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The process of extracting Hericium erinaceus polysaccharides from Hericium erinaceus extract powder.

2024-11-30
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Hericium erinaceus extract powder
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Hericium erinaceus extract powder

1. Introduction

Hericium erinaceus, also known as the "lion's mane mushroom," has been recognized for its various health - promoting properties. Among the bioactive components in Hericium erinaceus, polysaccharides play a significant role. Extracting Hericium erinaceus polysaccharides from Hericium erinaceus extract powder is of great importance in the fields of food, medicine, and health products. This process, though complex, can be optimized to obtain high - quality polysaccharides with good yields.

2. Preparation of Hericium erinaceus extract powder

2.1 Quality assessment

Before starting the extraction process, it is crucial to ensure the quality of the Hericium erinaceus extract powder. This involves several aspects. Firstly, the source of the Hericium erinaceus should be verified. High - quality raw materials are the foundation for obtaining good polysaccharides. The powder should be free from contaminants such as heavy metals, pesticides, and other harmful substances. Analytical methods such as spectroscopy and chromatography can be used to detect potential contaminants.

2.2 Particle size adjustment

The particle size of the Hericium erinaceus extract powder can also affect the extraction efficiency. Finer particles generally offer a larger surface area, which is beneficial for the interaction between the powder and the solvent during extraction. If the powder has large particles, it may be necessary to grind it to an appropriate size. This can be achieved using mechanical grinding devices such as ball mills or crushers. However, excessive grinding should be avoided as it may damage the structure of the polysaccharides in the powder.

3. Selection of solvents

3.1 Water as a solvent

Water is a commonly used solvent for extracting Hericium erinaceus polysaccharides. It has several advantages. Firstly, it is a green and environmentally friendly solvent, which is in line with the current trend of sustainable development. Water can effectively dissolve many types of polysaccharides due to the presence of hydroxyl groups in polysaccharides, which can form hydrogen bonds with water molecules. However, the extraction using water may also extract other water - soluble substances simultaneously, which may require further purification steps in the later stage.

3.2 Alcohol - based solvents

Alcohol - based solvents, such as ethanol, are also considered for extraction. Ethanol has a lower polarity compared to water. It can selectively extract polysaccharides while reducing the extraction of some impurities. The use of alcohol - based solvents can also help in the precipitation of polysaccharides after extraction. For example, by gradually increasing the concentration of ethanol in the extract solution, polysaccharides can be precipitated out. However, alcohol - based solvents are flammable and require proper safety precautions during handling. In addition, the choice between different alcohol concentrations may also affect the extraction efficiency and the properties of the extracted polysaccharides.

4. Extraction methods

4.1 Hot - water extraction

  1. Sample - solvent ratio: The first step in hot - water extraction is to determine the appropriate ratio of Hericium erinaceus extract powder to water. A typical ratio may range from 1:10 to 1:50 (w/v), depending on the characteristics of the powder and the desired extraction efficiency. A higher ratio of water to powder may lead to a more complete extraction, but it may also increase the volume of the extract and subsequent processing difficulties.
  2. Temperature control: The extraction is usually carried out at an elevated temperature. Temperatures between 80 - 100°C are commonly used. Higher temperatures can accelerate the dissolution of polysaccharides, but excessive heat may cause degradation of the polysaccharides. Therefore, precise temperature control is essential. Heating can be achieved using water baths or heating mantles.
  3. Extraction time: The extraction time also affects the yield of polysaccharides. Generally, extraction times ranging from 1 - 3 hours are common. Longer extraction times may increase the yield, but it may also lead to the extraction of more impurities. Regular sampling and analysis during the extraction process can help to determine the optimal extraction time.

4.2 Ultrasonic - assisted extraction

  1. Equipment setup: Ultrasonic - assisted extraction requires an ultrasonic generator and a suitable reaction vessel. The ultrasonic generator emits ultrasonic waves with a certain frequency and power. The reaction vessel should be able to withstand the ultrasonic vibration and be made of materials that do not react with the solvent and the sample.
  2. Parameters adjustment: The key parameters in ultrasonic - assisted extraction include ultrasonic power, frequency, and extraction time. Ultrasonic power typically ranges from 100 - 500 W, and frequencies between 20 - 50 kHz are often used. The extraction time is usually shorter compared to hot - water extraction, typically ranging from 15 minutes to 1 hour. Higher ultrasonic power and longer extraction times can increase the extraction yield, but they may also cause damage to the polysaccharides.
  3. Mechanism: The ultrasonic waves create cavitation bubbles in the solvent. When these bubbles collapse, they generate high - pressure and high - temperature micro - environments. These micro - environments can enhance the mass transfer between the powder and the solvent, break the cell walls of the Hericium erinaceus extract powder more effectively, and thus promote the release of polysaccharides.

4.3 Microwave - assisted extraction

  1. Microwave equipment: Microwave - assisted extraction utilizes microwave ovens or specialized microwave reactors. These devices can generate microwaves with specific frequencies, usually in the range of 900 - 2450 MHz.
  2. Power and time settings: The power of the microwave and the extraction time need to be carefully adjusted. Typical microwave powers range from 300 - 800 W, and extraction times may range from 5 - 30 minutes. Microwaves can rapidly heat the solvent and the sample, which can significantly shorten the extraction time compared to traditional extraction methods. However, improper power and time settings may lead to overheating and degradation of the polysaccharides.
  3. Heating mechanism: Microwaves cause the polar molecules in the solvent and the sample to oscillate rapidly, generating heat through dielectric loss. This rapid heating can effectively break the cell structures in the Hericium erinaceus extract powder and facilitate the release of polysaccharides.

5. Optimization of extraction conditions

5.1 Single - factor experiments

Single - factor experiments are often carried out to study the influence of each individual factor on the extraction of Hericium erinaceus polysaccharides. For example, the effect of extraction temperature can be studied by keeping other factors (such as extraction time, solvent - to - sample ratio) constant while varying the temperature. The same approach can be applied to study the effects of extraction time, solvent - to - sample ratio, and other factors. Through these experiments, the approximate range of optimal values for each factor can be determined.

5.2 Response surface methodology

Response surface methodology is a more comprehensive optimization method. It takes into account the interactions between multiple factors. By designing a series of experiments based on a specific experimental design (such as central composite design), a mathematical model can be established to describe the relationship between the extraction yield of polysaccharides and various factors (such as temperature, time, and solvent - to - sample ratio). This model can then be used to predict the optimal combination of factors to achieve the highest extraction yield and the best quality of polysaccharides.

6. Purification of extracted polysaccharides

After extraction, the obtained extract usually contains not only polysaccharides but also other impurities. Therefore, purification steps are necessary.

6.1 Removal of proteins

Proteins are common impurities in the extract. Methods such as the Sevag method or trichloroacetic acid (TCA) precipitation can be used to remove proteins. In the Sevag method, a mixture of chloroform and n - butanol is added to the extract. After shaking and centrifugation, the proteins are transferred to the organic phase at the interface, while the polysaccharides remain in the aqueous phase. TCA precipitation involves adding a certain concentration of TCA to the extract to precipitate proteins, which can then be removed by centrifugation.

6.2 Removal of pigments

Pigments can also be present in the extract, which may affect the quality and appearance of the polysaccharides. Adsorption chromatography using materials such as activated carbon or macroporous resins can be used to remove pigments. Activated carbon has a large surface area and strong adsorption ability, which can effectively adsorb pigments. Macroporous resins can selectively adsorb pigments based on their molecular size and polarity.

6.3 Dialysis

Dialysis is used to remove small - molecule impurities such as salts and low - molecular - weight sugars from the extract. A semi - permeable membrane is used in dialysis. The polysaccharides, which are macromolecules, are retained inside the membrane, while small - molecule impurities can pass through the membrane and be removed.

7. Characterization of Hericium erinaceus polysaccharides

After purification, the Hericium erinaceus polysaccharides need to be characterized to understand their chemical structure and properties.

7.1 Chemical composition analysis

Chemical composition analysis can determine the types of monosaccharides that make up the polysaccharides. Methods such as high - performance liquid chromatography (HPLC) or gas chromatography - mass spectrometry (GC - MS) can be used. These methods can accurately identify and quantify the different monosaccharides in the polysaccharides, such as glucose, galactose, and mannose.

7.2 Molecular weight determination

The molecular weight of Hericium erinaceus polysaccharides is an important parameter. Techniques such as gel permeation chromatography (GPC) can be used to determine the molecular weight distribution of the polysaccharides. The molecular weight can affect the biological activities of the polysaccharides, such as their immunomodulatory and antioxidant activities.

7.3 Structural analysis

Structural analysis methods include nuclear magnetic resonance (NMR) spectroscopy and infrared (IR) spectroscopy. NMR spectroscopy can provide detailed information about the chemical bonds and the spatial arrangement of atoms in the polysaccharides. IR spectroscopy can identify the functional groups present in the polysaccharides, which can help in understanding their chemical structures.

8. Conclusion

The extraction of Hericium erinaceus polysaccharides from Hericium erinaceus extract powder is a multi - step process that involves careful preparation of the powder, selection of solvents, application of appropriate extraction methods, optimization of extraction conditions, purification of the extracted polysaccharides, and characterization of the final product. Each step plays a crucial role in obtaining high - quality Hericium erinaceus polysaccharides with good yields. With the continuous development of extraction and purification technologies, more efficient and environmentally friendly methods are expected to be developed for the extraction of Hericium erinaceus polysaccharides in the future.



FAQ:

What are the main factors affecting the extraction of Hericium erinaceus polysaccharides from Hericium erinaceus extract powder?

The main factors include extraction time, temperature, and solvent - to - sample ratio. Appropriate control of these factors can optimize the extraction yield and the quality of the polysaccharides obtained.

Why are water or alcohol - based solvents often considered for extracting Hericium erinaceus polysaccharides?

Water or alcohol - based solvents are often considered because they can effectively dissolve and separate the polysaccharides from the Hericium erinaceus extract powder.

What is the role of ensuring the purity and quality of Hericium erinaceus extract powder before extraction?

Ensuring the purity and quality of the powder before extraction is important as it can affect the extraction process and the quality of the final polysaccharides. Impurities may interfere with the extraction, and high - quality powder is more likely to yield better - quality polysaccharides.

How does ultrasonic - assisted extraction work in the process of extracting Hericium erinaceus polysaccharides?

Ultrasonic - assisted extraction uses ultrasonic waves to create cavitation bubbles in the solvent. These bubbles collapse and generate mechanical forces that can break the cell walls of Hericium erinaceus more effectively, thus facilitating the release of polysaccharides from the extract powder.

What are the advantages of hot - water extraction in extracting Hericium erinaceus polysaccharides?

Hot - water extraction is a relatively simple and environmentally friendly method. It can effectively dissolve the polysaccharides in the Hericium erinaceus extract powder under appropriate temperature conditions, and is suitable for large - scale extraction.

Related literature

  • Optimization of Hericium erinaceus Polysaccharides Extraction and Their Biological Activities"
  • "Studies on the Extraction and Structural Characterization of Hericium erinaceus Polysaccharides"
  • "Recent Advances in Hericium erinaceus Polysaccharides: Extraction, Purification and Application"
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