CN1268361C - Chinese traditional medicine composition for treating cardiovascular and cerebrovascular diseases - Google Patents

Chinese traditional medicine composition for treating cardiovascular and cerebrovascular diseases Download PDF

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Publication number
CN1268361C
CN1268361C CN 200310117309 CN200310117309A CN1268361C CN 1268361 C CN1268361 C CN 1268361C CN 200310117309 CN200310117309 CN 200310117309 CN 200310117309 A CN200310117309 A CN 200310117309A CN 1268361 C CN1268361 C CN 1268361C
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paeoniae rubra
radix paeoniae
radix
injection
radix puerariae
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CN1546137A (en
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张文芳
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Yunnan Biovalley Pharmaceutical Co ltd
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Abstract

The present invention discloses a medicine for treating cardiovascular and cerebrovascular diseases, and a preparation thereof. The medicine is composed of red peony root and kudzuvine root. By the experimental verification of medicine effect, the medicine has the obvious efficiency of improving cardiovascular and cerebrovascular blood-supply shortage, resisting thrombosis, etc.

Description

A kind of modern compound preparation for the treatment of cardiovascular and cerebrovascular disease
Affiliated field
The present invention relates to a kind of medicine and preparation thereof for the treatment of cardiovascular and cerebrovascular disease, belong to medical pharmaceutical field, particularly belong to the Chinese medicine antithrombotic, improve cardiovascular and cerebrovascular vessel blood supply insufficiency pharmaceutical technology field.
Background technology
Radix Puerariae is widely used as food for a long time, is medically doing the clearing away heat and expelling pathogen in the exterior agent, and the treatment flu finds that now Radix Puerariae contains various active compositions such as flavone, has effects such as the cerebral vascular resistance of reduction, cerebral blood flow increasing amount, lax nerve, allaying tiredness.Wherein Radix Puerariae flavone has a stronger inhibitory action to thrombin such as thrombin and partial prothrombinase are former, also has the effect that thrombus in vivo forms that suppresses.Its main functional component puerarin can promote the normal brain activity circulation and improve the local microcirculation obstacle, increases the amplitude of blood capillary motion, improves regional blood flow.
The main effective ingredient of Radix Paeoniae Rubra is paeoniflorin (Paeoniforin), peony lactone glycoside (Albiforin), hydroxypaeoniflorin (Oxy paeoniflorin), benzoylpaeoniflorin monoterpene glycoside compounds such as (Benzoyl paeoniflorin) is called for short the Radix Puerariae Radix Paeoniae Rubra extract.The modern plants chemistry thinks that Radix Paeoniae Alba total glycosides is the active component in the Radix Paeoniae, mainly is present in the root bark portion of Radix Paeoniae.Traditional medicine thinks, Radix Paeoniae Rubra can clearing away heat and cooling blood, and eliminating stasis to stop pain clinically, is diseases such as monarch drug prescription therapeutic ischemic angiocardiopathy and cerebrovascular with Radix Paeoniae Rubra or with Radix Paeoniae Rubra.
Theory of Chinese medical science thinks that two medicines mutually 5 have to rise to have and rush down, and has field headquarters blood, removes the function of arthralgia due to stagnation of blood, the meridian dredging.Modern effect experiment proves, two medicines 5 have mutual synergic effect mutually, and the preparation made of two flavor medicines has significant cardiovascular and cerebrovascular vessel blood supply insufficiency and the antithrombotic effect improved thus.
Summary of the invention
The invention discloses a kind of modern compound preparation for the treatment of cardiovascular and cerebrovascular disease, said preparation is made up of Radix Paeoniae Rubra and Radix Puerariae two flavor medicines, and its dosage form can be a solid preparation, also can be liquid preparation.Solid preparation comprises tablet, slow releasing tablet, capsule, slow releasing capsule, soft capsule and drop pill etc.Liquid preparation can be aqueous injection, injectable powder, infusion solution and fat milk injection.Various dosage forms are to make with conventional method, and wherein Radix Paeoniae Rubra extract and Radix Puerariae extract existence are solid, shaped or liquid, and administering mode is oral, intravenous or intramuscular injection
The solid constituent of Radix Puerariae Radix Paeoniae preparation is made up of Radix Puerariae extract and Radix Paeoniae Rubra extract and pharmaceutic adjuvant, two flavor medicine weight ratios are: Radix Paeoniae Rubra 0.5-0.9 part, Radix Puerariae 0.1-0.5 part also can be Radix Paeoniae Rubra 0.1-0.5 part, Radix Puerariae 0.5-0.9 part, such as: 1 part of Radix Puerariae, 2 parts of 2 parts of Radix Paeoniae Rubra or Radix Puerariaes, 1 part of Radix Paeoniae Rubra also can be 1 part of a Radix Puerariae, 1 part of Radix Paeoniae Rubra, various preparations are all made according to common process.
Below by embodiment modern compound preparation of cardiovascular medicament with antithrombotic acitivity of the present invention and preparation method thereof is described further.
Embodiment 1:
Preparation Radix Puerariae Radix Paeoniae Rubra extract aqueous injection, prescription ratio: 1 part of Radix Puerariae, 2 parts of Radix Paeoniae Rubra.
1kg is dissolved in the 100L water for injection with the Radix Puerariae Radix Paeoniae Rubra extract, is made into 10mg/ml, regulates PH to 6.0.After the microporous filter membrane ultrafiltration, replenish water for injection to ormal weight, fill is in ampoule bottle, and the sealing by fusing sterilization through after the assay was approved, is packed promptly.
Embodiment 2:
Preparation Radix Puerariae Radix Paeoniae Rubra extract aqueous injection, prescription ratio: 2 parts of Radix Puerariaes, 1 part of Radix Paeoniae Rubra.
1kg is dissolved in the 100L water for injection with the Radix Puerariae Radix Paeoniae Rubra extract, is made into 10mg/ml, regulates PH to 6.0.After the microporous filter membrane ultrafiltration, replenish water for injection to ormal weight, fill is in ampoule bottle, and the sealing by fusing sterilization through after the assay was approved, is packed promptly.
Embodiment 3:
Preparation Radix Puerariae Radix Paeoniae Rubra extract aqueous injection, prescription ratio: 1 part of Radix Puerariae, 1 part of Radix Paeoniae Rubra.
1kg is dissolved in the 100L water for injection with the Radix Puerariae Radix Paeoniae Rubra extract, is made into 10mg/ml, regulates PH to 6.0.After the microporous filter membrane ultrafiltration, replenish water for injection to ormal weight, fill is in ampoule bottle, and the sealing by fusing sterilization through after the assay was approved, is packed promptly.
Embodiment 4
Preparation Radix Puerariae Radix Paeoniae Rubra injectable powder, prescription ratio: 1 part of Radix Puerariae, 2 parts of Radix Paeoniae Rubra.。
Radix Puerariae Radix Paeoniae Rubra extract 1kg is dissolved in an amount of 100L water for injection, the pharmaceutic adjuvant that adds metering, regulate PH to 6.0, after the microporous filter membrane ultrafiltration, vacuum drying gets Radix Puerariae Radix Paeoniae Rubra extract aseptic powder, and aseptic powder is sub-packed in the cillin bottle, make every bottle and contain Radix Puerariae Radix Paeoniae Rubra extract aseptic powder 100mg, three specifications of 150mg, 200mg, roll lid, through after the assay was approved, packing promptly.
Embodiment 5
Preparation Radix Puerariae Radix Paeoniae Rubra lyophilized injectable powder, prescription ratio: 2 parts of Radix Puerariaes, 1 part of Radix Paeoniae Rubra.
With Radix Puerariae Radix Paeoniae Rubra extract 1kg, after the dissolving of 5 times of amount water for injection, add the injection water solublity pharmaceutic adjuvant of metering, regulate PH to 6.0, filter, be loaded in the ampoule bottle, every 10ml, after lyophilization, sealing by fusing, after the assay was approved, packing is promptly.
Embodiment 6
Preparation Radix Puerariae Radix Paeoniae Rubra lyophilized injectable powder, prescription ratio: 1 part of Radix Puerariae, 1 part of Radix Paeoniae Rubra.
With Radix Puerariae Radix Paeoniae Rubra extract 1kg, after the dissolving of 5 times of amount water for injection, add the injection water solublity pharmaceutic adjuvant of metering, regulate PH to 6.0, filter, be loaded in the ampoule bottle, every 10ml, after lyophilization, sealing by fusing, after the assay was approved, packing is promptly.
Embodiment 7
Preparation Radix Puerariae Radix Paeoniae Rubra lyophilized injectable powder, prescription ratio: 1 part of Radix Puerariae, 2 parts of Radix Paeoniae Rubra.
With Radix Puerariae Radix Paeoniae Rubra extract 1kg, after the dissolving of 5 times of amount water for injection, add the injection water solublity pharmaceutic adjuvant of metering, regulate PH to 6.0, filter, be loaded in the ampoule bottle, every 10ml, after lyophilization, sealing by fusing, after the assay was approved, packing is promptly.
Embodiment 8
Preparation Radix Puerariae Radix Paeoniae Rubra lipomul, prescription ratio: 1 part of Radix Puerariae, 2 parts of Radix Paeoniae Rubra.
With Radix Puerariae Radix Paeoniae Rubra extract 1kg, be dissolved in the 100L injection fat solvent (forming) by water for injection and emulsifying agent, be made into the solution of 10mg/ml, regulate PH to 6.0.After the microporous filter membrane ultrafiltration, be sub-packed in 2ml, the 5ml ampoule, after the assay was approved, packing is promptly.
Embodiment 9
Preparation Radix Puerariae Radix Paeoniae Rubra lipomul, prescription ratio: 2 parts of Radix Puerariaes, 1 part of Radix Paeoniae Rubra.
With Radix Puerariae Radix Paeoniae Rubra extract 1kg, be dissolved in the 100L injection fat solvent (forming) by water for injection and emulsifying agent, be made into the solution of 10mg/ml, regulate PH to 6.0.After the microporous filter membrane ultrafiltration, be sub-packed in 2ml, the 5ml ampoule, after the assay was approved, packing is promptly.
The pharmacological effect experiment
Experiment 1, Radix Puerariae Radix Paeoniae Rubra extract are to the thrombotic influence of rats in vitro
Experiment material
1. medicine: Radix Puerariae Radix Paeoniae Rubra extract powder pin: 100mg/ props up; The injection XUESHUANTONG: 50mg/ props up.
2. animal: 40 of healthy male Wistar rats, body weight 200.72 ± 9.0g.
Experimental technique
40 rats are divided into 4 groups (10 every group) at random: 1. matched group (0.9% sodium chloride injection, 5.0ml/kg), 2. Radix Puerariae Radix Paeoniae Rubra powder pin 20mg/kg dosage group, 3. Radix Puerariae Radix Paeoniae Rubra powder pin 10mg/kg dosage group, 4. injection XUESHUANTONG 20mg/kg dosage group.Each treated animal by described dosage with the injection volume of 5.0ml/kg through the tail vein injection administration, once a day, successive administration 3 days, 30min after the last administration with pentobarbital sodium (30.0mg/kg) anesthesia, is used for external thrombus from abdominal aortic blood 2ml and forms and measure.
External thrombus forms to be measured: according to the Chandler in vitro method, at once blood is injected in the rotating ring, the blood volume of injection is full of rotating ring below 1/2, rapidly sealing, put on the thrombosis instrument, rotation 10min, inclining thrombosis, the normal saline washing, measure length, the weighing weight in wet base is put 80 ℃ of baking oven 3h with the thrombosis bar, claims its dry weight after the constant weight.
Experimental result:
Table 1. Radix Puerariae Radix Paeoniae Rubra extract is to the thrombotic influence of rats in vitro (X ± SD)
Group Dosage (/kg) Number of animals Thrombosis
Length (mm) Weight in wet base (mg) Dry weight (mg)
Matched group 10 21.1±1.8 150.4±10.0 26.7±1.7
The injection XUESHUANTONG 20mg 10 16.1±2.0 130.6±16.3 20.4±3.7
Radix Puerariae Radix Paeoniae Rubra extract powder pin 10mg 10 20.9±1.5 134.1±12.0 23.3±6.1
Radix Puerariae Radix Paeoniae Rubra extract powder pin 20mg 10 16.6±3.1 130.7±20.4 19.3±4.5
Annotate: compare P<0.01 with matched group
By table 1 as seen, compare with matched group, the thrombosis length of Radix Puerariae Radix Paeoniae Rubra powder pin 20mg/kg and 10mg/kg dosage group all obviously shortens (P<0.01), and wet weight of thrombus and dry weight all obviously alleviate (P<0.01), and the thrombosis dry weight has the trend of alleviating; The thrombosis dry weight of injection XUESHUANTONG group obviously alleviates (P<0.05), and thrombosis length has shortening trend, and wet weight of thrombus has the trend of alleviating.Show that Radix Puerariae Radix Paeoniae Rubra powder needle set has the effect that suppresses thrombosis, blood viscosity lowering, to compare drug effect suitable with XUESHUANTONG.
Experiment 2: the Radix Puerariae Radix Paeoniae Rubra extract is to the influence of clotting time of mice
40 of kunming mices are divided into 5 groups at random, each treated animal by described dosage with the injection volume of 5.0ml/kg through the tail vein injection administration, once a day, successive administration 3 days, behind the 1h, abdominal aortic blood is used the determination of tube method clotting time after the last administration.The result: three kinds of dosage all obviously prolong the clotting time of mice.
Experimental result:
Table 2 Radix Puerariae Radix Paeoniae Rubra extract is to the influence of clotting time of mice (n=10, x ± s)
Group Dosage (mg/kg) Clotting time (s)
Normal saline Radix Puerariae Radix Paeoniae Alba extract (greatly) Radix Puerariae Radix Paeoniae Alba extract (in) Radix Puerariae Radix Paeoniae Alba extract (little) aspirin Deng capacity 20 10 5 10 57.1±9.8 69.8±12.2 63.5±12.0 57.6±11.7 67.1±10.6
Compare P<0.01 with the normal saline group
Experiment 3: Radix Puerariae Radix Paeoniae Rubra injection is to Medulla Leporis seu Oryctolagi circulation and the metabolic influence of brain
1.1 animal: 32 of new zealand rabbits, body weight 2.0~3.0kg, male and female dual-purpose.
1.2 medicine: Radix Puerariae Radix Paeoniae Rubra injection (self-control) is made into 10mg/ml.
1.3 instrument: MF-1200 type electromagnetic flowmeter, STAT-PROFILE-5 type electrolyte analyser.
Experimental technique:
2.1 animal preparation: animal via urethane (1.0g/kg) auricular vein injecting anesthetic, the circulation of qi promoting cannula separates two side femoral artery, sidelights record blood pressure, opposite side extracts arterial blood.Separate a side common carotid artery and internal carotid artery and external carotid artery simultaneously, ligation external carotid artery and branch thereof are in order to laying the electromagnetic flowmeter probe at the common carotid artery place.The rabbit head is fixed on the stereotaxic instrument, cuts cranium item skin, expose posterior lambdoid suture place, boring is in order to extracting cerebral veins, venae cerebri blood above torcular.
2.2 animal grouping: animal is divided into 4 groups at random, i.e. the heavy dose of group of Radix Puerariae Radix Paeoniae Rubra (44mg/kg), Radix Puerariae Radix Paeoniae Rubra small dose group (22mg/kg), nimodipine group (3 μ g/kg) and normal saline matched group.8 of every treated animals.The auricular vein drug administration by injection.
2.3 hemodynamics is measured: the left side femoral arteriography is connected in AP-621G carrier amplifier recording blood pressure through pressure transducer, with the AT-611G Cardiotacs heart rate is carried out the integration record.
2.4 ICAF quantitative determination: use the method for measuring the ICAF amount and judge cerebral blood flow (CBF).The probe that bore is suitable places on the side common carotid artery, and is connected in MF-1200 type electromagnetic flowmeter, judges CBF by the ICAF amount.
Experimental result proves, Radix Puerariae Radix Paeoniae Rubra injection can the cerebral blood flow increasing amount, improves brain oxygen consumption and glucose uptake amount, illustrates that it has the cerebral circulation of improvement and the metabolic dual function of brain.

Claims (2)

1, a kind of solid preparation of cardiovascular and cerebrovascular disease or modern compound preparation of liquid preparation form for the treatment of is characterized in that being made by the crude drug of pharmaceutic adjuvant and following weight fraction:
Radix Paeoniae Rubra 1-2 part
Radix Puerariae 1-2 part.
2, according to the preparation of claim 1, described solid preparation form is tablet, slow releasing tablet, capsule, slow releasing capsule, soft capsule or drop pill, and described liquid preparation form is aqueous injection, injectable powder, infusion solution or fat milk injection.
CN 200310117309 2003-12-08 2003-12-08 Chinese traditional medicine composition for treating cardiovascular and cerebrovascular diseases Expired - Lifetime CN1268361C (en)

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Application Number Priority Date Filing Date Title
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CN1268361C true CN1268361C (en) 2006-08-09

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