Sodium valproate compound preparation and use thereof
A technology of sodium valproate and compound preparations, which is applied in the direction of pharmaceutical formulas, medical preparations of non-active ingredients, active ingredients of anhydride/acid/halide, etc., to achieve enhanced therapeutic effect, fast absorption, and prevention of liver function damage
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Embodiment 1
[0029] The preparation of embodiment 1 test medicine
[0030] The present invention will be further described below in conjunction with specific experimental groups, but it should not be understood that the scope of the above subject of the present invention is limited to the following experimental groups. All technologies realized based on the above contents of the present invention belong to the scope of the present invention. The excipients in the following experimental groups can be replaced, reduced or increased with pharmaceutically acceptable similar excipients.
[0031] Experimental group 1
[0032]
[0033] Preparation Process:
[0034] (1) Take purified water accounting for 40% of the total amount, slowly add hydroxyethyl cellulose, stir until it swells completely, and obtain solution A.
[0035] (2) Take 20% of the total amount of purified water to dissolve sodium valproate, preservatives, correctives, fragrances and coloring agents to obtain solution B.
[0...
Embodiment 2
[0053] Embodiment 2 active investigation
[0054] 1. Purpose of the test
[0055] Through the test, the degree of control of epileptic seizures, learning and memory functions and changes in liver tissue cells were observed in rats after using the medicine of the present invention and the medicine of the control group respectively.
[0056] 2. Test materials
[0057] 1. Test drug: the drug of the present invention, sodium valproate oral solution (registration number H20041435), polyene phosphatidylcholine capsules (registration number H20059010).
[0058] 2. Animals: healthy male SD rats with a body weight of 235-268 g.
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