Uncultured Amniotic Cell Separation via Filtration

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for preparing amniotic cell products from amniotic fluid are costly, time-consuming, and often result in lower concentrations of amniotic cell populations due to contamination with blood cells and other components, limiting their therapeutic effectiveness for regenerative medicine and wound healing.

Innovation Solution

A method involving the use of cell-separation filters to isolate uncultured amniotic cells and protein fractions from amniotic fluid, removing contaminants like blood cells, urea, and electrolytes, thereby producing products that are substantially free of these components, which can be used for tissue regeneration and wound healing.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If centrifugation methods are used to prepare uncultured amniotic cell products, then cell separation is achieved, but the product contains blood cells, cellular debris, and other contaminants that reduce therapeutic effectiveness

Engineering Contradiction:
Improvetherapeutic effectivenessVSAvoidcontaminants (blood cells, cellular debris)
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent applies the extraction principle by removing harmful components (blood cells, cellular debris, urea, electrolytes) from the amniotic fluid through a multi-step process involving filtration and centrifugation. The harmful substances are separated and discarded, leaving a purified amniotic cell product that maintains therapeutic effectiveness without contamination.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent segments the amniotic fluid into distinct components through sequential processing steps. Different cell types and molecular components are separated based on their physical and chemical properties, allowing selective isolation of amniotic cells while removing contaminants like blood cells and cellular debris.

Inventive Principle:
Principle #1Segmentation

2Quantity of substance

If cultured amniotic cell products are prepared through expansion in culture, then cell population increases, but the process is costly, time-consuming, and results in lower concentrations of some amniotic cell populations

Engineering Contradiction:
Improvecell population concentrationVSAvoidculture time
Core Design Contradiction:
Quantity of substanceVSLoss of time

Solution Approach 1:

The patent applies preliminary action by collecting and processing amniotic fluid immediately after amniocentesis or C-section, preserving cells in their natural state before culture. This eliminates the need for time-consuming expansion cultures while maintaining high cell population concentrations and diversity, as the cells are processed fresh rather than grown in culture over time.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent uses fresh amniotic cells directly from the fluid as a natural copy of the therapeutic product, eliminating the need for artificial culture expansion. The cells retain their native characteristics and concentrations without requiring prolonged cultivation periods.

Inventive Principle:
Principle #26Copying

3Quantity of substance

If cultured amniotic cell products are prepared through expansion in culture, then cell numbers increase, but the process is costly

Engineering Contradiction:
Improvecell population concentrationVSAvoidmanufacturing cost
Core Design Contradiction:
Quantity of substanceVSEase of manufacture

Solution Approach 1:

The patent employs a simplified, cost-effective processing protocol that uses basic filtration and centrifugation equipment rather than expensive culture systems. The method processes amniotic fluid quickly and directly, avoiding costly culture media, incubators, and extended processing time, thereby reducing manufacturing costs while maintaining high cell population concentrations.

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

4Quantity of substance

If amniotic cells are cultured, then some populations divide more slowly than others, but this leads to lower concentrations of slower-dividing cell populations in the final product

Engineering Contradiction:
Improveamniotic cell population concentrationVSAvoidcell population diversity
Core Design Contradiction:
Quantity of substanceVSStability of the object's composition

Solution Approach 1:

The patent extracts all amniotic cell populations directly from the fresh amniotic fluid before culture, preserving the natural diversity and relative concentrations of different cell types. By processing cells immediately rather than allowing differential proliferation during culture, the method maintains the original stable composition of the cell population.

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

This method provides a cost-effective and efficient way to produce amniotic cell products with higher concentrations of stem cells and proteins, suitable for therapeutic applications, including topical administration for skin, eye, joint, and spine treatments, enhancing tissue regeneration and healing.

Implementation Method 1

A method involving the use of cell-separation filters to isolate uncultured amniotic cells and protein fractions from amniotic fluid

Methodology Applied
Scientific EffectFiltration: Filter (physical)

Data Source

PatentUS20230126319A1Products Derived from Amniotic Fluid and Methods of Use
Publication Date: 2023.04.27 STIMLABS LLC
  • US20230126319A1 patent drawing
  • US20230126319A1 patent drawing

AI summary

Uncultured amniotic cell and protein fraction products derived from amniotic fluid and methods of preparing and using those compositions are provided. According to the methods of the present invention, uncultured amniotic cell and protein products may be derived from a large sample of amniotic fluid to provide a higher concentration of tissue regeneration components. Described are methods for separating uncultured amniotic cells or protein fractions from other components of amniotic fluid and the resulting uncultured amniotic cell and protein products. Furthermore, the present invention includes methods for delivering the uncultured amniotic cell and protein products to the skin and eye, including before, during, or after a treatment procedure.