CN104336596A - Medicine composition capable of lowering blood lipid and preparation method thereof - Google Patents
Medicine composition capable of lowering blood lipid and preparation method thereof Download PDFInfo
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Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Botany (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The invention relates to a medicine composition capable of lowering blood lipid. The medicine composition comprises the following raw medicines in parts by weight: 50 parts of commelina communis, 50 parts of Curculigo orchioides, 50 parts of Salvia miltiorrhiza, 50 parts of ginkgo leaves, 35 parts of Alisma plantago-aquatica, 35 parts of Kudzuvine root, 10 parts of hives, and 20 parts of gynostemma pentaphyllum. The low, middle and high dosage groups of the medicine composition all can effectively lower the blood lipid in the human body, and are safe to use and have remarkable curative effect.
Description
Technical field
The present invention relates to pharmaceutical composition of a kind of reducing blood lipid and preparation method thereof, belong to field of health care food.
Background technology
Along with the raising of people's lives, the expanding day of people with hyperlipidemia, and the diabetes caused by high fat of blood, blood circulation system disease is increasing to human health risk.Along with the market demand, the health food with auxiliary antilipemic also increases gradually, but works mainly with the form of one-component greatly, and act synergistically poor, effect is not obvious, still can not meet the needs in market.
Summary of the invention
Object of the present invention is just to provide a kind of pharmaceutical composition of more efficiently auxiliary antilipemic effect.
The compositions of reducing blood lipid of the present invention forms primarily of the Chinese medicine of following weight portion: dayflower 30-70 part, thizoma curculiginis 30-70 part, red sage root 30-70 part, ginkgo leaf 30-70 part, rhizoma alismatis 20-50 part, root of kudzu vine 20-50 part, honeycomb 5-15 part, gynostemma pentaphylla 10-30 part.
Preferably, each Chinese medicine and weight portion thereof are respectively: dayflower 40-60 part, thizoma curculiginis 40-60 part, red sage root 40-60 part, ginkgo leaf 40-60 part, rhizoma alismatis 30-40 part, root of kudzu vine 30-40 part, honeycomb 8-12 part, gynostemma pentaphylla 15-25 part.
More preferably, each Chinese medicine and weight portion thereof are respectively: dayflower 50 parts, thizoma curculiginis 50 parts, the red sage root 50 parts, ginkgo leaf 50 parts, rhizoma alismatis 35 parts, the root of kudzu vine 35 parts, 10 parts, honeycomb, gynostemma pentaphylla 20 parts.
The present invention also provides the preparation method of above-mentioned Antilipidemic pharmaceutical compositions:
1) by the root of kudzu vine pulverize, cross 100 mesh sieves, every prescription collect 50g fine powder (
60co radiation, dosage < 5ky), all the other meal are for extraction.
2) red sage root, ginkgo leaf, rhizoma alismatis, the root of kudzu vine, gynostemma pentaphylla, dayflower, thizoma curculiginis, honeycomb 80% alcohol reflux extract 2 times, first time adds 10 times amount solvent extraction 2h, second time adds 8 times amount solvent extraction 1.5h, merge twice filtrate (the another device of the dregs of a decoction is preserved), decompression (-0.065 ~-0.075Mpa; 60 DEG C) concentrated, reclaim ethanolic solution and be concentrated into relative density 1.32 ~ 1.35(60 DEG C) medicinal extract 1 for subsequent use.
3) the above-mentioned dregs of a decoction add 8 times amount soak by water 1 time, and the time, 1.5h considered, filtrate decompression (-0.065 ~-0.075Mpa; 60 DEG C) to be concentrated into relative density be 1.32 ~ 1.35(60 DEG C) medicinal extract 2 for subsequent use.
4) medicinal extract 1 and medicinal extract 2, root of kudzu vine fine powder are mixed, dry, pulverize 80 mesh sieves with less than 65 DEG C reduce pressure (-0.075 ~-0.085Mpa).
5) above-mentioned fine powder 85% appropriate amount of ethanol makes softwood, 20 mesh sieves granulate less than 60 DEG C dry, the whole grain of 16 mesh sieve, loads No. 0 capsule and get final product.
Beneficial effect
The traditional Chinese medical science thinks that hyperlipidemia genus " this void table is real " is demonstrate,proved, and with the internal resistance of the phlegm stasis of blood for mark, the dirty functional disturbance of liver,spleen,kidney three is originally.
Rhizoma alismatis, the clearing heat and detoxicating soothing the liver clearing gallbladder of dayflower, to help the transporting of taste; Gynostemma pentaphylla, thizoma curculiginis tonifying middle-Jiao and Qi, invigorating the spleen production of sperm, with Zhi Qiben; Ginkgo, the root of kudzu vine, the red sage root, honeycomb eliminates the phlegm and stomach promotes the production of body fluid, resolving turbidity and eliminating dampness control altogether its mark.
Detailed description of the invention
Following examples for illustration of the present invention, but are not used for limiting the scope of the invention.
Embodiment 1
Prescription forms:
Dayflower 60 parts, thizoma curculiginis 40 parts, the red sage root 60 parts, ginkgo leaf 40 parts, rhizoma alismatis 40 parts, the root of kudzu vine 30 parts, 12 parts, honeycomb, gynostemma pentaphylla 15 parts.
The preparation method of the pharmaceutical composition of reducing blood lipid of the present invention:
1) by the root of kudzu vine pulverize, cross 100 mesh sieves, every prescription collect 50g fine powder (
60co radiation, dosage < 5ky), all the other meal are for extraction.
2) red sage root, ginkgo leaf, rhizoma alismatis, the root of kudzu vine, gynostemma pentaphylla, dayflower, thizoma curculiginis, honeycomb 80% alcohol reflux extract 2 times, first time adds 10 times amount solvent extraction 2h, second time adds 8 times amount solvent extraction 1.5h, merge twice filtrate (the another device of the dregs of a decoction is preserved), decompression (-0.065 ~-0.075Mpa; 60 DEG C) concentrated, reclaim ethanolic solution and be concentrated into relative density 1.32 ~ 1.35(60 DEG C) medicinal extract 1 for subsequent use.
3) the above-mentioned dregs of a decoction add 8 times amount soak by water 1 time, and the time, 1.5h considered, filtrate decompression (-0.065 ~-0.075Mpa; 60 DEG C) to be concentrated into relative density be 1.32 ~ 1.35(60 DEG C) medicinal extract 2 for subsequent use.
4) medicinal extract 1 and medicinal extract 2, root of kudzu vine fine powder are mixed, dry, pulverize 80 mesh sieves with less than 65 DEG C reduce pressure (-0.075 ~-0.085Mpa).
5) above-mentioned fine powder 85% appropriate amount of ethanol makes softwood, 20 mesh sieves granulate less than 60 DEG C dry, the whole grain of 16 mesh sieve, loads No. 0 capsule and get final product.
Embodiment 2
Prescription forms:
Dayflower 40 parts, thizoma curculiginis 60 parts, the red sage root 40 parts, ginkgo leaf 60 parts, rhizoma alismatis 30 parts, the root of kudzu vine 40 parts, 8 parts, honeycomb, gynostemma pentaphylla 25 parts.
The preparation method of the pharmaceutical composition of reducing blood lipid of the present invention is with embodiment 1
Embodiment 3
Prescription forms:
Dayflower 50 parts, thizoma curculiginis 50 parts, the red sage root 50 parts, ginkgo leaf 50 parts, rhizoma alismatis 35 parts, the root of kudzu vine 35 parts, 10 parts, honeycomb, gynostemma pentaphylla 20 parts.
The preparation method of the pharmaceutical composition of reducing blood lipid of the present invention is with embodiment 1
Embodiment 4
Health food hard shell capsules auxiliary lipid-lowering function Report on Animal of the present invention
1. materials and methods
1.1 samples and test liquid preparation: pharmaceutical composition medicine of the present invention, by Shaanxi, century-old healthy pharmaceutcal corporation, Ltd provides, and for content sepia capule size is 0.35g/ grain, human body recommends consumption for adult (everyone) every day 2 times, each 3, convert 35mg/kgBW by body weight 60kg.Room temperature preservation.Before experiment with 5% starch solution sample dispense become 17.5,35.0, the solution of 70.0mg/ml is for trying out.
1.2 experimental animals: male rat 60 in cleaning grade (II grade) Wistar selecting Guangxi medical pharmaceutical university Experimental Animal Center [ approval number is osmanthus dynamic (2000) the 001st ] to breed, body weight 207 ± 22.6g.This center experimental animal room quality certification number: dynamic No. 23003rd, the word of osmanthus doctor.Animal housing's temperature 22 ~ 25 DEG C, relative humidity 55 ~ 70%.
1.3 dosage choice and animal subject give mode: human body day per sample recommends consumption, 700,350 if, 175mg/kgBW(is equivalent to 20,10,5 times of human body recommended amounts respectively) 3 dosage groups, separately establish a basal feed control group and a high model control group (high fat group).Often organize 14 animals.Give test solution in per os mode, gavage amount is 1.0ml/100g BW.
1.4 key instruments and reagent:
Instrument: Hitachi KY2000 type semi-automatic biochemical analyzer, centrifuge, whirlpool are mixed device and water bath with thermostatic control etc.
Reagent: T-CHOL (TC), triglycerides (TG), HDL-C (HDL-C) kit (Zhongsheng Beikong Biological Science & Technology Co., Ltd. produces, and lot number is respectively 181091,222062,190161)
1.5 test methods: according to the auxiliary lipid-lowering function method of inspection in " health food inspection and assessment technical specification-2003 ", employing hyperlipoidemia method-preventative to given the test agent.Rat observes 5 days at the indoor nursing basal feed of SPF level zoopery, and the intraocular corner of the eyes gets hematometry every blood fat observation index normal value.According to TC level, adopt stratified random smapling mode that rat is divided into 5 groups, often group 14 also suitably adjusts and makes TC, HDL-C of each group of rat and original body mass balanced as far as possible.After starting test, except basal feed is according to except group, all the other are respectively organized equal high lipid food and feed and raise.Each rats in test groups per os gavage gives test solution, and two control group gavages give 5% starch solution, and gavage amount is 1.0ml/100g BW.Once a day, continuous 30 days, weigh once weekly, and according to body weight adjustment gavage amount.After test to fasting 16h during whole end, blood sampling measures serum TC, TG, HDL-C content.Serum TC, TG, HDL-C content.The mensuration of serum TC, TG and HDL-C content all uses enzyme reagent-end-point method.
1.6 experimental data processing: carry out statistical disposition with variance analysis.
1.7 results judge: in serum total cholesterol, monoglyceride, HDL-C three indexs, and serum total cholesterol and the triglycerides binomial index positive, can judge that given the test agent auxiliary lipid-lowering function animal experiment is positive.
2 result of the tests
2.1 samples are on the impact of rat body weight
Each group rat body weight no significant difference before test, body weight and the gain in weight of respectively organizing rat when process of the test each week and off-test compare, and difference does not all have significant (P>0.05), table
The growth of this sample bright to tested rat body weight does not have a significant effect, in table 1.
The changes of weight of front and back rat tested by table 1
Note: in table between each group comparing difference there are no significant (P>0.05).
2.2 samples are on the impact of serum total cholesterol TC content.
The tested rat experiment of table 2 is front and terminate TC content
Note: * * represents to have pole conspicuousness (P<0.01) with high fat control group comparing difference
Before experiment, each group Serum TC content is basically identical, the no significant difference (P<0.05) between each group.Experiment terminates the TC content of high fat control rats apparently higher than Basal control group, and difference has pole conspicuousness (P<0.01), shows that hyperlipidemia model is set up; At the end of experiment, the TC content of sample each dosage group is all lower than high fat control group, and the difference of each dosage group and negative control group all has pole conspicuousness (P<0.01), in table 2, show that this sample has the serum total cholesterol content effect reducing hyperlipidemia model rat.
2.3 samples are on the impact of serum glyceride (TG) content
Before experiment, respectively organize rat blood serum (TG) content basically identical, the no significant difference (P>0.05) between each group.The TG content of off-test height fat control rats is all higher than Basal control group, and difference has conspicuousness (P<0.01), shows that hyperlipidemia model is set up; During off-test, the TG content of sample each dosage group rat is all lower than high fat control group, and the difference of each dosage group and negative control group all has pole conspicuousness (P<0.01), in table 3, show that this sample has the effect reducing rat blood serum triglycerides.
The tested rat experiment of table 3 is front and terminate TG content
Note: * * represents to have pole conspicuousness (P<0.01) with high fat control group comparing difference
2.4 samples are on the impact of serum High Density Lipoprotein Cholesterol (HDL-C) content
The tested rat experiment of table 4 is front and terminate HDL-C content
Note: * and * * represents to have pole conspicuousness (P<0.05) and pole conspicuousness (P<0.01) with high fat control group comparing difference respectively
Before experiment, each group serum HDL-C level is basically identical, the no significant difference (P<0.05) between each group.The HDL-C content that experiment terminates high fat control rats is starkly lower than Basal control group, and difference has pole conspicuousness (P<0.01), shows that hyperlipidemia model is set up; During off-test, the HDL-C content of each dosage group is all higher than high fat control group, and the difference of each dosage group and negative control group all has conspicuousness (P<0.05 or P<0.01), in table 4, show that this sample has the effect of the serum High Density Lipoprotein Cholesterol content raising hyperlipidemia model rat.
3. result judges
Respectively with 175,350,700mg/kg BW(be equivalent to human body recommended amounts 5,10,20) blood fat lowering capsule of dosage is to the continuous gavage of hyperlipidemia model rat 30 days, serum total cholesterol (TC) and triglycerides (TG) content of rat can be reduced, improve the content of the serum High Density Lipoprotein Cholesterol (HDL-C) of rat, the body weight of rat is increased and has no significant effect.As can be seen here, this sample has auxiliary lipid-lowering function effect.
Embodiment 5
Health food hard shell capsules auxiliary lipid-lowering function of the present invention-human feeding trial report
1. materials and methods
1.1 samples: the auxiliary antilipemic capsule provided by the century-old healthy pharmaceutcal corporation, Ltd in Shaanxi, specification 0.35g/ intragranular is tolerant is sepia.Human body recommended amounts is adult (everyone) every day 2 times, each 3.
1.2 study subjects:
1.2.1 experimenter's inclusive criteria: the crowd of simple dyslipidemia, keeps usual diet, blood sampling 2 times in half a year.(1) twice serum total cholesterol (TC) is >=5.2mmol/L; (2) or twice serum glyceride (TG) >=1.65mmol/L.
1.2.2 Subject Exclusion Criteria: (1) age is under-18s or over-65s person; (2) gestation or women breast-feeding their children, to health food allergy sufferers: the serious diseases such as (3) merge intentionally, liver, kidney and hemopoietic system, cyclothymic patient; (4) take the article relevant with tested function in a short time, have influence on the judgement person to result; (5) do not meet inclusive criteria, not by the edible given the test agent of regulation, effect or data not umbra sound effect or security judgement person cannot be judged.
1.3 experimental design and grouping: adopt two kinds of control design between self and group.Requirement according to randomized double-blind is divided into groups.Connect experimenter's blood lipid level and be divided into test-meal group and control group at random, the principal element considering as far as possible affect result as age, sex, diet, carry out harmony and check, to ensure the comparativity between group.Often organize experimenter and be no less than 50 examples.
1.4 edible dosage and the times: test-meal group 2 times for each person every day; Each 3, control group adopts blank.Continuous Time of Administration is no less than 30 days, if desired can proper extension to 45 day.
1.5 key instruments, reagent and test environment require: electrocardiogram, X-ray examination machine, B ultrasonic scanner, Biochemical Analyzer, blood counting instrument, sphygmomanometer etc.
1.6 observation index:
1.6.1 safety indexes
1.6.1.1 ordinary circumstance: comprise the state of mind, sleep, diet, stool and urine etc., every day is by experimenter's record.
1.6.1.2 blood routine examination: apply full-automatic blood counting instrument and detect routine blood indexes, before experiment, tests and terminates respectively to do once.
1.6.1.3 blood pressure and liver, kidney, functional check: take blood pressure with blood pressure measuring, application automatic clinical chemistry analyzer measures blood Main Biochemical, and before experiment, experiment terminates respectively to do once.
1.6.1.4 Chest X-rays, electrocardiogram, Abdominal B type ultrasonography: before experiment starts, carry out a fluoroscopy of chest, electrocardiogram and Abdominal B type ultrasonography inspection.
1.6.2 efficiency index:
1.6.2.1 index: serum total cholesterol (TC) level and reduction percentage, triglycerides (TG) level and reduction percentage, HDL-C (TDL-C) level and ascensional range.
1.6.2.2 effect criterion: effectively: TC reduces >10%; TG reduces >15%; >0.104mmol/L is invalid in TDL-C rising: do not reach effective standard person.Observation serum total cholesterol (TC) is efficient, triglyceride (TG) is efficient, HDL-C (TDL-C) is efficient and total effective rate.The computational methods of total effective rate: each study subject only has index (TC, TG, a TDL-C) display effectively, namely counts efficiently individual quantity, efficiently individual quantity both obtained total effective rate divided by this group number.
1.7 data statistics: all own control data can adopt paired t-test, two groups of means compare and adopt into t inspection, the latter need carry out homogeneity test of variance, suitable variable transitions is carried out to the data of Non-Gaussian Distribution or heterogeneity of variance, after meeting normal state variance and be neat, carry out t inspection by the data of conversion; If translation data still can not meet the neat requirement of normal state variance, use t ' inspection or rank test instead, the neat side of variance but the logging data application rank test of the coefficient of variation too large (as CV>50%).Efficient and total effective rate adopts X
2inspection is tested.The total number of cases of four fold table is less than 40, or total number of cases is equal to or greater than 40 but occurs that theoretical value is equal to or less than 1, should use exact method method instead.
1.8 results judge: (1) serum total cholesterol and the triglycerides binomial index positive, HDL-C, not significantly lower than control group, can judge that this given the test agent has auxiliary lipid-lowering function effect.(2) an index positive in serum total cholesterol, triglycerides, two indexs, HDL-C, not significantly lower than control group, can judge that this given the test agent has auxiliary reduction serum total cholesterol or the effect of auxiliary reduction triglycerides.
2. result
2.1 ordinary circumstances: before test-meal, the age, mental status, sleep quality, diet situation etc. of test-meal group and control group crowd are basically identical, and the fluoroscopy of chest of two groups of crowds, electrocardiogram and Abdominal B type ultrasonography check result are showed no obvious abnormalities.Serum TC, TG, TDL-C there are no significant difference (P<0.05), in table 5
Two groups of crowd's serum TCs, TG, TDL-C comparision contents before table 5 test-meal
2.2 samples are on the impact of people with hyperlipidemia efficacy measures
After test-meal, serum TC and the TG content of test group crowd all have obvious reduction, self compare and with more all there is between control group pole significant difference (P<0.01); The serum HDL-C level of experimental group and control group compares, no significant difference (P>0.05); The total effective rate of test group auxiliary antilipemic is 74%, compares have pole significant difference (P<0.01) with 24% of control group, in table 6 ~ table 9, shows that this sample has and reduces the examination serum TC of trencherman, the effect of TG content.
Two groups of crowd's serum TC comparision contents before and after table 6 test-meal
Two groups of crowd's serum TG comparision contents before and after table 7 test-meal
Two groups of crowd serum T DL-C comparision contents before and after table 8 test-meal
Two groups of effective situations of crowd's auxiliary antilipemic after table 9 test-meal
2.3 samples are on the impact of safety indexes
2.3.1 sample is on the impact of blood pressure
The assay of two groups of crowd's blood pressures after table 10 test-meal
Before and after test-meal, the systolic pressure of experimental group and control group crowd and diastolic pressure, all in normal range (NR), in table 10, show that the blood pressure of this sample to experimenter has no adverse effects.
2.3.2 sample is on the impact of urine, feces routine
Before and after test-meal, the urine acid-base value of experimental group and control group crowd, transparency, color and urinary sediment microscopy no abnormality seen, Urine proteins is all unnegative, the stool colour of two groups of crowds, shape and microscopy are showed no exception, in table 11, table 12, show that the stool, urine routine of this sample to experimenter has no adverse effects.
The two groups of crowd's routine urinalysis assays in front and back tested by table 11
The assay of the two groups of crowd's stool routine examinations in front and back tested by table 12
2.3.3 sample is on the impact of routine blood test
Before and after test-meal, the erythrocyte number of experimental group and test-meal group crowd; Leukocyte count and content of hemoglobin, all in normal range (NR), in table 13, show that the routine blood indexes of this sample to experimenter has no adverse effects.
The assay of two groups of crowd's routine blood tests after table 13 test-meal
2.3.4 sample is on the impact of blood Main Biochemical.
The assay of two groups of crowd's blood parameters after table 14 test-meal
Before and after test-meal, the blood parameters check result of test group and control group crowd and all in normal range (NR), in table 14, show that the Liver and kidney function of this sample to experimenter has no adverse effects.
2.3.5 the bad reaction of sample, in experimentation test-meal sample person all do not occur feeling sick, the bad reaction such as flatulence, diarrhoea and allergy.
3. brief summary
3.1 meet this people with hyperlipidemia 100 example testing tested inclusion criteria (man 39 example, female 61 example), wherein experimental group 50 example takes blood fat lowering capsule of the present invention 30 days (2 times for each person every day continuously, each 3, specification is 350mg/ grain) after, result test-meal sample person TC, TG content obviously reduces, and test-meal sample person self compares and more all has conspicuousness (P<0.01) with control group; TDL-C content is without obviously changing (P>0.05), and total effective rate is 74%, has pole significant difference (P<0.01) with 24% of control group; Show that this sample has auxiliary lipid-lowering function effect.
Before and after 3.2 experiments, every check result such as erythrocyte number, leukocyte count, hemoglobin, stool and urine routine, total serum protein, albumin, glutamic-oxalacetic transaminease, glutamic-pyruvic transaminase, urea nitrogen, creatinine, blood sugar of test-meal sample sets crowd, all in normal range (NR), shows that this sample has no adverse effects to experimenter's health.
In 3.3 processs of the test, test-meal sample person is the bad reactions such as appearance is felt sick, flatulence, diarrhoea and allergy.
Claims (4)
1. a pharmaceutical composition for reducing blood lipid, it is made up of the bulk drug of following weight portion: dayflower 30-70 part, thizoma curculiginis 30-70 part, red sage root 30-70 part, ginkgo leaf 30-70 part, rhizoma alismatis 20-50 part, root of kudzu vine 20-50 part, honeycomb 5-15 part, gynostemma pentaphylla 10-30 part.
2. the pharmaceutical composition of reducing blood lipid according to claim 1, it is characterized in that, the weight portion of each bulk drug is respectively: dayflower 40-60 part, thizoma curculiginis 40-60 part, red sage root 40-60 part, ginkgo leaf 40-60 part, rhizoma alismatis 30-40 part, root of kudzu vine 30-40 part, honeycomb 8-12 part, gynostemma pentaphylla 15-25 part.
3. the pharmaceutical composition of reducing blood lipid according to claim 1 and 2, it is characterized in that, the weight portion of each bulk drug is respectively: dayflower 50 parts, thizoma curculiginis 50 parts, the red sage root 50 parts, ginkgo leaf 50 parts, rhizoma alismatis 35 parts, the root of kudzu vine 35 parts, 10 parts, honeycomb, gynostemma pentaphylla 20 parts.
4. a preparation method for the pharmaceutical composition of reducing blood lipid described in any one of claim 1-3, is characterized in that comprising the following steps: by the root of kudzu vine pulverize, cross 100 mesh sieves, every prescription collect 50g fine powder (
60co radiation, dosage < 5ky), all the other meal are for extraction; The red sage root, ginkgo leaf, rhizoma alismatis, the root of kudzu vine, gynostemma pentaphylla, dayflower, thizoma curculiginis, honeycomb 80% alcohol reflux extract 2 times, first time adds 10 times amount solvent extraction 2h, second time adds 8 times amount solvent extraction 1.5h, merges twice filtrate (the another device of the dregs of a decoction is preserved), decompression (-0.065 ~-0.075Mpa; 60 DEG C) concentrated, reclaim ethanolic solution and be concentrated into relative density 1.32 ~ 1.35(60 DEG C) medicinal extract 1 for subsequent use; The above-mentioned dregs of a decoction add 8 times amount soak by water 1 time, and the time, 1.5h considered, filtrate decompression (-0.065 ~-0.075Mpa; 60 DEG C) to be concentrated into relative density be 1.32 ~ 1.35(60 DEG C) medicinal extract 2 for subsequent use; Medicinal extract 1 and medicinal extract 2, root of kudzu vine fine powder are mixed, dry, pulverize 80 mesh sieves with less than 65 DEG C reduce pressure (-0.075 ~-0.085Mpa); Above-mentioned fine powder 85% appropriate amount of ethanol makes softwood, 20 mesh sieves granulate less than 60 DEG C dry, the whole grain of 16 mesh sieve, loads No. 0 capsule and get final product.
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CN105031045A (en) * | 2015-09-15 | 2015-11-11 | 曾盛钊 | Heart protecting and liver nourishing tea |
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WO2018072276A1 (en) * | 2016-10-19 | 2018-04-26 | 广西中医药大学 | Health-care food and preparation method therefor |
CN109528827A (en) * | 2019-01-09 | 2019-03-29 | 武汉百理王生物工程有限公司 | A kind of promoting blood circulation, reducing blood lipid, the pharmaceutical composition of auxiliary adjustment cardiovascular and cerebrovascular disease and preparation method thereof |
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