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A kind of preparation technology of compound medicine for treating chronic nephritis

A technology for chronic nephritis and a preparation process, which is applied in directions such as drug combinations, medical preparations containing active ingredients, and pharmaceutical formulations, can solve the problems of easy rejection, loss of active ingredients, and single preparation method, and achieves a simple and feasible preparation process. , improve profits, good effect

Active Publication Date: 2020-02-21
XIANGYU PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The applicant found in the pharmaceutical process that the preparation method of the drug is relatively simple, and the same extraction process is used for various raw materials, which has the defect of loss of active ingredients, and the Cordyceps Qishen Capsules need to be taken 4 capsules each time, three times a day, and the dosage is too large , some patients find it hard to accept and prone to rejection

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] A preparation process for a compound drug for the treatment of chronic nephritis, comprising the steps of:

[0018] 1) Weighing: Weigh each raw material according to the weight part for later use, including 80g of Cordyceps sinensis, 1200g of Astragalus membranaceus, 600g of Salvia miltiorrhiza, 600g of safflower, and 320g of jujube seed;

[0019] 2) Preparation of component A: take Cordyceps sinensis and grind it into a fine powder of Cordyceps sinensis, which is component A;

[0020] 3) Preparation of component B: Take astragalus, crush it, pass through a 200-mesh sieve, put it in a container, add three times the weight of 85% (v / v) ethanol, stir and extract at 300rpm, control the microwave power to 500W during the extraction process, The extraction time is 90 minutes; then placed at 4°C for 12 hours, filtered, and the filter residue is used for later use; the filtrate is evaporated under reduced pressure to recover ethanol, and the filtrate is concentrated to the ext...

Embodiment 2

[0035] Animal Toxicity Test

[0036]60 healthy Kunming strain mice, half male and half female, body weight 18.9±2.6g, 60 mice were randomly divided into two groups, half male and half female in each group, 30 of them were the control group, fed with normal water; the other 30 Only mouse is given the preparation prepared by embodiment 1, dosage is 200mg / kg, every day three times, application mouse is carried out toxicity experiment and shows: compare with matched group, mouse does not see obvious difference after administration, experiment observes continuously for two weeks, little The general condition, food intake, drinking water and weight gain of the rats were all normal. On the day of administration and within two weeks after administration, no animal died, suggesting that the drug has low toxicity and is safe for clinical use.

Embodiment 3

[0038] Drug efficacy comparison test

[0039] Animals: 120 SD male rats, weighing 221±19g, healthy and clean, raised in the experimental animal center of our company.

[0040] Grouping treatment: 120 SD male rats, 30 were randomly selected as the blank control group according to no significant difference in body weight, and the remaining 90 were prepared for adriamycin nephropathy model. The model rats were randomly divided into model control group (gastric administration of normal saline, dose 100 mg / kg), Example 1 group (gastric administration of the preparation produced in Example 1, dose 100 mg / kg), control group 1 (gastric administration of control The preparation produced in Example 1, dose 100mg / kg), 30 rats in each group. Gastrointestinal administration once a day for one month in a row. The rats in each group were collected 24h urine volume at the beginning and end of the experiment to measure the 24h urine protein (sulfallic acid method).

[0041] Observation indi...

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PUM

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Abstract

The invention belongs to the technical field of traditional Chinese herbal medicine extraction, and discloses a preparation process for a compound medicine for treating chronic nephritis. The preparation process comprises the following steps: 1) weighing; 2) preparing a component A; 3) preparing a component B; 4) preparing a component C; 5) preparing a component D; and 6) uniformly mixing, crushing and granulating. The preparation process is improved on the basis of a conventional cordyceps ginseng capsule preparation process, the leaching efficiency of effective components of the raw materials is improved, and the medicinal effect is improved.

Description

technical field [0001] The invention belongs to the technical field of Chinese herbal medicine extraction, and in particular relates to a preparation process of a compound medicine for treating chronic nephritis. Background technique [0002] Chronic nephritis, also known as chronic glomerulonephritis, is a group of glomerular diseases with various etiologies, different pathological forms and similar clinical manifestations. , accompanied by varying degrees of renal dysfunction, often recurrent, protracted and difficult to heal, anemia, retinopathy and uremia may occur in the later stage, and even life-threatening. The main manifestations are: (1) edema; (2) high blood pressure; (3) pain in the renal area and renal colic; (4) urinary tract irritation (ie urgency, dysuria, frequent urination); (5) abnormal urination (Including decreased urine output, proteinuria, hematuria, casturia, leukocyturia, pyuria and bacteriuria, positive renal function tests, etc. According to the in...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K36/725A61K9/48A61P13/12
CPCA61K9/4841A61K36/068A61K36/286A61K36/481A61K36/537A61K36/725A61K2236/19A61K2236/331A61K2236/333A61K2236/39A61K2300/00
Inventor 林凡友郭增光张海雷王文天秦承盟
Owner XIANGYU PHARMA