Luteolin chewable tablet and preparation method thereof
A technology of luteolin and chewable tablets, which is applied in the direction of pharmaceutical formulas, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc., which can solve the problems of low drug bioavailability, poor water solubility and stability of luteolin Low-level problems, to achieve the effect of reducing mental burden, good bioavailability, and good taste
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Embodiment 5
[0062] Example 5 Preparation of luteolin chewable tablet of the present invention
[0063] Preparation of luteolin solid dispersion: accurately weigh a certain mass of luteolin in a small beaker, add a small amount of ethanol and heat appropriately to dissolve luteolin. Accurately weigh a certain mass of PEG4000, place it in an electric heating mantle and heat it until it melts, quickly pour the luteolin solution into the PEG4000 melt, wash the small beaker containing the luteolin solution several times with a small amount of ethanol, and pour it into the PEG4000 melt. in the oil bath at a constant temperature of 55°C and stirring for about 30 minutes to fully disperse the drug in the carrier, volatilize most of the ethanol, and place it on an ice-salt bath immediately. Freeze it in a -80°C refrigerator for 24 hours, take it out, dry it in a 40°C drying box for 24 hours, remove the residual solvent, and pulverize to obtain a yellowish powder, which is dried and stored for late...
Embodiment 6
[0065] Example 6 Preparation of luteolin chewable tablet of the present invention
[0066] The same method as Example 5, but the formula ratio is adjusted to luteolin solid dispersion (weight ratio of luteolin and PEG4000 is 1:2) 30g, mannitol 150g, xylitol 150g, vitamin C 10g, orange essence 1mL. Preparation of Luteolin Chewable Tablets
[0067] 30g of solid dispersions in Table 1 were respectively used, and the remaining auxiliary materials were: 150g of mannitol, 150g of xylitol, 10g of vitamin C, and 1mL of orange essence. Chewable tablets were made according to the method of Example 5, and the dissolution rate of each chewable tablet was measured respectively. The measurement results showed:
[0068] The performance of the chewable tablet made of luteolin and PEG4000 is better than that of other chewable tablets, especially the comprehensive performance (dissolution and stability) of the chewable tablet of luteolin and PEG4000 when the weight ratio of luteolin and PEG400...
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