CN100340268C - Synergistic medicinal composition containing tiopronin and Chinese medicine extract - Google Patents
Synergistic medicinal composition containing tiopronin and Chinese medicine extract Download PDFInfo
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- CN100340268C CN100340268C CNB2006100985028A CN200610098502A CN100340268C CN 100340268 C CN100340268 C CN 100340268C CN B2006100985028 A CNB2006100985028 A CN B2006100985028A CN 200610098502 A CN200610098502 A CN 200610098502A CN 100340268 C CN100340268 C CN 100340268C
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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 method basis of the Chinese medicine extract of said composition according to claim 1-2 among the Chinese patent CN1259944C, and is as follows:
The medicine material combination back of following proportioning is dropped in the extractor, add 10 liters in water, under 50 ℃ of-70 ℃ of temperature, decoct and obtained the water extract in 45 minutes, gained water extract proportion is 1.04-1.05, and drying under reduced pressure water extract gets dry extract; Described medicine material mixing ratio by weight is: Herba Hyperici Japonici: Herba Sedi: Herba Patriniae: Radix Salviae Miltiorrhizae: Fructus Schisandrae Chinensis: Fructus Crataegi: Semen Cassiae: Rhizoma Alismatis: Radix Bupleuri: Radix Glycyrrhizae=6: 6: 4: 4: 3: 3: 3: 2: 2: 1.
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 1.07g/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 1.07g/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 | 173.85±59.74 | 229.38±51.21 |
| The tiopronin group | 10 | 113.96±40.85 | 201.35±30.98 |
| The compositions group | 10 | 87.85±28.57 | 98.52±38.96 |
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: 107.
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: 107.
Claims (2)
1 one kinds of Pharmaceutical compositions that are used for adjuvant treating hepatitis, it is made up of with weight ratio tiopronin and Chinese medicine extract at 1: 107, and described Chinese medicine extract prepares by following method:
The medicine material combination back of following proportioning is dropped in the extractor, add 10 liters in water, under 50 ℃ of-70 ℃ of temperature, decoct and obtained the water extract in 45 minutes, gained water extract proportion is 1.04-1.05, and drying under reduced pressure water extract gets dry extract; Described medicine material mixing ratio by weight is: Herba Hyperici Japonici: Herba Sedi: Herba Patriniae: Radix Salviae Miltiorrhizae: Fructus Schisandrae Chinensis: Fructus Crataegi: Semen Cassiae: Rhizoma Alismatis: Radix Bupleuri: Radix Glycyrrhizae=6: 6: 4: 4: 3: 3: 3: 2: 2: 1.
The purposes of 2 compositionss as claimed in claim 1 in the medicine of preparation adjuvant treating hepatitis.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100985028A CN100340268C (en) | 2006-07-04 | 2006-07-04 | Synergistic medicinal composition containing tiopronin and Chinese medicine extract |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100985028A CN100340268C (en) | 2006-07-04 | 2006-07-04 | Synergistic medicinal composition containing tiopronin and Chinese medicine extract |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1899467A CN1899467A (en) | 2007-01-24 |
| CN100340268C true CN100340268C (en) | 2007-10-03 |
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| Application Number | Title | Priority Date | Filing Date |
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| CNB2006100985028A Expired - Fee Related CN100340268C (en) | 2006-07-04 | 2006-07-04 | Synergistic medicinal composition containing tiopronin and Chinese medicine extract |
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Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106491916A (en) * | 2016-12-07 | 2017-03-15 | 郑州郑先医药科技有限公司 | Chinese and western medicinal composition for the treatment of hepatitis containing throatroot extract and preparation method thereof |
| CN108420895A (en) * | 2018-05-22 | 2018-08-21 | 王宏奎 | For reducing the pharmaceutical composition and preparation method thereof of glutamic-pyruvic transaminase |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1404827A (en) * | 2002-10-08 | 2003-03-26 | 河南省新谊药业股份有限公司 | Tiopronin preparation |
| CN1509745A (en) * | 2002-12-25 | 2004-07-07 | 天津市汉沽区中医医院 | Preparation of wutian liver caring liquid |
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2006
- 2006-07-04 CN CNB2006100985028A patent/CN100340268C/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1404827A (en) * | 2002-10-08 | 2003-03-26 | 河南省新谊药业股份有限公司 | Tiopronin preparation |
| CN1509745A (en) * | 2002-12-25 | 2004-07-07 | 天津市汉沽区中医医院 | Preparation of wutian liver caring liquid |
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| Publication number | Publication date |
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| CN1899467A (en) | 2007-01-24 |
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