Concentrated Clotting Factor Composition for Adhesion Prevention

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Solution Overview

Problem

Postoperative adhesions following abdominal surgery are common and can lead to serious medical consequences such as pain, infertility, and bowel obstruction, as they are formed due to excessive activity of cells producing extracellular matrix proteins, and existing solutions fail to effectively prevent or reduce their severity.

Innovation Solution

A purified composition comprising fibrinogen-depleted plasma-derived clotting factors like proaccelerin (factor V), prothrombin (factor II), proconvertin (factor VII), and Stuart-Prower factor (factor X), concentrated to enhance clotting at surgical sites and applied topically to reduce adhesion formation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional adhesion prevention methods are used, then adhesion formation is reduced, but the effectiveness is insufficient to prevent serious medical consequences

Engineering Contradiction:
Improveadhesion prevention effectivenessVSAvoidadhesion severity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent concentrates specific clotting factors (V, VII, X, and prothrombin) to high levels (300%-2000% above normal plasma concentrations) to enhance the coagulation response at the surgical site, creating a more reliable adhesion prevention effect through parameter optimization rather than using standard concentrations

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent extracts and isolates specific clotting factors (V, VII, X, and prothrombin) from plasma while deliberately removing or depleting fibrinogen, creating a targeted composition that provides adhesion prevention without the harmful effects of excessive fibrin deposition associated with conventional plasma-based solutions

Inventive Principle:
Principle #2Taking out (Extraction)

2Strength

If fibrinogen-rich plasma is applied to promote clotting, then clot formation is enhanced, but excessive fibrin deposition occurs leading to increased adhesion formation

Engineering Contradiction:
Improveclotting capabilityVSAvoidfibrin deposition
Core Design Contradiction:
StrengthVSObject-generated harmful factors

Solution Approach 1:

The patent converts the potential harm of fibrinogen (which can lead to excessive fibrin deposition and adhesion formation) into a benefit by completely depleting fibrinogen from the composition, while retaining and concentrating other clotting factors that promote clotting through alternative pathways, thus achieving clot formation without the harmful fibrin byproduct

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Solution Approach 2:

The patent creates a localized clotting environment by applying a composition with highly concentrated specific clotting factors directly at the surgical site, where these factors activate the coagulation cascade locally to form clots that prevent adhesion without causing systemic or widespread fibrin deposition

Inventive Principle:
Principle #3Local quality

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 composition effectively reduces adhesion severity by forming a local clot at the wound site, preventing excessive fibrin deposition and adhesion formation, thereby improving healing and reducing long-term complications.

Implementation Method 1

The composition effectively reduces adhesion severity by forming a local clot at the wound site

Methodology Applied
Scientific EffectCoagulation: Coagulation

Data Source

PatentEP3400029B1Compositions for reducing tissue adhesions
Publication Date: 2022.03.02 EIO BIOMEDICAL LTD
  • EP3400029B1 patent drawingFigure 1
  • EP3400029B1 patent drawingFigure 2A
  • EP3400029B1 patent drawingFigure 2B

AI summary

The present invention provides a composition, comprising: proaccelerin (factor V) and at least one factor selected from the group consisting of: prothrombin (factor II), proconvertin (factor VII), and Stuart-Prower factor (factor X), wherein an amount of the proaccelerin in the composition is between 75% to 750% compared to an amount of proaccelerin in a blood plasma, and wherein an amount of the at least one factor is from 150% to 3000% compared to an amount of the at least one factor in the blood plasma; wherein the amount of proaccelerin and the at least one factor in the composition is determined by extrapolating an observed activity of the composition at a concentration of 500mM NaCl, using a prothrombin complementation assay using a standard curve constructed using the blood plasma.