fragments are more readily broken down by proteolytic enzymes in the body, accelerating degradation while maintaining sufficient durability for the intended application duration.

Inventive Principle:
Principle #35Parameter changes

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 peptone-based foam exhibits higher tensile strength, reduced immunogenicity, increased adhesiveness, and faster in-vivo degradation, making it more suitable for medical applications such as wound healing, hemostasis, and anti-adhesion, while maintaining stability and structural integrity over time.

Implementation Method 1

peptones prepared by enzymatic hydrolysis of a full-length protein

Methodology Applied
Scientific EffectEnzymatic hydrolysis: Hydrolysis

Implementation Method 2

an amphiphilic agent is required i.e. a molecule which has both a hydrophilic group and a hydrophilic group, allowing the strands of denatured proteins to form micelles, within which gas, such as air, is trapped

Methodology Applied
Scientific EffectMicelle formation: Amphiphiles

Implementation Method 3

the addition of a surfactant is generally required in order to reduce the surface tension of the liquid, enabling mixing of the gas with the liquid to form a stable foam

Methodology Applied
Scientific EffectSurface tension reduction: Surface Tension

Data Source

PatentUS11938165B2Stable pharmaceutical foam
Publication Date: 2024.03.26 OMRIX BIOPHARMACEUTICALS LTD
  • US11938165B2 patent drawing
  • US11938165B2 patent drawing
  • US11938165B2 patent drawing

AI summary

Provided are pharmaceutical foam compositions comprising a peptone, a peptide hydrolysate or an enzymatically-hydrolyzed protein prepared by enzymatic hydrolysis of a full-length protein; methods of preparation and uses thereof.