阅读说明：本技术 桦褐孔菌总三萜的高效提取方法及其精粉的制备方法 (High-efficiency extraction method of total triterpenoids of inonotus obliquus and preparation method of fine powder of total triterpenoids ) 是由 李振江 郎双静 王立东 刘莹 王长远 张东杰 于 2021-09-20 设计创作，主要内容包括：本发明涉及的是桦褐孔菌总三萜的高效提取方法及其精粉的制备方法,它包括：将桦褐孔菌原料粉碎得到桦褐孔菌粗粉；桦褐孔菌粗粉在液氮低温环境下利用球磨机进行研磨处理,得到桦褐孔菌微粉；桦褐孔菌微粉配置成桦褐孔菌悬浊液；桦褐孔菌悬浊液采用剪切超细粉碎处理,得到桦褐孔菌超微粉悬浊液；桦褐孔菌超微粉悬浊液离心得到沉淀,将沉淀烘干得到桦褐孔菌超微粉；桦褐孔菌超微粉置于汽爆试验装置中,得到超微破壁粉；超微破壁粉中添加乙醇,真空结合超声微波辅助浸提,得到桦褐孔菌总三萜粗提液；真空浓缩,得到桦褐孔菌总三萜浓缩浸提液。本发明在相同提取率下降低乙醇用量和提取时间,得到的三萜的纯度高,桦褐孔菌总三萜的生物活性高。(The invention relates to a high-efficiency extraction method of total triterpenoids in inonotus obliquus and a preparation method of fine powder thereof, which comprises the following steps: crushing inonotus obliquus raw materials to obtain inonotus obliquus coarse powder; grinding the inonotus obliquus coarse powder in a liquid nitrogen low-temperature environment by using a ball mill to obtain inonotus obliquus micro powder; preparing the inonotus obliquus micro powder into inonotus obliquus suspension; shearing and ultrafine grinding the inonotus obliquus suspension to obtain an inonotus obliquus ultrafine powder suspension; centrifuging the inonotus obliquus superfine powder suspension to obtain a precipitate, and drying the precipitate to obtain the inonotus obliquus superfine powder; placing the Inonotus obliquus superfine powder in a steam explosion test device to obtain superfine wall-breaking powder; adding ethanol into the ultramicro wall-broken powder, and performing vacuum extraction with ultrasonic microwave assistance to obtain a crude extract of the total triterpenes of the inonotus obliquus; vacuum concentrating to obtain concentrated extractive solution of total triterpene of Inonotus obliquus. The method reduces the ethanol dosage and extraction time at the same extraction rate, and the obtained triterpenoids have high purity and the total triterpenoids of the inonotus obliquus have high biological activity.)

1. An efficient extraction method of inonotus obliquus total triterpenes is characterized by comprising the following steps:

step one, crushing an inonotus obliquus raw material by using a universal crusher, and sieving the crushed material by using a 60-80-mesh sieve to obtain inonotus obliquus coarse powder;

step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under a liquid nitrogen low-temperature environment to obtain inonotus obliquus micro powder, wherein the particle size of the micro powder after grinding is 10-30 microns;

step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 10-20 mL to prepare inonotus obliquus suspension;

step four, shearing superfine grinding is carried out on the inonotus obliquus suspension obtained in the step three, the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus superfine suspension is obtained;

step five, centrifuging the inonotus obliquus superfine powder suspension obtained in the step four to obtain a precipitate, and drying the precipitate to obtain inonotus obliquus superfine powder;

putting the inonotus obliquus superfine powder obtained in the fifth step into a steam explosion test device, maintaining the pressure of 90-210 MPa for 90-210 s, and then carrying out explosion treatment to obtain ultramicro wall-broken powder with the particle size of 5-10 microns;

step seven, vacuum and ultrasonic microwave combined auxiliary extraction, adding 50-90% by volume of ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g: 10-20 mL, keeping the vacuum degree at 0.08-0.1 MPa, extracting at the temperature of 30-60 ℃, extracting for 400-1000 s, microwave power of 200-400W, ultrasonic frequency of 2450MHz and extracting times of 2-4 times; centrifuging and removing residues by using a low-temperature centrifuge at a centrifugal set temperature of 0-4 ℃, pre-cooling for 10min in advance, centrifuging and removing residues, wherein the centrifugation speed is 5000-10000 r/min, and the centrifugation time is 10min to obtain a crude extract of the total triterpenoids of the inonotus obliquus;

and step eight, carrying out vacuum concentration on the crude extract of the total triterpenoids of the inonotus obliquus obtained in the step seven, wherein the vacuum degree of the vacuum concentration is 0.08-0.1 MPa, the temperature is 30-50 ℃, and the vacuum concentration is dried until the mass concentration of ethanol is 10-20%, so as to obtain a concentrated extract of the total triterpenoids of the inonotus obliquus, wherein the extraction rate of the total triterpenoids of the inonotus obliquus is 2.9-5.1%, and the DPPH free radical clearance rate is 91.23-93.46%.

2. The method for efficiently extracting the total triterpenes from inonotus obliquus according to claim 1, which is characterized in that: the grinding conditions in the second step are as follows: the grinding time is 1-4 h, the material ball ratio is 1: 1-3, and the rotating speed is 300-500 r/min.

3. The method for efficiently extracting the total triterpenes from inonotus obliquus according to claim 2, which is characterized in that: the fifth step is specifically as follows: and C, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three, wherein the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus ultrafine suspension is obtained.

4. A preparation method of inonotus obliquus total triterpene fine powder is characterized by comprising the following steps:

step one, crushing an inonotus obliquus raw material by using a universal crusher, and sieving the crushed material by using a 60-80-mesh sieve to obtain inonotus obliquus coarse powder;

step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under a liquid nitrogen low-temperature environment to obtain inonotus obliquus micro powder, wherein the particle size of the micro powder after grinding is 10-30 microns;

step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 10-20 mL to prepare inonotus obliquus suspension;

step four, shearing superfine grinding is carried out on the inonotus obliquus suspension obtained in the step three, the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus superfine suspension is obtained;

step five, centrifuging the inonotus obliquus superfine powder suspension obtained in the step four to obtain a precipitate, and drying the precipitate to obtain inonotus obliquus superfine powder;

putting the inonotus obliquus superfine powder obtained in the fifth step into a steam explosion test device, maintaining the pressure of 90-210 MPa for 90-210 s, and then carrying out explosion treatment to obtain ultramicro wall-broken powder with the particle size of 5-10 microns;

step seven, vacuum and ultrasonic microwave combined auxiliary extraction, adding 50-90% by volume of ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g: 10-20 mL, keeping the vacuum degree at 0.08-0.1 MPa, extracting at 30-60 ℃, extracting for 400-1000 s, microwave power of 200-400W, ultrasonic frequency of 2450MHz and extracting times of 2-4 times; centrifuging and removing residues by using a low-temperature centrifuge at a centrifugal set temperature of 0-4 ℃, pre-cooling for 10min in advance, centrifuging and removing residues, wherein the centrifugation speed is 5000-10000 r/min, and the centrifugation time is 10min to obtain a crude extract of the total triterpenoids of the inonotus obliquus;

step eight, carrying out vacuum concentration on the crude extract of the total triterpenoids of the inonotus obliquus obtained in the step seven, wherein the vacuum concentration is 0.08-0.1 MPa, the temperature is 30-50 ℃, and drying is carried out until the mass concentration of ethanol is 10-20% to obtain a concentrated extract of the total triterpenoids of the inonotus obliquus, the extraction rate of the total triterpenoids of the inonotus obliquus is 2.9-5.1%, and the DPPH free radical clearance rate is 91.23-93.46%;

and step nine, freezing and drying the inonotus obliquus total triterpene concentrated leaching liquor obtained in the step eight at the vacuum degree of 0.08-0.1 MPa and the temperature of-40 to-60 ℃ to obtain the inonotus obliquus total triterpene fine powder.

5. The method for efficiently extracting the total triterpenes from inonotus obliquus according to claim 4, wherein the method comprises the following steps: the grinding conditions in the second step are as follows: the grinding time is 1-4 h, the material ball ratio is 1: 1-3, and the rotating speed is 300-500 r/min.

6. The method for efficiently extracting the total triterpenes from inonotus obliquus according to claim 5, wherein the method comprises the following steps: the fifth step is specifically as follows: and C, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three, wherein the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus ultrafine suspension is obtained.

The technical field is as follows:

the invention relates to the technical field of extraction of functional components of inonotus obliquus, in particular to an efficient extraction method of total triterpenoids of inonotus obliquus and a preparation method of fine powder of the total triterpenoids.

Secondly, background art:

inonotus obliquus (A) (B)Inonotus obliquus(Fr.) Pilat) is also called as Inonotus obliquus, Fiberella obliquus and the like, is mainly distributed in regions with north latitude of 40-50 degrees in the northern hemisphere, such as Russia, Japan and Finland, is mainly distributed in Changbai mountain regions of Jilin province, great Xinglojiang and Xiaoxing AnLing and other regions in China, and has regional characteristics. Currently, researchers in the united states, japan, korea, etc. are actively researching inonotus obliquus, especially russia, folks for treating various diseases using wild inonotus obliquus fruiting bodies. Inonotus obliquus has attracted considerable attention and interest worldwide. Important active ingredients of inonotus obliquus include polysaccharides, inonotus obliquus alcohol, various oxygenated triterpenoids, various lanosterol-type triterpenoids, folic acid derivatives, aromatic vanillic acid, syringic acid and gamma hydroxybenzoic acid, and tannin compounds, steroids, alkaloid compounds, melanin, low-molecular polyphenols and lignin compounds have been reported to be separated. Research shows that the inonotus obliquus has the effects of resisting tumor, improving immunity, reducing blood sugar, blood pressure and blood fat and resisting bacteria. In russian folk, inonotus obliquus is regarded as a psychotropic drug for treating tumors, and has high medicinal value. With the reconcognition of human beings on fungus drugs, the inonotus obliquus has a wide development prospect in the global range.

The triterpenes are bioactive components with high content, have the effects of resisting tumor, resisting oxidation, resisting inflammation, reducing blood sugar and the like, and have wide application prospect. Triterpenes have good functional properties, but their use is limited because they are mainly dissolved in organic solvents such as ethanol and are heat sensitive. The main body is as follows: firstly, people eat the inonotus obliquus mainly by adopting a hot water soaking mode, and triterpenoids cannot be dissolved out in a water solution and are discarded along with residues; the triterpene is a heat-sensitive component, and the extraction temperature is generally over 70 ℃ in the extraction process, so that the triterpene is influenced by high temperature and is oxidized by oxygen; thirdly, the content of triterpenes in the inonotus obliquus is low and is 20-60 mg/g, so that the intake of a human body is insufficient.

At present, the extraction method of triterpenes is more and the process is different. The Chinese patent application CN101849973A discloses a method for preparing an ultrasonic-assisted triterpene extract. The method comprises the steps of crushing inonotus obliquus, sieving, ultrasonic ethanol extraction, concentration, drying, extraction and purification, and finally obtaining the triterpenoid. The method comprises the steps of adding 70-95% ethanol into a raw material and ethanol in a ratio of 1g to 8-12mL, performing extraction for 2-4 times with ultrasonic power of 100W and 2-4h each time, wherein the ethanol extract and water are used in an amount of 1g to 20-50mL during purification, the weight of petroleum ether is 10-30 times that of the ethanol extract, the weight of n-butanol is 10-30 times that of the ethanol extract, the highest triterpene yield is 6.3%, and the purity is 11.57%. The method has the advantages of excessive organic solvent consumption and low extraction purity during processing, and can affect triterpene activity at high temperature and in contact with air for a long time during extraction.

Chinese patent application CN107841523A discloses a method for extracting triterpenes from inonotus obliquus by quorum sensing molecule induction. The method comprises the steps of activating inonotus obliquus strains, preparing a culture medium, inoculating, fermenting, adding a molecular inducer, separating and extracting thallus fermentation liquor, and purifying to obtain the triterpenoid substances of the inonotus obliquus, wherein the highest extraction rate of the method is 11.473mg/100 mL. The method can realize industrialized continuous production, but the fermentation method has the disadvantages of complicated operation, more uncontrollable factors, larger fluctuation of extraction efficiency and higher cost.

Chinese patent application CN112790382A discloses a method for extracting triterpenes from inonotus obliquus by using dynamic high-pressure microjet. The method comprises the steps of drying and crushing inonotus obliquus, adding an extractant, homogenizing, carrying out dynamic high-pressure microjet treatment, centrifuging, concentrating, and carrying out freeze drying to obtain the total triterpenoid of the inonotus obliquus, wherein the extraction rate of the triterpenoid can reach over 25 mg/g. The method has the advantages of reducing the granularity of materials, increasing the penetrating power of a solvent and the like. However, the method has the problems of high production cost, small treatment capacity and the like.

The triterpenoids prepared in the patents are respectively processed by different processing technologies such as ultrasonic-assisted ethanol extraction, quorum-sensing molecular induction, dynamic high-pressure microjet and the like, and a certain extraction effect is achieved, but the method still has certain defects in the production and processing aspects, such as large solvent demand, long extraction time, more uncontrollable factors, small treatment capacity, poor product bioactivity and the like.

Thirdly, the invention content:

the invention aims to provide a high-efficiency extraction method of inonotus obliquus total triterpenes, which is used for solving the problems of low extraction rate, high reaction temperature and easy oxidation of triterpenes in the prior art; the invention also aims to provide a preparation method of the inonotus obliquus total triterpene refined powder.

The technical scheme adopted by the invention for solving the technical problems is as follows: the high-efficiency extraction method of the inonotus obliquus total triterpene comprises the following steps:

step one, crushing an inonotus obliquus raw material by using a universal crusher, and sieving the crushed material by using a 60-80-mesh sieve to obtain inonotus obliquus coarse powder;

step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under a liquid nitrogen low-temperature environment to obtain inonotus obliquus micro powder, wherein the particle size of the micro powder after grinding is 10-30 microns;

step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 10-20 mL to prepare inonotus obliquus suspension;

step four, shearing superfine grinding is carried out on the inonotus obliquus suspension obtained in the step three, the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus superfine suspension is obtained;

step five, centrifuging the inonotus obliquus superfine powder suspension obtained in the step four to obtain a precipitate, and drying the precipitate to obtain inonotus obliquus superfine powder;

putting the inonotus obliquus superfine powder obtained in the fifth step into a steam explosion test device, maintaining the pressure of 90-210 MPa for 90-210 s, and then carrying out explosion treatment to obtain ultramicro wall-broken powder with the particle size of 5-10 microns;

step seven, vacuum and ultrasonic microwave combined auxiliary extraction, adding 50-90% by volume of ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g: 10-20 mL, keeping the vacuum degree at 0.08-0.1 MPa, extracting at 30-60 ℃, extracting for 400-1000 s, microwave power of 200-400W, ultrasonic frequency of 2450MHz and extracting times of 2-4 times; centrifuging and removing residues by using a low-temperature centrifuge at a centrifugal set temperature of 0-4 ℃, pre-cooling for 10min in advance, centrifuging and removing residues, wherein the centrifugation speed is 5000-10000 r/min, and the centrifugation time is 10min to obtain a crude extract of the total triterpenoids of the inonotus obliquus;

and step eight, carrying out vacuum concentration on the crude extract of the total triterpenoids of the inonotus obliquus obtained in the step seven, wherein the vacuum degree of the vacuum concentration is 0.08-0.1 MPa, the temperature is 30-50 ℃, and the vacuum concentration is dried until the mass concentration of ethanol is 10-20%, so as to obtain a concentrated extract of the total triterpenoids of the inonotus obliquus, wherein the extraction rate of the total triterpenoids of the inonotus obliquus is 2.9-5.1%, and the DPPH free radical clearance rate is 91.23-93.46%.

A preparation method of Inonotus obliquus total triterpene refined powder comprises the following steps:

step one, crushing an inonotus obliquus raw material by using a universal crusher, and sieving the crushed material by using a 60-80-mesh sieve to obtain inonotus obliquus coarse powder;

step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under a liquid nitrogen low-temperature environment to obtain inonotus obliquus micro powder, wherein the particle size of the micro powder after grinding is 10-30 microns;

step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 10-20 mL to prepare inonotus obliquus suspension;

step four, shearing superfine grinding is carried out on the inonotus obliquus suspension obtained in the step three, the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus superfine suspension is obtained;

step five, centrifuging the inonotus obliquus superfine powder suspension obtained in the step four to obtain a precipitate, and drying the precipitate to obtain inonotus obliquus superfine powder;

putting the inonotus obliquus superfine powder obtained in the fifth step into a steam explosion test device, maintaining the pressure of 90-210 MPa for 90-210 s, and then carrying out explosion treatment to obtain ultramicro wall-broken powder with the particle size of 5-10 microns;

step seven, vacuum and ultrasonic microwave combined auxiliary extraction, adding 50-90% by volume of ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g: 10-20 mL, keeping the vacuum degree at 0.08-0.1 MPa, extracting at 30-60 ℃, extracting for 400-1000 s, microwave power of 200-400W, ultrasonic frequency of 2450MHz and extracting times of 2-4 times; centrifuging and removing residues by using a low-temperature centrifuge at a centrifugal set temperature of 0-4 ℃, pre-cooling for 10min in advance, centrifuging and removing residues, wherein the centrifugation speed is 5000-10000 r/min, and the centrifugation time is 10min to obtain a crude extract of the total triterpenoids of the inonotus obliquus;

step eight, carrying out vacuum concentration on the crude extract of the total triterpenoids of the inonotus obliquus obtained in the step seven, wherein the vacuum concentration is 0.08-0.1 MPa, the temperature is 30-50 ℃, and drying is carried out until the mass concentration of ethanol is 10-20% to obtain a concentrated extract of the total triterpenoids of the inonotus obliquus, the extraction rate of the total triterpenoids of the inonotus obliquus is 2.9-5.1%, and the DPPH free radical clearance rate is 91.23-93.46%;

and step nine, freezing and drying the inonotus obliquus total triterpene concentrated leaching liquor obtained in the step eight at the vacuum degree of 0.08-0.1 MPa and the temperature of-40 to-60 ℃ to obtain the inonotus obliquus total triterpene fine powder.

The grinding conditions in the second step of the scheme are as follows: the grinding time is 1-4 h, the material ball ratio is 1: 1-3, and the rotating speed is 300-500 r/min.

The fifth step of the scheme is specifically as follows: and C, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three, wherein the shearing rotating speed is 10000-20000/min, and the time is 5-10 min, so that the inonotus obliquus ultrafine suspension is obtained.

Has the advantages that:

1. according to the invention, the inonotus obliquus is crushed by liquid nitrogen ultralow temperature ball milling superfine crushing equipment, so that the inonotus obliquus is embrittled, the ball milling crushing difficulty is reduced, and the inonotus obliquus is easier to crush; the problem of powder agglomeration caused by a ball milling process can be solved by combining with wet ultrafine grinding, so that the particle size is further reduced, and meanwhile, water-soluble substances in the powder can be removed, so that the purity of the triterpene is improved; the steam explosion can destroy the cell wall of Inonotus obliquus, so that the cell content can flow out more easily, and the extraction rate is further improved. Since the boiling point of the substance can be lowered in the vacuum environment, low-temperature extraction can be realized to reduce the damage of the temperature to the active substance.

2. The invention can solve the problems of powder agglomeration and cell wall constraint caused by ball milling, reduce the ethanol dosage and extraction time at the same extraction rate, and simultaneously can reduce the discharge of waste water and the production cost of products.

3. The invention applies vacuum to ultrasonic microwave assisted extraction, can reduce extraction temperature and avoid the reduction of the activity of the total triterpenoids of inonotus obliquus due to air oxidation.

4. The method realizes the high-efficiency extraction and high-activity retention of the total triterpenoids of the inonotus obliquus, and has good market popularization prospect.

5. The method adopts the methods of ultramicro wall breaking treatment, vacuum combined ultrasonic microwave assisted extraction and the like to the inonotus obliquus raw material, breaks through the key technology of high-efficiency extraction of the total triterpenoids of the inonotus obliquus, and obtains the high-efficiency extraction and preparation method of the total triterpenoids of the inonotus obliquus.

6. According to the invention, ultra-low temperature ball milling is combined with wet shearing superfine grinding, so that the particle size of the inonotus obliquus can be reduced, the ball milling grinding time and the grinding difficulty are reduced, the heat generated by ball milling is absorbed, the powder keeps a lower temperature, the bioactive components in the powder are protected, and meanwhile, the powder agglomeration caused by ball milling can be avoided; the vacuum combined ultrasonic microwave assisted extraction can keep the high efficiency of ultrasonic microwave synergistic extraction, simultaneously the vacuum environment can reduce the boiling point of the solution, reduce the extraction temperature, ensure that the activity of the solution cannot be influenced by high temperature, simultaneously the vacuum environment can prevent the extracted triterpenoids from being oxidized by air, and improve the biological activity of the total triterpenoids of the inonotus obliquus.

Fourthly, explanation of the attached drawings:

FIG. 1 is a block flow diagram of the present invention.

The fifth embodiment is as follows:

example 1:

the extraction rate of the total triterpenes of the inonotus obliquus prepared by the extraction method of the total triterpenes of the inonotus obliquus is 3.4%, and the DPPH free radical clearance rate is 93.20%. As shown in figure 1, the extraction method of the inonotus obliquus fine powder comprises the following steps:

step one, crushing the inonotus obliquus raw material by using a universal crusher, and sieving by a 60-mesh sieve to obtain inonotus obliquus coarse powder.

And step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under the low-temperature environment of liquid nitrogen to obtain the inonotus obliquus micro powder. The grinding conditions were: grinding for 1h, wherein the material ball ratio is 1:1, the rotating speed is 300r/min, and the particle size of the ground micro powder is 28-30 mu m.

And step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 10mL to prepare suspension.

And step four, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three, wherein the shearing rotating speed is 10000/min, and the time is 5min, so that the inonotus obliquus ultrafine powder suspension is obtained.

And fifthly, centrifuging the suspension of the inonotus obliquus superfine powder obtained in the step four at 5000r/min for 10min to obtain a precipitate, and drying the precipitate at 45 ℃ for 24h to obtain the inonotus obliquus superfine powder.

And step six, placing the inonotus obliquus superfine powder into a steam explosion test device, maintaining the pressure for 90 seconds under 90MPa, and then carrying out explosion treatment to obtain superfine wall-broken powder with the particle size of 8-10 microns.

Step seven, adding 50 volume percent ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g to 10mL, keeping the vacuum degree at 0.1MPa, the extraction temperature at 30 ℃, the extraction time at 400s, the microwave power at 200W, the ultrasonic frequency at 2450MHz and the extraction times at 2 times; centrifuging at 4 deg.C for 10min, pre-cooling, centrifuging at 8000r/min for 10min to obtain crude extract of total triterpenes of Inonotus obliquus.

And step eight, carrying out vacuum concentration on the crude extract of the total triterpenes of the hepta-inonotus obliquus in the step seven, wherein the vacuum degree of the vacuum concentration is 0.1MPa, the temperature is 40 ℃, and drying until the mass concentration of ethanol is 15% to obtain the concentrated extract of the total triterpenes of the hepta-inonotus obliquus.

And step nine, freezing and drying the concentrated leaching liquor of the total triterpenes of the inonotus obliquus in the step eight under the vacuum degree of 0.1MPa and at the temperature of minus 60 ℃ to obtain the refined powder of the total triterpenes of the inonotus obliquus.

Example 2:

the extraction rate of the total triterpenes of the inonotus obliquus prepared by the extraction method of the total triterpenes of the inonotus obliquus is 4.2 percent, the DPPH free radical clearance rate is 92.60 percent, and the extraction method of the fine inonotus obliquus powder comprises the following steps:

step one, crushing the inonotus obliquus raw material by using a universal crusher, and sieving by using a 70-mesh sieve to obtain inonotus obliquus coarse powder.

And step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under the low-temperature environment of liquid nitrogen to obtain the inonotus obliquus micro powder. The grinding conditions were: the grinding time is 2 hours, the material ball ratio is 1:2, the rotating speed is 400r/min, and the particle size of the ground micro powder is 18-22 mu m.

And step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 15mL to prepare suspension.

And step four, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three at the shearing speed of 15000/min for 8min to obtain the inonotus obliquus ultrafine suspension.

And fifthly, centrifuging the suspension of the inonotus obliquus superfine powder obtained in the step four at 5000r/min for 10min to obtain a precipitate, and drying the precipitate at 45 ℃ for 24h to obtain the inonotus obliquus superfine powder.

And step six, placing the inonotus obliquus superfine powder into a steam explosion test device, maintaining the pressure for 120s under 120MPa, and then performing explosion treatment to obtain superfine wall-broken powder with the particle size of 7-9 microns.

Step seven, adding 70 volume percent ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g to 15mL, keeping the vacuum degree at 0.1MPa, the extraction temperature at 45 ℃, the extraction time at 700s, the microwave power at 300W, the ultrasonic frequency at 2450MHz and the extraction times at 3 times; centrifuging at 4 deg.C for 10min, pre-cooling, centrifuging at 8000r/min for 10min to obtain crude extract of total triterpenes of Inonotus obliquus.

And step eight, carrying out vacuum concentration on the crude extract of the total triterpenes of the hepta-inonotus obliquus in the step seven, wherein the vacuum degree of the vacuum concentration is 0.1MPa, the temperature is 40 ℃, and drying until the mass concentration of ethanol is 15% to obtain the concentrated extract of the total triterpenes of the hepta-inonotus obliquus.

And step nine, freezing and drying the concentrated leaching liquor of the total triterpenes of the inonotus obliquus in the step eight under the vacuum degree of 0.1MPa and at the temperature of minus 60 ℃ to obtain the refined powder of the total triterpenes of the inonotus obliquus.

Example 3:

the extraction rate of the total triterpenes of the inonotus obliquus prepared by the extraction method of the total triterpenes of the inonotus obliquus is 4.8 percent, the DPPH free radical clearance rate is 91.52 percent, and the extraction method of the fine inonotus obliquus powder comprises the following steps:

step one, crushing the inonotus obliquus raw material by using a universal crusher, and sieving by a 80-mesh sieve to obtain inonotus obliquus coarse powder.

And step two, grinding the inonotus obliquus coarse powder obtained in the step one by using a ball mill under the low-temperature environment of liquid nitrogen to obtain the inonotus obliquus micro powder. The grinding conditions were: grinding for 4 hours, wherein the material ball ratio is 1:3, the rotating speed is 500r/min, and the particle size of the ground micro powder is 10-12 mu m.

And step three, adding deionized water into the inonotus obliquus micro powder obtained in the step two according to the proportion of 1g to 20mL to prepare suspension.

And step four, shearing and ultrafine grinding the inonotus obliquus suspension obtained in the step three at the shearing speed of 20000/min for 10min to obtain the inonotus obliquus ultrafine suspension.

And fifthly, centrifuging the suspension of the inonotus obliquus superfine powder obtained in the step four at 5000r/min for 10min to obtain a precipitate, and drying the precipitate at 45 ℃ for 24h to obtain the inonotus obliquus superfine powder.

And step six, placing the inonotus obliquus superfine powder into a steam explosion test device, maintaining the pressure for 210 seconds under 210MPa, and then carrying out explosion treatment to obtain superfine wall-broken powder with the particle size of 5-7 microns.

Step seven, adding 90 volume percent ethanol into the ultramicro wall-broken powder obtained in the step six according to the proportion of 1g to 20mL, keeping the vacuum degree at 0.1MPa, the extraction temperature at 60 ℃, the extraction time at 1000s, the microwave power at 400W, the ultrasonic frequency at 2450MHz and the extraction times at 4 times; centrifuging at 4 deg.C for 10min, pre-cooling, centrifuging at 8000r/min for 10min to obtain crude extract of total triterpenes of Inonotus obliquus.

And step eight, carrying out vacuum concentration on the crude extract of the total triterpenes of the hepta-inonotus obliquus in the step seven, wherein the vacuum degree of the vacuum concentration is 0.1MPa, the temperature is 40 ℃, and drying until the mass concentration of ethanol is 15% to obtain the concentrated extract of the total triterpenes of the hepta-inonotus obliquus.

And step nine, freezing and drying the concentrated leaching liquor of the total triterpenes of the inonotus obliquus in the step eight under the vacuum degree of 0.1MPa and at the temperature of minus 60 ℃ to obtain the refined powder of the total triterpenes of the inonotus obliquus.