CN103637179A - Food composition with functions of lowering blood sugar and blood fat and improving fatty liver - Google Patents
Food composition with functions of lowering blood sugar and blood fat and improving fatty liver Download PDFInfo
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- CN103637179A CN103637179A CN201310469837.6A CN201310469837A CN103637179A CN 103637179 A CN103637179 A CN 103637179A CN 201310469837 A CN201310469837 A CN 201310469837A CN 103637179 A CN103637179 A CN 103637179A
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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Abstract
The invention relates to a food composition with functions of lowering blood sugar and blood fat and improving fatty liver, belongs to the functional food field, and concretely provides a food composition with functions of lowering blood sugar and blood fat and improving fatty liver and a preparation method therefor. The food composition contains 3-6 parts of roots of kudzu vine, 3-6 parts of polygonatum rhizome, 3-6 parts of raspberries, 2-4 parts of medlars, 2-4 parts of haws, 1-3 parts of platycodon grandiflorum and 1-2 parts of lalang grass rhizome. Experiment research on mice with impaired glucose regulation shows that, the composition can raise sugar tolerance, increase insulin sensitivity, lower fasting blood glucose, lower blood fat and improve fatty liver substantially. The composition can be used for preparation of auxiliary health-care food lowering blood sugar and blood fat and improving fatty liver, and has substantial advantages of no toxic or side effects, high safety and economy and the like.
Description
Technical field
The invention belongs to functional food technical field, be specifically related to a kind of hypoglycemic, reducing blood lipid and improve functional food composition formula and the production method of fatty liver.
Background technology
Raising along with people's living standard, due to the change of people's dietary structure, rhythm of life and the few impact of moving the factors such as life style of sitting that day is becoming tight more, whole world onset diabetes rate increases year by year, has become the fourth-largest disease that causes population in the world death.According to latest data statistics, diabetes mellitus in China crowd is approximately 1.13 hundred million at present, and prediabetes is 4.93 hundred million.IGR (IGR) is the transition state of glycometabolism between normal and diabetes B, is the preliminary stage of diabetes.IGR is carried out to generation, the development that effective intervention could prevent and delay diabetes, delay the complication of capilary and trunk, thereby will obviously reduce crowd's the death rate.Diabetes belong to traditional Chinese medicine " diabete " category, and IGR should be early stage or the commitment of " diabete " mutually.Therefore for deficiency of both qi and yin, the internal resistance of the phlegm stasis of blood, carries out treating a disease by looking into both its root cause and symptoms, to reversing patient's condition, improves insulin resistance very crucial.In IGR crowd, complication is as high fat of blood and fatty live lesions also ubiquity.After Liver fatty deposition, be prone to sugar and absorb extremely, and cause more serious IGR.Therefore regulate high fat of blood and fatty liver, for delaying IGR, to develop into diabetes significant equally simultaneously.
Generally believe at present, although it is slightly disorderly to have there is glycometabolism in the IGR stage, but still can not think a kind of disease, but a kind of sub-health state, if so the method that adopts treatment diabetes is regulated and controled to tend to exceed the proper limits in righting a wrong as taken Western medicine etc., cause the side effects such as hypoglycemia, gastrointestinal reaction.Theoretical according to Traditional Chinese medical theory integration of drinking and medicinal herbs, the present invention is theoretical in conjunction with traditional Chinese medicine and pharmacy, and selection function food carries out rational proportion, forms patent formulation.Formulations composition is integration of drinking and medicinal herbs food, is suitable for every day edible, makes the adjusted blood sugar of Impaired Glucose Regulation and fat metabolism, protection and raising organ function, improves the multiple benefits such as physical function.
Summary of the invention
In the present invention, for the deficiencies in the prior art, propose a kind of food composition that reduces blood sugar, reducing blood lipid and improve fatty liver, effect is remarkable, and has no side effect.
The technical solution adopted for the present invention to solve the technical problems is: this kind of food composition that reduces blood sugar, reducing blood lipid and improve fatty liver, is characterized in that in described food composition that effectively raw material forms and weight proportion is: root of kudzu vine 3-6 part, sealwort 3-6 part, raspberry 3-6 part, matrimony vine 2-4 part, hawthorn 2-4 part, balloonflower root 1-3 part, cogongrass rhizome 1-2 part.
Preferably, the raw material of making this food composition active ingredient forms and weight proportion is: 4 parts of the roots of kudzu vine, 4 parts of sealworts, 4 parts of raspberries, 3 parts of matrimony vines, 3 parts of hawthorn, 2 parts of balloonflower roots, 1 part of cogongrass rhizome.
During proportioning, preferably the described root of kudzu vine, sealwort and raspberry are added by equivalent.
During proportioning, preferably described matrimony vine and hawthorn are added by equivalent.
The present invention also provides the preparation technology of this food composition active ingredient, specifically adopts following steps:
Steps A: by weight the selected root of kudzu vine, sealwort, raspberry, matrimony vine, hawthorn, balloonflower root, cogongrass rhizome, mechanical disintegration, crosses 60 mesh sieves, obtains medicinal material particle;
Step B: add 70% ethanol of 8 times of medicinal material particle weight, ultrasonic wave extracts 30min at 50 ℃, extracts three times, filters merging extract;
Step C: decompression and solvent recovery, temperature, lower than 55 ℃, obtains alcohol extracting paste, is further dried as flour.
Above-mentioned food composition extracts powdered thing can be made into powdery or granular nutrient powder or tablet or capsule.
The root of kudzu vine, taste is sweet, pungent, cool in nature, returns spleen, stomach warp, has and promotes the production of body fluid to quench thirst, and rises the merit of positive antidiarrheal; In < < Sheng Nong's herbal classic > >, just there is the record of " root of kudzu vine smell is sweet flat nontoxic, main quenching one's thirst "; The folk prescription that kudzuvine root juice in < < General Records of Holy Universal Relief > > is quenched one's thirst for treatment, with the root of kudzu vine is clearing heat and detoxicating simply, promote the production of body fluid to quench thirst, moisturize relieving restlessness, invigorating the spleen rises clear, to help body fluid source and defeated cloth.The main component Puerarin of the root of kudzu vine, has and suppresses interior free yl, hypoglycemic and improve microangiopathies texts.
Sealwort, taste is sweet, property is flat, returns spleen, lung, kidney channel.The effect with tonifying spleen moistening lung, supplementing qi and nourishing yin, for nourishing and fit keeping function and treatment suffer from a deficiency of the kidney, the deficiency syndrome of the lung and weakness of the spleen and the stomach disease.Modern pharmacology research is found, contains multiple steroid saponin constituents and Flavonoid substances in sealwort, is conducive to strengthen immunity of organisms, has reducing blood lipid, the hypoglycemic and effect such as delay senility simultaneously.
Raspberry: warm in nature, the sweet acid of taste, flat.Return kidney, urinary bladder channel.Containing organic acid, carbohydrate and vitamin C, filling liver kidney, dwindles just, supporing yang, controlling nocturnal emission with astringent drugs, improving eyesight, consumptive disease.
The fruit of Chinese wolfberry, taste is sweet, property is flat, has the effects such as kidney tonifying, enriching yin, nourishing the liver, improving eyesight, beneficial gas.Modern study finds that the fruit of Chinese wolfberry has anticancer, AFL, hypotensive and promote body to regulate the effects such as immunologic function.Be usually used in improving diabetes, hepatopathy and health care for the aged.
Crataegolic acid is sweet, and merit is arrogated to oneself spleen benefiting and stimulating the appetite, promoting blood circulation to remove blood stasis, the promoting the circulation of qi of reducing phlegm, and the especially kind greasy meat of carburetion is stagnant.Hawthorn energy prevention and cure of cardiovascular disease, has softening blood vessel, hypotensive, reducing blood lipid, improves blood circulation effect.
Balloonflower root taste is arduous, and calmness, analgesia, antipyretic, eliminate the phlegm, and treats laryngopharynx bitterly, and sharp the five internal organs stomach, has hemangiectasis, reducing heart rate, hypoglycemic and reducing blood lipid, inducing diuresis to reduce edema, antiulcer, antiallergy, the effect such as antitumor.Mainly contain multiple triterpene glucoside as ursolic acid, oleanolic acid etc., flavonoids is as compounds such as rutin, large sweet-scented osmanthus grass elements.Modern pharmacological research shows that the composition such as saponin class, flavonoids in plant has the activity of anti-inflammatory.
Cogongrass rhizome: cold in nature, taste is sweet.Clear heat with drugs of sweet flavour and cold nature, the diuresis of promoting the production of body fluid.Often with single or compound treatment difficult urination, blood urine and chyluria, oedema and hepatitis etc.< < herbal classic > > has the record of " the empty win of main internal lesion caused by overexertion, tonifying middle-Jiao and Qi, except extravasated blood, blood close fever and chills, diuresis ".
Visible according to results of animal, food composition of the present invention, after long term administration, is lowering postprandial blood sugar and fasting blood-glucose, and the effect of improving hyperlipemia and fatty liver is remarkable.
Accompanying drawing explanation
Accompanying drawing is murine liver tissue steatosis pathological change figure (oil red O stain, * 200), wherein, and NC: Normal group (upper left); MC: model control group (upper); PC: positive controls (upper right); AMF: dosage group (bottom left) in formula alcohol extract; AHF: formula alcohol extract high dose group (bottom right); →, the red fat that dyes drips.
the specific embodiment
Below by specific embodiment, the present invention is described in detail.Following embodiment, only gives an example for representative of the present invention, should not be construed as limited range of the invention process.Every simple replacement or variation to formula of the present invention, production craft step and condition, all belongs to protection scope of the present invention.
Embodiment 1
Get root of kudzu vine 200g, sealwort 200g, raspberry 200g, matrimony vine 150g, hawthorn 150g, balloonflower root 100g, cogongrass rhizome 50g, mechanical disintegration, crosses 60 mesh sieves.70% ethanol that adds 8 times of medicinal material particle weight, ultrasonic wave extracts 30min at 50 ℃, extracts three times, merges extract, and decompression and solvent recovery, to suitable volumes, obtains alcohol extracting paste, is dried, and makes nutrition powder.
Embodiment 2
Get root of kudzu vine 300g, sealwort 300g, raspberry 300g, matrimony vine 200g, hawthorn 200g, balloonflower root 120g, cogongrass rhizome 60g, mechanical disintegration, crosses 60 mesh sieves.70% ethanol that adds 8 times of medicinal material particle weight, ultrasonic wave extracts 30min at 50 ℃, extracts three times, merges extract, and decompression and solvent recovery, to suitable volumes, obtains alcohol extract thick paste, adds appropriate dextrin, mix, granulation, dry, compacting is in blocks, makes tablet.
Embodiment 3
The Combined food of being prepared by above-described embodiment 1 to gained carries out following pharmacodynamic experiment:
The Combined food alcohol extract dried powder of being prepared by the embodiment of the present invention 1 to gained carries out hypoglycemic, reducing blood lipid and improves fatty liver effect experiment the IGR mouse model of the high fructose diet induced of high fat:
1. experiment material and method
Animal used as test: SPF level ICR mouse, 20-22g, male, Beijing Vital River Experimental Animals Technology Co., Ltd. provides, the quality certification number: SCXK(capital) 2007-0001.Mouse feed composition: carbohydrate 64%, protein 21%, fat 4%, fiber 5%, is purchased from zoopery center, Beijing.Mouse is raised in China Agricultural University's Food Science and nutrition engineering college zoopery center (SPF level).Room ventilation condition is good, normally changes round the clock, and relative humidity is 55 ± 5%, room temperature: 23 ± 2 ℃.
Experimental technique: mouse adaptability was fed after 7 days, and 50 mouse are divided into 5 groups at random,, does grouping as follows: Normal group (NC), gavage 7% Tween-80 solution by 10 every group; Model control group (MC), usings 15% fructose water as unique water source in the time of gavage Fat Emulsion; Melbine positive controls (PC); The embodiment of the present invention 1 is prepared dosage group (AMF) and high dose group (AHF) in the food compositions alcohol extract of gained.Each group is edible conventional feed all, and NC organizes drinking pure water; Except NC group, all the other respectively organize equal gavage Fat Emulsion, using 15% fructose water as unique water source.Fat Emulsion preparation method: lard 50g, cholesterol 1.5g, pig cholate 0.3g, Tween-80 7mL, adds water and is settled to 100mL, is made into Fat Emulsion ,-20 ℃ of preservations.
Every day gavage dosage (in)=amount ÷ body weight (in 60kg) * the weight of animals * 20 times formula (1)
Gavage dosage every day (height)=amount ÷ body weight (in 60kg) * the weight of animals * 30 times formula (2)
The gavage amount of the alcohol extract of formula is calculated with formula (1) and (2), is then diluted with distilled water into the adaptation gavage volume (0.2mL/10g b.w) of mouse, positive controls gavage 0.5g/kg b.w. melbine.
2. measure and observation index
Adaptation is carried out intervention experiment to each group according to above grouping after raising and finishing, and gavage is 10 weeks continuously, within every three days, weigh 1 time, and satellite recanalization dosage.Test and measure sugar tolerance the 9th weekend, test and measure insulin tolerance the 10th weekend.When experiment finishes, fasting 13h after animals administer, does not limit drinking-water, plucks eyeball blood sampling, measures TC, TG, HDL-C, LDL-C and FFA content.Dissect mouse, get after its liver weighs, wherein a part of liver carries out histotomy observation.
2.1. the mensuration of blood sugar
Mouse fasting (can't help water) 13h, cuts tail vein blood, by Johnson & Johnson's blood glucose meter, measures mouse blood sugar, directly reading out data.
2.2. oral glucose tolerance test (OGTT)
Mouse fasting (can't help water) 13h, each is organized its mouse oral and gives 2.0g/kg b.w. glucose solution.In 120min subsequently, at 0min, 30min, 60min, 120min, cut tail vein blood respectively, blood glucose meter is measured blood sugar.Area under glucose tolerance curve (AUC) adopts trapezoidal method to calculate:
TG-AUC=0.25 * (0min blood sugar+30min blood sugar)+0.25 * (30min blood sugar+60min blood sugar)+0.5 * (60min blood sugar+120min blood sugar)
2.3. insulin tolerance test (ITT)
Mouse fasting (can't help water) 4h, each organizes mouse peritoneal injection 0.6IU/kg b.w. short-acting insulin.In 90min subsequently, at 0min, 30min, 50min, 70min, 90min, cut tail vein blood respectively, blood glucose meter is measured blood sugar.
2.4. the mensuration of blood fat
Mouse fasting (can't help water) 13h, in the blood sampling of eyeball rear vein beard, in the centrifugal 15min of 4000g, separation of serum, measures TC, TG, LDL-C, HDL-C and FFA.
3. experimental result:
IGR mouse to the induction of Fat Emulsion associating fructose is intervened, and the sugar tolerance result after 9 weeks is as shown in table 1.
Table 1. is intervened the sugar tolerance (n=10) of mouse after 9 weeks
Note: with NC comparison, #P<0.05, ##P<0.01; With MC comparison, * P<0.05, * * P<0.01.
From table 1, model control group shows associating IGT after 9 weeks in diet induced, and fasting blood-glucose raises 28.6% than Normal group, has utmost point significant difference, and its AUC and Normal group relatively exist utmost point significant difference.Melbine reduces the fasting blood-glucose of mouse, has improved sugar tolerance, illustrates that antidiabetic drug shows lasting effectively preventive effect to mouse IGR.More all there were significant differences for the alcohol extract high dose group each point blood sugar of formula and AUC and model control group, reduce respectively 24.4%, 29.3%, 29.5%, 19.3% and 23.0%, wherein dosage group mouse fasting blood-glucose, 30min blood sugar and AUC reduce, and more all have utmost point significant difference with model control group.Relatively 9 weeks rear formula extracts of gavage found that the intervention of mouse IGR: the alcohol extract high dose of formula reduces fasting blood-glucose when improving IGT, lasting to the preventive effect of mouse IGR, is dose-effect relationship.
Formula extract is intervened and is carried out ITT on the 10th week IGR mouse, the results are shown in Table 2:
Table 2. is intervened the insulin tolerance (n=10) of mouse after 10 weeks
Note: with NC comparison, ##P<0.01; With MC comparison, * P<0.05, * * P<0.01.
From table 2, after model control group mouse peritoneal insulin injection, blood sugar declines, during 50min, blood sugar touches the bottom, blood sugar bottom out subsequently, during 90min, blood sugar reaches 63.6% of initial blood sugar, initial blood sugar respectively than Normal group mouse high 52.8% and 66.7%, has utmost point significant difference with 90min blood sugar.The initial blood sugar of positive controls declines 20.0% and 28.6% than model control group respectively with 90min blood sugar, and there were significant differences.Formula extract intervention group initial blood sugar is lower than model control group, and has significant difference; The alcohol extract high dose group 70min of formula and 90min blood sugar are all lower than model control group (P<0.05), and 90min blood sugar only reaches 32.1% of initial blood sugar; In formula alcohol extract, dosage group 70min blood sugar and model control group do not have difference, and the alcohol extract of filling a prescription is as seen improving in the effect of mouse islets element sensitiveness, and high dose is better than middle dosage, amount effect relationship.
Formula extract is intervened and is carried out lipid determination on the 10th week IGR mouse, the results are shown in Table 3.After model control group diet induced 10 weeks, mice serum LDL-C, TC and FFA level are significantly higher than Normal group.Melbine makes serum LDL-C and TC content have the trend of rising.In formula alcohol extract, dosage reduces FFA level, and high dose group reduces TC, TG and FFA level.
Table 3. is intervened the blood lipids index (n=10) of mouse after 10 weeks
Note: with NC comparison, ##P<0.01; With MC comparison, * P<0.05, * * P<0.01.
Through test in 10 weeks, each carried out oil red O stain after organizing mouse liver freezing microtome section, observed hepatic tissue fat deposition situation, and result as shown in the figure.Visible indivedual fat vacuoles not of uniform size only in Normal group liver cell, are negative.In model control group mouse liver cell, the visible little red fat vacuole that dyes of diffusivity, illustrates that fat deposition degree is serious in hepatic tissue, severe fatty liver.The visible red fat vacuole that dyes of diffusivity in positive controls mouse cell, and fat drop is larger, illustrates that melbine does not have obvious inhibitory action to fatty degeneration of liver.The visible little red fat vacuole that dyes in the about 30%-40% liver cell of dosage group mouse in formula alcohol extract, slight fatty liver; The little red fat vacuole that dyes in the visible about 20%-30% liver cell of hepatic tissue of formula alcohol extract high dose group mouse, hepatic cell fattydegeneration.Alcohol extract is dose-effect relationship to suppressing fat deposition in hepatic tissue, and high dose is better than middle dosage.This result of study alcohol extract that shows to fill a prescription has remarkable minimizing mouse liver fat deposition, prevents and alleviates the function that fatty liver forms.
Result is visible from the above mentioned, and this Combined food formula of the present invention can play good reduction blood sugar, reduce blood fat, alleviates the effect of fatty liver simultaneously.
Claims (6)
1. hypoglycemic, reducing blood lipid and improve the food composition of fatty liver, the raw material that it is characterized in that active ingredient in described food composition forms and weight proportion is: root of kudzu vine 3-6 part, sealwort 3-6 part, raspberry 3-6 part, matrimony vine 2-4 part, hawthorn 2-4 part, balloonflower root 1-3 part, cogongrass rhizome 1-2 part.
2. a kind of hypoglycemic, reducing blood lipid according to claim 1 and improve the food composition of fatty liver, the raw material that it is characterized in that active ingredient in described food composition forms and weight proportion is: 4 parts of the roots of kudzu vine, 4 parts of sealworts, 4 parts of raspberries, 3 parts of matrimony vines, 3 parts of hawthorn, 2 parts of balloonflower roots, 1 part of cogongrass rhizome.
3. a kind of hypoglycemic, reducing blood lipid according to claim 1 and improve the food composition of fatty liver, is characterized in that: the described root of kudzu vine, sealwort and raspberry add by equivalent.
4. a kind of hypoglycemic, reducing blood lipid according to claim 1 and improve the food composition of fatty liver, is characterized in that: described matrimony vine and hawthorn add by equivalent.
5. according to a kind of hypoglycemic, the reducing blood lipid described in claim 1-4 any one with improve the food composition of fatty liver, it is characterized in that the preparation technology of active ingredient comprises the steps:
Steps A: by weight the selected root of kudzu vine, sealwort, raspberry, matrimony vine, hawthorn, balloonflower root, cogongrass rhizome, mechanical disintegration, crosses 60 mesh sieves, obtains medicinal material particle;
Step B: add 70% ethanol of 8 times of medicinal material particle weight, ultrasonic wave extracts 30min at 50 ℃, extracts three times, filters merging extract;
Step C: decompression and solvent recovery, temperature, lower than 55 ℃, obtains alcohol extracting paste, is further dried as flour.
6. a kind of hypoglycemic, reducing blood lipid according to claim 5 and improve the food composition of fatty liver, is characterized in that described food composition to make powdery or granular nutrient powder or tablet or capsule.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104095234A (en) * | 2014-07-04 | 2014-10-15 | 凯泽(武汉)健康管理有限公司 | Functional food for conditioning fatty liver |
CN107625129A (en) * | 2017-09-06 | 2018-01-26 | 如皋市滋生堂生物科技有限公司 | A kind of hypoglycemic and the health food and its production method of reducing blood lipid |
CN110506822A (en) * | 2019-10-10 | 2019-11-29 | 湖北民族大学 | A kind of rhizoma polygonati Poria cocos teabag drink and preparation method thereof |
CN114668813A (en) * | 2022-01-24 | 2022-06-28 | 安徽富韵生物科技有限公司 | Application of polygonatum sibiricum and nitraria tangutorum composition in regulating blood sugar and blood fat |
CN114831197A (en) * | 2022-05-23 | 2022-08-02 | 湖南楚茗茶业有限公司 | Composite dark tea and preparation method and application thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1899446A (en) * | 2006-07-05 | 2007-01-24 | 吉林农业大学 | Wolfberry fruit tablet health product and its preparing method |
CN101112525A (en) * | 2006-07-26 | 2008-01-30 | 郁华军 | Health products having functions of invigorating qi and blood and restoring consciousness and refreshing oneself |
CN101263901A (en) * | 2008-04-29 | 2008-09-17 | 刘跃明 | Plant health care wine |
CN102551140A (en) * | 2012-01-13 | 2012-07-11 | 唐新秀 | Sobering and liver-protecting kudzu vine root beverage |
-
2013
- 2013-10-10 CN CN201310469837.6A patent/CN103637179B/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1899446A (en) * | 2006-07-05 | 2007-01-24 | 吉林农业大学 | Wolfberry fruit tablet health product and its preparing method |
CN101112525A (en) * | 2006-07-26 | 2008-01-30 | 郁华军 | Health products having functions of invigorating qi and blood and restoring consciousness and refreshing oneself |
CN101263901A (en) * | 2008-04-29 | 2008-09-17 | 刘跃明 | Plant health care wine |
CN102551140A (en) * | 2012-01-13 | 2012-07-11 | 唐新秀 | Sobering and liver-protecting kudzu vine root beverage |
Non-Patent Citations (1)
Title |
---|
王慧芳 等: "药食两用中药降血糖作用研究进展", 《中国煤炭工业医学杂志》 * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104095234A (en) * | 2014-07-04 | 2014-10-15 | 凯泽(武汉)健康管理有限公司 | Functional food for conditioning fatty liver |
CN104095234B (en) * | 2014-07-04 | 2015-10-28 | 凯泽(武汉)健康管理有限公司 | A kind of functional food nursing one's health fatty liver |
CN107625129A (en) * | 2017-09-06 | 2018-01-26 | 如皋市滋生堂生物科技有限公司 | A kind of hypoglycemic and the health food and its production method of reducing blood lipid |
CN110506822A (en) * | 2019-10-10 | 2019-11-29 | 湖北民族大学 | A kind of rhizoma polygonati Poria cocos teabag drink and preparation method thereof |
CN114668813A (en) * | 2022-01-24 | 2022-06-28 | 安徽富韵生物科技有限公司 | Application of polygonatum sibiricum and nitraria tangutorum composition in regulating blood sugar and blood fat |
CN114831197A (en) * | 2022-05-23 | 2022-08-02 | 湖南楚茗茶业有限公司 | Composite dark tea and preparation method and application thereof |
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