Bovine Hemoderivative Production via Inert Atmosphere and Segmented Extraction

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Solution Overview

Problem

Existing methods for producing bovine hemoderivatives face issues such as energy loss, chemical instability due to oxidizing atmospheres, low selectivity in etheric preparation, and microbial contamination, leading to incomplete removal of undesirable substances and potential explosions during ether evaporation.

Innovation Solution

A biotechnological method involving multi-phase fermentation, controlled drying, and ethanol extraction with Soxhlet extraction, followed by vacuum inspissation and repeated etheric preparation to achieve high concentration and separation of bovine hemoderivative, using a nitrogen atmosphere to prevent oxidation and microbial contamination.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If ethanol extraction is performed with the extract placed outside the boiler, then the extraction process can proceed, but energy is lost and the temperature of the extract reduces

Engineering Contradiction:
Improveextraction process feasibilityVSAvoidenergy loss
Core Design Contradiction:
Ease of manufactureVSLoss of energy

Solution Approach 1:

The patent combines the extraction process with the heating system by placing the extraction vessel inside the boiler, allowing the extract to be heated during extraction. This merges two previously separate operations (extraction and heating) into one integrated process, eliminating energy loss and temperature reduction issues.

Inventive Principle:
Principle #5Merging (Combining)

2Device complexity

If one-step etheric preparation is used to separate phospholipids, then the process is simpler, but the selectivity is low and undesirable substances remain in the precipitate

Engineering Contradiction:
Improvepreparation process complexityVSAvoidpurification selectivity
Core Design Contradiction:
Device complexityVSManufacturing precision

Solution Approach 1:

The patent divides the etheric preparation into multiple sequential steps: first etheric extraction to remove phospholipids, then a second etheric treatment of the precipitate to further purify it. This segmentation of the preparation process into distinct stages achieves high purification selectivity while maintaining reasonable process complexity.

Inventive Principle:
Principle #1Segmentation

3Loss of substance

If ether evaporation is performed to remove ether after etheric preparation, then ether can be removed from the precipitate, but there is risk of explosion and ether contamination of the environment

Engineering Contradiction:
Improveether removalVSAvoidexplosion risk and environmental contamination
Core Design Contradiction:
Loss of substanceVSObject-affected harmful factors

Solution Approach 1:

The patent performs ether evaporation in an inert atmosphere (nitrogen or carbon dioxide) to eliminate oxygen, thereby preventing explosion risks. The inert gas environment also prevents ether contamination of the surrounding atmosphere, addressing both safety and environmental concerns while effectively removing ether from the precipitate.

Inventive Principle:
Principle #39Inert atmosphere (Inert environment)

4Quantity of substance

If the evaporation residue is left after ether removal, then the concentrated extract is obtained, but it becomes susceptible to microbial contamination and oxidative cleavage

Engineering Contradiction:
Improveextract concentrationVSAvoidchemical and microbial stability
Core Design Contradiction:
Quantity of substanceVSReliability

Solution Approach 1:

The patent maintains the evaporation residue in an inert atmosphere (nitrogen or carbon dioxide) to prevent both microbial contamination and oxidative cleavage. The inert gas creates a protective environment that preserves the chemical stability of the concentrated extract while preventing microbial growth, ensuring long-term reliability of the product.

Inventive Principle:
Principle #39Inert atmosphere (Inert environment)

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 results in a high-quality, microbially and chemically stable product with minimal undesirable phospholipids and blood salts, ensuring efficient separation and stability, reducing process time and environmental risks.

Implementation Method 1

using a nitrogen atmosphere to prevent oxidation and microbial contamination

Methodology Applied
Scientific EffectOxidation prevention through inert atmosphere: Oxidation

Implementation Method 2

The extract of the blood fermentations product is subjected to one vacuum inspissation, usually to a final concentration 20 times higher then the original concentration

Methodology Applied
Scientific EffectVacuum evaporation: Evaporation

Implementation Method 3

the condensed blood fermentation product is subjected to precipitation through diethyl ether, and the obtained precipitate is separated from the solution of undesirable phospholipids dissolved in the ether

Methodology Applied
Scientific EffectPrecipitation: Precipitation

Implementation Method 4

ethanol extraction of the blood fermentation product in several phases

Methodology Applied
Scientific EffectSolvent extraction: Absorption (physical)

Data Source

PatentEP2400857B1A method of biotechnological production of bovine hemoderivative
Publication Date: 2016.03.23 SVUS PHARMA A S
  • EP2400857B1 patent drawing

AI summary

The method of biotechnological production of bovine hemoderivative is presented in the following overview providing a summary of individual technological operations in time sequence (Flow-Sheet).