NZ551135A - A composition capable of treating chronic stable angina pectoris comprising Danshensu, sanchinoside and ginsenoside Rg1 - Google Patents

Abstract

A composition capable of treating chronic stable angina pectoris comprising Danshensu, sanchinoside and ginsenoside Rg1. Also disclosed is a method for obtaining the composition.

Description

*10052741420* 551135 NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION Title: HERBAL COMPOSITION FOR ANGINA PECTORIS, METHOD TO PREPARE SAME AND USES THEREOF TIANJIN TASLY PHARMACEUTICAL CO., LTD., CHINA of No. 1 Liaohedong Road, Xinyibai Avenue, Beichen District,Tianjin 300402, China hereby declare(s) the invention, for which it pray(s) that a patent may be granted to it, and the method by which it is to be performed, to be particularly described in and by the following statement: 1 la HERBAL COMPOSITION FOR ANGINA PECTORIS, METHOD TO PREPARE SAME AND USES THEREOF This application is a divisional application of New Zealand patent application No. 526995 , the' entire 5 disclosure of which is incorporated herein by reference.

Throughout this application, various publications are referenced and full citations for these publications may be found in the reference at the end of the specifications preceding the claims. The disclosures of these publications are hereby incorporated 10 by reference into this application in order to more fully describe the state of the art as known to the skilled therein as of the date of the invention described and claimed herein.

BACKGROUND OF THE INVENTION Chronic stable angina pectoris is due to transit myocardial 15 ischemia. Aspirin, nitrates, beta-adrenoceptor blocking drugs, and calcium channel blocking drugs used alone or in combination with one another are the commonly used drugs for angina pectoris.

Aspirin as an antithrombotic agent is a symptomatic treatment for chronic stable angina pectoris.

Nitrates are used to treat an anginal episode and can be successfully used in prophylaxis by patients with predictable symptoms. With all nitrates, troublesome headache can prevent their use in certain susceptible individuals.

Beta-adrenoceptor blocking drugs, although established as a 25 cornerstone in the treatment of angina, are specifically contraindicated in patients with obstructive airways diseases and severe ventricular dysfunction, and relatively contraindicated in diabetes and in those with peripheral vascular disease, bradycardia or heart block.

Calcium antagonists are certainly effective in angina, achieving 30 their effects by smooth muscle relaxation in the coronary arteries and peripheral circulation, increasing myocardial supply and reducing myocardial work.

* Although there is progress in. drug combination therapy in angina, which most patients begin treatment with nitrates and a beta-adrenoceptor blocking drug or a calcium antagonist, there is a need of drug for chronic stable angina pectoris which is 5 very effective, can be taken for a long period of time and has very low toxicity.

In view of the problems of relating to the above mentioned drugs, notable efforts have been made to apply herbal Medicine as an 10 alternative to the standard treatment of chronic stable angina pectoris. Traditional Chinese Medicine (TCM) has contributed much in this respect.

US Pat. No. 5288485 and 5433957 refer to an extract from hypericum 15 erectum thurib for curing or preventing diseases caused by disorder in blood circulation such as angina pectoris.

US Pat. No. 5776463 refers to an oral pharmaceutical composition containing petals of borage or extract of borage petals for the 20 prevention and treatment of stress which is associated with circulatory heart diseases including angina.

In addition to hypericum erectum thunb and borage petals, many other herbal plants have also been used to treat angina. One such 25 plant is Valeriana officinalis latifolia. Yang GY et al (1994) Reported that 82 patients with angina pectoris had been treated with Valeriana officinalis latifolia, among whom ST-T ischemic changes appeared on ECG in 50 cases before treatment. Its total effective rate for simple angina (without detectable ischemic 30 findings) was 87.80%; the angina with ischemic findings, 88.00%. In addition, it was discovered that Valeriana officinalis latifolia could lower plasma lipids as well. No toxic actions to liver, kidney, and hemopoietic tissue, have been found.(1) Wu Y (1990) reported that in a setting of 267 patients with angina pectoris, 93.3% of the patients treated with xintongkang capsule was effective.

Another herbal preparation called Shenshao tongguan plan was used in treating angina pectoris. In 1990, Hu JX et al. Reported that the Shenshao tongguan pian is composed chiefly of saponin from 5 the stem and leaves of Ginseng and Radix Paeoniae Alba, etc. The total effective rate for treating angina pectoris was 94.71%. And the ECG improvement rate was 63.38%. In addition, laboratory examination also revealed that Shenshao tongguan pian could promote the left ventricular output, lower the blood viscosity 10 and inhibit the aggregation of blood platelet. Both acute and chronic toxicity tests showed that Shenshao tongguan pian has no toxicity or side effects.

Kuo-guan granule is another herbal preparation for angina 15 pectoris. Li Y et al. (1990) reported that the changes of the plasma zinc, copper and erythrocyte glutathione peroxidase were measured by atomic absorption spectrometry and DTNB color development in 31 patients suffering from coronary heart disease with angina pectoris before and after taking Kuo-Guan granule 20 for one month. The results indicated that the plasma zinc and erythrocyte glutathione peroxidase were lower and copper was higher in the patients than the normal control group before treatment (P <0.01) , the plasma zinc and erythrocyte glutathione peroxidase increased and copper decreased after treatment (P 25 <0.0l). These suggest that therapeutic mechanism of Kuo-Guan granule for coronary heart disease with angina pectoris may relate to its regulation on trace elements disturbance in body.

Saponin of Tribulus terrestris was another herbal composition 30 for treating angina pectoris.

Fufang Danshen Pian is a folk prescription of Dan Shen Tablet which indicate for treating chronic stable angina pectoris due to coronary artery ischemia and has been officially listed in 35 the editions of Chinese Pharmacopoeia since 1977 and applied to clinical use for decades.

Fufang Danshen Pian contains multiple active extracts of botanical including Danshen (Radix Salviae Miltiorrhizae) , and Sanchi (Radix Notoginseng) . Both of the botanical were first documented in Shen Nong Ben Cao Jing (Shen-nong's Herbal Pharmacopoeia) completed in 200. Fufang Danshen Pian also contains synthetic borneol, aversion of a natural borneol (Bingpian) . Natural borneol was first documented in Tang Ben Cao (Herbal Pharmacopoeia of the Tang Dynasty) compiled around 659.

Li Cheng-zhu et al (1979) reported in (Acta Acad Med Prim Shanghai) on an experimental study of thrombotic inhibition effect of Radix Silviae Miltiorrhizae. Effects on in vitro thrombosis, functions of platelet and coagulation, fibrinolysis were observed in rabbits. After injection of Radix Silviae Miltiorrhizae, 3 links were found to play an important role in inhibition of in vitro thrombosis: (1) inhibition of platelet function; (2) inhibition of coagulation function; and (3) promote fibrinolysis. Of which, the former two mechanisms function more intensely. The results conform to those in the treatment of thrombotic diseases, especially arterial thrombotic diseases.

Chiang WT et al (1982) reported in (Acta Acad Med Prim Shanghai) the effects of "Danshensu" and other two water-soluble components of salvia miltiorrhiza on dog ischemic myocardium and isolated pig coronary artery. The effect of 3 new water-soluble components i.e. Danshensu (DS-182, D(+)-3,4-dihydroxyphenyl lactic acid) , protocathu-aldehyde (PCAD) and an impure diterpene acid (DS-187) isolated from Salvia miltiorrhiza Bunge, were compared with those of dipyridamole. Results revealed (1) in mice, DS-182 gave significant protection against hypoxia, whereas PCAD was ineffective; (2) DS-182 could nullify the pituitrin-induced electrocardiographic ischemic ST-T elevation but had no influence on the reduced heart rate. DS-187, PCAD and dipyridamole only showed incomplete protection; (3) in the acutely infarcted dog model prepared by ligation of the anterior descending branch of the left coronary artery, the benefits achieved by intravenous injection of DS-182 proved superior to DS-187 and PCAD in respect to the left ventricular function, left ventricular peak systolic pressure(LVPSP) and left ventricular end diastolic pressure(LVEDP) . PCAD, on the contrary, produced adverse effects on LVPSP and LVEDP. Intravenously administered dipyridamole, though it did not change LVEDP, 'suppressed LVPSP significantly with marked hypotensive effect. All these components of Salvia and dipyridamole significantly reduced the ultimate myocardial infarct size (N-BT assessment); Ds-182 was most effective, dipyridamole and DS-187 the next, while PCAD the least; (4) in the isolated perfused pig coronary artery preparation, DS-182 significantly reduced the resistance of the coronary vessel, whereas either DS-187, PCAD or sodium Tanshinone 11 -A sulfonate (DS-201) , another component of Salvia, incx-eased it. The constrictory action of morphine and propranolol on the isolated coronary artery preparation was antagonized by the prior administration of DS-182. All of these suggested that Danshensu might be the main active principle of Salvia miltiorrhiza in treating ischemic heart disease and that its concomitant use with propranolol or morphine would be beneficial.

Li Cheng-zhu et al (1983) reported in (Chin J Integr Med) the anti-coagulation effect of Radix Silviae Miltiorrhizae. Danshensu is a water-soluble monomer extracted from Radix Silviae Miltiorrhizae. It is also the main ingredient of commercially sold Injection Radix Silviae Miltiorrhizae. The present study proved that Danshensu inhibits thrombosis in vitro, aggregation of platelet (induced by ADP) ,and internal and external coagulation systems; diminishes the number of platelets and promotes the degradation of fibrin or fibrinogen. The effects peaked 30 minutes after a single injection of 2.0 mg/kg in rabbits, lasted for 1 hour, and recovered gradually. 4.5 hours after injection, all recovered to normal but thrombosis test in vitro.

Chen Zhanghua (1987) reported in Acta Acad Med Prim Shanghai on effects of *Danshensu" on experimental microcirculatory disturbances and plasm lactic acid concentrations. Natural Danshensu is a water soluble monomer extracted from Radix Salviae Miltiorrhizae(RSM). Microcirculatory disturbances in rabbits were induced by intravenous injection of high molecular weight dextran. Natural Danshensu (dosage 4-5 .rng/kg) markedly increased the number of capillary vessels in the bulbar conjunctiva, and also decreased the concentration, of plasm lactic acid in the rabbits. Mesenteric microcirculatory disorders were produced by local noradrenaline (4 g) drip in mice. Natural Danshensu dilated the arteries and accelerated the speed of blood flow, thus eliminating microcirculatory blood stasis. In our experiments, effects of synthetic Danshensu were observed concomitantly. The results showed that there was no significant difference between natural and synthetic Danshensu in relieving microcirculatory disturbances.

Sun Xi-ming et al (1991) reported a new pharmacological action of an extract of Danshen (Salvia miltiorrhiza) . The paper reports that an extract of Danshen (Salvia miltiorrhiza) which contains the sodium salts of D ( + ) - (3,4-dihydroxy phenyl) lactic acid was found to possess a new pharmacological action of decreasing the biosynthesis of cholesterol in cells and anti-lipoprotein oxidation, by cell cultural studies. When compared with the control, its electrophoretic migration rate was markedly lowered and MDA content and cytotoxicity decreased obviously. These results indicated that salts of D(+)-(3,4-dihydroxy phenyl) lactic acid may be effective in the prevention and treatment of atherosclerosis.

Zheng Ruo-xuan et al (1992) reported in (Chin J Integr Med) the preservation effect of Radix Silviae Miltiorrhizae on myocardial ischemia induced by coronary ligation in mice. Obvious preservation effect on acute myocardial ischemia in mice by coronary ligation could be obtained after i.p. water-extract of Radix Silviae Miltiorrhizae (5 g crude drug/kg). S-T segment elevation on EGG due to myocardial ischemia in the treatment group was much lower, ischemic size of the left ventricle was smaller and the survival rate was higher when compared with the control.

Wu Yao-zhong et al (1995) reported in (Acta Nanjing Univ Trad Chin Mater Med) on effects of Radix Silviae Miltiorrhizae in promoting blood circulation by removing blood stasis. Pharmacological research of Radix Silviae Miltiorrhizae is common. However, rheological studies on Radix Silviae Miltiorrhizae by assessing PGI2, ET, and TXA2 produced by platelet are seldom. Influence of Radix Silviae Miltiorrhizae on thrombosis, changes of PT, KPTT, FG, ESR and HCT, and aggregation of platelet in rabbits are evaluated in the present study. Conclusions are that Radix Silviae Miltiorrhizae reduces the synthesis of TXA2 and decreases the effects of enhancement of platelet aggregation and thrombosis.

Shi Lin et al (1990) reported in (Acta Pharmcol Sin) on the effects of total saponins of Panax Notoginseng on increasing PGI2 in carotid artery and decreasing TXA2 in blood platelet. Total saponins of Panax notoginseng (PNS) were given orally 100 rog/ (kg'day) to rabbit for 8 wk. Aortic atherosclerotic plaque formation was restrained as compared that of to the control group. Radioimmunoassay was used to investigate the effects of PNS on the contents of prostacyclin in carotid artery and thromboxane A2 in rats' blood platelet. Oral administration of PNS 25, 50, 100 mg/ (kg'day) for 10 days caused an increase of prostacyclin in carotid artery and a decrease of thromboxane A2 in blood platelet as compared with the control group. These results showed that the anti-atherosclerotic action of PNS maybe a result of the correction of the imbalance between prostacyclin and thromboxane A2.

Li Xing et al (1990) reported in (Acta Pharmacol Sin) the Protective effects of Panax Notoginseng saponin on experimental myocardial injury induced by ischemia and reperfusion in rats. Effects of total saponin of Panax Notoginseng (PNS) and purified ginsenoids Rbi and Rgi from PNS on myocardial injury induced by cardiac ischemia and reperfusion were studied using rat hearts in situ and in vitro. In. pentobarbital-anesthetized rats, PNS pretreatment (100 and 2 00 mg/kg) provided significant reduction in myocardial .infarcted size after left descending coronary artery ligation (40 min) and reperfusion (120 min) in comparison with the control. PNS 12 . 5 and 25 mg/L, Rbi 10 mg/L and Rgi 10 mg/L significantly decreased cardiac CPK release, attenuated myocardial Ca++ accumulation, reduced malondialdehyde (MDA) production and prevented reduction of superoxide dismutase (SOD) activity in comparison with the control in perfused isolated rat hearts with global ischemia (40 min) and reperfusion (15 min) . The results showed that PNS, Rbi and Rgi prevented cardiac ischemia and the action was considered to be related to the inhibition of lipid peroxidation.

Huang Cong et al (1991) reported in (Chin Bull Pharmacol)the effects of Panax Notoginseng Saponin on myocardial ischemia and reperfusion injury in conscious rabbits. The effects of Panax Notoginseng saponin (PNGS) on myocardial ischemia and •reperfusion injury in conscious rabbits were studied with observation of changes in electrocardiogram (ECG), the activities of creatine phosphokinase (CPK) and lactate dehydrogenase (LD) and the size of ischemic area. PNGS at the dose of 50 mg/kg and 100 mg/kg significantly reduced the size of myocardial ischemic area. These results suggested that PNGS have the protective effects on myocardial ischemia and reperfusion injury.

Mo Qi-xian et al (1987) reported in (Propriet Trad Chin Med Res) the dynamics of 3H-Borneol. In order to highlight the mechanism of inducing resuscitation of Borneol aromaticity, dynamics of 3H-Borneol were conducted by intraveneous injection and oral administration. The results revealed that the half-life time was 2.8 min after a single intraveneous injection of 3H-Borneol. it suggested that the drug distributed rapidly to the relevent organs and tissues after administration and produced prompt effect. In vivo distribution concentrated on organs and tissues which are abundant in blood flow, such as heart, lung, liver, kidney and brain, etc. This provided clinical application certain theoratical basis . Since the diminishing half-life time was 5.3 hours after oral administration of the drug, this suggested that oral Borneol could not lead to accumulation, but poor bioavailability. Further studies should be taken to discusse the relationship with drug dose and dosage form.

Chen Tie-feng et al (1990) reported in (Acta Pharmacol Sin) the enhancement of absorption of tetramethylpyrazine by synthetic borneol. Sprague-Dawley rats were given ig tetramethylpyrazine phosphate (TMP) 5 mg/kg with or without previous borneol 5 mg/kg. The plasm TMP concentrations were analysed by GC method, and the data were treated by NONLIN program. The Cmax were 931 and 562 ng/ml, respectively, (p<0. 01) ; while the AUC were 68849 and 37174, respectively, (P<0.05). It is suggested that the borneol enhances the absorption of the TMP but not in elimination.

Xu Wei et al (1995) reported in (Pharmacol Chin Med Clin) the effect of menthol and borneol on the distribution of sulfadiazine sodium and Evan's blue in the rat and mouse brain. Menthol (1.5 g/kg, ig) and Borneol (1.5 g/kg) prolonged the sulfadiazine sodium distribution half-life tx/7. in rats. The above dosage of menthol and borneol given orally also increased the concentration of sulfadiazine sodium in the rat brain. Menthol (ig 0.5g/kg for 3 days) and borneol (ig 0.5 g/kg for 3 days) promoted the concentration of Evan's blue in the mouse brain, but the value of concentration was significantly lower than that of the mice suffering from the ischemia-reperfusion injury. The results suggested that the menthol and borneol could enhanced the sulfadiazine sodium transfer in brain-blood barrier with no damage to brain-blood barier.

In the United States, coronary atherosclerotic heart disease is the commonest cause of cardiovascular disability and death.

Atherosclerosis is an arterial disorder characterized by yellowish plagues of cholesterol, lipids, and cellular debris 5 in the inner layers of the walls of large and medium-size arteries . The condition begins as a fatty streak and gradually builds to a fibrous plaque or atheromatous lesion. The blood vessel walls become thick, fibrotic, and calcified. The artery lumen narrows.

Many atherosclerotic plaques remain stable or progress gradually. Others may rupture resulting in hemorrhage, platelet activation, and thus intravascular thrombosis. Coronary thrombosis causes partial or complete vessel occlusion, impairs blood flow, thus leads to unstable angina or myocardial infarction. Alternately, 15 the ruptured plaques may become restabilized, often more severe stenosis.

Exercise and mental stresses increase myocardial oxygen demand. Under normal physiological condition, increased myocardial 20 oxygen demand is met by the arterioles dilating thus increasing blood flow. In the presence of atherosclerosis, the arterioles may dilate maximally to meet basic demand. Such dilated arterioles may be unable to meet the increased myocardial oxygen demand. When oxygen demand exceeds oxygen supply, the ischemia 25 of myocardium occurs. Alternately, severe vessel occlusions may limit blood flow thus cause myocardial ischemia. Clinical manifestations of transient myocardial ischemia is angina pectoris which is a paroxysmal thoracic pain, frequently spread to the arms, particularly to the left arm, with or without 3 0 accompanied by a feeling of suffocating and impending death.

Angina pectoris is subdivided in to two: stable and unstable. Stable angina pectoris is caused by the increased myocardial oxygen demand in most cases. Stable angina thus attacks in the 35 predictable frequency and duration upon provocation which increases myocardial oxygen requirements such as exercise, mental stress, etc. In contrast, unstable angina pectoris attacks without provocation and usually caused by decreased oxygen supply to myocardium. Plaque disruption, platelet plugging, and coronary thrombosis decrease oxygen supply to myocardium.

Angina pectoris is treated with various drugs, surgical procedure, coronary artery bypass graft, balloon-angioplasty, stent placement, etc. Therapy for stable angina pectoris is primarily to minimize myocardial oxygen demand as well as a preventive measure. Therapy for the acute syndrome unstable angina pectoris is primarily to inhibit platelet activation and thrombolysis.

Current therapeutic agents for chroni-c stable angina pectoris are nitroglycerine, other nitrates, calcium channel blockers, and beta-adrenergic receptor blockers. These drugs, administered alone or in combination with other drugs, alleviate or prevent rather than cure angina.

When angina attacks, nitroglycerine is administered sublingually to alleviate symptoms. Nitroglycerine is also applied to prevent anginal attacks caused by exertion and stress. Nitrates are applied to prevent angina attacks. Nitroglycerine and nitrates mediate their effect primarily by relaxing vascular smooth muscle, reducing myocardial activity, and thus reducing myocardial oxygen demand. The side effects are throbbing headache, dizziness, weakness, orthostatic hypotension, tachycardia, etc.

Beta-adrenergic receptor blockers such as propranolol are applied to prevent angina pectoris by reducing myocardial oxygen requirements during exertion and stress. The major contraindications arebronchospastic disease, bradyarrhythmias, and overt heart failure. In individuals with asthma and other forms of airway obstruction, beta-blockers may worsen their condition.

Calcium antagonists are applied to prevent angina pectoris by reducing the oxygen demand of myocardium. Myocardium is dependent on calcium influx for normal functions. By inhibiting calcium inf lux, calcium antagonists may relax smooth muscle of the blood vessel, decrease myocardium activity, reduce oxygen demand by myocardium, and thus prevent angina pectoris. Calcium antagonists have adverse side effects. The mild side effects are flushing, edema, dizziness, nausea, etc. Excessive inhibition of calcium influx to myocardium may cause severe side effects such as cardiac arrest, bradycardia, atrioventricular block, congestive heart failure, etc. Combined with beta-adrenergic drugs, the side effects of calcium antagonists are often augmented.

In China, Panax Notoginseng and Radix Salviae Miltorrhizae have been used for treating cardiovascular disease since 20 0 AD (Shen-nong's Herbal Pharmacopoeia) . Panax Notoginseng has been used for treating angina pectoris. Radix Salviae Miltiorrhizae has been used for promoting blood circulation and dispersing blood stasis. Numerous preclinical and clinical studies demonstrate the efficacy and safety of Panax Notoginseng and Radix Salviae Miltiorrhizae.

Traditional Chinese medicine is the mixture of several herbs requiring decoction. A modified form of Chinese medicine for treating coronary heart disease is Dan Shen tablet. Dan Shen tablet is a large unctuous ball, often as large as 1 cM in diameter. Dan Shen tablets are made of the extract of Radix Salviae Miltiorrhizae, powder of Panax Notoginseng and synthetic borneol, have been listed in the Chinese Pharmacopoeia since 1977, and have been used to treat cardiovascular disease for decades.

The disclosed Danshen pill (DSP) or called cardiotonic pill is a new generation Chinese medicine for coronary heart diseases. Chinese medicine consists of various herbs which vary from prescription to prescription in regard'to the type of herbs as well as the proportion of herbs. To control the quality, DSP is manufactured with the standarized formula. The therapeutic components of DSP are the water-soluble extracts of Radix Salviae Miltiorrhizae 10-30 % and sometimes, approximately 20 %, the water-soluble extracts of Panax Notoginseng (2-6 %) , and borneol (1-3 %). Furthermore, to alleviate angina quickly, DSP been manufactured as a small pill which, can be dissolved immediately upon sublingual administration, delivered to myoc ardium quickly, and thus alleviate angina fast.

DSP has been proven to be nontoxic and effective for the prevention and treatment of cardiovascular disease caused by coronary artery ischemia in preclinical and clinical studies. Furthermore, the superior efficacy of DSP to Dan Shen tablets for treating coronary arterial disease has been demonstrated in preclinical as Well a's in clinical studies.

DSP has been listed in the Supplement Edition of Chinese Pharmacopoeia since 1998, approved by the Chinese Ministry of Health, marketed as a drug in China since 1993, and used by more than five million people.

I 14 SUMMARY OF THE INVENTION Dan Shen Pill (DSP) is a new generation of Chinese medicine for treating coronary heart disease manufactured with the standardised formula. New Zealand 5 Patent Application 526995 discloses a composition capable of treating chronic stable angina pectoris, comprising 5-40% water soluble phenolic acid extracted from Radix Salviae Miltorrhizae, 1-10% water soluble saponin extracted from Panax Notoginseng and 1-5% of Borneol.

Panax Notoginseng is included to alleviate and to prevent angina. Radix 10 Salviae Miltorrhizae is included to inhibit platelet activation, to prevent coronary thrombosis, and thus to promote blood circulation. Borneol is included for the effective delivery of therapeutic components to myocardium.

DSP is manufactured as a small pill, approximately 25 mg, which can be dissolved immediately upon sublingual administration and thus to mediate its 15 therapeutic effects quickly. The efficacy of DSP alleviating and preventing angina has been proven in preclinical and clinical studies.

New Zealand 526995 also provides methods of obtaining the relevant herbal composition for treating chronic stable angina pectoris.

According to the present invention there is provided a composition capable of treating chronic stable angina pectoris comprising Danshensu, sanchinoside and ginsenoside Rgi which produces eight peaks as shown in the following table, Retention Relative Appearance Area Peak No.

Time Retention Time Probability Area ratio Area Ratio Range 1 8.289 0.672 100% 1034.276 0.572 0.572±0.096 2 12.343 1.000 100% 1817.065 1.000 1.000±0.000 -■> J> 17.493 1.417 100% 376.547 0.208 0.208±0.040 4 18.664 1.512 100% 328.011 0.181 0.181±0.059 24.883 2.016 100% 486.626 0.267 0.267±0.097 6 27.586 2.235 100% 525.432 0289 0.289±0.052 7 29.714 2.407 100% 940.963 0.516 0.516±0.125 8 34.030 2.757 100% 1547.495 0.850 0.850±0.163 when subjected to steps of: * 14a a) dissolving a suitable amount of said composition with internal standard para-aminobenzonic acid solvent; b) using Danshensu and protocatechuic aldehyde as the standards; 5 c) performing the HPLC assay; and d) calculating according to the internal standard method.

According to a further embodiment of the present invention there is provided a method for obtaining a herbal composition capable of treating chronic stable angina 10 pectoris which contains Danshensu, sanchinoside, ginsenoside Rgi comprising the steps of: a) Extraction. Put Radix Salviae Miltorrhizae into the multifunction extraction tank; add water until it is 15-20cm over the herb (about 5-7 times the quantity of the herb); heat them up to boiling with steam, while the inside air pressure should be controlled in between 0.04-0.06 mPa; keep the tank in boiling condition. Boiling twice, first for 2 hours and then for 1.5 hours. The extract is filtrated at the bottom of the extraction tank through a 100-mesh net into a stock tank. The remaining is discarded. b) Concentration. Transfer the solution from the stock tank into a vacuum tank. The 20 steam is controlled at below 0.05 mPa. In the mean time, adjust the vacuum to 0.076—0.088 mPa to keep the tank in boiling condition. The solution is concentrated to about the solution volume(Liter) to the herb quantity(kilogram) in the ratio of 1:1. c) Ethanol precipitation. After the concentration, the solution was filtrated at the 25 bottom of the vacuum concentration tank through a 100 order net into a precipitation tank. Add 95% ethanol to the solution with slow stirring until the ethanol concentration of the solution reaches 70% measured by ethanol gravimeter. Leave it for 24 hours. d) Ethanol recovery. Open the tank, transfer the supernate of the ethanol precipitated solution through 100 mesh net into a vacuum concentration tank.

Adjust the air input to 0.04-0.06 mPa and the vacuum to 0.076-0.088 mPa to keep the tank boiling but bumping. Recover the ethanol to the herb solution to about the solution volume (Liter) to the herb quantity(kilogram) in the ratio of 1:1. 14b e) Refinery by polyamide chromatography. Load the solution from the step (d) into the pre-treated polyamide chromatography. The loading volume is 5 ml/gram polyamide. After washing the column with 3 volume times water, elute the 5 column with 5-10 times 95% ethanol. Recover the ethanol as in the step (d) to concentrate the eluant to the density of 1.33-1.35.

According to another embodiment of the present invention, there is provided a method for obtaining a herbal composition capable of treating chronic stable angina 10 pectoris comprising steps of: (a) Extraction. Put Radix Notoginseng into the multi-function extraction tank; add water until it is 15-20 cm over the herb (about 5-7 times the quantity of the herb; heat up to boiling with steam, while the inside,air pressure should be controlled in between 0.04-0.06 MPa; keep the tank in boiling condition."Boiling twice, first for 2 hours and then for 1.5 hours. The extract is filtrated at the bottom of the extraction tank through a 100 mesh net into a stock tank. The remaining is discarded. (b) Macroporous adsorption resin. i. Pre-treatment of macroporous adsorption resin: After being soaked in 95% 20 ethanol for 24 hours, non-polarity macroporous adsorption resin ZTC-1, with particle size 0.3-1.2 mm and average aperture 130-300 A, is filled into a column. Wash the column with ethanol and equal volume of water until the eluant is clear with equal volume of water; or after washing the column with 0.1-1 mol/L NaOH or HCL, wash the column with water until the eluant has no ethanol smell or is 25 close to pH neutral. ii. Loading. Load the extract of Radix Notoginseng from Step (a), 1 g/1 g resin. The flow rate is 0.5-5 cm/cm2/min. After loading, wash the column until the eluant is clear. Elute with 70% ethanol. The flow rate is 0.5-5 cm/cm2/min. Collect the eluant. iii. Recovery resin. Wash the column with 95% ethanol until the eluant is without color and clear after adding equal volume of water. Then wash the column with water until there is no ethanol smell. (c) Concentration of the notoginseng eluant. Open the vacuum pump. Put the 75% ethanol eluant through 100 mesh net to a vacuum concentration tank. Adjust the 14c air input to 0.04-0.06 mPa and the vacuum to 0.076-0.088 mPa to keep the tank boiling but bumping.Recover the ethanol until the density of the eluant reaches 1.33-1.35. The extract of Notoginseng saponin is obtained.

DETAILED DESCRIPTION OF THE FIGURES Figure 1. Batch No.: 19990806 Figure 2. Batch No.: 19990815 Figure 3. Batch No.: 19990823 The position of fingerprint peaks: Group I consisting of peak 1 and 2 (retention time ranging from 7 to 15min) ; Group IIconsisting of peak 3 and 4 (retention time ranging from 15 to 20min) ; Group HI consisting of peak 5% 6n 7 and 8 (retention time ranging from 20 to 40min) . From whole sight, the abundance of peaks in the group T is largest, and that the height of peak l is close to the peak 2. The peaks in the group Ilstand side by side, posses same heights almost and the abundance is very small. The group III is composed of 4 peaks, and their height increase step by step. These three groups compose the representative fingerprint of Compound Danshen Dripping pills.

DETAILED DESCRIPTION OF THE INVENTION This invention discloses a composition of the medicament Dan Shen Pill (DSP) comprising: (a) [water-soluble]" extracts of Radix Salviae Miltorrhizae, [water-soluble] extracts of Panax Notoginseng, and [synthetic] Borneol; (b) Radix Salviae Miltorrhizae, Notoginseng, borneol, and carriers; and (c) Radix Salviae Miltorrhizae, Panax Notoginseng, borneol, and pharmaceutical carriers.

In an embodiment of the above medicament, Radix Salviae Miltorrhizae and Panax Notoginseng are employed as they are used in China for treating coronary heart disease since 200 AD. Panax Notoginseng has been used to treat angina and Radix Salviae Miltorrhizae has been used to promote blood circulation. Borneol is employed to facilitate the fast delivery of therapeutic components to target organs. Natunal Borneol has been used in China since 600 AD. As Borneol is almost extinct, DSP comprises synthetic borneol.

This invention provides the use of DSP for: (a) treating coronary heart disease; (b) treating coronary heart disease in conjunction with other drugs; (c) primary prevention of coronary heart disease; (d) primary prevention of coronary heart disease in conjunction with other drugs; (e) secondary prevention of coronary heart disease,- (f) secondary prevention of coronary heart disease in conjunction with other drugs; and (g) reducing nitrates intake by angina patients; and (h) reducing serum cholesterol level.

In an embodiment of DSP, the indication is for coronary artherosclerotic disease such as, but not limited, to alleviate angina pectoris, to prevent angina pectoris caused by exertion and stress, and to promote blood circulation by inhibiting platelet aggregation thus to preventing coronary thrombus formation. DSP can be applied to reduce nitroglycerine intake which is frequently used to alleviate and to prevent angina. DSP can be also applied to reduce plasma cholesterol level thus to prevent the formation of new atherosclerosis lesions. Atherosclerosis is often initiated by cholesterol streak deposited on vessel walls.

This inventions discloses a method for controlling the quality of medicaments by standarizing the composition and the concentration of therapeutic substances in a medicament by analyzing and identifying therapeutic components using analytical techniques comprising the steps of: (a) fractionating a medicament using analytical techniques; and (b) identifying and quantitating therapeutic substances contained in a medicament by comparing with the analytical profile of the relevant purified substances as standard.

In an embodiment of the above invention, examples of analytical techniques are thin-layer chromatography, high performance liquid chromatography, and others. The purified standard of therapeutic components are the major identified active components in medicaments. For example, the purified standards of active components for DSP are, but not limited to, saponins, phenolic acid such as Danshensu, borneol, etc. Active components in DSP are identified by comparing the position of DSP fractions such as retention time in high performance liquid chromatography or the position and the color of DSP fractions in thin-layer chromatography, etc. with the characteristic of purified standards. Active components of DSP is quantitated by comparing the size of active fractions of DSP with the size of the known amount of standards. For example, the amount of saponin contained in DSP is determined by comparing with the standard curve of the known amount of purified saponin.

In another embodiment, DSP comprises 5-4 0% water-soluble phenolic acid of Radix Salviae Miltorrhizae, 1-10 % water soluble saponin of Panax Notoginseng, and 1-5% borneol.

In another embodiment, DSP comprises 10-30 % water-soluble 10 phenolic acid of Radix Salviae Miltorrhizae, 2-6 % water soluble saponin of Panax Notoginseng, and 1-3 % borneol.

This invention discloses a dropping machine for manufacturing a small-sized medicament, which can be readily dissolved thus 15 readily delivered to organs, comprising the parts of: (a) [a dropping pot] [dropping pots] of which temperature ranges [60-100] [more preferably 89-93 °C] ; (b) liquid paraffin cooling solution of which temperature is lower than 8°C; (c) a dropping head with 1.8mm inner diameter and 2.35 outer diameter; (d) [a dropping head] distanced from the surface of cooling solution by approximately [15 m]; and 2.S In an embodiment of the use of the above machine is to manufacture small-sized pills which can be dissolved immediately upon administration.

In another embodiment, the size of small pills are: 30 (a) 0.33-0.34 cm in diameter; (b) 21.25-28.75 mg in weight; and (c) 1.13-1.40 mg/mm3 in density.

EXPERIMENTAL DETAILS Manufacturing of Dan Shen Pill (DSP) DSP is a small pill, approximately 25 mg, of which therapeutic components comprise water-soluble extracts of Notoginseng, water soluble extracts of Salviae, and synthetic borneol.

For manufacturing DSP, Notoginseng and Salviae are extracted separately with hot water in circulating systems and filtered. The filtrates are condensed under decompressed conditions, filtered and precipitated. The concentrates are refined using resin columns and concentrated under decompressed conditions. The refined water-soluble extracts thus obtained were mixed with synthetic Borneol and pharmaceutical carriers. The mixture is made to a small pill using a special dropping machine. The quality of DSP is controlled by standarizing the quantity as well as the proportion of its major therapeutic components Saponon, phenolic acid such as Danshensu and Borneol. Thin-layer chromatography, high performance liquid chromatography, fingerprinting and other analytical techniques are used to identify and quantitate therapeutic components in DSP.

Manufacturing of DSP 1. Extraction of water-soluble component: of Panax Notoginseng (a) Dilution of herbs with 5-7 times of water. (b) Extraction of water-soluble components of Panax Notoginseng by boiling in a tank with the air pressure between 0.04-0.06 mPa for 2 hours. (c) Repeat extraction under the same condition for 1.5 hours. (d) Filtration of the extraction with 100-mesh net. (e) Refine the filtrate using macroporous adsorption resin eluting with ethanol. (g) Concentration of the eluted extracts under decompressed condition with the air input to 0 .04-0 .06 mPa and the vacuum to -0.076--0.088 mPa until the density is 1.33-1.35. 2. Extraction of water-soluble components of Radix Salviae Miltorrhizae (a) Dilution of herbs vv:.th 5-7 times of water. (b) Extraction of water-soluble components of Radix Salviae Miltorrhizae by boiling in a tank with the air pressure between 0.04-0.06 mPa for 2 hours. (c) Repeat extraction under the same condition for 1.5 hours. (d) Filtration of the extraction with 100-mesh net. (e) Concentration of the filtrates under decompressed conditions with the vacuum pressure is-0.076—0.088 mPa until one Kg initial herb becomes one liter.] (f) Precipitation of the concentrates with ethanol. (g) Filtration of the ethanol precipitates solution through 100-mesh net. (h) Concentration of the filtrates under decompressed conditions with input air pressure is 0.04-0.06 mPa and the vacuum pressure is 0.076--0.088 mPa. (i) Refine the concentrates by polyamide chromatography eluting with ethanol. (j) Concentrate the refined extracts to the density of 1.33-1.35.

DSP production (a) Mix the extracts of Panax Notoginseng, the extracts of Radix Salviae Miltorrhizae, synthetic boneol and polyethylene glycol 6000 at the ratio of 4.0:20.6:1.9:79.5. (b) Melting the mixture. (c) Manufacturing the melted mixture to DSP using the dropping machine with the following characteristics: the temperature of dropping pot is constantly 89-93°C, the cooling solution is liquid paraffin of which the temperature is lower than 8 °C, the inner diameter of the dropping head is 1. 8mm, the outer diameter of the dropping head is 2.4mm, the distance between the dropping head and the surface of cooling solution is 15 cm. (d) Centrifugation of the pills at 80C-1100 rpm for 15 minutes to remove oils.

Quality control of DSP DSP contains the identified therapeutic components protocatechuic aldehyde and saponin as well as various other components. The contents of these compounds in herbs vary from lot to lot of herbs. To standarize the contents of therapeutic components in DSP and thus to control the quality of DSP, a method to identify and to quantitate therapeutic agents in medicaments has been developed. An example of the procedures comprises: (a) Dissolve 30 DSPs in 3 ml methanol and ultrasonicate for 10 minutes. (b) Centrifugation for 5 minutes. (c) Fractionate the supernatant using standard analytical techniques using thin layer chromatography, high performance liquid chromatography, etc. (d) Identification of the therapeutic components of DSP such as Sodium Danshensu, protocatechuic aldehyde, saponin, etc. by comparing DSP fractions with the relevant purified standards in regard to the position, size and color. (e) Identifying and quantitating.therapeutic components in DSP by comparing the position, size, and color of DSP fractions with the position, size and color of the relevant purified standards. (f) Identifying therapeutic components in DSP by comparing the relative retention time and relative area of peaks in fingerprints with the relative retention time and relative area of peaks in standard fingerprint.

TLC identification of DSP A method for identifying Sodium Danshensu and protocatechuic aldehyde of a herbal composition capable of treating chronic stable angina pectoris by thin layer chromatography comprising the steps of: a) preparing the assay comprising the steps of: i. putting 30 pellets of the said composition in 3 ml methanol and dissolve by ultrasonation for 10 minutes to form a solution; ii. centrifuging the solution for 5 minutes and collect the supernatant; iii. contacting 10 ul the solution onto a silicon G gel plate containing 0.5% CMC-Na; iv. developing the plate with a developing solution comsisting of Chloroform, acetone and methane acid in the ratio of 10:4:1.6; v. drying and fumigating the plate with ammonia and laying the plate up for 15 minutes; vi. checking the plate under ultraviolet light, the spot representing the said composition should be at the corresponding position of the standards and show the same color. b) . using Sodium Danshensu and protocatechuic aldehyde as the standards.

A method for identifying gypenoside of a herbal composition capable of treating chronic stable angina pectoris by thin layer chromatography comprising the steps of: a) preparing the assay comprising the steps of: i. Put 30 pellets of the said composition in 5 ml ammonia solvent and dissolve by ultrasonation to form a solution; ii Put the said solution into the macroporous adsorption resin column; the speed is 0.5/minute; iii. After washing the macroporous adsorption resin column with 20 ml distilled water, the macroporous adsorption resin column is eluted with 2 ml methanol solution; iv. collecting the eluant; v. contacting 10 ul said eluant onto a silicon G gel plate containing 0.5% CMG-Na; vi. developing the plate with 10 ml developing solution which is a lower layer clarificant of the solution of Chloroform, acetone and water in the ratio of 6:3:1 after 2 hours at 10DC; vii. After being dried and sprayed with 10% ethanol sulfate, the plate is baked at 105DC for several minutes; viii. Check the plate under normal light, the spot representing the said composition should be at the corresponding position of the standards and show the same color. b) . using total gypenoside, Saponin R1 and ginsenoside Rgi as the standards.

Fingerprints of Cardiotonic Pill 1. Preparation of fingerprints (1) Chromatographic system and system suitability Alkyl silan-linking silico-18 was used as the stationary phase, and the mixture of A and B as mobili phase. A was methanol and B was the mixture of water- MN,N-dimethyl-formamide" -glacial acetic acid (100: 45: 4). The concentration of A changes from 5% to 30% when time of gradient elution elapses from 0 to 25 minutes. The detective wavelength was set at 281nm. The number of theoretical plates of the column was not less than 2000 when calculated with the peak of Danshensu.' (2) Apparatus and reagents Chromatograph: HP 1100 Liquid Chromatograph Detector: HP VWD-stile ultraviolet detector Column: Alltech Company 5u, 250X4.6mm, ODS column Pre-column: Alltech Company, Alltima Ci8 5u pre-column Temperature of the column: 3 0°C (3) Preparation of the control sample Salvianic acid B, Danshensu and protocatechuic aldehyde were dissolved respectively in methanol to produce three control solutions each ml containing 50 u g, 40 u g and 10 U g correspondingly. (4) Preparation of the test sample Put 10 pills of Cardiotonic Pill into a 25 ml measuring flask, 5 add 20ml of methanol, ultrasonicate for 20 minutes, allow to cool, dilute the solution to the scale-line with methanol, centrifugate and take the supernate as the test solution. (5) Procedure Accurately inject 10 U 1 each of the control solutions and the test 10 solution, respectively, into the column, record the chromatograph chart and calculate the content. 2. Fingerprints of different batches of Cardiotonic Pill Twenty batches of Cardiotonic Pill samples were tested with the 15 above-described method, and statistical data is shown as Table 1, Table 2 and Table 3 . These data revealed that Cardiotonic Pill had specific fingerprint of its own and the fingerprints contained eight common peaks, that is, these peaks should exist simultaneously in each batch of DSP. Taking protocatechuic 20 aldehyde peak as reference peak, whose relative retention time was 1, the average value of relative retention time of the eight peaks was 0.672, 1.000, 1.417, 1.512, 2.016, 2.235, 2.407, 2.757. The values of relative retention time and relative area of the eight peaks were very stable, and among the eight common peaks, 25 peak No.l was Danshensu, peak No.2 protocatechuic aldehyde and peak No. 7 Salvianic acid B, and the ratio of relative area value was 0.476-0.668: l: 0.391-0.641, respectively.

Fingerprints of three batches of Cardiotonic Pill are also 3 0 provided as Figures 1 through 3.

Table 1. The peak retention time & relative retention time of 20 batches of DSP Common sPeaks Peak No. 1 Peak No. 2 Peak No. 3 Peak No. 4 Peak No. 5 Peak No. 6 Peak No. 7 Peak No. 8 Batch No.

Retention time Relative retention time Retention time Relative retention time Retention time Relative retention time Retention time Relative retention time Retention time Relative retention time Retention time Relative retention time 19990806 19990815 19990823 19990921 19990928 19991014 19991026 19991109 19991127 19991205 20000106 20000216 20000323 20000406 20000422 20000513 20000606 20000726 20000728 20000804 Average value RSD% 8. 347 8. 313 8.285 8. 302 8.299 8. 290 8.295 8.286 8.291 8.291 8. 287 8.294 8. 256 8.272 8.274 8.276 8.273 8.283 8. 287 8.274 8.289 0.225 0.676 0.676 0.672 0.672 0.672 0.672 0.672 0.672 0.672 0.672 0.672 0.671 0.670 0.670 0.670 0.670. 0.67Q . 0.670 0.670 0.670 0. 672 0.266 12.341 12. 305 12. 338 12. 350 12.352 12. 344 12.337 1Z. 329 12.341 12.340 12.338 12. 352 12.329 12. 349 12. 348-12. 350: 12. 347 12. 356 12. 368 12. 351 12. 343 0.104 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1.000 1. 000 1.000 1.000 1.000 1.000 0.000 17.662 17.631 17.498 17.553 17. 549 17.4% 17. 513 17.477 17.502 17. 500 17. 503 17.536 17. 402 17.428 17.425 17.439 17.421 17.413 17.487 17.434 17. 493 0.398 1.431 1.433 1. 418 1.421 1. 421 1. 417 1.420 1. 418 1.418 1.418 1.419 1.420 1.411 1.411 1.411 1.412 1.411 1.409 1.414 1.412 1.417 0.447 18.802 18.769 18.673 18.739 18.727 18. 677 18.673 18. 642 18.660 18.659 18.664 18.687 18. 606 18.628 18.609 18.611 18.597 18.598 18.653 18. 597 18.664 0.313 1.524 1.525 1.513 1.517 1.516 1.513 1.514 1.512 1.512 1.512 1.513 1.513 1.509 1.508 1.507 1.507 1.506 1.505 1.508 1.506 1. 512 0. 362 .090 25. 072 25. 034 25. 005 24. 968 24. 903 24.889 24. 852 24. 882 24.862 24.867 24.887 24. 869 24. 843 24. 799 24.791 24.755 24. 744 24.807 24. 746 24.883 0.416 2.033 2.038 2.029 2.025 2.021 2.017 2.017 2.016 2.016 2.015 2.015 2.015 2.017 2.012 2.008 2.007 2.005 2.003 2.006 2.004 2. 016 0.476 27.805 27. 793 27.742 27.715 27.661 27.604 27.600 27.571 27. 594 27. 569 27. 576 27.590 27.561 27. 534 27.493 27. 479 27.451 27. 440 27. 500 27. 441 27.586 0.399 2.253 2. 259 2.249 2. 244 2.239 2. 236 2. 237 2.236 2.236 2.234 2.235 2.234 2. 235 2. 230 2.227 2.225 2.223 2.221 2.223 2.222 2.235 0.463 Retention time Relative retention time Retention time Relative retention, time .047 30.046 29. 897 29.875 29. 804 29. 743 29. 747 29.722 29. 737 29.708 29.721 29. 730 29.644 29. 613 29. 572 29. 553 29. 524 29. 513 29. 573 29. 515 29.714 0. 540 2.435 2.442 2.423 2.419 2. 413 2. 410 2. 4li 2. 411 2.410 2.407 2.409 2.407 2.404 2. 398 2.395 2. 393 2. 391 2. 389 2. 391 2.390 2. 407 0.606 34.146 34.092 34.186 34.155 34. 070 34.019 34. 017 34.014 34.026 34.007 34.026 34.066 34.067 34.012 33. 975 33.944 33. 918 33.925 34. 001 33.941 34. 030 0.219 2. 767 2.771 2. 771 2.766 2. 758 2.756 2.757 2.759 2.757 2. 756 2.758 2.758 2.763 2.754 2.751 2. 749 2.747 2.746 2.749 2.748 2.757 0.273 N> ■Jl Table 2. The peak area value & area ratio of 20 batches of DSP Common Peak No. 1 Peak No. 2 _Peak No. 3 Peak No. 4 Peak No. 5 Peak No. 6 Peak No. 7 Peak No. 8 iaks Area Area . Area , Area , Area . Area . Area , Area Batch Area ratio Area ratio Area ratio Area ratio Area ratio Area ratio Area ratici Area ratio 19990806 1044.800 0.668 1563.800 1.000 269.790 0.173 240.540 0.154 266.040 0.170 583.830 0.373 1001.800 0.641 1568.000 1.003 19990815 834.300 0.576 1448.900 1.000 359.860 0.248 347.080 0.240 340.390 0.235 348.490 0.241 600.210 0.414 994.740 0.687 19990823 1036.100 0.576 1800.300 1.000 409.060 0.227 334.160 0.186 486.430 0.270 495.600 0.275 323.430 0.457 1632.800 0.907 19990921 980.840 0.568 1726.000 1.000 379.050 0.220 317.920 0.184 498.570 0.289 479.530 0.278 875.440 0.507 1518.700 0.880 19990928 1068.000 0.549 1943.800 1.000 397.230 0.204 329.450 0.169 514.290 0.265 595.650 0.306 1092.700 0.562 1828.100 0.940 19991014 984.660 0.589 1670.700 1.000 353.250 0.211 297.610 0.178 504.860 0.302 504.900 0.302 879.420 0.526 1378.000 0.825 19991026 978.100 0.556 1758.900 1.000 348.520 0.198 282.550 0.161 451.380 0.257 416.600 0.237 800.660 0.455 1303.700 0.741 19991109 974.320 0.603 1617.100 1.000 334.350 0.207 275.050 0.170 477.390 0295 491.810 0.304 836.830 0.517 1302.800 0.806 19991127 1053.800 0.565 1865.300 1.000 413.960 0.222 327.640 0.176 499.750 0.268 521.160 0.279 1047.200 0.561 1643.800 0.881 19991205 1089.600 0.564 1931.200 1.000 391.970 0.203 334.240 0.173 468.210 0142 521.600 0.270 890.080 0.461 1659.100 0.859 20000106 1130.800 0.571 1979.800 1.000 408.490 0.208 347.890 0.176 512.040 0.259 519.150 0.262 891.890 0.450 1747.000 0.882 20000216 1114.900 0.548 2034.600 1.000 419.800 0.206 426.030 0.209 570.720 0.281 521.100 0.256 1232.200 0.606 1767.500 0.869 20000323 1080.000 0.599 1801.900 1.000 323.240 0.179 2S4.760 0.164 562.520 0.312 602.060 0.334 1041.600 0.578 1544.700 0.857 20000406 1132.600 0.583 1943.200 1.000 431.080 0.222 374.840 0.193 609.180 0.313 655.030 0.337 .1166.600 0.600 1642.400 0.845 20000422 1124.400 0.508 2212.300 1.000 378.160 0.171 356.690 0.161 574.650 0.260 692.970 0.313 1189.700 0.538 1758.300 0.795 20000513 1088.200 0.564 1928.200 1.000 390.250 0.202 331.510 0.172 466.050 0.242 518.200 0.269 886,300 0.460 1750.200 0.908 20000606 1033.200 0.575 1796.300 1.000 408.200 0.227 333.210 0.185 485.200 0.270 492.920 0.274 821.520 0.457 1613.200 0.898 20000726 985.250 0.569 1730.200 1.000 382.510 0.221 322.210 0.186 502.350 0.290 483.060 0.279 880.210 0.509 1523.200 0.880 20000728 1120.320 0.521 2148.500 1.000 410.920 0.191 385.540 0.179 621.250 0.289 672.250 0.313 1178.200 0.548 1692.300 0.788 20000804 831.320 0.577 1440.300 1.000 321.250 0.223 301.280 0.209 321.240 0.223 392.720 0.273 683.270 0.474 1081.360 0.751 Average value 1034.276 0.572 1817.065 1.000 376.547 0.208 328.011 0.181 486.626 0.267 525.432 0.289 940.963 0.516 1547.495 0.850 RSD% 8.486 5.612 11.452 0.000 10.914 9.354 12.553 11.003 18.592 12.698 16.851 11.766 18.292 12.061 14.739 8.647 Table 3 . The statistical data of eight peaks derived from fingerprints of 20 batches of DSP Peak No.

Retention Time Relative Retention Time Appearance Probability Area Area Ratio Area Ratio Range 1 8.289 0.672 100% 1034. 276 0.572 0. 572+0.096 O £j 12. 343 1.000 100% 1817. 065 1.000 1. 000+0.000 3 17. 493 1.417 100% 376. 547 0. 208 0. 208+0.040 4 18. 664 1. 512 100% 328.011 0.181 0. 181+0.059 24. 883 2.016 100% 486. 626 0. 267 0. 267+0.097 6 27. 586 2. 235 100% 525. 432 0. 289 0. 289+0.052 7 29. 714 2. 407 100% 940. 963 0.516 0.516+0.125 8 34. 030 2. 757 100% 1-S47. 495 0.850 0. 850+0.163 Quantitative analysis of Danshensu in DSP Chromatography and systemic adaptive conditions, apparatus and reagents: 1. Preparation of fingerprints 10 (1) The parameters of Chromatogram & system adjustment.

Alkyl silan-linking silico-18 was used as filling material, and water-acetonitrile-glacial acetic acid (87: 12: 1) as mobile phase. Detective wave length was set at 281 nm. The number of theoretical plate should not be less than 2500 when calculated 15 with the peak of Danshensu, and the degree of separation should meet the requirements. (2) Apparatus & reagents Chromatograph: HP 1100 Liquid Chromatograph 20 Detector: HP VWD-stile ultraviolet detector Column: Alltech Company 5u, 250 x 4.6 mm, ODS column Pre-column: Alltech Company, Alltima C18 5u pre-column Temperature of the column: 3 0°C Acetonitrile: chromatographically pure, Tianjin Siyou 25 Biomedical & Technical Co. Ltd.

Glacial acetic acid: analytically pure, Tianjin Tianhe Reagent Company. (3) Preparation of the control sample.

Use 25.0 rag of sodium salvianic acid and 5.0mg of protocatechuic aldehyde as the control samples: Weigh both of the samples accurately and put them into the 50 ml measuring flasks. Add mobile phase to dissolve them and dilute the solutions up to the scale-line of the flasks, shake them thoroughly and save them as the stock solutions. Weigh a little amount of paraaminobenzoic acid accurately, dissolve it as a solution of 0.2 mg/ml with the mobile phase and take it as the internal standard stock solution. Pipit proper amounts of sodium salvianic acid A, protocatechuic aldehyde and internal standard solutions whit their volumes accurately read, dilute them with the mobile phase to prepare a solution that contained 50 ug of sodium salvianic acid A, 10 ug of protocatechuic aldehyde and 80 ug of paraaminobenzoic acid. The prepared solution was taken as the control solution. (4) Preparation of the test sample.

Take 10 pills of Cardiotonic Pill and 1 ml of internal standard stock solution, put them into a 25 ml measuring flask, dissolve them with mobile phase, and dilute the solution to the scale-line.

Take 10 ml of the control and the test sample solutions, respectively, make the injection and record the chromatograph chart.

Preparation of the control solution: Take and weigh accurately 25.0mg of sodium tanshinol, and put it into a measuring flask. Add the mobile phase, and dissolve and dilute it to the scale. Shake the solution up, and keep it as the control stock solution. Weigh para-aminobenzoic acid accurately and dilute it into a 0.2mg/ml solution with the mobile phase. Keep the solution as the internal standard stock solution. Take appropriate doses of the control stock solution and the internal standard stock solution, and make them into the control solution comprising 50 P g of sodium tanshinol and 80 Ug of para-aminobenzoic acid per milliliter.

Preparation of the test solution: Take 10 pills of this article and 1ml of the internal stock solution. Put them in a 25ml measuring flask, dissolve them to the scale and make them into the test solution.

Take 101 of the control solution and 101 of the test solution respectively, take down the fingerprints and calculate the results.

The herbal composition comprising DSP should contains 0.14-0.18mg Danshensu per pill.

Quantitative analysis of Ginsenoside Rgi and Sanchinoside R1 in DSP (1) Chromatographic system and system suitability Alkyl silan-linking silico-18 was used as the stationary phase, and the mixture of water and acetonitrile as mobile phase. The concentration of acetonitrile was 25% from 0 to 15 minutes, and 35% after 15th minute. Nebulizer gas flowrate was 2.5 liter per minute and drift tube temperature was set at 93.8°C. The number of theoretical plates of the column was not less than 5000 when calculated with the peak of Ginsenoside Rgi. (2) Apparatus and l-eagents Chromatograph: Agilent 1100 Liquid Chromatograph Detector: Alltech ELSD 2000 detector (evaporative light scattering detector) Column: Alltech Company 5u, 250X4.6mm, ODS-Cis column Pre-column: Alltech Company, Alltima CiB 5u pre-column Temperature of the column: 30°C (3) Preparation of the control sample Ginsenoside Rgi and Sanchinoside R1 were dissolved respectively in methanol to produce two control solutions each ml containing 0.98mg and 0.25mg correspondingly. (4) Preparation of the test sample Put 50 pills of Cardiotonic Pill into a 5 ml measuring flask, add 4% ammonia to the scale-line, ultrasonicate for 20 minutes, and apply the solution to a previously prepared small Ci8 column (STRATA C18-E column of Phenomenex Company, 500mg and 3cc tube) , elute 10ml of water, discard the eluate, then elute 2ml of 5 methanol, collect the eluate in a measuring flask and dilute it to the scale-line with methanol, take the solution as the test solution. (5) Procedure Accurately inject 10 u 1 each of the control solutions and the test solution, respectively, into the1 column, record the chromatograph chart and calculate the content. (6) Result Twenty batches of Cardiotonic Pill samples were tested with the above-described method, and statistical data is shown as Table 4. Drawn on above table, the herbal composition comprising DSP contains 0.401%-0.712%, average 0.550% Sanchinoside R1 and 2 . 069%-4.044%, average 2.847% Ginsenoside Rgi.

Table 4. Quantities of Ginsenoside Rgi and Sanchinoside R1 in DSP Sanchinoside R1 (ii Ginsenoside Rgi (n Batch No. g/pill) g/pill) 20000106 17. 22 80.93 20000216 16. 92 80. 78 20000323 .16 70.76 20000406 13. 65 62.51 20000422 14. 24 68.72 20000513 . 27 71.16 20000606 14. 86 68.21 20000726 14. 59 72. 35 20000728 14. 25 57. 37 20000804 . 30 70.55 Average value .15 70. 33 RSD% 7. 53 9.67 not less than 12.12 56.26 The characteristics of DSP thus manufactured are as follows: (a) DSP contain b-3, 4-dihydroxyphenyl lactic acid, sodium danshensu, saponin, and borneol, (b) negative for bacteria: contains less than 1,000 bacteria, (c) negative for fungi: contains less than 100 fungi, (d) negative for heavy metalcontains less than the safety amount defined by the Chinese government. (e) The shelf-life of DSP is four years at room temperature.

CLINICAL STUDIES OF DSP Angina pectoris is evaluated by the history of angina, serum lipid level, electrocardiography (ECG), exercise ECG, scintigraphic assessment of ischemia, coronary angiography, etc. Assessing therapeutic efficacy using these end points, DSP has been shown to be effective for treating angina pectoris.

DSP is effective for angina pectoris , 157 patients with coronary heart disease were treated with 10 DSPs per t.i.d., oral administration for 4 weeks. Assessing the frequency, intensity and duration of ang.i.na, oppressed feeling in chest and palpitation, the symptoms were disappeared or remitted in 95.3% patients.

DSP is more efficient than Dan Shen tablets in alleviating angina. Dan Shen tablet is another Chinese medicament for treating angina pectoris currently used in China. The efficacy of DSP and Dan Shen tablet was compared. Coronary heart disease patients were randomly divided into two groups. 107 patients were treated with DSP and 50 patients were treated with Dan Shen Tablet. Comparing the frequency of angina attacks and the consumption of nitrates, DSP was more effective than Dan Shen Tablets for treating angina pectoris. See Table 5 below.

Table 5. Comparison of DSP and Dan Shen tablet Number of patients Total Responsive DSP 107 102 (95.3%) Dan Shen tablet 50 3 8 (76%) Having proven that DSP is more effective than Dan Shen tablets, the efficacy of DSP was compared with various drugs which are currently used for treating chronic stable angina pectoris in the US.

Comparison of DSP and nitroglycerine Nitroglycerine is the frequently used to relieve angina. The efficacy of DSP and nitroglycerine relieving angina was compared. At the onset of angina, patients were treated with either DSP 15 or nitroglycerine, and the time required to alleviate angina was compared. Both DSP and nitroglycerine alleviate angina in all patients within 15 minutes. The efficacy of DSP was slightly lower than nitroglycerine. See Table 6 below.

Table 6. Comparison of DSP and nitroglycerine # patients responded within 1-5 minutes 6-10 minutes 11-15 minutes DSP 11 14 5 Nitroglycerine 17 12 1 Total-. 30 patients per group DSP does not change heart rate The data demonstrate that DSP effectively alleviate angina. It 3 0 was examined whether DSP relieves anginal by increasing heart rate. The heart rate after DSP treatment was equivalent to the pretreatment rate, which indicates that DSP relieves angina without affecting heart rate (Table 7).

Table 7. DSP does not affect heart rate Heart rate Pretreatment Post - treatment DSP 84.3 + 23.1 82.8 + 22.8 Comparison of the efficacy of DSP with the nitrate isosorbide dinitrate Having proven that DSP alleviate angina as efficiently as nitroglycerin, it was examined whether DSP can prevent angina. The efficacy of DSP and the nitrate isosorbide dinitrate was compared. Isosorbide dinitrate is a long-acting nitrate frequently used for preventing chronic stable angina pectoris in the US. Patients were treated with either DSP chree times per day orally 10 pills per treatment or Isosorbide dinitrate three times per day orally 10 mg per treatment. Cardiac function and Electrocardiogram was examined.

Cardiac function.

The efficacy of DSP and nitrates on cardiac function was evaluated by measuring cardiac output per stroke (CO), stroke volume per minute (SV) , eject blood fraction (EF) , fraction of shortened rate of left ventricular short axis (FS) . DSP improves cardiac function more efficiently than nitrates. See Table 8 below.

Table 8. The effect of DSP and nitrates on cardiac function DSP Isosorbide initrate Pre- Post- Pre- Post SV 75.38 + 8.32 83.45 + 9.11 74.96 + 8.44 79.47 + 8 . 72 CO .61 + 1.34 6.94 + 1 .36 6.54 + 1.36 6.12 + 1 .41 EF 0.57 + 0.02 0.79 + 0 .02 0.59 + 0.03 0.70 + 0 .03 FS 17.14 + 3.4 16.69 + 3.6 17.32 + 3.1 18.46 + 4.2 Pre- : preteatment Post-: post-treatment DSP improves ECG The ST-T effective rate was evaluated by recording the frequency of change in the ST-T segment. Both DSP and isosorbide dinitrates decreased the frequency of change in ST-T significantly. DSP, 5 however, was more efficient. See Table 9 below.

Table 9. Comparison of the effect of DSP and nitrate on ECG The frequency of ST-T change Pretreatment Post-treatment DSP 131 35 isosorbide dinitrate 129 42 Comparison of DSP and aspirin in reducing blood stasis 15 Hemorrhage at the atherosclerotic lesions induces platelet activation, coronary thrombosis and blood stasis resulting in impaired blood flow. Thus to improve blood flow, chronic administration of the platelet-activation inhibitor aspirin .is recommended for patients with angina. The efficacy of DSP and aspirin 20 improving blood flow was compared by evaluating [Hb, Lb, P and air flow] . DSP improves blood flow as efficiently as aspirin. DSP improves blood flow as efficiently as aspirin. See Table 10 below.

Table 10. DSP and aspirin improve blood flow DSP aspirin Pre- Post- Pre- Post- Hb 6.23 + 1.67 4 . ,35 + 1. , 02 6.12 + 1.56 4 , .28 + 1, .07 LB .92 + 2.21 8 .30 + 1 .14 .38 + 1.96 8. .21 + 0 , .3 P 1.95 + 0.08 1, .77 + 0. , 08 1.89 + 0.12 1. . 67 + 0. . 7 Air flow 1.79 + 0.13 1. .39 + 0. .11 1.82 + 0.17 1, .40 + 0. . 10 Total number of patients: 25 for DSP and 28 for aspirin DSP reduces blood stasis by inhibiting platelet activation Thromboxane B2 activates platelet. Activated platelets release various substances including 6 platelet microglobulin, which causes blood stasis, thus impairing blood flow. The efficacy of DSP inhibiting platelet activation was examined. DSP lowers thromboxane B2 concentration and inhibits platelet aggregation efficiently. Isosorbide dinitrate, which is known to be unable to inhibit platelet activation thus used as control, did not reduce thromboxane B2 or inhibit, platelet activation. See Table 11 below.

Table 11. DSP inhibits platelet activation Pretreatment Post-treatment P PM DSP 62.44 + 14.37 45.65 + 12.25 nitrates 59.89 +15.42 54.36 + 13.18 Txj82 DSP 1312 + 535 738 + 384 nitrates 1315 + 507 1218 + 445 DSP lowers plasma cholesterol level Increased plasma cholesterol has been implicated in the initiation of atherosclerosis. To prevent the formation of new atherosclerotic lesions, the decrease of plasma cholesterol either by modifying diets. or drugs was recommended. It was examined whether DSP decreases plasma cholesterol. DSP lowered the cholesterol level by 0.3 mmol/L, which is statistically significant at the P value 0.05. See Table 12 below.

Table 12. DSP decreases plasma cholesterol Plasma cholesterol (mmol/L) Pretreatment Posttreatment DSP 5.15+0.16 4.84 +.0.2 Number of patients: 80 Cardiotonic Pill's Effect on LPO and SOD in the Blood Serum of Patients Suffering from Coronary Heart Disease The method: In the treatment group, 24 patients, in accordance with China Reference Diagnosis Standards for Coronary Heart Disease amended in 1979, are administered with Cardiotonic Pill, 10 pills/time, and 3 times/day. In the normal group, 20 healthy people do not receive any medical treatment.

The results: The level of LPO of the patients suffering from coronary heart disease is clearly higher than that of the healthy 5 people, while the content of SOD is clearly lower (p<0.01) . After the patients are treated with Cardiotonic Pill, their LPO evidently decreases (p<0.01) , and their SOD evidently increases (p<0.01). See Table 13 below.

Table 13 . A Comparison of the Contents of SOD and LPO in the Normal and the Treatment Groups (x±s) Groups Patients SOD (ng/ml) LPO (nmol/ml) Normal group 348±106 4.64±1.52 Treatment group 24 Before treatment 261±16* 7.16±1.48* After treatment 309+87#. 4.68+1.72## Note: In comparison with the normal group, *p<0.05. In comparing with those of pre-treatment, #p<0.05, ##p<0.01.

The conclusion: Chronic ischemia of cardiac muscles of patients suffering from coronary heart disease and tissue anoxia lead to the reduction of the activity of SOD, especially that of extra cellular SOD, and the increase of oxygen free radicals, which causes the elevation of LPO and consumption of SOD further. After 20 the patients are treated with Cardiotonic Pill, the ievel of LPO decreases evidently, while the content of the SOD increases obviously. This proves that Cardiotonic Pill has a strong action of clearance on oxygen free radicals, which is also one of the mechanisms to treat coronary heart disease.

The Effect of Cardiotonic Pill on the Activities of LPO and Antioxidases in Treatment of Pulmonary Heart Disease The method: The subjects: 48 patients suffering from pulmonary heart disease are randomly divided into 3 groups. In the normal 30 group, 16 patients are treated with a complex of therapies, such as anti-inflamatory therapy, antiasthma, oxygen inhalation, and so on. In the Cardiotonic Pill group, 14 patients are treated with Cardiotonic Pill, 10 pills/time, and 3 times/day. In the Gantangzhi group , 18 patients are treated with the intravenous drip 200mg of Gantangzhi dissolved in 250ml of 5% glucose injection, 1 time/day, and 10 days/period.

The results: After treatment with Cardiotonic Pill, the value of GSH-Px goes up, the value of LPO goes down, and, therefore, GSH-Px/LPO goes up. In comparison with the normal treatment group, there is a significant difference. See Table 14 below.

Table 14. Indices before and after Treatments GSH-Px (U/mgHb) PAT (U/gHb) SOD (U/gHb) LPO (nmolAnT) GSH-Px/LPO Healthy people group 140.6+35.2 312.7 + 58.1 5799.8 +948 4.2+1.2 34.2+8.7 Normal group Before treatment 101.3 + 23.6 300.4+ 107.7 5740.5 + 939.0 .6 + 1.9 .4+8.8 After treatment 120.6± 20.6* 390 + 184.3" 6076.8 + 1091 4.3 + 1.2** 31.3 + 15.1** Cardiotonic Pill group Before treatment 108.8+28.3 233.1 + 70.2 5863.3 + 1072.7 .9+2.0 18.5+7.6 After treatment 158.2+ 40.7**** 328.4 + 7.8.5"* 5582.8 + 1094.7** 4.1 ± 1.6**** 36.4 + 6.7"** Note: Comparing those before treatment with those after treatment, #p>0.05, ##p<0.05, *p>0.05, **p<0.05.

The conclusion: Cardiotonic Pill has the function of 15 antioxidation, and can lighten the lipid peroxidation reaction and raise the ability of antioxidation of human body.

Treatment with Cardiotonic Pill for Essential Hypertension The method: (1) The choice of patients: Select those patients 20 suffering from Phase I or II essential hypertension, but without secondary hypertension or cardiac, hepatic and renal insufficiencies. (2) The administration: Stop the patients from taking any western 25 and traditional Chinese medicines (except for hypotensors) for two weeks, and then, in the third week, measure their blood pressures and blood rheologyical indices and take down their clinical manifestations. The double blind method is adopted. In the Cardiotonic Pill group, the subjects take orally Cardiotonic 30 Pill, 10 pills/time, and 3 times/day. In Compound Danshen Tablet group, the subjects take orally Compound Danshen Tablet, 5 tablets/time, and 3 times/day. The subjects in the control group take placebos, and the period of treatment is six weeks.

The results: (1) Effect on the viscosity of whole blood. After treatment, the viscosities of whole blood of patients in both the Cardiotonic Pill group and the Compound Danshen Tablet group drop remarkably, but the curves of the viscosities of whole blood in the Cardiotonic Pill group at any shear rates go down more sharply than those in the Compound Danshen Tablet group. See Table 15.

Table 15. Effect of Cardiotonic Pill on the Viscosity of Whole Blood (mPas, x±s) Groups 3.83s-' N> 00 00 192 s'1 Cardiotonic group (30 subjects) Before treatment 18.27 + 2.85 .82 + 0.93 4.54+0.78 After treatment 11.79 + 3 75*<w#&& 4.78 + 0.84*™ 3.98+ 0.65**s&& Compound Danshen Tablet group (30 subjects) Before treatment 17.69+1.96 ■ .86+0.79 4.69+0.54 After treatment 14.68+ 3.41 **&& .69 + 0.81*& 4.42 + 0.59**&& Control group (15 subjects) Before treatment 17.65+2.07 .69 + 0.79 : 4.75+0.58 After treatment 18.02+2.32 .71 + 2.76 4.86+0.65 Note: In comparison with those of the same group before treatment, *p<0.05, **P<0.01. Comparing with those of the Cardiotonic Pill group after treatment, #p<0.05, ##p<0.01. Comparing with those of the control group after treatment, &p<0.05, &&p<0.01. (2) Effect on the deformation and the aggregation of erythrocytes. After treatment, the deformation of erythrocytes in Cardiotonic Pill group is markedly greater than that before treatment, and the area and the index of aggregation are observably smaller than those before treatment. And comparing with the Compound Danshen Tablet group, the Cardiotonic Pill group declines much faster (p<0.01). See Table 16.

Table 16. Effect o£ Cardiotonic Pill on the Deformation and the Aggregation o£ Erythrocytes (x±s) Groups Index of Deformation Index of Aggregation Area of Aggregation(integral) Cardiotonic group (30 subjects) Before treatment 0.4115 + 0.0360 4.06+0.39 841.12+67.68 After treatment 0.4274+ 0.034*& 3.41 + 0.36"#&& 683.52+69.09**#&& Compound Danshen Tablet group (30 subjects) Before treatment 0.4066+ 0.0290 3.98+0.34 806.90+66.30 After treatment 0.4180+ 0.0281*& 3.64+ 039«&& 716.12+84.29**& Control group (15 subjects) Before treatment 0.4091 + 0.0376 4.02 + 0.41 812.52+65.64 After treatment 0.4001 + 0.0381 4.01+0.39 804.44+68.06 Note: In comparison with those of the same group before treatment, *p<0, with those of (lie Cardiotonic Pill group after treatment, #p<0.05, ##p<0.01 the control group after treatment, &p<0.05, &&p<0.01. 05, **P<0.01. Comparing . Comparing with those of (3) Effect on Blood Pressure. After treatment, the systolic pressures and the diastolic pressures of patients in both the Cardiotonic Pill group and the Compound Danshen Tablet group drop markedly (p<0.01), and there is no evident difference between the two groups. See Table 17. (4) Effect on symptoms of hypertension. The patients in both the Cardiotonic Pill group and the Compound Danshen Tablet group 15 improve a lot in terms of such symptoms as headache, dizziness, and numb extremities (p<0.01) , but do not improve in insomnia. See Table 18.

Table 17. Effect of Cardiotonic Pill on Blood Pressure (imnHg, x±s) Groups Systolic pressure Diastolic pressure Cardiotonic group (30 subjects) Before treatment 155.00±8.08 90.70+7.93 After treatment 149.20±8.89**&& 86.59+8.30**&& Compound Danshen Tablet group (30 subjects) Before treatment 152.93+9.59 92.59±8.30 After treatment 146.02±10.20**&& 88.55+7.22**&& Control group (15 subjects) Before treatment 154.06±7.05 90.90±9.10 After treatment 152.08 ±9.25 91.10+8.70 of the control group after treatment, &&p<0.01.

Table 18. Effect of Cardiotonic Pill on Clinical Symptoms of Hypertension (patients) Groups Headache Dizziness Numb extremities Insomnia Yes No Yes No Yes No Yes No Cardiotonic group (30 subjects) Before treatment 16 14 12 18 8 22 After treatment 7 23' 2 28" 3 27' 4 26 Compound Danshen Tablet group (30 subjects) Before treatment 22 8 17 13 6 24 After treatment * 8 22* 3 27* 6 248 Control group 05 subjects) Before treatment 8 7 6 9 4 11 4 11 After treatment 7 8 3 12 2 13 Note: In comparison with those of the same group before treatment, *P<0.01.

The conclusion: The rheological property of erythrocytes of patients suffering from essential hypertension is clearly abnormal. The deformation of erythrocytes debases clearly, while the aggregation rises distinctly. The experiment shows that Cardiotonic Pill has the functions oi: markedly reducing the 10 viscosity of whole blood and the index of and the area of aggregation of erythrocytes, and greatly raising the ability of deformation of erythrocytes. Cardiotonic Pill can also lower the blood pressure and improve clinical symptoms of the patients. And thus, Cardiotonic Pill is of great benefi t to preventing or 15 postponing the occurrence of essential hypertension and cardio-cerebral syndrome.

Toxicity DSP is safe and nontoxic. In China, over 5 million patients have 20 been treated with DSP without severe side effects. Mild side effects, headache or dizziness, have been reported in a minor portion of patients.

Summary of clinical studies 25 DSP is a new generation Chinese medicine for treating coronary heart disease. Clinical studies demonstrate that DSP alleviates as well as prevent angina by improving cardiac function, reducing myocardial ischemia, inhibiting platelet activation thus reducing blood stasis, and decreasing plasma cholesterol. The therapeutic efficacy of DSP was superior to another form of 5 Chinese medicament Dan Shen tablets. DSP is as efficient as drugs used in the USA. DSP is aleviate angina as efficiently as nitroglycerine, prevents angina as efficiently as the long-acting nitrate isosorbid dinitrate, and inhibits platelet aggregation as effectively as aspirin. DSP is nontoxic: over 5 10 million people have been treated without noticeable side effects in most cases.

PRECLINICAL STUDIES Preclinical studies reveal the mechanism by which DSP prevent 15 as well as alleviate angina.

DSP alleviate angina by increasing blood flow.

Wistar rats, approximately 260 g, were anesthetized by urethane, opened the chest, excise the heart, perfused in 20 the Langendorff. mode at 3 7 °C. And constant coronary perfusion pressure of 65 cm H20.

After stabilized the heart rate, various amounts of DSP or Danshen tablet were applied each time through lateral branch of aorta 25 cannula. Subsequently, the coronary flow and the heart rate were measured. DSP increased coronary flow in a wide dosage. Danshen tablet, on the other hand, increased coronary flow at a narrow dosage. See Table 19 below.

Table 19. DSP increases coronary flow Coronary flow Dose (mg/ml) Pretreatment post-treatment None 7 . .0 + 1, . 1 7. , 1 + 0. .97 DSP .8 7. .2 + 1, . 1 7. , 0 + 1. ,4 290 6. .7 + 1. ,6 8. , 7 + 1. .4 580 6 . .7 + 1. .5 9. .3 + 2 . .9 DS Tablet .8 6 , •7 > / + T J, , A ■ ** 7 , , 1 + 1. . 5 290 7 .3 + 1. .7 9. .1 + 2. . 1 580 6 .8 + 1. .4 7 . .1 + 1. . 5 The effect of DSP and Danshen tablets on heart rate was examined. Neither DSP nor Danshen tablet changes heart rate. See Table 20 below.

Table 20. DSP does not increase heart rate Heart rate Dose (mg/ml) Pretreatment post-treatment None 194 + 1? 193 + 12 DSP 5.8 180 + 11 189 + 9 290 188 + 7 184 + 8 580 173 + 14 167 + 13 5.8 DS tablet 5.8 180 + 11 189 + 9 290 189 + 16 183 + 14 580 186 + 23 171 + 8 DSP increases coronary flow by relaxing vascular smooth muscle thus dilating vessels.

The effect of DSP on potassium-induced vasocontraction of rabbit aortic strip was examined. DSP relaxed smooth muscle thus dilating vessels significantly. Similar effects were observed in the experiments using pig coronary artery rings.

DSP inhibits platelet aggregation The effect of DSP on platelet aggregation was examined. Rabbit platelets were treated with DSP and aggregation was examined. DSP inhibited platelet aggregation sign^ficar.iiy. See Table 21 below.

Table 21. DSP inhibits plate-Let aggregation DSP(mg/ml) #animals Aggregation ratio(%) inhibition(%) 0 8.3+4.5 23 . 6+6.7* 37.6+5.9* 69.0+6.9* Table 22 shows micronucleus rates in mice at Different Time After treatment with the herbal composition of this invention (8400 mg/kg).

Table 22.

Time(h) Polychromatic RBCs Micronucleus Cells Micro-rates(%) (x±SD) 12 6, 000 9 1.5+0.8 24 6,000 11 1.8±0.7 36 6,000 11 1.8+1.2 48 6,000 11 1.8+1 .5 72 6,000 13 2 . 2±0 . 7.

Solvent 2 4 6,000 9 1. 5±1.. 4 Table 23 shows the micronuleus rates in ivies it 24 "~rs after DSP & CP Administration. 2 0 Table 23.

Dose(mg/kg) Polychromatic RBCs Micronucleus Cells Micro-rates(%) (x+SD) „ . 8, 400 6, 000 12 2.0±0.6 . . 840 6,000 9 1.5+1.0 84 6, 000 11 1.8+1.0 Solvent 6, 000 9 1.5+1.4 CP (80mg/kg) 6, 000 138 23.0+4.0* * Compare with solvent P<0.01. 0 6 6.7+4.4 1.8 6 42. 7±2.5 3.5 6 33.4+3.4 7 6 25.3±2.1 14 6 15.8+3.0 Table 24 shows assessment criteria f;:r graded effectiveness of tested drugs.

Table 24.

Parameters\ Effects Very high effect High Effect Effect No effect RBC aggregation status No A little Marked Severe onset Time <90 90-180 180-300 >300 Micro-blood flow status Better than normal Turn to normal Improved Deteriorated Duration(min) >15 -10 -5 <5 DSP improves microcirculation The effect of DSP on microcirculation in Chinese hamsters was examined. DSP improved microcirculation for 23 minutes within 111 minutes of buccal administration in all animals. See Table 10 25 below.

Table 25. DSP improves microcirculation onset Time(min) Duration (min) Effect rate (%) DSP 111 23 1 100 Table 26 shows the protective effect of DSP on the myocardium induced by pituitrin in. rats (second period).

Table 26. (n=8) Group Dosage (g/kg) Before medication After medication Before pituitrin After pituitrin(40s-15 minutes) Number of rats with abnormal ECG Control Normal Normal 7 DSP 0.4 Normal Normal 3* 0.8 Normal Normal 1** 1.2 Normal Normal 1** DST 0.4 Normal Normal 4 0.8 Normal Normal 1** Compared with the control. *p<0.05; **p<0.01.

Table 27 shows the inhibitory effect of DSP on myocardial ischemia induced by pituitrin in rat.

Table 27.

Group Dosage(g/kg) Inhibition(%) DSP 0.4 71.4* 0.8 85.7* 1.2 71.4* DST 0.4 42.8* 0.8 85.7* As compared with the control. *p<0.05.

Table 28 shows the protective effect of DSP on the myocardial ischemia induced by pituitrin in rats (first period).

Table 28 (n=8) Group Dosage (g/kg) Changes in T-ST of.ECG- (lead II) in the first period Before medication After medication Before pituitrin After pituitrin (0-40s.) Number of rats with abnormal ECG elevated T inverte d T Total Control - Normal Normal 4 3 7 DSP 0.4 v Normal Normal 3 0 3* 0.8 Normal Normal 1 1 2* 1.2 Normal Normal 2 , j 3* DST 0.4 Normal NorrT.1 2 t 0.8 Normal Normal j 2* As compared with control. *p<0.05.

Cardiotonic Pill's Action of Clearance on Oxygen Free Radicals The study of Cardiotonic Pill's action of clearance on oxygen free radicals is carried out by using electron paramagnetic resonance (EPR) and spin trapping, with superoxide anions and hydroxy radicals produced by using the xanthine- xanthine oxidase system and the H202-Fe2+ system respectively.

The method: (l) Production of hydroxy radicals. Set up a test model according to the Fenton Principle. Mix up H202, ferrisulphas and DMPO (5,5-dimethyl-pyrroline-l-oxide), and then carry out the EPR testing. The resulting signals serve as the control. Add Cardiotonic Pill in the treatment group. (2) Production of superoxide anions. Set up a test model based on the xanthine- xanthine oxidase reaction. Mix up xanthine, 5 Dietrylene triamine Pentacetic acid, DMPO and xanthine oxidase, and then carry out the EPR testing. The resulting signals serve as the control. Add Cardiotonic Pill in the treatment group.

Ten samples for each of the four groups are tested, and the results 10 are expressed in terms of the average. T-test is applied in the statistical analysis.

The Results: (1) Cardiotonic Pill's action of clearance on hydroxy radicals produced by the H202-Fe2+ system. An adduct 15 DMPO-OH will be generated when a hydroxy radical is captured by a DMPO. The peak value of the adducts in the control group is 11.8±0.6 relative units , while that in the Cardiotonic Pill group is 4.1 ±0.5 relative units. There is a significant difference between them (p<0.01), and the clearance rate of 20 Cardiotonic Pill is over 65%. (2) Cardiotonic Pill's action of clearance on superoxide anions produced by the xanthine- xanthine oxidase system. An adduct DMPO-OOH will be generated when a superoxide anion is captured 25 by a DMPO. The peak value of the adducts in the control group is 10. 6±0.67 relative units , while the spectral signals in the Cardiotonic Pill group disappear completely. In comparison with the control group, there is a significant difference (p<0.01), and the clearance rate of Cardiotonic Pill is 100%.

The above experiments show that Cardiotonic Pill has an effective action of clearance on superoxide anions produced by the xanthine- xanthine oxidase system and hydroxy radicals produced by the H202-Fe2+ system.

Cardiotonic Pill's Effect on Free Radicals of Cerebral Ischemia Reinfusion Injury Tissue o£ Rats The method: Take 30 SD rats, and randomly divide them into 3 groups, which are the feigned operation group (An operation is 5 performed, but the blood vessels and nerves are not ligated), the cerebral ischemia reinfusion model group and the Cardiotonic Pill group (4g/kg). After the 3-day continuous intraperitoneal (Ip) administration, and two hours after the administration on the third day, the rats are anaesthetized with the 20% 10 Ethylurethanm and their conducting arteries in both sides of their necks and vagus nerves are separated and ligated. After a 3 0-minute reinfusion, cut off their heads and get their brains . Take about 500mg of cortical tissues of their left-brains and hippocampus tissues in both sides, and put them into the liquid 15 nitrogen for homogenization. After they are made into a homogenate with freezing physiological saline, centrifugate the homogenate. Take the supernatant and determine the activities of CAT and SOD and the contents of MAD and GSH.

The results: See Table 29. (1) Cardiotonic Pill's effect on the activity of CAT and the content GSH of brain tissues. The activities of CAT of brain cortex and hippocampus tissues and the content of GSH of the brain cortex in the cerebral ischemia reinfusion model group are much lower than those in the feigned 25 operation group. Both the activity of CAT of h.ippocc"ipus tissues and the content of GSH of the brain cortex in the Cardiotonic Pill group are significantly greater than those in the model group.

Table 29. The Activities of CAT and SOD and the Contents of MDA and GSH of Brain Tissues of the Rats (mPas, x±s) (n=10) Groups CAT Activity (U/mg Protein) GSH (U mol/rag Protein) SOD Activity (U/mg Protein) MDA (nmol/mg Protein) Brain Cortex Hippocampus Brain Cortex Hippocampus Brain j Hippocampus Coreex j Brain Cortex Hippocampus Feigned Operation Group 2.94 + 0.17 2.78±0.14 18.49 ±0.70 16 .87± C .92 ' { -J- a t .34± 0 .74 0.502 ± 0.054 1.084± 0.117 Model Group 2.17± 0.24° 1.97 + 0 .23° 14.76 i 1.12s 13.3Ci0.74 ID .44 4- 0.79s 18.18 + 0.S28 0.718 + 0.070s 1.449± 0.140s Cardiotonic Pill Group 2 -55± 0.35 2.79±0.213 17.14 ±0.76 .76± 1.183 13.31 + 0.773 .59± 0.593 0.483 ± 0.0653 1.069± 0.1315 Note: In comparison with the feigned operation group, *p<0.05; in comparison with the model group, SJp<0.05 (2) Cardiotonic Pill's effect on the activity of SOD and the content MDA of brain tissues. The activity of SOD of brain tissues in the model group is significantly lower than that in the feigned operation group, while the content of MDA is significantly 10 higher. The activities of SOD of brain cortex and hippocampus tissues in the Cardiotonic Pill group increase significantly, while the content of MDA decreases significantly.

The conclusion: After cerebral ischemia reinfusion, the content 15 of MDA in the brain tissues increases, while the content of GSH decreases. The activities of CAT and SOD, two important enzymes for clearing oxygen free radicals in the tissues, decrease significantly, which shows that during the course cf cerebral ischemia reinfusion, a great lot of oxygen free radicals occur 20 due to the failure of the function of the iree -radical clearance system. This leads to the lipid peroxidation, and then leads to the brain injury. Cardiotonic Pill can decrease the contents of MDA in the brain cortex and hippocampus tissues of reinfused rats and increase the content of GSH and the activities of CAT and 25 SOD greatly, which shows that Cardiotonic Pill has the functions of markedly restraining the reactions of oxygen free radicals, controlling the lipid peroxidation and protecting damaged brain cells caused by ischemia reinfusion. 3 0 The Antioxidation of Cardiotonic Pill in Chronic Hepatic Injury The method: The CCL4-high-fat-low-protein induced mild chronic hepatic injury model of the Wister rat is adopted. In the Cardiotonic Pill group, perfuse Cardiotonic Pill into the rats' stomachs at the dose of 4g/kg, while in the normal and the model groups, perfuse the same amount of physiological saline. The activity of SOD is determined by using the xanthine oxidase method, while the content of the MDA is determined by using the improved thiobarbituric acid method.

The results: See Table 30. Comparing the model group with the normal group, the activity of SOD degrades, while that of MDA increases. In the Cardiotonic Pill group, however, the activity of SOD increases, while that of MDA degrades, making the Cardiotonic Pill group go back to the normal.

Table 30. The Activities of SOD and the Contents of MDA in Chronic Hepatic Injury Groups Rats SOD (NU/mg.pr) MDA (nM/mg.pr) Normal group 12 1.717±0.521 .21±4.35 Model group 12 1.326±0.3218 19.39±4.62* Cardiotonic Pill group 11 1.710±0.415# .16±4.29# Note: In comparison with the normal group, *p<0.05. In comparison with the model group, #p<0.05 The conclusion: MDA is a major degradation product of the lipid peroxidation. MDA can badly damage the structure of the cell membrane, and then hepatic cells. SOD is a scavenger of super-oxide anion free radicals, and it. can restrain the lipid peroxidation caused by free radicals. Cardiotonic Pill can significantly increase the activity of SOD and decrease the content of MDA, which will degrade the level of the lipid peroxidation and lighten the hepatic injury.

DSP is not mutagenic It was examined whether DSP is mutagenic in the Ames assay. DSP was not mutagenic. See Table 31 below.

Table 31. The mutagenicity of DSP (Ames test) colony number per dish S9 TA97 Ta98 TA100 TA102 DSP - 0.0 - 141±13 36+3 161 + 21 303+44 0.5 - 140+17 +2 148 + 21 .288 + 15 - ■ 136+14 34+4 154+26 280±16 50 - 133+20 33 + 5 142+25 292+37 500 - 109+15 34±3 154+16 311+32 5000 - 67+8* +4 149 ±27 298 ±32 0.0 + 141 + 13 44+6 176+19 296+39 0.5 + 148+13 42+9 161 ± 27 296+37 .0 + 152+11 44+7 161 ± 16 292 ±38 50.0 + 140+18 .37+6 166±9 307 ±55 500.0 + 135+21 42+7 152±22 287 ±16 5000. 0 + 119+17 38+7 162+17 363 ±57 Dexon 50 - 2155+814 952± 187 831±114 1510±211 2-AF 40 - 125+18 38±3* 161 + 16 + 1404+644* 1598 + 124 1222 ± 309 DAN 100 - 364+50 " - + 943 + 102* Production of crude drugs 1. Dan shen 5 (1) Quality control Crude drug Dan Shen was sampled from production aris.3 throughout China. Chemical analysis was conducted on chose samples from different bases for their chief components. The results showed that the quality of Dan Shen from an aria named Shangluo was the 10 best of all and it proved that the climate of Shangluo is most suitable for the growth of Dan Shen. The active ingredients of Dan Shen such as tanshinone and salvianic acid A. were approved the best in quantity. (2) Topography Shangluo is geographically located at the East Longitude 108°34' 20' ' ~lll°l' 25" and North Altitude 33°2' 30 " - 34°24' 40" with an average sea level of 900 meters. The region is an area with low and median high mountains and is free of pollutions. The unpolluted clean air circumstance makes it ideal for the growth of drug plants. (3) Climate It is warm and semi-humid in climate, typical for the mountainous areas of transitional zone from the subtropics to the temperate. Affected by the South-eastern monsoons, it has obvious divisions for seasons and a great amount of rain. The precipitation of rainfall of the year in this area is estimated at 733.9-899 mm. The sunshine period is around 1874.1-2185 hours a year, with an annual sun irridiance of 119.57-124.36 kilocalories/cm2. The temperature varies from 18 °C - 40.8 °C. A frost-free period lasts 198-218 days of the year. (4) Soil 80% of the soil in Shangluo is arenaceous, most of the arable land comprises of neutral and alkalescent soil with a pH value of 6.5-8. Within 0-20 cm of the tillage layer, the soil nutrients consist of the following: 1.36% organic matter; 0.085% nitrogen; 18 ppm fast-effective phosphor; 136 ppm fast-effective potassium; and 60 ppm alkaline-hydrolyzed nitrogen. Heavy metals and other toxic matters contained in the soil do not exceed the agricultural standards set by the country. The region is rich in plants and animals. Local farmers use organic fertilizers. (5) Heavy Metals: The .eight metals, including Lead, cadmium, mercury, arsenic, etc. , the pesticide residues, air and water all meet the country environment standards. (6) Standardization The planting and plowing of Dan Shen follow the standard of Good Agriculture Practice (GAP) . Technological know-how relevant to the growing of Dan Shen is compiled into a booklets and distributed among the Dan Shen growers in the base. During the planting seasons, technicians are sent to the fields to give growers training on the spot and offer technical support, so as to standardize the planting of Dan Shen on a large plantation-like scale. (7) The Shangluo production base had bred and cultivated 20 different breeds of Dan Shen. Different Dan Shens were observed and compared in their growth situations., yield; ■appearance and chemical components for three years. The best breeds in quality chosen for large-scale plantation. (8) Tissue cultivation and clone technology are adopted in the Dan Shen cultivation to accelerate the procedure and shorten the circle of growth. (9) After a 30-day period of test-tube planting, an enlarged reproduction procedure is taken. It lasts 40 days before the root period. The root period will takes another 10 days that is for the plants to generate and enrich their roots. The rate of rooting usually reaches 90% or above. The plant can then be transferred to the nursery, where advanced spray irrigation device and conditions are controlled by computer technology. The plants can be transplanted to the outside field after a month cultivation in the nursery. (10) According to the experts, the cultivated Dan Shen from our product base are not only in high quality but also productive for their productive roots (50% more in root weight than those from other areas), and high chemical composition (70% higher in active drug ingredients than samples fro- other places). 2. Natural Borneol (1) Growth Conditions The growth areas of natural Borneol are Xinhuang county of Hunan province, China, a region with mid-height hills at a sea level of 300-600m. 60% of the area is covered by forest. The land consists of yellow and red sand soil with pH 5-6. No air or water pollutions are found within the region. (2) Biological Characteristics of the tree Extremely strong growth capability, it grows in brushwood field, 300-400 trees per mu (equal to 666. 7 m2) ; Parts above branch leaves are collected; net gain is 1000 kg per mu. (3) Reproduction and transplant Use grafting and cuttage technology for eprc duct ion. The Plant grows in the nursery garden durir.g the first year and is transplanted to the filed in the spring of the second year. The filed need to be fertilized and scarified periodically. (4) The plant may grow up to 30 cm in height and 80-100 cm for the largest diameter. It contains natural Camphor in different parts of the plant: leafs, branches, trunk and roots. Among all, the leaves contain the most of Camphor content. (5) The Borneol-type Camphor from Xinghuang is one of the natural variation of Cirnamonium glandullferm (wall) Noes. The Camphors trees vary in contents of Camphor and Borneol, Some are low in Borneol, high in Camphor while others high in Borneol and low in Camphor. Through an assay with large amount of samples and many HPLC analyses, we finally choose a kind of Camphor trees that contains over 80% Borneol with less impurity. 3. Radix Notoginseng a. Seeds of the plant (1) Determination of Radix Notoginseng With the PCR reaction for molecular mass marking, Radix Notoginseng can be stained observed, Radix Notoginseng has its characteristic DNA fingerprinting. (2) Shape and properties The Radix Notoginseng seed has a round, circular body. For seeds of different growth period, Radix Notoginseng has 2-year or 3-year seeds. The. 2-year seed is 0.45-0.55 cm in diameter and 95-103 grams in weight for its dried grain. The 3-year seeds is 0.54-0.65 cm in diameter and 98-109 grams in weight for its dried grain. (3) Suitable Temperature for seed sprouting The appropriate temperature for seed sprouting is 10-30 °C, the ideal temperature is 15-20 °C. (4) Water Content The amount of water contained should be 60-70%, if water content is below 20% for a long period of time, the seeds will lose vivacity. (5) Dormancy The seeds have a tendency to go through dormancy for 45-60 days after collection. (6) Life Span The seeds have a life span of 15 days in natural state after they are collected. (7) Requirements for storage of Seed Seeds for storage should be collected from the plants that grow more than two years and the tree should be growing prosperously for parts above the earth and pest-free. It is recommended that seeds be collected from three-year plants. (8) Management for the seed reservation field Seed reservation field should be better managed than the regular production fields, contaminated plants should be disposed of at all times, pests should not come in contact with the buds under any circumstances . During period of sprouting of buds and leafs, 3000 ppm of YunDa-120 and 400 times solution of Yang Kang biological fertilizer should be sprayed twice. And, during florescence and fruit period, Phytokinin is sprayed. (9) Harvest Period of the seed The harvest period of Radix Notoginseng seed is from the end of October to the beginning of December. (10) Methods for Collection of Seeds The collection of the seeds is decided dependant upon the levels of maturity of the seeds. The seeds from trees that grow stronger will be collected and stored separately. The base strictly prohibits collection of immature plants. (11) Processing Plants are washed immediately after collection while pulps and blighted seeds are picked out. Dry the plants in the sun after washing. (12) Storage Use 3 00 times solution of 58% metalaxyl manganous zinc dissolvable liquid to treat Radix Notoginseng seeds for 30 minutes, let the surface of the seeds become dry, and store the seeds with wet sand containing 20% water. It is a crucial step for the process. (13) Packaging Pinal products are packaged in uncontaminated containers, There should be signs that indicate the date of collection, processing, and the product batch number. (14) Transporting Clean, waterproof and ventilated transportation vehicles instruments should be used for transportation in order to prevent the product being contaminated with toxic matters . If it takes more than 8 hours for transportation, the product seed should be with the wet sand. (15) Test for vitality of the seeds Use the TTC methods: weigh accurately 1 g of tetrazolium powder and dissolve it in 1000 mL of distilled water to make up the solution of 0.1% TTC. Immerse the sample into the solution and keep it for 24 hours, take it out and cut it into half and place ' - 56 - one-half into a culture disk. Use the prepared 0.1% TTC to dye the sample for 30 minutes. The vitality of the seeds can be determined by the color of the seeds (16) Inspection of Pests i. Observe the seed with human eyes while placing 500-1000 sample pellets on a white sheet of paper or glass. If unusual spots or pests appear on the surface of the sample, the contamination can be decided. Contaminated 10 samples should be taken apart and be identified for its level of contamination. ii. Cutting and Inspect: use. a scalpel to cut and open 2 sample sets each contain 100 seeds. Calculate the 15 number of contaminated seeds to determine the level of contamination. iii. Smell to inspect samples-, place them in hand and detect them by nose for any moldy odor. Or simply 20 leave sample in a cup containing heated water (60-70 °C) , and covered for 2-3 minutes, pour out the water and smell the seeds. The seeds should send forth a delicate fragrance, if not, it is probably contaminated. (17) Color Inspection An uncontaminated seed should have light yellow and white color. (18) Microscopic Inspection 3 0 Pick out 5 test sample sets by random (each sample contains no less than 50 ceeds), place the samples.in a culture disk for 24 hours. Observe them under a microscope to detect them for any pathogenic bacteria, if so, calculate the level of contamination. b. Seedling of the plant (1) Temperature for sprouting The temperature for Radix Notoginseng's sprouting is 1-20 °C, the ideal temperature is 15°C. (2) Water Content The water content of the soil used for seedling plant is 20-25%. (3) Storage The development of Radix Notoginseng from resting bud to sprouting requires 90 days of dormancy period. 100 ppm of gibberellin can help shorten the Radix Notoginseng's dormancy period. (4) Refining Radix Notoginseng's refinery period is from the beginning of December to the end of January. While refining, the roots should be handled with care. Plant immediately after refinery. (5) Transportation Radix Notoginseng cannot be transported over long distance, otherwise it will be damaged. If unavoidable, Radix Notoginseng should be placed in a ventilated container with soil, without direct exposure to sunlight. (6) Quality Inspection i. For weight of each unit, choose 300-500 seedling plant as samples, put each 100 seedling plants in a group, weigh them on the balance and calculate the unit weight. ii. For pesticide inspection: set up four groups of samples each contains 100 seedling plants. Place samples on a glass disk and observe the samples with human eyes or 5-10 times magnifying lens to check for their pesticide. iii. Set up four groups of sample each contains 100 plants, slice the samples for an observation under the microscope. c. Culture of the seedling (1) Field condition Radix Notoginseng seedling plants are cultured in the best-conditioned areas. The base uses centered culture and 5 large-scaled cultural method. (2) Environment The area is totally free of pollutions. The air quality is above level 2 of GB 3059-96 standard. (3) Water Resources The water resources consist of rainwater, underground water, and natural running water. Water quality in the area is monitored with the GB 5084-92 standard. (4) Soil Radix Notoginseng cannot be planted i'ri oozy soil, the amount of heavy metals in the soil chosen for Radix Notoginseng must be within relevant country standard. (5) Ideal Soil For a good result expected, we choose acidic soil (pH 5.5-7.0) with a slope no more than 15°. A level no more than 1600 m above the sea should be with 8-12% of sunshine, and level more than 25 1600 m above sea level should be 10-20% of sunshine. (6) Temperature During sprout period the atmospheric temperature should be at 20- 25°C, and the earth temperature is at 10-15°C. During bearing 30 period is the best atmospheric temperature that is 20-25°C, and the best soil temperature that is 15-20°C. (7) Water Content Water content of soil should be at 25-30%. (8) Soil Preparation Soil plotting should be repeated for 3 times before planting, and soil be exposed under sunlight, it helps to exterminate bacteria substance in the soil. (9) Handle with Soil For prevention of root damage, 75-100g of lime is used each square meter before transplanting. (10) Construction and management of Shade The shade is 1.8m above ground with a 2m deep trench below the ground. Sunlight penetration is best at 8-10% if in area of no more than 1600 m above sea level, or 10-15% if it is more than 1600 m. The ground should be flat; deep layer of the earth should be lose; while the surface level of the earth should be rigid. Planting season is best at the end of December to the end of January. Before planting, the seeds should be immersed in 58% metalaxylic zinc (500-800x) or 1.5% antimycin (200ppm) for 30-50 minutes and dip out to let dry. This is to protect the plant from diseases (Coated seeds do not have to undergo the above procedures). Density of planting is to be 4 x 5 cm pr 5 x 5 cm, with 100-200 thousand seeds per mi of land. Use special tools to create a shallow gutter and use machine or hands to seed and plant. Seeds are covered with fine soil completely.

After all, fertilizing, watering and weeding tasks are performed. Weeds should be eliminated all the time. If the shade is broken, it should be repaired immediately and ensured the correct penetration of sunlight. Natural fertilizers including poultry waste, stove dust, and bone dust (human waste should not apply) . d. Radix Notoginseng Cultivation (1) Topology The ground is best be with a moderate slope under 15° and a good exposure to sunshine. (2) Soil Texture It is the best if the ground is deeply seated with loose and sand soil. (3) Soil pH should be at 5.5-7. (4) Pre-planted Crops Corns, wheat, and beans are pre-planted in new fields in avoid of soil destruction. (5) Sea Level 1400-1800m above sea level near an altitude of 23,5° is the location of the most suitable Radix Notoginserig area for cultivation. (6) Sunshine Radix Notoginseng is a kind of plant that requires only 8-20% of sunshine. The amount of sunshine should be varied increased in respect to different period of its growth. However, too much sunshine exposure will result in stagnant plants. (7) Water Content The water content within the soil should be at 25-30%. (8) Fertilizer Organic fertilizers are used along with compound fertilizers, micronutrient fertilizers, or trace-element fertilizers. (9) Temperature The average temperature is estimated at 15-18 °C during the year in the Radix Notoginseng area. During sprout period, atmospheric temperature should be, the most suitable, at 20-25°C, and soil temperature 15 °C. During nutrient development and blooming period, temperature is better be kept at 25°C. If the temperature is below 15 °C, florescence will be affected. (10) Filed Division Before cultivation, the field should be ploughed and loosened 3 times until its structure becomes powderized. (11) Soil Management Before sowing and transplanting, apply 75-100g of quick lime to soil for sterilization purposes. (12) Standards of the bed Flat ground soil bed of 20-25 cm in height, at slope area it should be 15-20 cm. The width of the bed is between 120 and 140 cm in a shape of a tile. The soil at the bottom of the base should be loose and that on the top should be solid, that is for better penetration. (13) Seed Soaking During transplanting, soak seed for 30-50 minutes in 58% metalaxyl (500-800x) and then let dry, this will prevent plant from diseases and eliminate pests. (14) Density of planting Keep a distance of 10 x 12.5 cm - 10 x 15 cm in plant density. That is 26-32 thousand plants every mu. (15) Methods for Transplanting Seedlings are planted facing the same direction for management purposes. In case of slope grounds, seedlings are planted from low end to the high ground. The first row of seedlings is facing up while the second row faces down. Buds are also to face upward, and the bottom is to face inward. (16) Covering of Soil Use powdered, loose, and moistures soil to cover the seedlings completely, without exposing the roots or the buds. (17) Fertilization Use poultry waste, stove ash, bone ash, Calcium Magnesium Phosphate, etc as specialized fertilizer.

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. Chen ZH et al. , "Studies on effects of "Danshensu" on experimental microcirculatory disturbances and plasm lactic acid concentrations" Acta Acad Med Prim Shanghai 1987; 14: 25-29. 31. Huang C et al. , "Effects of Panax Notoginseng Saponins on myocardial ischemia and reperfusion injury in conscious rabbit" Chin Bull Pharmacol 1991; 7: 190-3. 32 . Shi L et al., "Effects of total saponins of Panax Notoginseng on increasing PG12 in carotid artery and decreasing TXA2 in blood platelets" Acta Pharmcol Sin 1990; 11: 29-32. 33. Xu W et al., "Effect of menthol and borneol on the distribution of sulfadiazine sodium and Evan's blue in the rat and mouse brain" Pharmacol Chin Med Clin 1995; (6): 31-33. 34. Chen TF et al., "Enhancement of absorption of tetramethylpyrazine by synthetic borneol" Acta Pharmacol Sin 1990; 11:42-44.

. Li X et al., "Protective effects of Panax notoginseng saponins on experimental myocardial injury induced by ischemia and reperfusion in rat" Acta Pharmacol Sin 1990;11:26-29. 36. Pan JG et al. , "Chemical Studies on Essential oils from six Artemisia Species" Chin J Chin Mater Med 1992; 17: 741-6. 37 . Wu YZ et al., "An assessment of Radix Silviae Miltiorrhizae in promoting blood circulation by removing blood stasis" Acta Nanjing Univ Trad Chin Mater Med 1995; 11:35-6. 38. Wang NS et al. , "Experimental studies of "Benifits of Borneol as an Assistant or a guide," J Trad Chin Med 1994; 35:46-7. 39. Li CZ et al., "Anti-coagulation effect of Radix Silviae Miltiorrhizae" Chin J Integr Med 1983; 3: 297-9. 40. Li CZ et al. , "An experimental study on thrombotic 15 inhibition effect of Radix Silviae Miltiorrhizae" Acta Acad Med Prim Shanghai 1979;6:145-9. 41. Mo QX et al., "Dynamics of 3H-Borneol" Propriet Trad Chin Med Res 1982; 8 : 5-7. 42. Zheng RX et al. , "Preservation effect of Radix Silviae Miltiorrhizae on myocardial ischemia induced by coronary ligation in mice" Chin J Integr Med 1992;12:424-6.

Claims (7)

What is claimed is: 67

1. A composition capable of treating chronic stable angina pectoris comprising 5 Danshensu, sanchinoside and ginsenoside Rgi which produces eight peaks as shown in the following table, Retention Relative Appearance Area Peak No. Time Retention Time Probability Area ratio Area Ratio Range 1 8.289 0.672 100% 1034.276 0.572 0.572±0.096 2 12.343 1.000 100% 1817.065 1.000 1.00010.000 3 17.493 1.417 100% 376.547 0.208 0.208±0.040 4 18.664 1.512 100% 328.011 0.181 0.181 ±0.059 5 24.883 2.016 100% 486.626 0.267 0.267±0.097 6 27.586 2.235 100% 525.432 0.289 0.28910.052 7 29.714 2.407 100% 940.963 0.516 0.516±0.125 8 34.030 2.757 100% 1547.495 0.850 0.85010.163 when subjected to steps of: a) dissolving a suitable amount of said composition with internal standard para- aminobenzonic acid solvent; 10 b) using Danshensu and protocatechuic aldehyde as the standards; c) performing the HPLC assay; and d) calculating according to the internal standard method.

2. A composition capable of treating chronic stable angina pectoris comprising about 15 0.14 to about 0.18 mg Danshensu, more than 12.12jxg sanchinoside R1 and more than 56.26(ag ginsenoside Rgi.

3. A method for obtaining a herbal composition capable of treating chronic stable angina pectoris which contains Danshensu, sanchinoside, ginsenoside Rgi 20 comprising the steps of: (A) Extracting Radix Salviae Miltiorrhizae herb, including: placing Radix Salviae Miltiorrhizae in an extraction tank; adding water until the water level is 15-20cm over the herb (or about 5-7 times the quantity of the herb); heating the water and 68 Radix Salviae Miltiorrhizae herb to boiling with steam and with pressure between about 0.04-0.06 mPa to form a first water and herb mixture; maintaining the first water and herb mixture in boiling condition; boiling twice, first for 2 hours and then for 1.5 hours; filtering the first water and herb mixture through 100-mesh net into a stock tank to obtain a first extract solution; (B) Concentrating the first extract solution, including: transferring the first extract solution from the stock tank into a vacuum tank, maintaining the steam pressure at below 0.05 mPa; adjusting the vacuum to 0.076—0.088 mPa to keep the first extract solution in boiling condition; concentrating the first extract solution to 1:1 ratio of volume of solution (liter) to quantity of herb (kilogram) to obtain a concentrated solution; (C) Performing ethanol precipitation, including: filtering the concentrated solution through 100-mesh net into a precipitation tank, adding 95% ethanol to the concentrated solution; stirring slowly until the concentration of the ethanol in the concentrated solution reaches 70% as measured by ethanol gravimeter to obtain a ethanol solution; storing the ethanol solution for 24 hours; (D) Performing ethanol recovery, including: filtering the ethanol solution through 100-mesh net into a vacuum concentration tank; adjusting the air input to 0.04-0.06 mPa and the vacuum to 0.076-0.088 mPa to maintain the ethanol solution in boiling condition; recovering the ethanol from the ethanol solution to 1:1 ratio of volume of solution (liter) to quantity of herb (kilogram) to obtain a crude first extract of Radix Salviae Miltiorrhizae-, (E) Refining the crude first extract by performing polyamide chromatography, including: loading the crude first extract into the pre-treated polyamide chromatography chamber, wherein the loading volume is 5 ml/gram polyamide; washing the column with water; eluting the column with 95% ethanol for 5-10 times; recovering ethanol from the crude first extract until the density of the crude first extract reaches 1.33-1.35 to from the extract of Radix Salviae Miltiorrhizae;

4. A method for obtaining a herbal composition capable of treating chronic stable angina pectoris comprising steps of: 69 (A) Extracting Radix Notoginseng herb, including: placing Radix Notoginseng herb into an extraction tank; adding water until it is 15-20 cm over the Radix Notoginseng herb (or about 5-7 times the quantity of the herb); heating water and Radix Notoginseng herb to boiling with steam and with the pressure between 0.04-0.06 mPa to form a second water and herb mixture; keeping the second water and herb mixture in boiling condition; boiling twice, first for 2 hours and then for 1.5 hours; filtering the second water and herb mixture 100-mesh net into a stock tank to obtain a second extract solution; (B) Macroporous adsorption resin i. Pre-treating of macroporous adsorption resin, including: filling a column with non-polarity macroporous adsorption resin ZTC-1 having a particle size 0.3-1.2 mm and average aperture 130-300 A after being soaked in 95% ethanol for 24 hours; washing the column with ethanol and equal volume of water until an eluant is clear with equal volume of water; or washing the column with 0.1-1 mol/L NaOH or HCL, then washing the column with water until an eluant has no ethanol smell or is close to pH neutral; ii. Loading the second extract solution in the column with 1:1 weight ratio of the second extract solution to resin, wherein the flow rate is 0.5-5 cm/cm2/min, washing the column until the eluant is clear; eluting the column with 70% ethanol, wherein the the flow rate is 0.5-5 cm/cm2/min; collecting the eluant; iii. Washing the column with 95% ethanol until the eluant is without color and clear after adding equal volume of water; washing the column with water until there is no ethanol smell; and (C) Concentrating the eluant, including: filtering the eluant through 100-mesh net to a vacuum concentration tank; adjusting the air input to 0.04-0.06 mPa and the vacuum to 0.076~0.088 mPa to keep the eluant at boiling condition; recovering the ethanol until the density of the eluant reaches 1.33-1.35 to form the extract of Notoginseng saponin.

5. The method of claim 4, wherein the macroporous resins are packed in columns. 69a

6. The method of claim 4, wherein the chromatographic material is selected from porous polymer, silicon gel, aluminum oxide, polyamide, activated charcoal, cellulose or sephadex in addition to macroporous resin (model D101).

7. The method of claim 4, wherein the chromatographic column eluate is concentrated at reduced pressure under 60°C to a relative density of 1.33-1.35.