CN1899515A - Synergistic medicinal composition for treating hepatitis - Google Patents
Synergistic medicinal composition for treating hepatitis Download PDFInfo
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- CN1899515A CN1899515A CNA2006100909823A CN200610090982A CN1899515A CN 1899515 A CN1899515 A CN 1899515A CN A2006100909823 A CNA2006100909823 A CN A2006100909823A CN 200610090982 A CN200610090982 A CN 200610090982A CN 1899515 A CN1899515 A CN 1899515A
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Abstract
The present invention discloses synergistic medicinal composition of tiopronin and Chinese medicine extract and the application of the composition in preparing medicine for auxiliary treatment of hepatitis.
Description
Invention field
The present invention relates to the Pharmaceutical composition formed by tiopronin and Chinese medicine extract, and the purposes of said composition in the medicine of preparation adjuvant treating hepatitis.
Background technology
Hepatitis has multiple sorting technique clinically, classifies as (1) nosetiology: viral hepatitis can be divided into five types is first, second, third, fourth, penta.(2) clinical classification can be divided into following a few type: 1. acute anicteric hepatitis, this is a modal type in the viral hepatitis, see with B-mode, third type, hepatitis D more, general this type of hepatitis clinical symptoms is less, and transaminase's elevated levels is lower, and Histological change is light, mortality rate is lower, but the course of disease can be delayed the long period, and " three is slow " characteristics are arranged, and morbidity is slow, recovery is slow, delay also slow (referring to the long meaning slowly); 2. acute icterohepatitis is less relatively compared with anicteric hepatitis, and the state of an illness is a self limiting often, and how good prognosis is, but minority can develop into hepatitis gravis; 3. chronic hepatitis: relevant experts in 1994 propose the name and the suggestion of chronic hepatitis again, with the cause of disease is the diagnosis name that chronic hepatitis is determined on the basis, simultaneously ordered grade scale, formulated standard by stages according to degree of hepatic fibrosis again according to the downright bad order of severity of hepatitis inflammation; 4. hepatitis gravis can be divided into acute heavy type, severe subacute and chronic heavy type again; 5. cholestatic hepatitis.
Wherein hepatitis B is caused by hepatitis B virus, serves as main a kind of infectious disease that also can cause multiple organ injury with the liver inflammatory lesion.China is the most popular country of hepatitis B, reaches more than 35% some local crowd infection rate, and be the most serious infectious disease of current harm people ' s health.According to investigations, China's hepatitis B patient is about 2,700 ten thousand, and annual New Development patient about 9,000,000.
The hepatitis B clinical manifestation is various, easily develops into chronic hepatitis and liver cirrhosis, and a few peoples finally develop into hepatocarcinoma.Hepatic fibrosis is the total pathological change of many chronic hepatopathy evolutions, and the damage of chronic, persistence is the prerequisite that hepatic fibrosis forms.Cause the factor of hepatic injury a lot,, hepatitis B, liver cirrhosis, take some drugs for a long time and can cause acute and chronic liver injury generally because of factors such as medicine, a large amount of ethanol, allergy cause acute liver damage.By reducing detrimental effect to liver function, can adjuvant treating hepatitis.
The medicine that is used for the treatment of the acute and chronic hepatic injury at present, commonly used have tiopronin, a diammonium glycyrrhizinate etc.These chemicalses generally have certain side effect, and cause that therapeutic effect at a specified future date is poor, problem such as Strain produces after drug resistance phenomenon, the drug withdrawal relapse rate height.
The curative effect of Chinese medicine hepatitis B is proved by a large amount of clinical trials.Chinese medicine all can be brought into play curative effect preferably at aspects such as antiviral, adjusting immunity of organisms, protection hepatocyte.But Chinese medicine preparation ubiquity onset at present is slow, needs problems such as life-time service.
Therefore, Western medicine and Chinese Medicine and Clavicular need be got up, i.e. synergism is played in Chinese medicine and western medicine combination, solves the problem that above-mentioned Western medicine and Chinese medicine exist in auxiliary treatment all kinds hepatitis separately, produces synergistic therapeutic effect simultaneously.
Summary of the invention
One object of the present invention is to provide the Pharmaceutical composition of being made up of tiopronin and a kind of Chinese medicine extract, wherein prepares on the basis of the Chinese medicine extract of said composition according to claim 1 method among the Chinese patent CN1058163C, and is as follows:
15 parts of Radix Pseudostellariaes, 15 parts of Radix Ophiopogonis, 15 parts of structure Fructus Lyciis, 15 parts of Rhizoma Polygonatis, 10 parts of Radix Angelicae Sinensis, 15 parts of the Radix Paeoniae Albas, 10 parts in Poria, 15 parts of Herba Artemisiae Scopariaes, 15 parts of Flos Loniceraes, 6 parts of Fructus Forsythiaes, 10 parts of Radix Isatidis, 15 parts of Radix Dipsaci, 10 parts of Fructus Schisandrae Chinensis, 10 parts of Rhizoma Cyperis, 6 parts of Radix Bupleuri, 6 parts of Radix Notoginseng, 15 parts of Carapax Trionycis, 15 parts of Squama Maniss, Radix Glycyrrhizae are decocted with water three times for 6 parts, heat and after 100 ℃, boiled 20-30 minute, making medicinal liquid leaches, merge three times filtrate, moisture is removed in decompression, drying obtains the water extracted immersing paste.
One object of the present invention is to provide the purposes of above-mentioned Pharmaceutical composition in preparation auxiliary treatment all kinds hepatitis medicament.
This Chinese medicine the water extracted immersing paste is called " the described Chinese medicine extract of this paper (or above) " hereinafter.
Above-mentioned composition and mixing acceptable accessories can be made acceptable forms clinically, as tablet, capsule, granule, oral liquid, subcutaneous administration preparation, suppository etc.
Pharmacological research
The main pharmacodynamics of Pharmaceutical composition of the present invention studies confirm that it has strong transaminase lowering effect, i.e. function for protecting liver and reducing enzyme activity.
Edit with reference to Zhang Juntian, " modern pharmacology test method " (volume two), combined publication society of China Concord Medical Science University of Beijing Medical University, the 1397-1398 page or leaf, disclosed method in " first segment chmice acute chemical liver injury model ", set up the acute chemical liver injury model of mouse carbon tetrachloride, carry out the pharmacodynamics test of Pharmaceutical composition anti-liver injury of the present invention.
The test grouping:
1 normal control group: animal does not do any processing, and normal physiological saline is irritated stomach;
2 model control group: after the animal model modeling success, normal physiological saline is irritated stomach;
2 pure Chinese drug-treated group: the water extracted immersing paste 0.83g/kg body weight as indicated above
3 tiopronin groups: the 10mg/kg body weight is irritated stomach
4 compositions groups: 10mg/kg body weight tiopronin+the water extracted immersing paste 0.83g/kg body weight mentioned above is irritated stomach.
Following table has shown the influence of each group to Mouse Liver function leading indicator GOT, GPT.
| Group | Number of animals | GOT (active unit) | GPT (active unit) |
| The normal control group | 10 | 20.78±16.75 | 48.31±17.35 |
| Model control group | 10 | 250.76±76.58 | 306.25±59.47 |
| Pure Chinese drug-treated group | 10 | 171.59±55.34 | 228.69±49.25 |
| The tiopronin group | 10 | 96.74±32.56 | 188.96±21.56 |
| The compositions group | 10 | 74.41±19.54 | 99.29±37.68 |
This table shows that all there is significant difference (P＜0.05) in each group (pure Chinese drug-treated group, tiopronin group, compositions group) of treatment with model control group, and all there are significant difference (P＜0.05) in compositions group and pure Chinese drug-treated group, compositions group and tiopronin group.Show that there are cooperative effect in tiopronin and described Chinese medicinal components in the compositions group.
The pharmaceutics test
Can produce the tablet that contains following component in a conventional manner:
Component Mg/ sheet
Pharmaceutical composition 200-1000 of the present invention
Corn starch 125.0
Pulvis Talci 75.0
Magnesium stearate 1.0
Wherein compositions is made up of with weight ratio tiopronin and Chinese medicine extract mentioned above at 1: 83.
Can produce the capsule that contains following component in a conventional manner:
Component Mg/ sheet
Pharmaceutical composition 200-1000 of the present invention
Lactose 10.0
Corn starch 20.0
Talcum 5.0
Wherein compositions is made up of with weight ratio tiopronin and Chinese medicine extract mentioned above at 1: 83.
Claims (2)
1 one kinds of Pharmaceutical compositions, it is made up of with weight ratio tiopronin and Chinese medicine extract at 1: 83, and described Chinese medicine extract prepares by following method:
With 15 parts of Radix Pseudostellariaes, 15 parts of Radix Ophiopogonis, 15 parts of structure Fructus Lyciis, 15 parts of Rhizoma Polygonatis, 10 parts of Radix Angelicae Sinensis, 15 parts of the Radix Paeoniae Albas, 10 parts in Poria, 15 parts of Herba Artemisiae Scopariaes, 15 parts of Flos Loniceraes, 6 parts of Fructus Forsythiaes, 10 parts of Radix Isatidis, 15 parts of Radix Dipsaci, 10 parts of Fructus Schisandrae Chinensis, 10 parts of Rhizoma Cyperis, Radix Bupleuri 6
Part, 6 parts of Radix Notoginseng, 15 parts of Carapax Trionycis, 15 parts of Squama Maniss, Radix Glycyrrhizae decoct with water three times for 6 parts, heat and boil 20-30 minute after 100 ℃, make medicinal liquid and leach, and merge three times filtrate, and moisture is removed in decompression, and drying obtains the water extracted immersing paste.
2 compositionss as claimed in claim 1 using in the medicine of preparation adjuvant treating hepatitis.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100909823A CN100356960C (en) | 2006-07-06 | 2006-07-06 | Synergistic medicinal composition for treating hepatitis |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100909823A CN100356960C (en) | 2006-07-06 | 2006-07-06 | Synergistic medicinal composition for treating hepatitis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1899515A true CN1899515A (en) | 2007-01-24 |
| CN100356960C CN100356960C (en) | 2007-12-26 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100909823A Expired - Fee Related CN100356960C (en) | 2006-07-06 | 2006-07-06 | Synergistic medicinal composition for treating hepatitis |
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| Country | Link |
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| CN (1) | CN100356960C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101797337A (en) * | 2010-04-15 | 2010-08-11 | 张大宇 | Medicine containing Guadisu |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106241738A (en) * | 2016-08-05 | 2016-12-21 | 江苏河海新能源股份有限公司 | Carbon dioxide and hydrogen separation device |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1058163C (en) * | 1995-06-02 | 2000-11-08 | 丁殿利 | Yigan Kangyangsan powder for curing hepatitis B |
| CN1115157C (en) * | 2000-08-24 | 2003-07-23 | 张汉三 | Method for preparing liver recovery decoction for curing liver disease |
-
2006
- 2006-07-06 CN CNB2006100909823A patent/CN100356960C/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101797337A (en) * | 2010-04-15 | 2010-08-11 | 张大宇 | Medicine containing Guadisu |
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| Publication number | Publication date |
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| CN100356960C (en) | 2007-12-26 |
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