Medicinal composition for treating diabetes
The technology of a diabetes drug and composition, applied in the field of medicine, can solve the problems of low bioavailability, small molecular weight of ligands, large required dose, etc., and achieve the effects of promoting normal progress, lowering blood sugar level, and simple processing method
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Embodiment 1
[0025] (Example 1) The pharmaceutical composition of the present embodiment is made up of pharmaceutically active component and adjuvant, wherein the pharmaceutically active component is chromium chloride and adenosine triphosphate ATP, and the mol ratio of chromium chloride and ATP is 1: 1, and the pharmaceutical activity The weight ratio of the components in the composition is 1%-95% (33% in this embodiment). Excipients consist of water, lactose, corn starch, hydroxypropylmethylcellulose and magnesium stearate.
[0026]The dosage form of the pharmaceutical composition of the present embodiment is a tablet, and materials: 100 grams of the above-mentioned pharmaceutical active components (7.8 grams of chromium in it), 35 grams of water, 100 grams of lactose, 55 grams of cornstarch, hydroxypropyl methylcellulose 44 grams of vegetable matter, 1 gram of magnesium stearate; wherein, water acts as a wetting agent and a binding agent, lactose and cornstarch are diluents, and cornsta...
Embodiment 2
[0030] (Embodiment 2) The pharmaceutically active component in the pharmaceutical composition of the present embodiment is chromium chloride and adenosine triphosphate ATP, and the mol ratio of chromium chloride and ATP is 1: 2, and the weight of pharmaceutically active component is in composition The proportion is 1% to 95% (4.5% in this embodiment).
[0031] The dosage form of the pharmaceutical composition of this embodiment is an injection. In every 1 ml of injection, there are 9 mg of sodium chloride, a total of 45.5 mg of active pharmaceutical components (including 2 mg of chromium), and the vehicle is high-purity water for injection.
[0032] Specific embodiments of the present invention can transform some technical features of the above-mentioned embodiment 2 to obtain other embodiments. For example, the chromium in the above-mentioned pharmaceutical active ingredients can be replaced by other pharmacologically soluble chromium salts, such as chromium sulfate and chrom...
Embodiment 3
[0035] (Example 3) The pharmaceutical composition of the present example differs from Example 1 in that: the pharmaceutically active component is chromium sulfate and adenosine diphosphate, and the molar ratio of chromium sulfate and adenosine diphosphate is 1:3, The proportion of the weight of the active pharmaceutical component in the composition is 15%.
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