Method for extracting total chlorogenic acid from photinia fraseri

文档序号:1823158 发布日期:2021-11-12 浏览:29次 中文

阅读说明:本技术 一种从红叶石楠中提取总绿原酸的方法 (Method for extracting total chlorogenic acid from photinia fraseri ) 是由 邹敏亮 菅保森 邓思 姚宏 于 2021-08-23 设计创作,主要内容包括:本发明公开了一种从红叶石楠中提取总绿原酸的方法,属于天然活性物提取技术领域。以红叶石楠红色嫩芽叶或红色鲜叶为原料,包括以下步骤:将原料干燥,得到干品;将所得干品粉碎,用溶剂进行提取,过滤;滤液经陶瓷膜精滤,RO膜低温浓缩,浓缩液喷雾干燥或冷冻干燥得红叶石楠提取物。RO膜浓缩液,经大孔树脂柱吸附,乙醇水梯度洗脱,得洗脱液;含绿原酸类似物洗脱液经RO膜浓缩、浓缩液经干燥得总绿原酸活性物。通过选择红色嫩芽为原料、经过纯物理处理工艺,实现简单、高效的从红叶石楠叶中获得高含量总绿原酸活性物。(The invention discloses a method for extracting total chlorogenic acid from photinia fraseri, belonging to the technical field of natural active matter extraction. The method takes red tender bud leaves or red fresh leaves of photinia fraseri as raw materials and comprises the following steps: drying the raw materials to obtain a dry product; pulverizing the dried product, extracting with solvent, and filtering; filtering the filtrate with ceramic membrane, concentrating at low temperature with RO membrane, and spray drying or freeze drying the concentrated solution to obtain Photinia fraseri extract. Adsorbing the RO membrane concentrated solution by a macroporous resin column, and performing gradient elution by ethanol water to obtain an eluent; concentrating the eluate containing chlorogenic acid analogue by RO membrane, and drying the concentrated solution to obtain total chlorogenic acid active substance. By selecting red tender shoots as raw materials and carrying out a pure physical treatment process, the high-content total chlorogenic acid active substance is simply and efficiently obtained from the photinia fraseri leaves.)

1. A method for extracting total chlorogenic acid from photinia fraseri is characterized in that red tender bud leaves or red fresh leaves of photinia fraseri are used as raw materials, and the method comprises the following steps:

(1) drying the raw materials to obtain a dry product;

(2) crushing the dried product obtained in the step (1), extracting with a solvent to obtain an extracting solution, centrifuging and filtering the extracting solution to obtain a centrifugal solution, finely filtering the centrifugal solution by using a ceramic membrane, concentrating the centrifugal solution at a low temperature by using an RO (reverse osmosis) membrane to obtain a concentrated solution, and drying the concentrated solution to obtain the photinia fraseri leaf extract.

2. The method as claimed in claim 1, wherein in step (1), the drying is selected from drying in the shade, drying in the sun, direct drying or drying after deactivation of enzymes, preferably drying after deactivation of enzymes, further, the temperature of deactivation of enzymes is 180 ℃ and 220 ℃, and the temperature of drying is 80-90 ℃.

3. The method according to claim 1, wherein in the step (2), the solvent is ethanol water or purified water, preferably, the ethanol water is ethanol water with a volume fraction of 40-60%, the temperature of the purified water is 50-100 ℃, further, the ethanol water is ethanol water with a volume fraction of 50%, and the temperature of the purified water is 85-95 ℃, and most preferably, the purified water is 85-95 ℃.

4. The method according to claim 1, wherein in the step (2), the ratio of the extracted material to the liquid is 1:5-30, preferably 1:12, and the extraction temperature is 20-100 ℃, preferably 85 ± 5 ℃.

5. The Photinia fraseri extract prepared according to any one of claims 1-4, wherein the total chlorogenic acid content is 20-61%.

6. A preparation method of a high-content total chlorogenic acid extract is characterized in that red tender leaves or red fresh leaves of photinia fraseri are used as raw materials, and the method comprises the following steps:

(1) drying the raw materials to obtain a dry product;

(2) crushing the dried product obtained in the step (1), extracting with a solvent to obtain an extracting solution, centrifuging and filtering the extracting solution to obtain a centrifugal solution, finely filtering the centrifugal solution by a ceramic membrane, and concentrating the centrifugal solution at a low temperature by an RO membrane to obtain a concentrated solution;

(3) adsorbing the obtained concentrated solution with macroporous resin column, gradient eluting with ethanol water, mixing eluates containing chlorogenic acid and its analogues, concentrating the eluates at low temperature with RO membrane, and drying the concentrated solution to obtain high content total chlorogenic acid extract.

7. The method as claimed in claim 6, wherein in step (1), the drying is selected from drying in the shade, drying in the sun, direct drying or drying after deactivation of enzymes, preferably drying after deactivation of enzymes, further, the temperature of deactivation of enzymes is 180 ℃ and 220 ℃, and the temperature of drying is 80-90 ℃.

8. The method according to claim 6, wherein in the step (2), the solvent is ethanol water or purified water, preferably the ethanol water is ethanol water with a volume fraction of 40-60%, the temperature of the purified water is 50-100 ℃, preferably the ethanol water is ethanol water with a volume fraction of 50%, and the temperature of the purified water is 85-95 ℃, and most preferably the purified water is 85-95 ℃.

9. The method according to claim 6, wherein in step (3), the macroporous resin column is selected from any one of XAD1600, D101, DiaonHP-20, XDA-7 and AB-8, the gradient elution is a gradient elution with 5-30% ethanol water, and the low-temperature concentration is a low-temperature concentration to 15-40% of solid content through a nanofiltration membrane.

10. The total chlorogenic acid active substance prepared by any one of the methods of claims 7 to 9, characterized in that the total chlorogenic acid content is above 80%.

Technical Field

The invention belongs to the technical field of natural active matter extraction, and particularly relates to a method for extracting total chlorogenic acid from photinia fraseri leaves.

Background

Chlorogenic acid (5-O-caffeoylquinic acid, 5-CQA) is depsides formed by condensation of carboxyl of caffeic acid and hydroxyl of quinic acid, is a phenylpropanoid substance synthesized by plant cells through a shikimic acid pathway, and an isomer analogue 3-CQA thereof is neochlorogenic acid, and 4-CQA thereof is cryptochlorogenic acid. The chemical structures of chlorogenic acid and analogues thereof are as follows:

chlorogenic acid has pharmacological actions in various aspects such as oxidation resistance, antibiosis, antivirus, antitumor, blood fat reduction, blood sugar reduction, weight control, immunoregulation and the like, and is widely applied to the fields of food, medicine, chemical industry and the like [ Wangqinghua and the like, the pharmacological action and mechanism research progress of chlorogenic acid, pharmaceutical science reports 2020,55(10),2273 and 2280 ].

Chlorogenic acid and analogues thereof have simple chemical structures, but chemical synthesis is difficult because of the existence of a plurality of chiral centers, and chlorogenic acid and analogues thereof are mainly prepared by extracting, enriching and separating from plants. The content of chlorogenic acid in folium Eucommiae (dried product) is generally 0.4-4.8%, the content of chlorogenic acid in green coffee bean (dried product) is generally 1-4%, and the content of higher chlorogenic acid and its analogues in Compositae plants such as flos Chrysanthemi and flos Chrysanthemi Indici, sweet potato leaf (1.97%), and sunflower seed meal (2.48%).

However, although the plants such as eucommia leaves, chrysanthemum, green coffee beans and the like contain higher chlorogenic acid analogues, the plants also contain other plant secondary metabolites, the prepared active ingredients are complex, and the cost for preparing high-purity chlorogenic acid by separation and purification is high. The invention has the following patent: CN 201710876351.2: a method for extracting chlorogenic acid from honeysuckle flower is characterized by that the honeysuckle flower is a rare medicinal material, and its chlorogenic acid content is generally less than 4%, and the honeysuckle flower is used as raw material to extract chlorogenic acid, so that its cost is high and practicability is low. The invention patent US 2011/0223281 a1 discloses a weight control effect of decaffeinated green coffee bean extract, which is characterized by high cost of preparing high content of total chlorogenic acid active of decaffeinated since green coffee beans contain caffeine.

Chinese herbal medicine records: the Photinia serrulata is leaf or twig with leaf of Photinia serrulata (P.serula) belonging to Rosaceae, has pungent, bitter and neutral properties, and has effects of dispelling pathogenic wind and removing dampness, relieving itching, strengthening tendons and bones, and benefiting liver and kidney. At present, the fresh leaves of the photinia fraseri are rich in resources, new buds can be induced after the photinia fraseri is pruned, and red tender bud leaves can be harvested for a plurality of times after the photinia fraseri is pruned and harvested for a plurality of times under the unnatural condition. In view of the above, the invention uses photinia fraseri tender shoots and fresh leaves thereof as raw materials to prepare the high-content total chlorogenic acid extract with high efficiency and low cost.

Disclosure of Invention

The invention aims to provide a method for extracting total chlorogenic acid from photinia fraseri leaves.

In order to achieve the purpose, the technical scheme of the invention is as follows:

on one hand, the invention provides a method for extracting total chlorogenic acid from photinia fraseri, which takes red tender bud leaves or red fresh leaves of photinia fraseri as raw materials and comprises the following steps:

(1) drying the raw materials to obtain a dry product;

(2) crushing the dried product obtained in the step (1), extracting with a solvent to obtain an extracting solution, centrifuging and filtering the extracting solution to obtain a centrifugal solution, finely filtering the centrifugal solution by using a ceramic membrane, concentrating the centrifugal solution at a low temperature by using an RO (reverse osmosis) membrane to obtain a concentrated solution, and drying the concentrated solution to obtain the photinia fraseri leaf extract.

In the invention, the total chlorogenic acid refers to neochlorogenic acid (3-CQA) and chlorogenic acid (5-CQA).

The red tender leaves of the photinia fraseri are in the period of 1 bud and 2 leaves; the red fresh leaves are 3-6 leaves, and are mostly dark red; the old leaves turn green. The inventor finds that the red photinia fraseri red tender bud leaves and the red fresh leaves are used as raw materials to obtain the extract with higher total chlorogenic acid content, wherein the red tender bud leaves are the best. Red tender bud leaves are therefore preferred. The red tender bud leaves can be new tender bud leaves in early spring, natural new tender bud leaves in other periods or new tender bud leaves after trimming.

Preferably, in the step (1), the drying manner is selected from drying in the shade, drying in the sun, directly drying or drying after enzyme deactivation, and further preferably drying after enzyme deactivation, further more preferably, the temperature of the enzyme deactivation is 180 ℃ and 220 ℃, and the temperature of the drying is 80-90 ℃. The inventor finds that the content of the total chlorogenic acid is higher than that of the dry product prepared by drying the tender leaves of the photinia fraseri after high-temperature enzyme deactivation in the sun and in the shade.

Preferably, in the step (2), the mixture is ground and sieved by a sieve with 10-20 meshes.

Preferably, in the step (2), the solvent is ethanol water or purified water, further preferably, the ethanol water is ethanol water with a volume fraction of 40-60%, the temperature of the purified water is 50-100 ℃, further preferably, the ethanol water is ethanol water with a volume fraction of 50%, and the temperature of the purified water is 85-95 ℃, and most preferably, the purified water is 85-95 ℃.

Preferably, in the step (2), the material-liquid ratio of the extraction is 1:5-30, preferably 1:12, and the extraction temperature is 20-100 ℃, preferably 85 +/-5 ℃.

Preferably, in the step (2), the extraction is performed in two times, and the time for the first extraction is 30-90min, and more preferably 60 min; the time for the second extraction is 15-50min, preferably 30 min.

Preferably, in the step (2), the centrifugal filtration is performed by a horizontal centrifuge, a butterfly centrifuge or a tubular centrifuge.

Preferably, in the step (2), the drying manner is spray drying or freeze drying.

In another aspect, the invention also provides the photinia fraseri extract prepared by the method, wherein the content of the total chlorogenic acid is 20-61%.

On the other hand, the invention also provides a preparation method of the extract with high content of total chlorogenic acid, which takes red tender leaves or red fresh leaves of photinia fraseri as raw materials and comprises the following steps:

(1) drying the raw materials to obtain a dry product;

(2) crushing the dried product obtained in the step (1), extracting with a solvent to obtain an extracting solution, centrifuging and filtering the extracting solution to obtain a centrifugal solution, finely filtering the centrifugal solution by a ceramic membrane, and concentrating the centrifugal solution at a low temperature by an RO membrane to obtain a concentrated solution;

(3) adsorbing the obtained concentrated solution with macroporous resin column, gradient eluting with ethanol water, mixing eluates containing chlorogenic acid and its analogues, concentrating the eluates at low temperature with RO membrane, and drying the concentrated solution to obtain high content total chlorogenic acid extract.

Preferably, in the step (1), the drying manner is selected from drying in the shade, drying in the sun, directly drying or drying after enzyme deactivation, and further preferably drying after enzyme deactivation, further more preferably, the temperature of the enzyme deactivation is 180 ℃ and 220 ℃, and the temperature of the drying is 80-90 ℃. The inventor finds that the content of the total chlorogenic acid is higher than that of the dry product prepared by drying the tender leaves of the photinia fraseri after high-temperature enzyme deactivation in the sun and in the shade.

Preferably, in the step (2), the mixture is ground and sieved by a sieve with 10-20 meshes.

Preferably, in the step (2), the solvent is ethanol water or purified water, further preferably, the ethanol water is ethanol water with a volume fraction of 40-60%, the temperature of the purified water is 50-100 ℃, further preferably, the ethanol water is ethanol water with a volume fraction of 50%, and the temperature of the purified water is 85-95 ℃, and most preferably, the purified water is 85-95 ℃.

Preferably, in the step (2), the material-liquid ratio of the extraction is 1:5-30, preferably 1:12, and the extraction temperature is 20-100 ℃, preferably 85 +/-5 ℃.

Preferably, in the step (2), the extraction is performed in two times, and the time for the first extraction is 30-90min, and more preferably 60 min; the time for the second extraction is 15-50min, preferably 30 min.

Preferably, in the step (2), the centrifugal filtration is performed by a horizontal centrifuge, a butterfly centrifuge or a tubular centrifuge.

Preferably, in the step (2), the drying manner is spray drying or freeze drying.

Preferably, in step (3), the macroporous resin column is selected from any one of XAD1600, D101, DiaonHP-20, XDA-7 and AB-8.

Preferably, in step (3), the gradient elution is 5-30% ethanol water gradient elution.

Preferably, in the step (3), the low-temperature concentration is performed until the solid content is 15-40% by the nanofiltration membrane, and more preferably 25-35%.

Preferably, in step (3), the drying manner includes, but is not limited to, spray drying, freeze drying, and the like.

On the other hand, the invention also provides the total chlorogenic acid active substance prepared by the method, and the content of the total chlorogenic acid is more than 80%.

The invention has the beneficial effects that:

(1) selecting tender leaves of photinia fraseri as an extraction raw material, and obtaining a chlorogenic acid product with high yield and purity;

(2) the loss of the total chlorogenic acid is reduced to the maximum extent by adopting a quick drying mode after enzyme deactivation;

(3) the extraction method is optimized, and water and ethanol are used as extraction solvents, so that the extraction effect is improved;

(4) purifying by macroporous resin column adsorption and gradient elution to further increase total chlorogenic acid content, wherein the total chlorogenic acid content in the obtained active substance is above 80%.

Drawings

FIG. 1 is an HPLC chromatogram of tender leaves of Photinia fraseri;

FIG. 2 is a DAD spectrum of HPLC characteristic peak (RT 7.26min, new chlorogenic acid) of tender leaves of Photinia fraseri;

FIG. 3 is the DAD spectrum of the HPLC characteristic peak (RT 10.12min, chlorogenic acid) of the tender leaves of Photinia fraseri.

Detailed Description

The following non-limiting examples are presented to enable those of ordinary skill in the art to more fully understand the present invention and are not intended to limit the invention in any way. The following is merely an exemplary illustration of the scope of the invention as claimed, and various changes and modifications of the invention of the present application may be made by those skilled in the art based on the disclosure, which also fall within the scope of the invention as claimed.

The present invention will be further described below by way of specific examples. The various chemicals used in the examples of the present invention were obtained by conventional commercial routes unless otherwise specified.

The young leaves of Photinia fraseri (2 leaves per bud), dark red fresh leaves (3-6 leaves), and green fresh leaves used in the following examples were collected from Photinia fraseri in the middle 3-10 months in different places of Wuhan Hubei.

The invention adopts an HPLC detection method to detect the content, and comprises the following steps:

using an Agilent 1260 hplc chromatograph, DAD detector, column Zorbax Eclipse Plus C18(250mm 4.6mm,5 um); the column temperature was 35 ℃; the flow rate is 1.0 ml/min; detection wavelengths 254nm, 280nm, and 327 nm; the sample size was 2 uL. Mobile phase a was 0.1% formic acid solution and B was 0.1% formic acid-acetonitrile solution, and the gradient elution procedure is shown in the following table:

TABLE 1 mobile phase gradient elution Condition Table (post run 15min)

Time/min 0 15.00 30.00 40.00 50.00 55.00 55.01 60.00
Proportion of A phase/%) 92 83 82 80 60 50 92 92
Proportion of B phase/%) 8 17 18 20 40 50 8 8

In the following examples, the materials were obtained from the following sources:

table 2.

Example 1 analysis experiment of Photinia fraseri composition

Taking the collected leaves in each stage back to the laboratory, sucking water drops and removing foreign matters by using clean filter paper as soon as possible, cutting the leaves by using scissors, weighing 5.00g of the cut leaves in a 50ml PET centrifugal tube with scales, adding 40ml of 75% ethanol/water solvent, screwing a tube cover, and carrying out ultrasonic extraction for 30 min. Filtering the extractive solution with 0.5um organic filter membrane, injecting 2ul filtrate, and analyzing by HPLC. The results of analyzing and detecting the content of the chlorogenic acid by comparing with the standard chlorogenic acid are shown in the following table:

table 3.

Sample numbering Chlorogenic acid (3-CQA) content Chlorogenic acid (5-CQA) content Total chlorogenic acid content
1 1.12% 6.02% 7.14%
2 1.32% 6.74% 8.06%
3 2.48% 3.56% 6.04%
4 3.30% 3.48% 6.78%
5 2.44% 2.84% 5.28%
6 1.20% 1.46% 2.66%
7 1.10% 1.04% 2.14%
8 0.75% 0.70% 1.45%

In the table, samples No. 1 to 4 were red tender leaves, samples No. 5 to 7 were red fresh leaves, and samples No. 8 were green fresh leaves

HPLC spectrogram of tender bud of Photinia fraseri is shown in FIG. 1, and main characteristic peak of Photinia fraseri tender bud HPLC spectrogram with retention time of 7.26min is neochlorogenic acid (3-CQA); the main characteristic peak at 10.02min is chlorogenic acid (5-CQA). The characteristic peak of the neochlorogenic acid is shown in figure 2, and the characteristic peak of the chlorogenic acid is shown in figure 3, so that the content of the total chlorogenic acid in the photinia rubra tender shoot leaves is the largest, which is the main reason for the good extraction effect by using the red tender shoot leaves as the raw materials.

Example 2 Dry mode screening experiment

67.5Kg of tender leaves of photinia fraseri are collected and divided into four batches. 1 batch of tender bud leaves 2.5Kg are directly dried in the sun; 1 batch of tender bud leaves are dried in the shade at 2.5 Kg; 2.0Kg of 1 batch of tender bud leaves are directly dried at 85 ℃; 60Kg of 1 batch of tender bud leaves are spread, aired and withered, then are subjected to enzyme deactivation at a high temperature of 200 ℃ by a tea leaf enzyme deactivation machine, and are dried by a tea leaf dryer at a temperature of 85 ℃. And detecting the content of chlorogenic acid in 4 batches of dried tender shoot leaves. The test results are as follows:

table 4.

Batches of Drying mode Weight of tender bud and leaf Weight of dried product Yield of dry product The dry product contains total chlorogenic acid
1 Drying in the shade 2.5Kg 0.780Kg 31.2% 6.8%
2 Dried in the sun 2.5Kg 0.755Kg 30.2% 10.2%
3 Direct drying at 85 DEG C 2.0Kg 0.596Kg 29.8% 16.8%
4 Quick drying after enzyme deactivation 60Kg 17.04Kg 28.4% 18.4%

Experiments show that the dry product prepared by drying the photinia fraseri tender buds and leaves after high-temperature enzyme deactivation has less loss amount and higher content of total chlorogenic acid compared with the dry product prepared by directly drying, drying in the sun and drying in the shade.

Example 3 Photinia fraseri tender leaf extract preparation

The preparation method is characterized by taking red tender leaves of photinia fraseri as a raw material and preparing the raw material according to the following steps:

(1) deactivating enzymes of photinia fraseri red tender buds and leaves at a high temperature of 200 ℃, and quickly drying the leaves and leaves at a temperature of 85 ℃ by a tea dryer to obtain a dry product;

(2) crushing 10kg of the dried product obtained in the step (1), sieving the crushed product by a 10-mesh sieve, adding 120 liters of pure water, stirring and extracting the mixture for 60min at 85 +/-5 ℃, filtering the mixture by a 100-mesh stainless steel sieve, adding 80 liters of pure water into filter residues, stirring the mixture for 30min at room temperature, filtering the mixture by a 100-mesh stainless steel sieve, and combining the secondary extraction filtrate;

(3) the combined filtrate is subjected to fine filtration by 0.3um ceramic membrane equipment (Shanghai Wobdy) to remove particulate impurities, the fine filtration permeate is subjected to low-temperature concentration by a reverse osmosis membrane (specification 2540-2, polyamide and polyether sulfone materials) until the solid content (Brix) is 25.8%, the concentrated solution is subjected to spray drying to obtain 2.4Kg of photinia fraseri tender leaf extract, and the total chlorogenic acid content of the extract is 56.8% through HPLC detection.

Example 4 preparation of extract from fresh leaves of photinia fraseri

The difference from example 3 is that the raw material used is red fresh leaves, and the rest steps are the same. 1.8Kg of photinia fraseri fresh leaf extract is obtained, and the total chlorogenic acid content of the extract is 23.6 percent by HPLC detection.

Example 5 Photinia fraseri extract preparation

Different from the example 3, the tender leaves of photinia serrulata are directly dried at 85 ℃, and the rest steps are the same.

2.5Kg of plant extract with high chlorogenic acid content is obtained, and the total chlorogenic acid content of the extract is 48.8 percent by HPLC detection.

Example 6 Photinia fraseri extract preparation

Different from the embodiment 3, 50 liters of 50 percent ethanol water is added in the first extraction, the extraction is carried out for 60min under stirring at 50 ℃, and the extraction is carried out for 30min under stirring at room temperature in the second extraction, wherein the filter residue is added with 30 liters of 50 percent ethanol water.

2.2Kg of plant extract with high chlorogenic acid content is obtained, and the total chlorogenic acid content of the extract is 33.6 percent by HPLC detection.

Example 7 preparation of high content Total chlorogenic acid active

(1) Deactivating enzymes of photinia fraseri red tender buds and leaves at a high temperature of 200 ℃, and quickly drying the leaves and leaves at a temperature of 85 ℃ by a tea dryer to obtain a dry product;

(2) crushing 10kg of the dried product obtained in the step (1), sieving the crushed product by a 10-mesh sieve, adding 120 liters of pure water, stirring and extracting the mixture for 60min at 85 +/-5 ℃, filtering the mixture by a 100-mesh stainless steel sieve, adding 80 liters of pure water into filter residues, stirring the mixture for 30min at room temperature, filtering the mixture by a 100-mesh stainless steel sieve, and combining the secondary extraction filtrate;

(3) microfiltering the combined extractive filtrates with ceramic membrane, adsorbing with macroporous resin column (Diaon HP-20), and gradient eluting with 5%, 10%, 20%, and 30% ethanol water for 3 column volumes respectively to obtain eluates;

(4) concentrating the eluate with RO membrane to recover ethanol water, concentrating the trapped concentrated solution under reduced pressure and vacuum to remove ethanol to obtain concentrated solution solid content of 30.8%, freeze drying the concentrated solution to obtain high content of active substance of total chlorogenic acid 980g, and detecting total chlorogenic acid 85.6% by HPLC.

The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.

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