CN101239099A - Application of Chinese medicinal composition in preparing medicament for treating chronic cardiac insufficiency - Google Patents
Application of Chinese medicinal composition in preparing medicament for treating chronic cardiac insufficiency Download PDFInfo
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Abstract
The invention is related to the use of a Chinese medicine composition serving for preparing drug for curing chronic cardiac insufficiency. The composition is formed of the following raw materials by weight: 22.2% to 66.8% of astragalus, 11.6% to 33.4% of salvia, 2.5% to 13.5% of panax notoginseng, 14.5% to 44.3% of lignum dalbergiae odoriferae.
Description
Technical field
The invention belongs to field of medicaments, be specifically related to the application of QISHEN YIQI DIWAN in the medicine of preparation prevention and treatment chronic cardiac insufficiency.
Background technology
Cardiac insufficiency claims congestive heart failure (being called for short heart failure or heart failure) again, be meant under the normal situation of venous return, because the overweight left cardiac output that causes of former heart damage or the long-term pressure of ventricle or volume load reduces and ventricular filling pressure raises, clinically with tissue blood hypoperfusion and pulmonary circulation and (or) body circulation blood stasis is a kind of clinical syndrome of principal character, show as cardiopalmus severe palpitation, shortness of breath and fatigue, dyspnea, limds edema, liver and swell and ache etc.Chronic cardiac insufficiency almost is all organic heart disease patients' final home to return to, and this disease clinical onset rate height is one of difficult medical problem of primary study.
The treatment of cardiac insufficiency, doctor trained in Western medicine medicine commonly used comprises diuretic, vasodilation, cardiac tonic, Folium Digitalis Purpureae, non-sample Radix Rehmanniae class positive inotropic medicament, converting enzyme inhibitor, beta receptor inhibitor etc., but side effect is in various degree all arranged or use taboo; Chinese patent medicine commonly used is mainly SHENFU ZHUSHEYE, SHENMAI ZHUSHEYE etc., but curative effect is not satisfactory, and untoward reaction in various degree occurs.
QISHEN YIQI DIWAN is made up of the Radix Astragali, Radix Salviae Miltiorrhizae, Radix Notoginseng and Lignum Dalbergiae Odoriferae, is produced by Tianjin Tasly Pharmaceutical Co., Ltd, and is evident in efficacy in order to the angina pectoris of treatment coronary heart disease with qi deficiency and blood stasis, do not have any obvious toxic and side effects.Chinese patent application CN1375316A discloses the composition of said preparation, method for making and the purposes aspect angina pectoris, Chinese patent application CN200510013503.3A, CN200510013504.8, CN200510013505.2, CN200510013506.7, CN200510013507.1 discloses said composition respectively at preparation control medicine for senile dementia, preparation suppresses the albumin outside leakage medicine, preparation suppresses the application in the mast cell degranulation medicine, preparation prevents and treats the application in the high altitude anoxia medicine, application in the preparation treatment acute pancreatitis medicine, but this medicine does not appear in the newspapers as yet in the effect aspect the control chronic cardiac insufficiency.
Summary of the invention
The purpose of this invention is to provide the purposes of a kind of Chinese medicine composition in the medicine of preparation treatment chronic cardiac insufficiency, said composition is prepared from by the following raw materials by weight percent medicine: the Radix Astragali 22.2%~66.8%, Radix Salviae Miltiorrhizae 11.6%~33.4%, Radix Notoginseng 2.5%~13.5%, Lignum Dalbergiae Odoriferae 14.5%~44.3%.
Chinese medicine composition of the present invention, person's left ventricle contractile function that can improve the chronic cardiac insufficiency, increase chronic cardiac insufficiency person's left ventricular ejection mark (LVEF) and shortening fraction (FS), the person's that improves the chronic cardiac insufficiency energy metabolism, showing as ATP raises, ATP/ADP ratio raises, and can close (energy charge, EC) rising.
Chinese medicine composition of the present invention, its preferred proportioning is the Radix Astragali 30.8%~57.2%, Radix Salviae Miltiorrhizae 15.4%~28.6%, Radix Notoginseng 3.5%~6.5%, Lignum Dalbergiae Odoriferae 20.6%~38.2%; Its best proportioning is the Radix Astragali 44.7%, Radix Salviae Miltiorrhizae 26.7%, Radix Notoginseng 6.3%, Lignum Dalbergiae Odoriferae 22.3%; Perhaps be the Radix Astragali 41.2%, Radix Salviae Miltiorrhizae 23.8%, Radix Notoginseng 4.5%, Lignum Dalbergiae Odoriferae 30.5%.
Chinese medicine composition of the present invention, can extract preparation to crude drug according to the method for routine or the method for prior art respectively, mix then, preferably, prepare: Radix Salviae Miltiorrhizae, the pseudo-ginseng of learning from else's experience and pulverizing according to following method, decocting boils, filter, filtrate suitably concentrates the back precipitate with ethanol, and supernatant reclaims ethanol, be condensed into extractum, i.e. Salvia miltiorrhiza and Panax notoginseng extractum; The Milkvetch Root that other learns from else's experience and pulverizes, decocting boils, and filters, and filtrate suitably concentrates the back precipitate with ethanol, precipitate with ethanol again after supernatant suitably concentrates, supernatant reclaims ethanol, is condensed into extractum, i.e. Radix Astragali extractum; Get the Lignum Dalbergiae Odoriferae medical material again, add water, reflux, extract, is collected volatile oil.With above two kinds of extractum and volatile oil and adjuvant mixed evenly after, make said dosage form on any pharmaceutics of preparation, wherein preferred dosage form is a drop pill.For example, the drop pill method for making: get the Polyethylene Glycol-6000 of 2~5 times of above-mentioned Salvia miltiorrhiza and Panax notoginseng extractum, Radix Astragali extractum and extractum gross weights, water-bath is dissolved, change even after, add volatile oil of Lignum Dalbergiae Odoriferae, mixing, the method for making drop pill routinely is prepared, promptly; More solito sheet agent method can be made into tablet; Or the like.
For a better understanding of the present invention, below by the influence of Chinese medicine composition of the present invention (to call " QISHEN YIQI DIWAN extractum " in the following text) to the chronic cardiac insufficiency rat, parallel excusing from death kinetocardiography is measured left ventricular ejection mark (EF) and shortening fraction (FS), ATP, ADP, AMP are measured in cardiac muscular tissue's homogenate, and the effect of QISHEN YIQI DIWAN in the treatment chronic cardiac insufficiency is described.
Test objective:
Observe the therapeutical effect of QISHEN YIQI DIWAN for the chronic cardiac insufficiency rat.
Material and method
1, animal: the SD rat, male, cleaning level, available from Shanghai Slac Experimental Animal Co., Ltd., the quality certification number: 0016807,0017299
2, be subjected to the reagent thing:
(1) QISHEN YIQI DIWAN extractum: according to the method preparation of embodiment 1, per 1 gram extractum contains the 14.3g crude drug, mouse experiment LD
50Be 25.807g/kg, convert and be rat LD
50For: 18.0649g/kg, the clinical using dosage of people is: 6.25mg/kg, Radix Astragali extractum: Salvia miltiorrhiza and Panax notoginseng extractum: volatile oil of Lignum Dalbergiae Odoriferae=1: 1: 0.0735.Deionized water dissolving.
(2) vasorel (energy metabolism regulator, VASOREL, Trimetazidine dihydrochloride): by French Les Laboratoires servier provide (SERVIER, France), every 20mg, batch number (Batch): 5J4515.Deionized water dissolving.
(3) acertil (renin angiotensin converting enzyme inhibitor, ACERTIL, Perindopril tablets): by provide by French Les Laboratoires servier (SERVIER, France), every 4mg, batch number (Batch): 5K0401.Deionized water dissolving.
Raised by the equal stomach of reagent thing route of administration, every Mus 1ml every day.
3, reagent and solution
(1) isoproterenol (Sigma, DL-Isoproterenol hydrochloride): No:15627-25G, the 055k1021 physiological saline solution, subcutaneous injection is used.
(2) heparin sodium injection (Chinese changzhou thousand red-face roleization pharmaceutical Co. Ltds): batch number: 051229,2ml:12500 unit is with normal saline dilution, 500 units/ml.
(3) chloral hydrate solution (Jiangsu TCM Hospital, the medicine system word H04001110 of Soviet Union): batch number: 060412, it is 7.5% stand-by diluting with normal saline.
4, experimental apparatus and equipment:
(1) the little processing pH meter of conventional equipment: Ph213 (HANNA), WS-1 magnetic stirring apparatus, rat oral gavage pin, shears, tweezers, vascular clamp, gauze etc.
(2) echocardiograph: the VIVID7 of GE company type
5, experiment modeling: except that rats in normal control group, model group and treatment group rat begin to carry out modeling in normal raising after 3-7 days, method is as follows: the 1st day different third kidney of subcutaneous injection (ISO) 20mg/Kg, the 2nd day different third kidney of subcutaneous injection (ISO) 10mg/Kg, the 3rd day ISO 5mg/Kg, 4-12 days ISO 3mg/Kg.
6, the experiment grouping:
142 of SD rats, body weight 201.86 ± 6.68g is divided into two groups at random: normal group (n=18) and model group (n=124).Test the model group rat that began in first day and give the modeling of ISO subcutaneous injection, method is the same, after one month, rat is ultrasonic in the test section, the model group rat that will partly survive at random is divided into stilbene ginseng QI invigorating high dose group (n=16), dosage group (n=16) in the stilbene ginseng QI invigorating, stilbene ginseng QI invigorating low dose group (n=16), vasorel group (n=15) and acertil group (n=15) residue model group (n=16), stilbene ginseng QI invigorating height, in, the every respectively Mus of low dose group rat is irritated stomach stilbene ginseng QI invigorating extractum 78.125mg/kg every day, 39.063mg/kg and 19.531mg/kg, the every Mus of vasorel group rat is irritated stomach vasorel 10mg/kg every day, and the every Mus of acertil group rat is irritated stomach 0.417mg/kg every day.Treatment continued for 4 weeks, once a day, put to death 6-10 rat for every group after 4 weeks of treatment, surplus SD rat continued treatment, and the 6th week put to death.
7, observation index:
(1) rat ordinary circumstance: mobility, body weight, death toll etc.
(2) the ultrasonic index of rat: rat chloral hydrate anesthesia before experiment finishes, row two-dimensional ultrasound record left ventricular ejection mark (EF) and shortening fraction (FS).
(3) cardiac muscular tissue's homogenate: measure ATP, ADP, AMP.Sample disposal:
A.ATP measures
A) reagent is prepared
Triethanolamine buffer (50mmol/L): pH7.2; NADP 10mmol/l; MgCl
20.1mol/l; Glucose 0.5mol/l;
Enzyme buffer liquid: G6P-DH (80U/ml): HK (100U/ml)=1: 1
ATP standard substance 100 μ mol/l; 200 μ mol/l; 400 μ mol/l.
Blank buffer TEA: NADP: MgCl
2: glucose=7: 1: 1: 1
Reaction buffer is the 1mmol/lATP that every milliliter of blank buffer adds 20 μ l
B) experimental procedure
Blank tube reaction pipe
Sample 200 μ l
Neutral perchloric acid 200 μ l
Blank buffer 1000 μ l
Reaction buffer 1000 μ l
Enzyme buffer liquid 20 μ l 20 μ l
Enzyme-added mixing is also put back in the ice bath, and it is abundant to put into 37 degree water after all adding together, and in wavelength 339nm place colorimetric, with the air zeroing, the blank pipe of note is A behind the 20min
0, reaction tube is A.ΔA=A-A
0
Δ A is directly proportional with the concentration of ATP.
B.ADP/AMP
A) reagent is prepared
Triethanolamine buffer (50mmol/L): PH8.0; PEP/MgSO
4/ KCl (PEP 14mmol/l, MgSO
40.5mol/l, KCl1.8mol/l); NADH (16mmol/l); LDH 2500U/ml; PK 2000U/ml; MK 100U/ml.
Reaction buffer TEA (600 μ l)+PEP/MgSO
4/ KCl (120 μ l)+NADH (35 μ l)+LDH (20 μ l)
Standard substance configuration: AMP 200 μ mol/l 300 μ mol/l 400 μ mol/l
The ATP that should contain same concentrations in the AMP standard substance
ADP?100μmol/l 150μmol/l 200μmol/l
B) experimental procedure
Blank tube reaction pipe
Sample 600 μ l
Neutral perchloric acid 600 μ l
Reaction buffer 600 μ l 600 μ l
The reading note A1 of mixing 5min 339nm place
PK 20μl 20μl
The reading note A2 of mixing 20min 339nm place
MK 100μl 100μl
The reading note A3 of mixing 20min 339nm place
Δ A
ADP=Δ A
Sample (A2-A1)-Δ A
Blank (A2-A1)Δ A
ADPBe directly proportional with ADP concentration in the sample
A
AMP=Δ A
Sample (A3-A2)-Δ A
Blank (A3-A2)Δ A
AMPBe directly proportional with AMP concentration in the sample
7, data analysis and statistics
Represent measurement data with mean ± standard deviation, measurement data relatively adopts ANOVA to analyze for many groups, relatively adopts the S-N-K check between group in twos; Two groups of means relatively adopt the T check; Enumeration data adopts X 2 test.All statistics utilize the SPSS12.0 software analysis to finish, and P<0.05 is for there being significant difference.
The result
(1) ordinary circumstance, body weight and mortality rate are relatively: death toll and body weight are compared with normal group and are seen Table 1 after the different third kidney modeling, and rats death digital display work is higher than normal group behind the different third kidney modeling type, and significant difference is arranged, modeling after the 28th day body weight alleviate than normal group.Drug therapy is carried out in modeling after 30 days, each treatment group death toll and weight ratio see Table 2.1 model group rats death only during the treatment, body weight does not have significant change between each group.
Normal group, model group mortality rate, body weight comparative result (body weight unit: g) before table 1 treatment
Through check, normal group and model group rats death are counted P=0.044 (Pearson Chi-square=4.620); * compare P<0.05 with normal group
Respectively organize (body weight unit: g) of death toll, weight ratio after table 2 treatment
(2) rat ultrasoundcardiogram comparative result: 30 days model group and normal group are respectively got 8 rats underwent echocardiography after the different third kidney modeling, the results are shown in Table 3, and model group EF and FS are starkly lower than normal group, and significant difference is arranged.Drug therapy is carried out in modeling after 30 days.
(testing 30 days) normal group and model group ultrasoundcardiogram are relatively before table 3 treatment
* compare P<0.05 with normal group;
After 4 weeks of treatment and 6 weeks, get 46 capable echocardiography of every group of rat respectively, each is organized ultrasoundcardiogram and relatively sees Table 4.Results suggest: model group and each medication therapy groups EF, FS all are lower than normal group, and each medication therapy groups FS all is higher than model group.Stilbene ginseng QI invigorating high dose group, vasorel group EF are higher than model group, and significant difference is arranged.Stilbene ginseng QI invigorating high dose group EF is higher than the acertil group significant difference.
Table 4 is respectively organized the rat ultrasoundcardiogram relatively after 6 weeks of treatment:
* compare P<0.05 with normal group; # compares with model group, P<0.05; $ compares P<0.05 with stilbene ginseng high dose group; ﹠amp; Compare P<0.05 with dosage group in the stilbene ginseng; % compares P<0.05 with stilbene ginseng low dosage; @ compares with the vasorel group, P<0.05
(4) rat heart muscle high-energy phosphate compound content relatively
Treat and respectively organize rat heart muscle high-energy phosphate compound content 6 weeks and see Table 5.
Table 5 treatment 6 all rat heart muscle high-energy phosphate compound content
* compare P<0.05 with normal group; # compares with model group, P<0.05; $ compares P<0.05 with stilbene ginseng high dose group; ﹠amp; Compare P<0,05 with dosage group in the stilbene ginseng; % compares P<0.05 with stilbene ginseng low dosage; @ compares with the vasorel group, P<0.05 result:
1. isoproterenol continues subcutaneous injection and can cause rat pathology to present between heart matter to be fibrosis, calcification, connective tissue proliferation, normal myocardium cell and to be island, the cardiac muscle fiber arrangement disorder, part is with inflammatory cell infiltration, ultrasonic cardiography diagram LVd, LVs, EDV, ESV obviously increase, EF, FS, IVS, LVPW obviously reduce, and similar chronic cardiac insufficiency changes.
2. in stilbene ginseng QI invigorating extractum treatment SD heart failure 6 weeks of rat, can improve heart failure rat cardiac function LVEF and FS.
3. the treatment of stilbene ginseng QI invigorating extractum can improve the energy metabolism of chronic heart failure rat, and results change and clinical Western medicine vasorel commonly used, acertil are similar.
To sum up, stilbene ginseng QI invigorating extractum can increase heart failure rat cardiac function LVEF and FS as can be seen, improves the left chamber contractility of chronic cardiac insufficiency rat, improves the energy metabolism of chronic heart failure rat.
The specific embodiment
Below in conjunction with embodiment medicine of the present invention is described further, following each embodiment only is used to the present invention is described and is not limitation of the present invention.
Embodiment one
Get Radix Astragali 86.5g, Radix Salviae Miltiorrhizae 21.3g, Radix Notoginseng 3.5g, Lignum Dalbergiae Odoriferae 20.6g, adjuvant Polyethylene Glycol-600030g.Will be through Radix Salviae Miltiorrhizae, the Radix Notoginseng of pulverizing, decocting boils 2 times, adds 7 times of water gagings at every turn, each 2 hours, merge decoction liquor, filter, filtrate is concentrated into 900ml, add 95% ethanol, make determining alcohol reach 70%, left standstill 12~24 hours, filter, reclaim ethanol, being condensed into relative density is the extractum of 1.32~1.38 (50~60 ℃); To decoct with water 2 times through the Radix Astragali of pulverizing, add 6 times of water gagings at every turn, extracted successively 2 hours, 1 hour, merging filtrate is when being concentrated into the 1500ml left and right sides, adding 95% ethanol, to make determining alcohol be 60%, left standstill 12~24 hours, filters, filtrate recycling ethanol, when being concentrated into the 400ml left and right sides, adding 95% ethanol, to make determining alcohol be 80%, left standstill 12~24 hours, filter, filtrate recycling ethanol, being condensed into relative density is the extractum of 1.32~1.38 (50~60 ℃); Get Lignum Dalbergiae Odoriferae, add 5 times of water gagings, reflux, extract, 5 hours is collected volatile oil; Get above-mentioned Salvia miltiorrhiza and Panax notoginseng extractum, Radix Astragali extractum, add volatile oil of Lignum Dalbergiae Odoriferae, mixing.
Embodiment two
Get Salvia miltiorrhiza and Panax notoginseng extractum, Radix Astragali extractum and the Polyethylene Glycol-6000 of embodiment one, water-bath is dissolved, and after change is even, adds volatile oil of Lignum Dalbergiae Odoriferae, and mixing moves in the drop pill machine, makes 1000 drop pill.
Embodiment three
Get Radix Astragali 40.6g, Radix Salviae Miltiorrhizae 44.8g, Radix Notoginseng 11.2g, Lignum Dalbergiae Odoriferae 38.6g, adjuvant Polyethylene Glycol-600030g makes 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment four
Get Radix Astragali 77.3g, Radix Salviae Miltiorrhizae 22.8g, Radix Notoginseng 4.8g, Lignum Dalbergiae Odoriferae 30.5g, adjuvant Polyethylene Glycol-600028g, make 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment five
Get Radix Astragali 42.3g, Radix Salviae Miltiorrhizae 39.2g, Radix Notoginseng 8.2g, Lignum Dalbergiae Odoriferae 46.8g, adjuvant Polyethylene Glycol-600025g, make 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment six
Get Radix Astragali 65.2g, Radix Salviae Miltiorrhizae 38.9g, Radix Notoginseng 9.3g, Lignum Dalbergiae Odoriferae 32.5g, adjuvant Polyethylene Glycol-600040g, make 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment seven
Get Radix Astragali 56.2g, Radix Salviae Miltiorrhizae 32.5g, Radix Notoginseng 6.2g, Lignum Dalbergiae Odoriferae 41.6g, adjuvant Polyethylene Glycol-600022g, make 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment eight
Get Radix Astragali 36.5g, Radix Salviae Miltiorrhizae 32.4g, Radix Notoginseng 6.2g, Lignum Dalbergiae Odoriferae 41.7g, adjuvant Polyethylene Glycol-600022g, make 1000 drop pill by the method for embodiment one and embodiment two.
Embodiment nine
Get Radix Astragali 65.6g, Radix Salviae Miltiorrhizae 25.8g, Radix Notoginseng 9.5g, Lignum Dalbergiae Odoriferae 46.4g, make extractum by the preparation technology of embodiment one, qinghuo reagent, sucrose and dextrin are made 200 in tablet by weight 1: 3: 1 ratio according to conventional method.
Embodiment ten
Get Radix Astragali 35.5g, Radix Salviae Miltiorrhizae 50.8g, Radix Notoginseng 16.3g, Lignum Dalbergiae Odoriferae 52.3g, make extractum by the preparation technology of embodiment one, qinghuo reagent, sucrose and dextrin are made 125 bags of granules in 1: 3: 1 ratio according to conventional method.
Embodiment 11
Get Radix Astragali 86.5g, Radix Salviae Miltiorrhizae 21.3g, Radix Notoginseng 3.5g, Lignum Dalbergiae Odoriferae 20.6g, make extractum by the preparation technology of embodiment one, qinghuo reagent, sucrose and dextrin are made granule in 1: 3: 1 ratio according to conventional method, record capsule according to conventional method.
Claims (8)
1. the Chinese medicine composition purposes in the medicine of preparation treatment chronic cardiac insufficiency, said composition is prepared from by the following raw materials by weight percent medicine: the Radix Astragali 22.2%~66.8%, Radix Salviae Miltiorrhizae 11.6%~33.4%, Radix Notoginseng 2.5%~13.5%, Lignum Dalbergiae Odoriferae 14.5%~44.3%.
2. purposes as claimed in claim 1 is characterized in that described Chinese medicine composition person's left ventricle contractile function that can improve the chronic cardiac insufficiency.
3. purposes as claimed in claim 2 is characterized in that the described Chinese medicine composition person's that can increase the chronic cardiac insufficiency left ventricular ejection mark.
4. purposes as claimed in claim 2 is characterized in that the described Chinese medicine composition person's that can increase the chronic cardiac insufficiency shortening fraction.
5. purposes as claimed in claim 1 is characterized in that the described Chinese medicine composition person's that can improve the chronic cardiac insufficiency energy metabolism.
6. as arbitrary purposes of claim 1~5, wherein said Chinese medicine composition is prepared from by the following raw materials by weight percent medicine: the Radix Astragali 30.8%~57.2%, Radix Salviae Miltiorrhizae 15.4%~28.6%, Radix Notoginseng 3.5%~6.5%, Lignum Dalbergiae Odoriferae 20.6%~38.2%.
7. purposes as claimed in claim 6, wherein said Chinese medicine composition is prepared from by the following raw materials by weight percent medicine: the Radix Astragali 44.7%, Radix Salviae Miltiorrhizae 26.7%, Radix Notoginseng 6.3%, Lignum Dalbergiae Odoriferae 22.3%.
8. purposes as claimed in claim 6, wherein said Chinese medicine composition is prepared from by the following raw materials by weight percent medicine: the Radix Astragali 41.2%, Radix Salviae Miltiorrhizae 23.8%, Radix Notoginseng 4.5%, Lignum Dalbergiae Odoriferae 30.5%.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102293822A (en) * | 2010-06-28 | 2011-12-28 | 天津天士力制药股份有限公司 | Application of traditional Chinese medicine composition in preparation of medicines used for reducing occurrence of cardiovascular events after acute myocardial infarction |
CN101675946B (en) * | 2008-09-19 | 2012-04-18 | 天津天士力制药股份有限公司 | Application of a traditional Chinese medicine in preparing a medicine for reducing inflammatory reaction after PCI |
CN110339202A (en) * | 2018-04-04 | 2019-10-18 | 天士力医药集团股份有限公司 | A kind of pharmaceutical composition and its application |
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2007
- 2007-02-06 CN CNA200710056720XA patent/CN101239099A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101675946B (en) * | 2008-09-19 | 2012-04-18 | 天津天士力制药股份有限公司 | Application of a traditional Chinese medicine in preparing a medicine for reducing inflammatory reaction after PCI |
CN102293822A (en) * | 2010-06-28 | 2011-12-28 | 天津天士力制药股份有限公司 | Application of traditional Chinese medicine composition in preparation of medicines used for reducing occurrence of cardiovascular events after acute myocardial infarction |
US9211310B2 (en) | 2010-06-28 | 2015-12-15 | Tasly Pharmaceutical Group Co., Ltd | Use of a Chinese medicine composition in preparing medicaments for treating secondary prevention of myocardial infarction |
CN110339202A (en) * | 2018-04-04 | 2019-10-18 | 天士力医药集团股份有限公司 | A kind of pharmaceutical composition and its application |
US11491173B2 (en) | 2018-04-04 | 2022-11-08 | Tasly Pharmaceutical Group Co., Ltd. | Pharmaceutical composition and application thereof |
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