Medicine composition for treating hyperlipemia and coronary disease and preparation method thereof
A composition and technology for coronary heart disease, applied in the directions of drug combination, pharmaceutical formulation, drug delivery, etc., can solve the problems of limited clinical application, slow effect, elevated blood lipids, etc.
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experiment example 1
[0032] Experimental Example 1: Anti-myocardial ischemia test of granules of the present invention
[0033] Test product: finished granules of the present invention Specifications: 27.3g crude drug / 3.2g powder / bag; dosage and administration: Clinically, adults (60kg body weight) take 1 bag each time, 3 times a day, that is, the daily dosage for adults It is: (1 bag / time×3 times / day×27.3g crude drug / bag)÷60kg body weight=1.365g crude drug / kg body weight; 30 days is a course of treatment. The following are calculated according to the original drug, see Table 1. Positive control drug: Di'ao Xinxuekang Capsules, produced by Chengdu Di'ao Pharmaceutical Group Co., Ltd. Batch number 00020501; specification: 100mg×20 capsules. Before use, distilled water was used to make the required concentration of liquid medicine for experimentation, and the following calculations were made according to this, as shown in Table 1. Modeling drug: vasopressin, produced by Shanghai Biochemical Pharm...
experiment example 2
[0039] Experimental example 2: the influence of granule of the present invention on rabbit plasma fibrin degradation product (FDP)
[0040] Granules of the present invention, urokinase for injection, are mixed with required concentration medicinal liquid with 0.996 sodium chloride injection during the test for subsequent use (see Table 3).
[0041]
group
Test substance
(g / ml)
Dosing volume
(ml / kg)
Dosage
(g / kg)
Days of administration
(sky)
medication
way
control group
urokinase group
Granule high dose group of the present invention
The middle dose group of granules of the present invention
Granules of the present invention low dose group
Urokinase for Injection
Granules of the present invention
Granules of the present invention
Granules of the present invention
--
1000U / ml
18.2
...
experiment example 3
[0047] Experimental Example 3: Determination of Rabbit Plasma Euglobulin Time (ELT)
[0048] 48 Japanese big-eared white rabbits were randomly divided into 6 groups, 8 rabbits in each group, half male and half male. According to the drugs and doses listed in Table 5, they were administered from the marginal ear vein once a day for 7 consecutive days. 30 minutes after the last administration of animals in each group, blood was taken from the ear vein, anticoagulated with 3.8% sodium citrate (1:9 ratio of anticoagulant and blood), and immediately centrifuged at 3000rpm / min for 10min to separate platelet-poor plasma (PPP) . Calcium addition method is used to measure ETL, the method is as follows: take a centrifuge tube with conical bottom, add 7.5ml of distilled water, add 0.12ml of 0.17mol / L acetic acid, make the pH about 4.5. Place in ice water bath. Add 0.5ml of the above PPP, mix well, continue to put in ice bath for 10min, and centrifuge (2500×g, 5min). Pour off the supe...
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