Pharmaceutical composition for reducing blood sugar and preparation method thereof
A composition and blood sugar-lowering technology, which can be applied in drug combinations, pharmaceutical formulas, plant raw materials, etc., and can solve problems that have not been reported in the literature
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Embodiment 1
[0024] Weigh 300g of dried ginseng, add 1 to 2 times the amount of 50% ethanol to soak for 1 hour, use ultrasonic extraction for 1 to 3 hours, filter and collect the filtrate; concentrate the filtrate with a rotary evaporator, collect the concentrate, let it cool, add 2-3 times the amount of water and stirred, let it stand at room temperature for 24 hours, precipitated, filtered or centrifuged to take the precipitate, heated the precipitate in a watch glass, removed ethanol and water, until there was no alcohol smell, and obtained the ginseng alcohol extract; The ginseng alcohol extract was subjected to 150 μm reversed-phase chromatography, and gradient elution was carried out with methanol / water (V / V, 0:10-10:0) as the mobile phase, and the collected separated components were detected by reversed-phase thin-layer chromatography. Separate components with the same composition were combined and concentrated to obtain ten separate components from F1 to F10. F2 (IC 50 =12.5μg / L) ...
Embodiment 2
[0027] Weigh 400g of dried ginseng, add 1 to 2 times the amount of 50% ethanol to soak for 1 hour, use ultrasonic extraction for 1 to 3 hours, filter and collect the filtrate; concentrate the filtrate with a rotary evaporator, collect the concentrate, let it cool, add 2-3 times the amount of water and stirred, let it stand at room temperature for 24 hours, precipitated, filtered or centrifuged to take the precipitate, heated the precipitate in a watch glass, removed ethanol and water, until there was no alcohol smell, and obtained the ginseng alcohol extract; The ginseng alcohol extract was subjected to 150 μm reversed-phase chromatography, and gradient elution was performed with methanol / water (V / V, 0:10-10:0) as the mobile phase, and the collected separated components were detected by reversed-phase thin-layer chromatography. Separate components with the same composition were combined and concentrated to obtain ten separate components from F1 to F10. F2 (IC 50 =12.5μg / L) an...
Embodiment 3
[0030] According to the conventional method of pharmacy, the dry powder prepared in Example 1 or 2 can be added with one or more pharmaceutically acceptable Carriers or excipients are mixed to prepare various conventional dosage forms suitable for gastrointestinal administration. For example, the dry powder prepared above is aseptically filled into capsules according to conventional methods to obtain the pharmaceutical composition of the present invention in the form of capsules. The pharmaceutical composition of the present invention may be formulated into tablets, capsules, pills, powders, suppositories and solutions and suspensions according to methods known in the pharmaceutical industry. Among them, capsules and tablets suitable for gastrointestinal administration are preferred. When preparing dosage forms suitable for oral administration, sucrose, lactose, galactose, corn starch, gelatin, microcrystalline cellulose, carboxymethyl cellulose, etc. can be used as carriers ...
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