Dihydromyricetin extraction and purification process

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Solution Overview

Problem

Existing dihydromyricetin extraction methods face challenges in high production costs due to complex processes, safety risks from high-temperature centrifugation, and introduction of impurities during ultrasonic oscillation, making industrialization difficult.

Innovation Solution

A process using acetone as an extraction solvent for reflux extraction, followed by crystallization with water and decolorization with activated carbon, minimizing energy consumption and reducing the need for costly materials, while ensuring high extraction rates and purity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If ultrasonic-assisted extraction method is used, then extraction efficiency is improved, but production cost increases and decolorization becomes difficult

Engineering Contradiction:
Improveextraction efficiencyVSAvoidproduction cost
Core Design Contradiction:
ProductivityVSEase of manufacture

Solution Approach 1:

The patent changes the extraction parameter from ultrasonic assistance to simple reflux extraction, and adjusts the solvent system to a mixed solvent containing acetone, ethanol, and water in specific proportions (acetone:ethanol:water = 1:(3-5):(8-12)). This parameter change maintains high extraction efficiency while avoiding the high equipment costs and operational complexity of ultrasonic extraction, thereby reducing production costs and improving decolorization ease.

Inventive Principle:
Principle #35Parameter changes

2Manufacturing precision

If high-temperature centrifugation is used, then purification is achieved, but safety risks increase and impurities are introduced

Engineering Contradiction:
Improvepurification effectVSAvoidsafety risks
Core Design Contradiction:
Manufacturing precisionVSObject-affected harmful factors

Solution Approach 1:

The patent performs preliminary filtration of the extraction solution before concentration and crystallization steps. This preliminary action removes large particles and impurities early in the process, eliminating the need for subsequent high-temperature centrifugation to achieve purification. The process achieves the desired purification effect through gentle filtration and controlled crystallization, avoiding safety risks associated with high-temperature centrifugation while preventing introduction of additional impurities.

Inventive Principle:
Principle #10Preliminary action

3Manufacturing precision

If complex purification processes are used, then product purity is improved, but process complexity and cost increase

Engineering Contradiction:
Improveproduct purityVSAvoidprocess complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent selectively extracts dihydromyricetin from the plant material using a specifically formulated mixed solvent system. The extraction process is designed to selectively dissolve the target compound while leaving impurities behind. Following extraction, simple filtration and controlled crystallization steps isolate the pure product. This approach achieves high product purity through selective extraction rather than through multiple complex purification steps, thereby reducing process complexity.

Inventive Principle:
Principle #2Taking out (Extraction)

4Ease of operation

If conventional extraction solvents are used, then extraction is simple, but energy consumption increases

Engineering Contradiction:
Improveextraction simplicityVSAvoidenergy consumption
Core Design Contradiction:
Ease of operationVSUse of energy by moving object

Solution Approach 1:

The patent modifies the conventional extraction approach by using a mixed solvent system with acetone as a key component, which has higher solubility for dihydromyricetin compared to conventional single solvents. This allows extraction to proceed efficiently at lower temperatures through reflux, reducing the energy input required. The mixed solvent system enhances extraction efficiency, enabling simpler operation with reduced energy consumption compared to conventional high-temperature extraction methods.

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 process achieves high dihydromyricetin content (>96%) with reduced costs and simplified operations, suitable for industrial production, and avoids the introduction of impurities, thus enhancing efficiency and safety.

Implementation Method 1

adding an extraction solvent in an amount 5 times that of the raw material to perform reflux extraction

Methodology Applied
Scientific EffectReflux extraction:

Implementation Method 2

acetone can be used to efficiently extract chlorophyll at room temperature through oscillation

Methodology Applied
Scientific EffectDissolution: Solvation

Implementation Method 3

adding water to the extract in proportion and resting for crystallization for 24 hours

Methodology Applied
Scientific EffectCrystallization: Crystallisation

Implementation Method 4

adding 5%-10% activated carbon for decolorization and impurity removing

Methodology Applied
Scientific EffectAdsorption: Adsorption

Implementation Method 5

performing suction filtration to obtain light-green sediment underneath

Methodology Applied
Scientific EffectFiltration: Filter (physical)

Data Source

PatentUS12617764B2Dihydromyricetin extraction and purification process
Publication Date: 2026.05.05 DR KANG INTERNATIONAL LTD
  • US12617764B2 patent drawing

AI summary

The present invention relates to the field of dihydromyricetin extraction and purification, and in particular to a dihydromyricetin extraction and purification process. Technical problem: the dihydromyricetin extraction and purification process aims to resolve the technical problems of increased cost of subsequent impurity removing and safety risks in high-temperature centrifugation in the prior art. Technical solution: a dihydromyricetin extraction and purification process: step 1: weighing a raw material, adding an extraction solvent in an amount 5 times that of the raw material to perform reflux extraction, concentrating the filtrate to an extract, and recovering acetone; step 2: resting for crystallization for 24 hours; step 3: performing suction filtration to obtain light-green sediment underneath, and dry the sediment; step 4: adding 5%-10% activated carbon for decolorization and impurity removing; step 5: performing suction filtration; step 6: drying to obtain white powder of dihydromyricetin; and step 7: detecting a content with HPLC.