CN108904643A - Mixture containing plant component and the preparation method and application thereof for reducing blood lipid - Google Patents
Mixture containing plant component and the preparation method and application thereof for reducing blood lipid Download PDFInfo
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- CN108904643A CN108904643A CN201810912912.4A CN201810912912A CN108904643A CN 108904643 A CN108904643 A CN 108904643A CN 201810912912 A CN201810912912 A CN 201810912912A CN 108904643 A CN108904643 A CN 108904643A
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- 239000011718 vitamin C Substances 0.000 description 1
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- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/39—Complex extraction schemes, e.g. fractionation or repeated extraction steps
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Abstract
The present invention is provided to mixtures containing plant component of reducing blood lipid and its preparation method and application.The mixture includes tea stem micro mist or tea stalk/tea stem extraction, and tea stalk/tea stem can effectively prevent and reduce Hyperlipemia rich in a variety of polyphenol compounds, controls weight, effectively prevention, mitigate and treat because of hyperlipidemia and complication caused by overweight.Zoopery proves, tea stem of the present invention, tea stalk extract are able to suppress the activity of intestine in rats lipase, reduce the decomposition of food source fat, reduce the absorption of intestinal fat, the triglyceride levels in fat loading rat blood are reduced, and then have the function that the blood lipid that loses weight and reduce.The preparation process of the mixture is simple, energy consumption is low, pollution-free.
Description
Technical field
The invention belongs to reducing blood lipid plant extracts technical fields, and in particular to tea stalk/tea stem extract.
Background technique
In recent years, with the improvement of material living standards, the fat intake of people is also rising year by year.High-caliber rouge
Fat intake has been found closely related with the morbidity of the lifestyle diseases such as obesity, hyperlipemia, artery sclerosis and diabetes.Although
The fat many factors such as with diet, heredity, living habit, mental element, exercise lack, disease are related, but to most overweight peoples
For, the accumulation of body fat caused by nutrition intake is excessive is one of the main reasons for this.Root Ju epidemiological survey, with normal person
It compares, the in-vivo tissue lipopexia of most overweight peoples is abnormal.In addition, hyperlipemia has proved to be, to form systemic arterial athero-
The Etiological of hardening, while being also the important risk factor of the diseases such as cerebral apoplexy, coronary heart disease, myocardial infarction, cardiac sudden death.By
Various lifestyle diseases caused by obesity have become the problem of people extremely pay close attention to.
The heat highest that fat constituent contains in known food, excess ingestion fat are to lead obesogenous immediate cause.Rouge
The absorption of fat firstly the need of being broken down into free fatty acid under the action of the lipase that pancreas is secreted, and after inhaled through small intestine
It receives, synthesizes neutral fat again in vivo and accumulated and utilized.Excessively accumulation can induce fatty liver to neutral fat in liver.It is neutral
Fatty acid is converted into Ultra Low Density Lipoprotein (Very low density lipoprotein, VLDL) into blood in liver
Liquid, excessive VLDL is one of clinical indices of hyperlipidemia in blood.Hyperlipidemia is not only the main of atherosclerosis
The cause of disease can also cause thrombosis, and induce a variety of circulatory system illness such as cerebral infarction, myocardial infarction.It is hard for prevention of arterial
Change, it is considered that blood lipid is reduced by limitation fat absorption or the metabolism of promotion body fat, especially reduction VLDL is
Very effective method.
Tea (Camellia sinensis (L.) O.Kuntze), Theaceae dungarunga or undershrub plant originate in me
State, the present whole world are more than that 60 countries have cultivation.Tealeaves has long applicating history, in addition to being world hobby drink
One of the raw material of material or the traditional medicine in China.Modern research shows that tea extract have preferable lipid-loweringing, weight-reducing,
Anti-oxidant, anti-inflammatory isoreactivity, tea extract have been widely used for production health food and functional food additives etc., use
In diseases such as adjuvant treatment hyperlipemia, obesity, diabetes, bacterium infections.However, having the tea of most of identical active constituent
Stalk, tea stem are not yet used for anti-curing hyperlipemia and obesity.Tea stem is the waste material of winter pruning tea tree, and crushing can add as animal feeding-stuff
Add agent;Tea stalk is the waste material after tealeaves production, has certain health value.
In this specification, tea stalk/tea stem refers to tea stalk or tea stem.
Summary of the invention
The present invention is provided to mixtures containing plant component of reducing blood lipid and the preparation method and application thereof, it is intended to solve tea
Stalk/tea stem is for the technical issues of preventing and treating hyperlipidemia.
Technical solution of the present invention first is that a kind of mixture containing plant component for reducing blood lipid, including tea stalk/tea stem are micro-
Powder or tea stalk/tea stem extraction.Tea stalk/tea stem contains epigallocatechin gallate, epi-nutgall acid catechu
The polyphenol compounds such as element, L-Epicatechin gallate, epicatechin.
It further, further include antioxidant, preservative and sweetener, the antioxidant is sulphite or Vitamin C
Acid or both above mixture, the preservative be dihydroxy acetic acid or methaform or more than both mixture, the sweet tea
Taste agent is the mixture of sucrose or lactose or PEARLITOL 25C or the above three.
Further, further include excipient and lubricant, the excipient be starch or avicel cellulose or more than both
Mixture, the lubricant is the mixture of magnesium stearate or calcium stearate or talcum powder or the above three.
Further, the dosage form of use is granule, tablet, capsule or pill.
Mixture containing plant component provided by the present invention for reducing blood lipid includes that tea stem micro mist or tea stalk/tea stem extract
Object, tea stalk/tea stem can effectively prevent and reduce Hyperlipemia rich in a variety of polyphenol compounds, control weight, effectively pre-
It is anti-, mitigate and treat because of hyperlipidemia and complication caused by overweight.Zoopery proves, tea stem of the present invention, tea stalk
Extract is able to suppress the activity of intestine in rats lipase, reduces the decomposition of food source fat, reduces the absorption of intestinal fat,
The triglyceride levels in fat loading rat blood are reduced, and then have the function that the blood lipid that loses weight and reduce.
Technical solution of the present invention second is that the preparation method of the above-mentioned mixture containing plant component for reducing blood lipid, including with
Lower three steps:S110 will trim tea stalk/tea stem that tea tree obtains and be mechanically pulverized into average grain diameter less than 0.85mm (20 mesh)
Powder, to obtain the tea stalk/tea stem micro mist;The tea stalk/tea stem the micro mist obtained in S120, step S110 adds with described
Agent is added to mix;S130 is prepared into scheduled dosage form for mixture is obtained in step S120.The dosage form is granule, tablet, glue
The clinical applications dosage form such as wafer.
Technical solution of the present invention third is that the preparation method of the above-mentioned mixture containing plant component for reducing blood lipid, including with
Lower three steps:S210 will trim tea stalk/tea stem that tea tree obtains and be mechanically pulverized into powder;S220 obtains step S210
Raw material powder is mixed with solvent, and the solvent is water, ethyl alcohol or hydrous ethanol, and the weight ratio of the raw material powder and solvent exists
1: (10~20) then obtain the tea stalk/tea stem extraction by heating extraction, Microwave Extraction or ultrasonic extraction;S230, step
The tea stalk/tea stem extraction that rapid S220 is obtained is mixed with the additive, is then prepared into scheduled dosage form.
Further, step S220 include following three step by step:The raw material powder and water that S221, step S210 are obtained are mixed
It closes, first-time filtrate and a filter residue is obtained by filtration after heating extraction;S222 mixes a filter residue with water again, heating
Secondary filtrate is obtained by filtration after second of extraction;S223 merges the first-time filtrate and the secondary filtrate, is concentrated to get described
Tea stalk/tea stem extraction.
Provided by the present invention for the two above preparation method of the mixture containing plant component of reducing blood lipid, one is first making
Standby average grain diameter is less than tea stalk/tea stem micro mist of 0.85mm, then mixes with additive, is then prepared into scheduled dosage form;Secondly
It is that solvent is first made using water, ethyl alcohol or hydrous ethanol, prepares tea stalk/tea stem extraction, then mix with additive, be then prepared into
Scheduled dosage form.The form of micro mist or solvent extractable matter using partial size less than 0.85mm convenient for digesting and assimilating, and prepares work
Skill is simple, energy consumption is low, pollution-free.
Technical solution of the present invention fourth is that the above-mentioned mixture containing plant component for reducing blood lipid is preparing antilipemic healthy
Application in product.
Technical solution of the present invention fifth is that the above-mentioned mixture containing plant component for reducing blood lipid preparation reducing blood lipid drug
In application.
Technical solution of the present invention sixth is that the above-mentioned mixture containing plant component for reducing blood lipid preparation blood fat reducing food
In application.
It is below the constituent analysis of the tea stalk/tea stem extraction and tea extract of one embodiment:
Experiment is analyzed using high performance liquid chromatography.DIONEX liquid phase analysis instrument is 3000 type of U1timate, electronics
Balance is ten a ten thousandth type of Sartorius BP211D, and thermostatic drying chamber is Germany's Memmert type, and ultrapure water instrument is Merck
Millipore company, micromill are Hangzhou Xiong Huo Science and Technology Ltd., and acetonitrile is Fisher (chromatographically pure), and formic acid is wide
State chemical reagent factory (analysis is pure).Reference substance caffeine (Caffeine, Caff), theobromine (Theobromine, Tb), does not eat
Sub- catechin and gallate ((-)-Gallocatechin gallate, GCG), Epigallo-catechin gallate (EGCG)
((-)-Epigallocatechin gallate, EGCG) is purchased from Japanese Wako Pure Chemicals Co., Ltd.;Gallic acid (Gallic
Acid, GA), catechin ((+)-Catechin, C) is purchased from Sigma Co., USA;Nutgall catechin ((-)-
Gallocatechin, GC), epigallocatechin (Epigallocatechin, EGC), epicatechin (Epicatechin,
EC) purchased from Japanese Kurita Water Industries Ltd;L-Epicatechin gallate ((-)-Epicatechin-3-gallate, ECG)
Purchased from Shanghai Jing Chun biochemical technology limited liability company.
Chromatographic condition, chromatographic column COSMOSIL 5C18-AR-II (4.6*250mm, 5 μm, Nacalai tesque.Inc.,
Japan), flow velocity 1ml/min, quantitative detection wavelength are 231nm, and column temperature is 35 DEG C, and sample volume is 20 μ l.Mobile phase A:H2O
(containing 0.1% formic acid);Mobile phase B:CH3CN (contains 0.1% formic acid), and gradient elution program is shown in Table one.Test sample is through distilled water
It is centrifuged, is analyzed through the laggard HPLC of 0.45 μm of water film filtering, each component content is shown in Table two in sample after dissolution.
Caffeine it can be seen from table two in the extract of tea stalk/tea stem and tealeaves, in tea extract
(Caffeine, Caff) content will be significantly larger than tea stalk/tea stem extract, may result in insomnia, excitement and palpitaition etc.
Adverse reaction;And tea stalk/tea stem extract is conducive to control blood lipid level rich in polyphenol active ingredients such as catechins, rule
Keep away caffeine bring adverse reaction.
Table one, HPLC gradient elution program
Table two, alkaloid and polyphenol compound content (%) in tea stalk/tea stem and young tea leaves extract
Extract component | Tealeaves | Tea stem | Tea stalk |
GA | 0.15 | 0.17 | 0.20 |
Tb | 0.26 | 0.05 | 0.03 |
GC | 0.71 | 0.17 | 0.06 |
EGC | 2.60 | 0.53 | - |
C | 0.27 | 0.24 | 0.16 |
Caff | 3.31 | 0.91 | 0.25 |
EC | 0.85 | 0.58 | 0.17 |
EGCG | 4.58 | 1.29 | - |
GCG | 1.55 | 0.08 | - |
ECG | 1.76 | 1.04 | 0.06 |
Note:Expression does not detect
Here is tea stalk/tea stem extraction on lipase in rat small intestine (lipase) active influence.
Experimental animal is (dynamic purchased from Guangdong Province's medical experiment using the 7 week old SD rat of SPE grade of male, 200~240g of weight
Object center, credit number SCXK (Guangdong) 2013-0002).Experimental animal is raised in cleaning grade laminar-flow rack, environment temperature be 23 ±
2 DEG C, relative humidity is 75 ± 10%, and lighting hours is 12 hours/day (7:00~19:00).
Experimental animal is randomly divided into control group, tea stem extraction 50mg/kg group, tea stem extraction 100mg/kg group, tea stem
Extract 200mg/kg group and tea stalk extract 50mg/kg group, tea stalk extract 100mg/kg group, tea stalk extract 200mg/
Kg group, every group 8.The fasting 12 hours before experiment starts, each administration group is through gastric infusion, and control group stomach-filling is to isometric distillation
Water.After administration 30 minutes, experimental animal opens abdomen after yellow Jackets are anaesthetized, and takes out small intestine respectively three equal parts from upper end, note
For small intestine -1, small intestine -2 and small intestine -3, intestinal contents taking-up is placed on coverslip respectively, and removes small intestinal mucosal and is placed in load
On slide.The small intestinal mucosal and the lipase active in intestinal contents for measuring different parts respectively, while measuring its protein
Content, and the enzymatic activity in calculating and more same albumen quality.Experimental data is indicated with Mean ± S.E.M, using SPSS
19.0 softwares carry out data processing, are examined using ANOVA and carry out statistical analysis, and p < 0.05 is statistically significant.
For experimental result as shown in table two to table five, the lipase active in small intestine lumen content is significantly larger than mucous membrane of small intestine
In lipase active, the tea stem or tea stalk extract of various dose have the activity of the intraluminal lipase of small intestine significant
Inhibiting effect, and show apparent dose-effect relationship, wherein 100mg/kg and 200mg/kg tea stem extraction is to small intestine upper section pipe
Intracavitary fatty enzyme inhibition rate is respectively 45% and 66%, 100mg/kg and 200mg/kg tea stalk extract is to small intestine upper section lumen
Interior fatty enzyme inhibition rate is respectively 38% and 61%.
Table two, influence (U/g protein) of the tea stem to lipase active in the small intestinal mucosal of experimental animal
Group | Dosage | Small intestine -1 | Small intestine -2 | Small intestine -3 |
Control group | - | 3157.6±455.9 | 2166.7±424.4 | 1024.1±234.6 |
Tea stem extraction group | 50mg/kg | 2748.3±420.2 | 1944.5±173.8 | 891.3±195.1 |
Tea stem extraction group | 100mg/kg | 2702.4±327.4 | 1298.7±257.4 | 940.7±122.2 |
Tea stem extraction group | 200mg/kg | 2640.8±361.8 | 1088.3±208.2 | 835.8±198.4 |
Table three, influence (U/g protein) of the tea stalk to lipase active in the small intestinal mucosal of experimental animal
Group | Dosage | Small intestine -1 | Small intestine -2 | Small intestine -3 |
Control group | - | 3157.6±455.9 | 2166.7±424.4 | 1024.1±234.6 |
Tea stalk extract group | 50mg/kg | 2968.7±437.5 | 1907.2±195.0 | 1036.0±113.6 |
Tea stalk extract group | 100mg/kg | 2852.1±369.2 | 1403.6±272.7 | 962.6±146.9 |
Tea stalk extract group | 200mg/kg | 2826.1±466.9 | 1175.3±246.1 | 902.7±202.4 |
Note:* indicate that P < 0.05, material indicate P < 0.01, there is statistical difference compared with the control group.
Table four, the measurement (U/g protein) of lipase active in experimental animal small intestine lumen content
Group | Dosage | Small intestine -1 | Small intestine -2 | Small intestine -3 |
Control group | - | 13607.9±856.2 | 3407.2±472.5 | 179.5±50.4 |
Tea stem extraction group | 50mg/kg | 9213.2±1029.4 | 2083.2±334.3 | 163.9±35.7 |
Tea stem extraction group | 100mg/kg | 7493.2±606.4** | 1533.3±194.9* | 137.5±63.8 |
Tea stem extraction group | 200mg/kg | 4577.2±494.8*** | 2085.3±609.6 | 147.5±49.6 |
Table five, the measurement (U/g protein) of lipase active in experimental animal small intestine lumen content
Group | Dosage | Small intestine -1 | Small intestine -2 | Small intestine -3 |
Control group | - | 13607.9±856.2 | 3407.2±472.5 | 179.5±50.4 |
Tea stalk extract group | 50mg/kg | 10341.3±1260.5 | 2338.3±357.1 | 183.9±38.1 |
Tea stalk extract group | 100mg/kg | 8378.0±653.9** | 2808.8±573.8 | 146.4±55.6 |
Tea stalk extract group | 200mg/kg | 5356.7±403.9*** | 1717.8±208.1* | 165.6±61.4 |
Note:*-P < 0.05, material-P < 0.01 expects *-P < 0.001, there is statistical difference compared with the control group.
Here is influence of the tea stalk/tea stem extraction to triglycerides (TG) level in fat loading rat blood.
Experimental animal is (dynamic purchased from Guangdong Province's medical experiment using the 7 week old SD rat of SPE grade of male, 200~240g of weight
Object center, credit number SCXK (Guangdong) 2013-0002).Experimental animal is raised in cleaning grade laminar-flow rack, environment temperature be 23 ±
2 DEG C, relative humidity is 75 ± 10%, and lighting hours is 12 hours/day (7:00~19:00).
Experimental animal is randomly divided into control group, tea stem extraction 100mg/kg group, tea stem extraction 200mg/kg group, tea stalk
Extract 100mg/kg group and tea stalk extract 200mg/kg group, every group 8.Fasting 12 hours, respectively gives before experiment starts
Medicine group gives isometric distilled water through gastric infusion, control group stomach-filling.After administration 30 minutes, 5ml/kg olive is given in stomach-filling respectively
Oil, and before olive oil load, 2 after load, 4,6,8 hours different time points take blood through tail vein, measure its difference
The TG of time is horizontal.Experimental data is indicated with Mean ± S.E.M, is carried out data processing using 19.0 software of SPSS, is used
ANOVA, which is examined, carries out statistical analysis, and p < 0.05 is statistically significant.
Experimental result is as shown in Table 6, and after giving rat 5ml/kg olive oil, the triglyceride levels in blood are significantly risen
Height, and reach peak value after 6 hours, it is then gradually reduced, tea stem, the tea stalk extract of various dose can be to a certain extent
Inhibit the rising of TG value.
Table six, the horizontal measured value of TG of the experimental rat after fat loading (mmol/L)
Note:* indicate that P < 0.05, material indicate P < 0.01, there is statistical difference compared with the control group.
Here is the influence of influence of the tea stalk/tea stem extraction to high sugar, Induced by High Fat Diet in Rats weight.
Experimental animal is (dynamic purchased from Guangdong Province's medical experiment using the 7 week old SD rat of SPE grade of male, 200~240g of weight
Object center, credit number SCXK (Guangdong) 2013-0002).Experimental animal is raised in cleaning grade laminar-flow rack, environment temperature be 23 ±
2 DEG C, relative humidity is 75 ± 10%, and lighting hours is 12 hours/day (7:00~19:00).
Experimental animal is randomly divided into control group, tea stem extraction 100mg/kg group, tea stem extraction 200mg/kg group, tea stalk
Extract 100mg/kg group and tea stalk extract 200mg/kg group, every group 10.Feed for nursing is containing lard 10%, cholesterol
2%, the high glucose and high fat fat feed of yolk powder 5%, propylthiouracil 0.2%, sucrose 10%, basal feed 72.8%.Respectively give
The daily gastric infusion of medicine group is primary, control group stomach-filling give isometric distilled water, Therapy lasted 24 days.It is measured daily simultaneously during experiment
Record the weight of rat.Experimental data is indicated with Mean ± S.E.M, is carried out data processing using 19.0 software of SPSS, is used
ANOVA, which is examined, carries out statistical analysis, and p < 0.05 is statistically significant.
Experimental result is as shown in Table 5, continuously gives high sugar, after high fat diet 24 days, the weight of experimental rat obviously increases
Add, compared with the control group, rat body weight increase can be significantly inhibited by giving tea stem, tea stalk extract.
Table seven, the influence (g) of high sugar, Induced by High Fat Diet in Rats weight
Note:Material indicates P < 0.01, there is statistical difference compared with the control group.
Specific embodiment
Specific embodiments of the present invention will be further explained below.It should be noted that for these implementations
The explanation of mode is used to help understand the present invention, but and does not constitute a limitation of the invention.In addition, invention described below
Technical characteristic involved in each embodiment can be combined with each other as long as they do not conflict with each other.
Tea stem and tea stalk used in following embodiment are provided by Guizhou Pu'an Hong Xin tea processing factory, have been cleaned and have tentatively been crushed.
Embodiment 1, for make blood fat reducing food containing tea stalk/tea stem micro mist mixture
Tea stem and tea stalk raw material are ground into the powder that average grain diameter is less than 0.85mm (20 mesh);Every above-mentioned tea of 100 parts by weight
1 part of ascorbic acid, 0.2 part of dihydroxy acetic acid, 2 parts of PEARLITOL 25C, 20 parts of cornstarch, stearic acid are added in stalk/tea stem micro mist
It 3 parts of calcium, 100 parts of water, dries after mixing;
It is particle of the average grain diameter less than 0.85mm to get the mixture that dried object, which crushes,.The mixture adds as bread
Add agent in use, 1~5g is added in every 100 grams of bread wheat flour speciallies.
Embodiment 2, make blood fat reducing health products containing tea stalk/tea stem micro mist mixture
Tea stem and tea stalk raw material are ground into the powder that average grain diameter is less than 0.85mm (20 mesh);Every above-mentioned tea of 100 parts by weight
1 part of ascorbic acid, 0.2 part of dihydroxy acetic acid, 2 parts of PEARLITOL 25C, 10 parts of avicel cellulose, tristearin are added in stalk/tea stem micro mist
3 parts of sour calcium, 90 parts of water, are dried after mixing.
Dried object is tabletted or pill, or records as capsule.Tablet/pill/the capsule makees blood fat reducing health products, temperature
Water takes oral, takes 1~5g after the meal.
Embodiment 3, the preparation of tea stalk/tea stem extraction
Raw material is ground into coarse powder, 500g coarse powder is taken, sets in extractor, adds 20 times of amount water refluxing extractions, keeps boiling 8 small
When, filtering, filter residue adds 20 times of amount water refluxing extractions, keeps boiling 1 hour, and filtering merges filtrate twice.Filtrate sets concentration
The liquid extract that relative density is 1.2 or so is concentrated under reduced pressure into for 60 DEG C in tank, and liquid extract, which takes out, is packed into pallet, so freeze-dried that mention
Take object about 50g.
Embodiment 4, the preparation of tea stalk/tea stem extraction
Raw material is ground into coarse powder, 500g coarse powder is taken, sets in extractor, 10 times of 50% ethanol water of amount reflux is added to mention
It takes, keeps boiling 2 hours, filtering, filter residue adds 10 times of 50% alcohol refluxs of amount and extracts, and keeps boiling 1 hour, filters, and closes
And filtrate twice.Filtrate sets in concentration tank and is concentrated under reduced pressure into the liquid extract that relative density is 1.0 or so for 60 DEG C, freeze-dried to obtain
Extract about 50g.
The extract, the tea extract prepared in aforementioned manners, be used for more than test analysis.
Embodiment 5, be used to prepare reducing blood lipid drug containing tea stalk/tea stem extraction mixture
The above tea stalk/tea stem extraction is prepared into a variety of pharmaceutical preparations, adds conventional excipient, lubricant, anti-oxidant
The additives such as agent, preservative, colorant, sweetener;Wherein, preferred excipient has lactose, white sugar, PEARLITOL 25C, starch, knot
Crystalline cellulose etc.;Preferred lubricant has magnesium stearate, calcium stearate, talcum powder etc.;Preferred antioxidant have sulphite,
Ascorbic acid etc.;Preferred preservative has dihydroxy acetic acid, methaform etc..Tea stalk/tea stem extraction is mixed evenly with additive
Afterwards, granule, tablet, capsule or pill etc. is made.The mode of taking of said medicine preparation is to take orally after the meal, each taking agent
In amount tea stalk/tea stem extraction content be 0.2~0.6g.
Above the embodiments of the present invention are described in detail, but the present invention is not limited to described embodiments.It is right
For those skilled in the art, in the case where not departing from the principle of the invention and spirit, these embodiments are carried out more
Kind change, modification, replacement and modification, still fall in protection scope of the present invention.
Claims (10)
1. a kind of mixture containing plant component for reducing blood lipid, characterized in that including tea stalk/tea stem micro mist or tea stalk/tea stem
Extract.
2. containing the plant component mixture according to claim 1 for reducing blood lipid, characterized in that further include anti-oxidant
Agent, preservative and sweetener, the antioxidant be sulphite or ascorbic acid or more than both mixture, the anti-corrosion
Agent be dihydroxy acetic acid or methaform or more than both mixture, the sweetener be sucrose or lactose or PEARLITOL 25C or with
The mixture of upper three.
3. containing the plant component mixture according to claim 2 for reducing blood lipid, characterized in that further include excipient and
Lubricant, the excipient be starch or avicel cellulose or more than both mixture, the lubricant be magnesium stearate or
Calcium stearate or talcum powder or the mixture of the above three.
4. containing the plant component mixture according to claim 2 or 3 for reducing blood lipid, characterized in that the dosage form of use
It is granule, tablet, capsule or pill.
5. a kind of method for preparing the mixture described in claim 1 containing plant component for reducing blood lipid, characterized in that including
Three steps below:The powder for being less than 0.85mm at average grain diameter is mechanically pulverized in tea stalk/tea stem by S110, thus described in obtaining
Tea stalk/tea stem micro mist;The tea stalk/tea stem the micro mist obtained in S120, step S110 is mixed with the additive;S130, will
Mixture is obtained in step S120 is prepared into scheduled dosage form.
6. a kind of method for preparing the mixture described in claim 1 containing plant component for reducing blood lipid, characterized in that including
Three steps below:
S210 will trim tea stalk/tea stem that tea tree obtains and be mechanically pulverized into powder;
S220 mixes the step S210 raw material powder obtained with solvent, the solvent be water, ethyl alcohol or hydrous ethanol, it is described
Raw material powder and solvent weight ratio 1: (1~20) then obtains institute by heating extraction, Microwave Extraction or ultrasonic extraction
State tea stalk/tea stem extraction;
The tea stalk/tea stem extraction that S230, step S220 are obtained is mixed with the additive, is then prepared into scheduled dose
Type.
7. the preparation method of the mixture according to claim 6 containing plant component for reducing blood lipid, characterized in that step
S220 include following three step by step:The powder that S221, step S210 are obtained is mixed with water, is obtained by filtration after heating extraction primary
Filtrate and a filter residue;S222 remixes a filter residue with water, and secondary filter is obtained by filtration after second of extraction of heating
Liquid;S223 merges the first-time filtrate and secondary filtrate, is concentrated to get the tea stalk/tea stem extraction.
8. containing the plant component mixture according to claim 1 for reducing blood lipid is preparing answering in blood fat reducing health products
With.
9. containing the plant component mixture according to claim 1 for reducing blood lipid answering in preparation reducing blood lipid drug
With.
10. containing the plant component mixture according to claim 1 for reducing blood lipid answering in preparation blood fat reducing food
With.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000327572A (en) * | 1999-05-18 | 2000-11-28 | Mitsui Norin Co Ltd | Squalene epoxidase inhibitor |
CN102068557A (en) * | 2009-11-25 | 2011-05-25 | 云南天士力生物茶科技有限公司 | Application of Pu'er tea extract in preparation of medicines for reducing blood fat |
CN102771593A (en) * | 2011-05-13 | 2012-11-14 | 贵州省生物研究所 | Ampelopsis grossedentata preparation for reducing blood sugar, blood lipid and blood pressure and its preparation method |
CN106924527A (en) * | 2017-03-07 | 2017-07-07 | 广州馥邦科技应用有限公司 | It is a kind of for medicine that is antifatigue, improving the health care of sleep food and preparation method thereof |
-
2018
- 2018-08-09 CN CN201810912912.4A patent/CN108904643A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000327572A (en) * | 1999-05-18 | 2000-11-28 | Mitsui Norin Co Ltd | Squalene epoxidase inhibitor |
CN102068557A (en) * | 2009-11-25 | 2011-05-25 | 云南天士力生物茶科技有限公司 | Application of Pu'er tea extract in preparation of medicines for reducing blood fat |
CN102771593A (en) * | 2011-05-13 | 2012-11-14 | 贵州省生物研究所 | Ampelopsis grossedentata preparation for reducing blood sugar, blood lipid and blood pressure and its preparation method |
CN106924527A (en) * | 2017-03-07 | 2017-07-07 | 广州馥邦科技应用有限公司 | It is a kind of for medicine that is antifatigue, improving the health care of sleep food and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
尚进 等: "响应面法优化铁观音茶梗中茶多糖提取工艺", 《基因组学与应用生物学》 * |
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