A kind of preparation method of drug preparation for female menopause depression
A technology of pharmaceutical preparations and depression, which is applied in the field of preparation of pharmaceutical preparations for female menopausal depression, can solve the problems of western medicines such as large toxic and side effects, easy repetition of drug withdrawal, and insignificant therapeutic effects, etc., achieves small toxic and side effects, relieves anxiety, and regulates reproduction endocrine effects
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Embodiment 1
[0031] A preparation method for female climacteric depression preparation, which is prepared from the following raw materials in weight ratio:
[0032] 35 parts of medlar, 35 parts of rehmannia, 35 parts of angelica, 30 parts of dodder, 30 parts of Anemarrhena,
[0033] Polygala 25, Poria 25, Morinda officinalis 25, Epimedium 20, Cnidium 20,
[0034] 20 parts of Chuanxiong, 15 parts of paeonol, 15 parts of Corydalis, 15 parts of Uncaria, 10 parts of mulberry,
[0035] 10 parts of Rhizoma Cyperi, 10 parts of Coix Seed, 10 parts of Angelica dahurica, 10 parts of Citrus aurantium, 8 parts of Polygonum multiflorum,
[0036] 8 parts of turmeric, 8 parts of Albizia Julibrissin, 5 parts of jujube seed, 5 parts of licorice, and 5 parts of hawthorn.
[0037] Its preparation method is:
[0038] 1) take each raw material and set aside;
[0039] 2) Take medlar, angelica, dodder, polygala, morinda officinalis, epimedium, chuanxiong, uncaria, angelica, aurantium citrus, turmeric, and al...
Embodiment 2
[0044]Acute toxicity test: 40 mice, half male and half female, weighing 30-40g, were subjected to acute toxicity test. The mice were randomly divided into 2 groups, i.e. a control group and a drug administration group (medicine preparation prepared in Example 1), 20 in each group, fasted for 12 hours before the experiment, and the drug administration group was given the drug prepared in Example 1 of the present invention The preparation was dissolved in water and administered by intragastric administration (a single administration dose of intragastric administration was 50g of crude drug / kg), and the control group was given the same amount of normal saline, administered twice a day, with an interval of 6 hours between administrations, and observed continuously for 14 hours after administration. days, and recorded the number of toxic reactions and deaths of the mice. The results of the experiment showed that compared with the control group, there was no significant difference i...
Embodiment 3
[0049] clinical information
[0050] The clinical data selected 102 clinical patients from the gynecological outpatient department of the hospital, aged 45-60 years, and were randomly divided into two groups: the treatment group and the control group were 51 cases. Statistical processing, no significant difference (P> 0.05), comparable.
[0051] Inclusion criteria: (1) Meet the relevant criteria of endogenous depression in the diagnostic criteria for functional mental disorders research and depressive episodes in the revision of the Chinese Mental Illness Classification Scheme and Diagnostic Criteria (2nd Edition); (2) Hamilton Depression Scale (HAMD, 24 items) the total score of the first seven items is ≥18 points; (3) no various organ diseases, endocrine, nervous system diseases, and severe malnutrition, while excluding those who are pregnant, breast-feeding, and drug abusers; (4) at least 1 Have not taken hormone drugs, contraceptives, and nerve blockers within one month, ...
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