CN101744844B - Fulvic acid or sodium fulvate substance with hypoglycemic function - Google Patents

Fulvic acid or sodium fulvate substance with hypoglycemic function Download PDF

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Publication number
CN101744844B
CN101744844B CN2009102183557A CN200910218355A CN101744844B CN 101744844 B CN101744844 B CN 101744844B CN 2009102183557 A CN2009102183557 A CN 2009102183557A CN 200910218355 A CN200910218355 A CN 200910218355A CN 101744844 B CN101744844 B CN 101744844B
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fulvic acid
sodium fulvate
sulfuric acid
acid ester
fulvate
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CN101744844A (en
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李宝才
毕艳艳
张惠芬
何静
李月梅
梅展青
李鹏
戴伟峰
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YUNNAN HIGH GRADE BIOTECHNOLOGY Co Ltd
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Kunming University of Science and Technology
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Abstract

The invention relates to a health care product and a drug, in particular to a fulvic acid or sodium fulvate substance health care product and a drug with hypoglycemic function; the fulvic acid or sodium fulvate substance with hypoglycemic function is provided, in particular to the health care product, and the health care product is oral solution, the ingredients of the oral solution are as follows by mass percentage: 1-10 percent of the fulvic acid or the sodium fulvate, 0.5-10 percent of polysaccharide sulfate and the remaining is water; the fulvic acid or sodium fulvate substance health care product can remarkably reduce the content of the blood sugar, total cholesterol and triglycercide of diabetics, increase the oral carbohydrate tolerance, and has a function of regulating blood sugar level; the fulvic acid or sodium fulvate substance health care product is a purely natural product, is safe and reliable and has no toxic and side effect, thereby being the health care product which can meet the needs of people.

Description

Fulvic acid or sodium fulvate material with hypoglycemic activity
Technical field
The present invention relates to a kind of health product and medicine, particularly relate to a kind of fulvic acid or sodium fulvate health product and medicine with hypoglycemic activity.
Background technology
Diabetes are a kind of more common chronic metabolic diseases of whole body by gene and the common decision of environment, and main feature is a chronic hyperglycemia, and follows sugar, protein and the fat metabolic disturbance that is caused by insulin secretion obstacle and insulin action defective.The classical symptom of diabetes is " three-many-one-littles ", i.e. drinking a lot of water, and diet is many; Frequent micturition and losing weight is controlled and badly will be caused many general complication, and for example: cardiovascular, kidney and neural chronic diseases become; Have a strong impact on human health, and threaten patient's life.
Along with the progress of society, great change has taken place in people's dietary structure, and diabetes prevalence also constantly rises.In many countries such as America and Europes, the mortality rate of diabetes is very high, after cardiovascular disease and tumor, classifies the 3rd as.At present, global diabetics reaches 1.5 hundred million people, expects onset diabetes rate in 2025 and will be outburst trend, will increase to 300,000,000, and wherein the diabetics number of China, India will reach 40% of the whole world.Because people constantly increase the needs of health, diabetes are paid close attention to by people day by day.
People are not limited only to blood sugar lowering to the requirement of antidiabetic drug now; Also requiring has blood fat reducing in blood sugar lowering, improve the functions such as carbohydrate tolerance of diabetics, has or not toxicity, action temperature with, slowly and lasting, the advantage of stable in properties.Because in the natural product, often multiple cofactor combined effect, multiple sugar-lowering components is also deposited.So it is significant in natural drug, to seek the medicine of blood sugar lowering safely and effectively and control diabetic complication.
Fulvic acid is that a kind of degree of oxidation is high, and it is many to contain active function groups, the utilization that is prone to be absorbed by the body, a kind of humic acids that medical effect is best.Before several thousand, Li Shizhen (1518-1593 A.D.) is the existing medicinal record of similar humic acids in Compendium of Material Medica, mainly reaches diseases such as all sores, incised wound are hemorrhage bitterly in order to treatment nosebleed, women's QI and blood.But do not see the report that fulvic acid and the effect of sodium fulvate aspect blood sugar lowering are arranged in the prior art.
Summary of the invention
The object of the present invention is to provide a kind of fulvic acid or sodium fulvate health product and medicine with hypoglycemic activity.
The present invention is based on theabrownin of Pu'er tea and fulvic acid aspect chemical property (structure and functional group) and have certain similarity; Infer that fulvic acid and sodium fulvate should have similarity in physiologically active and treatment function aspects and tea pigment; Should have function of blood sugar reduction; Therefore, develop following technical proposals of the present invention and realize the object of the invention:
Have the fulvic acid or the sodium fulvate material of hypoglycemic activity, this material is composed of the following components by mass percentage:
Fulvic acid or sodium fulvate 1% ~ 10%
Polysaccharide sulfuric acid ester 0.5% ~ 10%
Its surplus of water
The preferential content 2% of recommending fulvic acid or sodium fulvate, polysaccharide sulfuric acid ester 0.5, water surplus.
Fulvic acid of the present invention extracts with chemical method or bioanalysis; Sodium fulvate adopts the neutralisation preparation, and sodium fulvate serves as that the preparation of acid-base neutralization method is adopted on the basis with the fulvic acid that extracts.The polysaccharide sulfuric acid ester extracts with water extraction.
Fulvic acid or sodium fulvate health product that the present invention has hypoglycemic activity are the oral liquid formulations that contain fulvic acid or sodium fulvate.
The present invention also provides application and the application in the preparation health-caring product capable of reducing blood sugar in the preparation hypoglycemic drug of fulvic acid or sodium fulvate.
The method for preparing of fulvic acid of the present invention or sodium fulvate medicine comprises the steps:
1) preparation of fulvic acid and sodium fulvate:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate;
2) preparation of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester;
3) get 1) gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → by weight percentage fulvic acid or sodium fulvate 1% ~ 10%, polysaccharide sulfuric acid ester 0.5% ~ 10% adds polysaccharide sulfuric acid ester → mix → add pharmaceutical carrier by the conventional way of oral drugs to process fulvic acid or sodium fulvate drug oral medicament.
The method for preparing of fulvic acid or sodium fulvate health product is provided simultaneously, comprises the steps:
1) preparation of fulvic acid and sodium fulvate:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate;
2) preparation of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester;
3) get 1) gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → by mass percentage fulvic acid or sodium fulvate 1% ~ 10%, polysaccharide sulfuric acid ester 0.5% ~ 10% adds polysaccharide sulfuric acid ester → mix → fully dissolving → sterilization → bottling → fulvic acid or sodium fulvate health product.
The present invention compares with existing hypoglycemic drug, has the following advantages:
1, the present invention can obviously reduce the content of blood glucose, T-CHOL, triglyceride in the diabetes human body, increases diabetes patient's carbohydrate tolerance, has obvious hypoglycemic effect.
2, the invention belongs to all-natural product, safe and reliable, have no side effect, sour-sweet mouthfeel is arranged, be fit to drink.
3, method for preparing of the present invention is simple, and cost consumption is low, has economic advantage.
Description of drawings:
Fig. 1 is the result of variations of mice body weight in fulvic acid and the sodium fulvate acute toxicity testing.
Specific embodiments:
Below in conjunction with accompanying drawing, further specify essentiality content of the present invention with the embodiment of the invention, but do not limit the present invention with this.
Embodiment 1-8:
Embodiment 1-8 all carries out with following step:
1. prepare fulvic acid and sodium fulvate, its preparation technology's flow process is following:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate.
2. it is following to extract the technological process of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester.
3. the preparation technology of preparation health product of the present invention is following:
Get 1 gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → fulvic acid or sodium fulvate 1% ~ 10% by mass percentage, polysaccharide sulfuric acid ester 0.5% ~ 10% adds polysaccharide sulfuric acid ester → mix → fully dissolving → sterilization → bottling → fulvic acid or sodium fulvate health product.
The one-tenth component selections of the health product that embodiment 1-8 is prepared is seen table 1.
Table 1 health product composition of the present invention (in quality %)
In above-mentioned implementing process flow process, case study on implementation ratio, can process bottled oral liquid health product with sober-up and anti-drunk function.
Embodiment 9:
1) contain the medication preparation of fulvic acid and sodium fulvate:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate;
2) preparation of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester;
3) get 1) gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → by mass percentage fulvic acid or sodium fulvate 4%; Polysaccharide sulfuric acid ester 0.5% adding polysaccharide sulfuric acid ester → mix → add pharmaceutical carrier by the conventional way of oral drugs is processed fulvic acid or sodium fulvate drug oral medicament.
Can process bottled oral administration solution health product or the medicine with hypoglycemic activity of the present invention by the foregoing description.Do pharmacologic action and the pharmacological action that following animal experiment example is explained product of the present invention with above-mentioned health product of the present invention or medicine:
Test Example 1:
The animal experiment study of hypoglycemic activity of the present invention
1. main experimental apparatus and reagent material
1.1 main experimental apparatus
ELIASA: Molecular Devices company; Micro centrifuge: Anting Scientific Instrument Factory, Shanghai; Balance: the two outstanding test instrunment in Changshu factory; Liquid-transfering gun (2 μ L): Dragon Medical(Shanghai) Co., Ltd..
1.2 main agents and material
Alloxan: Sigma company; Glucose enzyme process blood sugar detection box, triglyceride test kit, cholesterol reagent box: ShangHai RongSheng Biology Pharmacy Co., Ltd; Glucose (analytical pure): Tianjin Fengchuan Chemical Reagent Science & Technology Co., Ltd.; Metformin hydrochloride: Shenzhen Haiwang Pharmaceutical Co., Ltd.
Humic acids, sodium fulvate and polysaccharide sulfuric acid ester: the preparation of this lab assistant.
" Handilong " sodium fulvate: provide by the logical Handilong humic acids company limited of Xinjiang remittance.
" two dragon " sodium fulvate: provide by Xinjiang Shuanglong Humate and Humic Acid Co., Ltd..
Kunming mice: buy the male mouse of kunming number of clean level from unming Medical College, adaptability is fed 2-3d, chooses body weight 18 ~ 22g mice and experimentizes.
2. experimental technique
2.1 acute toxicity testing
Get 20 kunming mices, body weight is 18-22g, is divided into 2 groups, 10 every group, and male and female half and half.Water 12h is can't help in fasting, irritates stomach respectively for two groups and gives fulvic acid and sodium fulvate with 5g/kg dosage, observes 14d, and the dead mouse number respectively organized in record, and measured the mice body weight in per two days.
2.2 influence to normal mouse blood sugar
Get 64 Male Kunming strain mice; Be divided into 8 groups at random; Every group 8; It is the blank group; The metformin hydrochloride positive controls, low (1% fulvic acid+0.5% polysaccharide sulfuric acid ester), in (2% fulvic acid+0.5% polysaccharide sulfuric acid ester), high (4% fulvic acid+0.5% polysaccharide sulfuric acid ester) concentration fulvic acid group (laboratory self-control), low (1% sodium fulvate+0.5% polysaccharide sulfuric acid ester), in (2% sodium fulvate+0.5% polysaccharide sulfuric acid ester), height (4% sodium fulvate+0.5% polysaccharide sulfuric acid ester) concentration sodium fulvate group (laboratory self-control).Each organizes mice by 0.2ml/10g body weight gastric infusion, and the blank group is irritated stomach equal-volume distilled water, every day gastric infusion, 7d continuously.After water 12h is can't help in fasting after the last administration, get blood, press blood sugar detection test kit time-and-motion study blood glucose value in mouse tail vein.
2.3 alloxan modeling experiment
Get male mice, water 12h is can't help in fasting.Alloxan is made into fresh 2% solution with physiological saline solution, and intraperitoneal injection, dosage are 250mg/kg.For preventing dead mouse 4.5~5h behind intraperitoneal injection, irritate the stomach mice with mass fraction 50% glucose, every dosage is the 0.2mL/10g body weight.After one week, getting tail vein and detect fasting glucose, is diabetic mice with the mice of blood glucose more than 11.1mmol/L, becomes the mould integral animal to show the symptom of " three-many-one-little ", promptly takes food, drinking-water and hydrouria, and diabetic symptom such as lose weight.To become the mould mice to include experiment in.
2.4 influence (carbohydrate tolerance test) to blood glucose in diabetic mice
The mice that modeling is successful is divided into 11 groups at random by blood glucose value and body weight; Every group 8: the blank group; Model control group; The metformin hydrochloride positive controls; " Handilong " (2% sodium fulvate+0.5% polysaccharide sulfuric acid ester) group; " two dragon " (2% sodium fulvate+0.5% polysaccharide sulfuric acid ester) group, low (1% fulvic acid+0.5% polysaccharide sulfuric acid ester), in (2% fulvic acid+0.5% polysaccharide sulfuric acid ester), high (4% fulvic acid+0.5% polysaccharide sulfuric acid ester) concentration fulvic acid group (laboratory self-control), low (1% sodium fulvate+0.5% polysaccharide sulfuric acid ester), in (2% sodium fulvate+0.5% polysaccharide sulfuric acid ester), height (4% sodium fulvate+0.5% polysaccharide sulfuric acid ester) concentration sodium fulvate group (laboratory self-control).Each organizes mice by 0.2ml/10g body weight gastric infusion, and blank group and model control group all give isopyknic distilled water, irritate stomach every day once, continuous irrigation stomach 12d.Water 12h is can't help in the mice fasting 11d evening, tail vein measuring blood sugar of blood extracting, triglyceride and cholesterol level behind the morning next day gastric infusion 1.5h.Experimental session respectively at 6d, 12d respectively fasting tail vein get blood examination and survey blood glucose.12d evening respectively to model group, matched group, basic, normal, high concentration fulvic acid group and sodium fulvate group (laboratory self-control) the mice fasting can't help water 12h, get blood from the tail vein and survey fasting glucose morning next day.Gastric infusion behind the survey blood glucose is irritated stomach 2.5g/kg glucose behind the 1h, respectively at 0.5h, and 1h, 2h measures blood glucose value by tail vein blood.
Assay method: the content of measuring blood glucose in the blood plasma, cholesterol and triglyceride according to the description of glucose enzyme process blood sugar detection box, triglyceride test kit and cholesterol reagent box respectively.
Blood extracting method: the tail vein is got blood, and 4 ℃ leave standstill centrifugal behind the 1h (3000r/min, 1min) preparation serum.
2.5 statistical procedures data
Adopt one factor analysis of variance or student-t inspection statistics in the spss statistical software to analyze result of experiment, represent, P<0.05 expression significant difference, P<0.01 expression difference highly significant with X ± S.
3. result and analysis
3.1 acute toxicity testing result
The filling stomach is given fulvic acid and the sodium fulvate with 5g/kg dosage, observes 14d, and dead phenomenon does not appear in two groups of mices of result.Two groups of mice body weight change results see accompanying drawing 1.Can get fulvic acid and sodium fulvate can be considered nontoxic by above result.
3.2 normal mouse blood sugar value influenced result's (seeing table 2).
Table 2 fulvic acid and sodium fulvate to the influence of normal mouse blood sugar (x ± s, n=10)
Figure G2009102183557D00081
Annotate: compare with blank control group: * * P<0.01; Compare #P<0.05, ##P<0.01 with matched group.
3.3 blood glucose in diabetic mice influenced result's (seeing table 3).
Table 3 humic acids and sodium fulvate to the blood glucose in diabetic mice value influence the result (x ± s, n=10)
Figure G2009102183557D00082
Figure G2009102183557D00091
Annotate: compare * P<0.05 with model group.
3.4 diabetic mice triglyceride, T-CHOL influenced result's (seeing table 4).
Table 4 fulvic acid and sodium fulvate to diabetic mice triglyceride, T-CHOL influence the result (x ± s, n=10)
Figure G2009102183557D00092
Annotate: compare with model group: * P<0.05, * * P<0.01.
3.5 the oral glucose tolerance experimental result (seeing table 5) of diabetic mice.
Table 5 fulvic acid and sodium fulvate to the diabetic mice oral glucose tolerance influence the result (x ± s, n=10)
Annotate: compare * P<0.05, * * P<0.01 with model group; Compare with matched group: #P<0.05.
4. conclusion:
Prove through above experiment; Fulvic acid and sodium fulvate health product can obviously reduce the content of blood glucose, T-CHOL, triglyceride in the mice body; Increase the carbohydrate tolerance of mice, therefore draw the effect that the health product that contain fulvic acid and sodium fulvate and medicine have blood sugar lowering.

Claims (10)

1. have the fulvic acid or the sodium fulvate material of hypoglycemic activity, this material is composed of the following components by mass percentage:
Fulvic acid or sodium fulvate 1%~10%
Polysaccharide sulfuric acid ester 0.5%~10%
Its surplus of water.
2. according to the described material of claim 1, wherein the content of fulvic acid or sodium fulvate is 2%, polysaccharide sulfuric acid ester 0.5%, water surplus.
3. according to the described material of claim 1, it is characterized in that fulvic acid extracts with chemical method or bioanalysis; Described sodium fulvate adopts the neutralisation preparation.
4. according to the described material of claim 1, it is characterized in that sodium fulvate is serves as that the preparation of acid-base neutralization method is adopted on the basis with the fulvic acid that extracts.
5. according to the described material of claim 1, described polysaccharide sulfuric acid ester extracts with water extraction.
6. the oral liquid formulations that contains claim 1 fulvic acid or sodium fulvate.
7. claim 1 fulvic acid or the sodium fulvate application in the preparation hypoglycemic drug.
8. claim 1 fulvic acid or the sodium fulvate application in the preparation health-caring product capable of reducing blood sugar.
9. the method for preparing of described fulvic acid of claim 1 or sodium fulvate medicine comprises the steps:
1) preparation of fulvic acid and sodium fulvate:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate;
2) preparation of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester;
3) get 1) gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → by weight percentage fulvic acid or sodium fulvate 1%~10%, polysaccharide sulfuric acid ester 0.5%~10% adds polysaccharide sulfuric acid ester → mix → add pharmaceutical carrier by the conventional way of oral drugs to process fulvic acid or sodium fulvate drug oral medicament.
10. the method for preparing of described fulvic acid of claim 1 or sodium fulvate health product comprises the steps:
1) preparation of fulvic acid and sodium fulvate:
Brown coal → crushing screening → get fine breeze → add hydrogen peroxide degrade → get upper strata liquid → centrifugal sucking filtration → get solution → drying → bullion fulvic acid → purification by macroporous resin → must make with extra care fulvic acid → add NaOH → sodium fulvate;
2) preparation of polysaccharide sulfuric acid ester:
Thallus Laminariae (Thallus Eckloniae) → add water heating extraction → get solution → concentrate → twice purification of bullion polysaccharide sulfuric acid ester → ethanol → must make with extra care the polysaccharide sulfuric acid ester;
3) get 1) gained fulvic acid or sodium fulvate → add water to stir → fully dissolving → by mass percentage fulvic acid or sodium fulvate 1%~10%, polysaccharide sulfuric acid ester 0.5%~10% adds polysaccharide sulfuric acid ester → mix → fully dissolving → sterilization → bottling → fulvic acid or sodium fulvate health product.
CN2009102183557A 2009-12-14 2009-12-14 Fulvic acid or sodium fulvate substance with hypoglycemic function Expired - Fee Related CN101744844B (en)

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CN103462085B (en) * 2013-09-24 2014-12-31 昆明理工大学 Spicy eel and preparation method thereof
CN103519214B (en) * 2013-10-12 2014-10-01 昆明理工大学 Low-salt flavor poultry meat and preparation method thereof
CN105832860A (en) * 2016-05-04 2016-08-10 昆明理工大学 Fulvic acid oral liquid capable of resisting altitude stress and preparation method thereof
JP7038424B2 (en) * 2018-01-29 2022-03-18 株式会社スタイルアンドバリュージャパン Food composition for improving or preventing lifestyle-related diseases

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101033231A (en) * 2007-04-29 2007-09-12 晋城市炬坤生物科技有限公司 Method of preparing high-purity medical xanthonumic acid

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101033231A (en) * 2007-04-29 2007-09-12 晋城市炬坤生物科技有限公司 Method of preparing high-purity medical xanthonumic acid

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
袁明霞等.黄腐酸钠对糖尿病大鼠视网膜病变的作用.《微循环学杂志》.2001,第11卷(第1期),11-13. *

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