Stem Cell Expansion Medium Using Carnitine and Heparin

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Solution Overview

Problem

Stem cells are present in minute quantities and are difficult to maintain in culture, especially in hard-to-reach organs, and there are ethical concerns with embryonic stem cells, necessitating methods for multiplying stem cells without differentiating into less potent forms.

Innovation Solution

A medium and method for culturing, expanding, and differentiating stem cells using a combination of human serum, O-acetyl-L-carnitine, N-desulphated-N-acetylated heparin, and specific cytokines such as thrombopoietin, flt-3 ligand, and stem cell factor, which supports the proliferation and differentiation of stem cells into primitive lineage-specific progenitor cells like natural killer and vascular progenitor cells.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If stem cells are cultured and multiplied, then the quantity of stem cells increases, but the cells may differentiate into less potent forms

Engineering Contradiction:
Improvequantity of stem cellsVSAvoidpotency of stem cells
Core Design Contradiction:
Quantity of substanceVSStability of the object's composition

Solution Approach 1:

The patent changes chemical parameters of the culture medium by adding specific compounds (O-acetyl-L-carnitine at 2-10 mmol/l, N-desulphated-N-acetylated heparin at 40-80 mg/l) and cytokine combinations to control stem cell differentiation and maintain potency during expansion

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses specific intermediary substances in the culture medium that mediate between the stem cells and the culture environment, preventing unwanted differentiation while allowing controlled proliferation and self-renewal

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If stem cells are maintained in culture, then the cells can be expanded, but the culture maintenance is difficult

Engineering Contradiction:
Improvestem cell expansionVSAvoidculture maintenance
Core Design Contradiction:
ProductivityVSEase of manufacture

Solution Approach 1:

The patent optimizes culture medium parameters including serum concentration (1-20%), specific cytokine combinations, and chemical additives to create ideal conditions for stem cell proliferation and maintenance

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses composite culture media combining multiple components (basic medium, serum, O-acetyl-L-carnitine, N-desulphated-N-acetylated heparin, cytokines) to achieve synergistic effects that simplify culture maintenance while enhancing productivity

Inventive Principle:
Principle #40Composite materials

3Quantity of substance

If embryonic stem cells are obtained, then stem cell production is achieved, but ethical concerns arise

Engineering Contradiction:
Improvestem cell productionVSAvoidethical concerns
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The patent extracts and expands stem cells from easily obtainable sources like umbilical cord blood and placenta, separating the stem cell acquisition process from embryonic destruction, thereby eliminating ethical concerns while maintaining stem cell production capability

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent utilizes readily available, non-controversial biological materials (umbilical cord blood, placental tissue) that are easily obtainable and do not raise ethical issues, replacing the need for embryonic stem cell harvesting

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Data Source

PatentUS9109202B2Methods and means for stem cell proliferation and subsequent generation and expansion of progenitor cells, as well as production of effector cells as clinical therapeutics
Publication Date: 2015.08.18 IPD THERAPEUTICS

AI summary

The invention provides means and methods for stem cell proliferation and subsequent generation and expansion of progenitor cells. The invention in particular provides media and other culture conditions for the same. The cells are preferably used as effector cells as clinical therapeutics.