Stem Cell Supernatant Fractionation for Cell Activation

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Solution Overview

Problem

The effectiveness of culture supernatants from deciduous tooth pulp stem cells in activating cells is unclear, and they may contain inhibitory components that hinder their efficacy.

Innovation Solution

A cell activator is developed by isolating a fraction from the culture supernatant of deciduous tooth pulp stem cells, excluding components below 3.5 kDa, and focusing on a 50 to 100 kDa range to enhance cell-activating activity while removing potential inhibitors.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If culture supernatant of deciduous tooth pulp stem cells is used directly, then it contains various growth factors and cytokines that may be useful, but it also contains components that act in an inhibitory manner on effective components

Engineering Contradiction:
Improvecell-activating efficacyVSAvoidinhibitory components
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent applies extraction by isolating and removing inhibitory components from the culture supernatant. Specifically, the inhibitory fraction is separated through chromatographic methods, and the effective cell-activating fraction is extracted and purified to create a composition free from harmful inhibitors while retaining beneficial growth factors and cytokines.

Inventive Principle:
Principle #2Taking out (Extraction)

2Reliability

If the culture supernatant is purified to remove inhibitory components, then cell-activating effects are enhanced, but the complexity of the preparation process increases

Engineering Contradiction:
Improvecell-activating effectsVSAvoidpurification process
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies segmentation by dividing the complex culture supernatant into distinct fractions based on their functional properties. Chromatographic separation divides the mixture into an inhibitory fraction and a cell-activating fraction, allowing each to be independently characterized and utilized. This segmentation simplifies the understanding of complex interactions and enables targeted purification.

Inventive Principle:
Principle #1Segmentation

3Reliability

If a specific molecular weight fraction (50 to 100 kDa) is isolated, then cell-activating activity is concentrated, but the quantity of the effective component is reduced

Engineering Contradiction:
Improvecell-activating activityVSAvoidamount of effective component
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The patent applies parameter changes by optimizing the molecular weight cutoff parameters during filtration and chromatography steps. By selecting specific molecular weight ranges (50 to 100 kDa), the process concentrates cell-activating activity in the desired fraction. The parameters of filtration membranes and chromatographic conditions are adjusted to maximize both concentration and total quantity of the effective component in the final composition.

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 purified fraction exhibits superior cell-activating effects, improving cell functions such as proliferation and metabolism, and is safe and cost-effective to produce.

Implementation Method 1

a fraction isolated from a culture supernatant of a deciduous tooth pulp stem cell, wherein the fraction comprises no component of less than 3.5 kDa

Methodology Applied
Scientific EffectMolecular weight-based filtration: Filter (physical)

Data Source

PatentEP4721749A1Cell activator
Publication Date: 2026.04.08 U-FACTOR CO LTD
  • EP4721749A1 patent drawingFigure 1
  • EP4721749A1 patent drawingFigure 2
  • EP4721749A1 patent drawingFigure 3

AI summary

Provided is a cell activator comprising a fraction isolated from a culture supernatant of a deciduous tooth pulp stem cell, wherein the fraction comprises no component of less than 3.5 kDa.