CN1234381C - Medicine compositions for treating hepatitis, and its prepn. method - Google Patents
Medicine compositions for treating hepatitis, and its prepn. method Download PDFInfo
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- CN1234381C CN1234381C CN 02153441 CN02153441A CN1234381C CN 1234381 C CN1234381 C CN 1234381C CN 02153441 CN02153441 CN 02153441 CN 02153441 A CN02153441 A CN 02153441A CN 1234381 C CN1234381 C CN 1234381C
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- radix
- hepatitis
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Abstract
The present invention discloses a medicine composition for treating hepatitis, which is characterized in that the medicine is prepared from the following raw material medicine by weight parts: 150 to 450 parts of Radix Codonopsis, 60 to 180 parts of prepared bupleurum root, 150 to 450 parts of white peony alba, 90 to 270 parts of Chinese angelica, 150 to 450 parts of indian bread, 60 to 180 parts of stir-frying largehead atractylodes rhizome, 90 to 270 parts of stir-frying Fructus Aurantii, 150 to 450 parts of dandelion, 120 to 360 parts of giant knotweed rhizome, 150 to 450 parts of Spica Prunellae, 90 to 270 parts of red sage root, 30 to 90 parts of peach kernel and 15 to 45 parts of turtle shell. The present invention also discloses a preparation method thereof.
Description
The present invention relates to a kind of pharmaceutical composition for the treatment of hepatitis and preparation method thereof.
Chronic hepatitis, liver cirrhosis are long with the course of disease, the symptom delay, and the impaired in various degree grade of liver function is a main feature.Conditions of patients is not healed repeatedly, and feelings will is lost smooth, the liver failing to maintain the normal flow of QI, and depression and stagnation of QI is then seen dull pain in liver; Prolonged illness must be empty, is added with that liver disease affecting spleen, and liver insulting spleen, weakness of the spleen and stomach, and dysfunction of the spleen in transportation, stomach loses and is received, and poor appetite is then seen by taste lifting mistake department, and big loose stool approaches; Spleen governing limbs muscle, weakness of the spleen and stomach, limbs fatigue then, fatiguability; Acute hepatitis is damp and hot for suffering from, the course of disease with the passing of time, damp and hot stopping over, weakness of the spleen and stomach loses in fortuneization increasingly, endogenous dampness accumulates heat-transformation of a specified duration, causes damp and hot accumulateing in middle Jiao eventually, so see bitter taste in the mouth and dry throat; Pathogen usually intruding into collateral in protracted disease, irritability stasis, hematogenous blockage, blood-stasis internal-depression, the then visible side of body is mass in the abdomen down, by do not move; Light purplish tongue has the tooth seal, yellow, thin and slightly greasy fur, and thready and stringy pulse is stagnation of liver-QI with deficiency of the spleen, presss from both sides resembling of damp and hot blood stasis.Primary disease pathology character is deficiency in origin and excess in superficiality, and the pathogenesis key is stagnation of liver-QI with deficiency of the spleen, the damp and hot blood stasis of folder of holding concurrently, control when soothing liver and strengthening spleen for earlier, assistant is with Qinghua dissipating blood stasis.
The object of the invention be to provide a kind of clinical efficacy significantly, the Chinese medicine of the treatment hepatitis that has no side effect of taking convenience and preparation method thereof.
Technical solution of the present invention is achieved in that
The raw material of weight portion as described below
150～450 parts of 60～180 portions of Radix Paeoniae Albas of Radix Codonopsis 150～450 parts of systems Radix Bupleuri
60～180 parts of 150～450 parts of Rhizoma Atractylodis Macrocephalae (parched)s of 90～270 parts of Poria of Radix Angelicae Sinensis
120～360 parts of 150～450 parts of Rhizoma Polygoni Cuspidati of 90～270 parts of Herba Taraxacis of Fructus Aurantii (parched)
30～90 parts in 90～270 parts of Semen Persicaes of 150～450 parts of Radix Salviae Miltiorrhizaes of Spica Prunellae
15～45 parts of Carapax Trionycis
Get the Rhizoma Atractylodis Macrocephalae, Radix Salviae Miltiorrhizae, system Radix Bupleuri, Radix Angelicae Sinensis, Fructus Aurantii, Rhizoma Polygoni Cuspidati, with 40%～80 alcohol reflux 2～3 times, each 1～3 hour, filter merging filtrate, decompression recycling ethanol, be concentrated into relative density and be 1.05～1.25 clear paste, measure temperature and be 50 ℃, standby; Medicinal residues after the alcohol extraction and Radix Codonopsis, the Radix Paeoniae Alba, Poria, Herba Taraxaci, Spica Prunellae, Semen Persicae, Carapax Trionycis decoct with water secondary, and each 1～3 hour, collecting decoction, filter, it is 1.05～1.20 that filtrate is concentrated into relative density, and measuring temperature is 60 ℃, be blended into above-mentioned clear paste, filtrate is concentrated into relative density and is about 1.25～1.35 thick paste, and measuring temperature is 60 ℃, drying is pulverized, and adds starch 50～150g and sucrose 150～450g, mixing, system granule, particle drying, make 1000g altogether, packing, promptly.
The present invention treats the pharmaceutical composition of hepatitis through laboratory observation, inhibition effect to infected duck serum DHBV-DNA level is remarkable, non-toxic reaction all has significant difference to the average suppression ratio of HbeAg in the 8th day supernatant of 2.25.15 cell culture, and tangible dose-effect relationship is arranged; Can make acute liver damage animal pattern Serum ALT, AST activity little than the matched group ascensional range, as seen the liver histological pathological observation obviously alleviates the rats'liver damage.The activity of ALT, AKP in the Rats with Acute Liver Injury serum is descended, ALB, BPC are raise, improve hepatic tissue pathology and change, reduce hydroxyprolin levels in the hepatic tissue; The immunologic liver injury mice there is function for protecting liver and reducing enzyme activity, can reduces ALT, AST unit of activity, reduce hepatosplenomegaly and organ coefficient thereof, alleviate the pathological lesion of hepatic tissue; Immune hyperfunction state to the immunologic liver injury mice has obvious inhibitory action, and the phagocytic percentage of peritoneal macrophage and phagocytic index are descended, and serum hemolysin HC50 reduces, and the inductive splenic t-cell propagation of ConA is reduced; The immunologic hypofunction mice there is facilitation, can improve mononuclear phagocyte carbon clearance index, improve the phagocytic percentage and the phagocytic index of peritoneal macrophage, improve serum hemolysin HC50, improve the inductive splenic t-cell propagation of ConA, improve the lymphoblastic percentage rate that PHA stimulates peripheral blood lymphocyte to transform, significance is all arranged.Above-mentioned experimental result shows that medicine of the present invention has soothing liver and strengthening spleen, heat-clearing and toxic substances removing, and the effect of softening the hard mass dissipating blood stasis is used for chronic active hepatitis, chronic persistent hepatitis, liver cirrhosis, hepatitis B virus carriers.
Clinical test results shows that the pharmaceutical composition that the present invention treats hepatitis has soothing liver and strengthening spleen, and heat-clearing and toxic substances removing, softening the hard mass loose and become silted up hepatoprotective, effects such as anti-hepatic fibrosis can be used for stagnation of liver-QI with deficiency of the spleen, the noxious dampness internal resistance, acute and chronic hepatitis, liver cirrhosis, treatment of conditions such as liver function injury.
Experimental example 1: the tetrachloro charcoal is caused the influence of rabbit experiment liver damage:
Rabbit is divided into 6 groups at random: normal control group, ccl4 (0.1ml/kg) model group, ccl4+ bifendate (60mg/kg) group, 3 dosage groups of ccl4+ pharmaceutical composition of the present invention.Behind the lumbar injection ccl4, the continuous gastric infusion of each treated animal 5 days was put to death animal in 1 hour after the last administration, got blood and dissection immediately, got liver and carried out histochemistry and pathological examination.The result shows: the heavy dose of group of pharmaceutical composition of the present invention has the SGPT of reduction value trend; LDH content is significantly increased than the damage group in the pathologic finding high dose group hepatic tissue, and lobules of liver central zone LDH content increases to some extent, and hepatic glycogen is evenly distributed, and lobules of liver central zone and paripheral zone glycogen increase to some extent than damage group; High dose group is loose to the hepatocyte endochylema, lipoid degeneration, acidophilia and necrosis all have obvious protective effect.The protective effect of pharmaceutical composition of the present invention is similar to the bifendate group, and latter's effect of reducing enzyme levels is stronger, sees the following form.
| Grouping | Number of animals | SGPT X±SD | The P value |
| Dosage group pharmaceutical composition low dose group of the present invention in the Normal group model control group DDB group pharmaceutical composition high dose group of the present invention pharmaceutical composition of the present invention | 10 10 9 10 9 10 | 35.43±7.93 502.08±32.22 211.41±50.42 237.38±38.90 339.68±46.22 489.91±64.00 | ＜0.01 ＜0.01 ＜0.05 |
Embodiment 1:
Radix Codonopsis 300g system Radix Bupleuri 120g Radix Paeoniae Alba 300g
Radix Angelicae Sinensis 180g Poria 300g Rhizoma Atractylodis Macrocephalae (parched) 120g
Fructus Aurantii (parched) 180g Herba Taraxaci 300g Rhizoma Polygoni Cuspidati 240g
Spica Prunellae 300g Radix Salviae Miltiorrhizae 180g Semen Persicae 60g
Carapax Trionycis 30g
Get the Rhizoma Atractylodis Macrocephalae, Radix Salviae Miltiorrhizae, system Radix Bupleuri, Radix Angelicae Sinensis, Fructus Aurantii, Rhizoma Polygoni Cuspidati, with 60% alcohol reflux secondary, each 1.5 hours, filter, merging filtrate, decompression recycling ethanol is concentrated into relative density and is 1.05～1.25 clear paste, measures temperature and is 60 ℃, and is standby; Medicinal residues after the alcohol extraction and Radix Codonopsis, the Radix Paeoniae Alba, Poria, Herba Taraxaci, Spica Prunellae, Semen Persicae, Carapax Trionycis decoct with water secondary, each 1.5 hours, collecting decoction, filter, it is 1.10～1.15 that filtrate is concentrated into relative density, and measuring temperature is 60 ℃, be blended into above-mentioned clear paste, filtrate is concentrated into relative density and is about 1.30～1.35 thick paste, and measuring temperature is 60 ℃, drying, pulverize, add starch 100g and sucrose 300g, mixing is made wetting agent system granule with 85% ethanol, particle drying, make 1000g altogether, packing, promptly.
Embodiment 2:
Radix Codonopsis 250g system Radix Bupleuri 100g Radix Paeoniae Alba 250g
Radix Angelicae Sinensis 200g Poria 250g Rhizoma Atractylodis Macrocephalae (parched) 100g
Fructus Aurantii (parched) 200g Herba Taraxaci 250g Rhizoma Polygoni Cuspidati 200g
Spica Prunellae 250g Radix Salviae Miltiorrhizae 200g Semen Persicae 80g
Carapax Trionycis 25g
Get the Rhizoma Atractylodis Macrocephalae, Radix Salviae Miltiorrhizae, system Radix Bupleuri, Radix Angelicae Sinensis, Fructus Aurantii, Rhizoma Polygoni Cuspidati, with 60% alcohol reflux secondary, each 1.5 hours, filter, merging filtrate, decompression recycling ethanol is concentrated into relative density and is 1.05～1.25 clear paste, measures temperature and is 60 ℃, and is standby; Medicinal residues after the alcohol extraction and Radix Codonopsis, the Radix Paeoniae Alba, Poria, Herba Taraxaci, Spica Prunellae, Semen Persicae, Carapax Trionycis decoct with water secondary, each 1.5 hours, collecting decoction, filter, it is 1.10～1.15 that filtrate is concentrated into relative density, and measuring temperature is 60 ℃, be blended into above-mentioned clear paste, filtrate is concentrated into relative density and is about 1.30～1.35 thick paste, and measuring temperature is 60 ℃, drying, pulverize, add starch 100g and sucrose 300g, mixing is made wetting agent system granule with 85% ethanol, particle drying, make 1000g altogether, packing, promptly.
Claims (7)
1, a kind of pharmaceutical composition for the treatment of hepatitis is characterized in that this medicine made by following bulk drugs:
150～450 parts of 60～180 portions of Radix Paeoniae Albas of Radix Codonopsis 150～450 parts of systems Radix Bupleuri
60～180 parts of 150～450 parts of Rhizoma Atractylodis Macrocephalae (parched)s of 90～270 parts of Poria of Radix Angelicae Sinensis
120～360 parts of 150～450 parts of Rhizoma Polygoni Cuspidati of 90～270 parts of Herba Taraxacis of Fructus Aurantii (parched)
30～90 parts in 90～270 parts of Semen Persicaes of 150～450 parts of Radix Salviae Miltiorrhizaes of Spica Prunellae
15～45 parts of Carapax Trionycis.
2, a kind of pharmaceutical composition for the treatment of hepatitis as claimed in claim 1 is characterized in that being made by following bulk drugs:
300 parts of 120 portions of Radix Paeoniae Albas of Radix Codonopsis 300 parts of systems Radix Bupleuri
120 parts of 300 parts of Rhizoma Atractylodis Macrocephalae (parched)s of 180 parts of Poria of Radix Angelicae Sinensis
240 parts of 300 parts of Rhizoma Polygoni Cuspidati of 180 parts of Herba Taraxacis of Fructus Aurantii (parched)
60 parts in 180 parts of Semen Persicaes of 300 parts of Radix Salviae Miltiorrhizaes of Spica Prunellae
30 parts of Carapax Trionycis.
3, a kind of preparation of drug combination method for the treatment of hepatitis as claimed in claim 1 or 2, it is characterized in that: get the Rhizoma Atractylodis Macrocephalae, Radix Salviae Miltiorrhizae, system Radix Bupleuri, Radix Angelicae Sinensis, Fructus Aurantii, Rhizoma Polygoni Cuspidati, with 40%～80 alcohol reflux 2～3 times, each 1～3 hour, filter merging filtrate, decompression recycling ethanol, be concentrated into relative density and be 1.05～1.25 clear paste, measure temperature and be 50 ℃, standby; Medicinal residues after the alcohol extraction and Radix Codonopsis, the Radix Paeoniae Alba, Poria, Herba Taraxaci, Spica Prunellae, Semen Persicae, Carapax Trionycis decoct with water secondary, and each 1～3 hour, collecting decoction, filter, it is 1.05～1.20 that filtrate is concentrated into relative density, and measuring temperature is 60 ℃, be blended into above-mentioned clear paste, filtrate is concentrated into relative density and is about 1.25～1.35 thick paste, and measuring temperature is 60 ℃, drying is pulverized, and adds adjuvant, mixing, system granule, particle drying, packing is made 1000g, promptly altogether.
4, a kind of preparation of drug combination method for the treatment of hepatitis as claimed in claim 3, it is characterized in that this method is: get the Rhizoma Atractylodis Macrocephalae, Radix Salviae Miltiorrhizae, system Radix Bupleuri, Radix Angelicae Sinensis, Fructus Aurantii, Rhizoma Polygoni Cuspidati, with 60% alcohol reflux secondary, each 1.5 hours, filter merging filtrate, decompression recycling ethanol, be concentrated into relative density and be 1.10～1.25 clear paste, measure temperature and be 50 ℃, standby; Medicinal residues after the alcohol extraction and Radix Codonopsis, the Radix Paeoniae Alba, Poria, Herba Taraxaci, Spica Prunellae, Semen Persicae, Carapax Trionycis decoct with water secondary, and each 1.5 hours, collecting decoction, filter, it is 1.10～1.15 that filtrate is concentrated into relative density, and measuring temperature is 60 ℃, be blended into above-mentioned clear paste, filtrate is concentrated into relative density and is about 1.30～1.35 thick paste, and measuring temperature is 60 ℃, drying is pulverized, and adds adjuvant, mixing, system granule, particle drying, make 1000g altogether, packing, promptly.
5, as claim 3 or 4 described a kind of preparation of drug combination methods for the treatment of hepatitis, make wetting agent with 85% ethanol when it is characterized in that making granule.
6, as claim 3 or 4 described a kind of preparation of drug combination methods for the treatment of hepatitis, it is characterized in that adjuvant is starch 50～150g and sucrose 150～450g.
7, a kind of preparation of drug combination method for the treatment of hepatitis as claimed in claim 6 is characterized in that adjuvant is starch 100g and sucrose 300g.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02153441 CN1234381C (en) | 2002-11-27 | 2002-11-27 | Medicine compositions for treating hepatitis, and its prepn. method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02153441 CN1234381C (en) | 2002-11-27 | 2002-11-27 | Medicine compositions for treating hepatitis, and its prepn. method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1418679A CN1418679A (en) | 2003-05-21 |
| CN1234381C true CN1234381C (en) | 2006-01-04 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 02153441 Expired - Lifetime CN1234381C (en) | 2002-11-27 | 2002-11-27 | Medicine compositions for treating hepatitis, and its prepn. method |
Country Status (1)
| Country | Link |
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| CN (1) | CN1234381C (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102743480B (en) * | 2012-07-27 | 2014-04-16 | 陕西步长高新制药有限公司 | Traditional Chinese medicine preparation for treating hepatitis and preparation method thereof |
| CN102743477B (en) * | 2012-07-27 | 2013-08-28 | 陕西步长高新制药有限公司 | Traditional Chinese medicine preparation for treating hepatitis and preparation method thereof |
| CN102743479A (en) * | 2012-07-27 | 2012-10-24 | 陕西步长制药有限公司 | Traditional Chinese medicine preparation for treating hepatitis and preparing method thereof |
| CN102743478A (en) * | 2012-07-27 | 2012-10-24 | 陕西步长制药有限公司 | Traditional Chinese medicine preparation for treating hepatitis and preparing method thereof |
| CN103735949A (en) * | 2013-12-30 | 2014-04-23 | 卢保健 | Traditional Chinese medicine for treating liver cancer and hepatic injury due to hepatitis B |
| CN105169274A (en) * | 2015-10-10 | 2015-12-23 | 崇州市地龙海龙生物制品开发研究所 | Preparation method of quick-acting liver pill |
| CN106620057A (en) * | 2016-12-12 | 2017-05-10 | 广西防城港常春生物技术开发有限公司 | Anti-hepatic fibrosis Zhuang medicine preparation and preparation method thereof |
| CN111214633A (en) * | 2020-03-09 | 2020-06-02 | 耿禄 | Formula for treating infectious hepatitis B |
-
2002
- 2002-11-27 CN CN 02153441 patent/CN1234381C/en not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| CN1418679A (en) | 2003-05-21 |
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| C06 | Publication | ||
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Owner name: QIYUANYIDE MEDICINES INST., BEIJING Free format text: FORMER OWNER: ZHANG HUIFANG Effective date: 20030812 |
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Effective date of registration: 20030812 Applicant after: Beijing Qi Yuan Yi De Pharmaceuticals Research Center Applicant before: Zhang Huifang |
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Owner name: XIANYANG BUCHANG PHARMACEUTICAL CO., LTD. Free format text: FORMER OWNER: QIYUANYIDE MEDICINES INST., BEIJING Effective date: 20040303 |
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Owner name: BAODING BUCHANG TIANHAO PHARMACEUTICAL CO., LTD. Free format text: FORMER OWNER: XIANYANG BUCHANG PHARMACEUTICAL CO., LTD. Effective date: 20100108 |
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Effective date of registration: 20100108 Address after: Hebei Dingxing 86188 army hospital Patentee after: BAODING BUCHANG TIANHAO PHARMACEUTICAL Co.,Ltd. Address before: The west section of Xianyang City Weiyang Road No. 123 Patentee before: BUCHANG Group |
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Owner name: BAODING TIANHAO PHARMACEUTICAL CO., LTD. Free format text: FORMER NAME: BAODING BUCHANG TIANHAO PHARMACEUTICAL CO., LTD. |
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Address after: Xinghua 072650 Hebei province Dingxing County Road No. 128 Patentee after: BAODING TIANHAO PHARMACEUTICAL Co.,Ltd. Address before: 072650 Hebei province Dingxing County 86188 army hospital Patentee before: BAODING BUCHANG TIANHAO PHARMACEUTICAL Co.,Ltd. |
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