A kind of pharmaceutical composition for preventing and treating neonatal jaundice, preparation method and application
A technology for neonatal jaundice and composition, applied in the field of pharmaceutical composition and preparation for preventing and treating neonatal jaundice, and the field of pharmaceutical composition for preventing and treating neonatal jaundice, which can solve the problem of lack of neonatal drug safety data and clinical experiment data, and potential safety hazards To achieve the effects of clear pharmacology, accelerated self-healing, and small side effects
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Embodiment 1
[0034] Example 1 Preparation of freeze-dried oral powder
[0035] Weigh 0.25g of geniposide, 4.0g of baicalin, 0.01g of p-hydroxyacetophenone, and 0.35g of chlorogenic acid, dissolve them in 800ml of purified water, adjust the pH value to 7.0 with 10% NaOH, add purified water to 1000ml, and filter , Packed into vials, 1ml per bottle. Move the vials to a vacuum freeze dryer for freeze drying. The temperature drops to -40°C within 1 hour, after 2 hours of heat preservation, the vacuum pump is turned on, the vacuum degree is maintained at 300 Pa, and the temperature is gradually raised to -5°C within 10 hours, the vacuum degree is reduced to 10 Pa, and the temperature is raised to +35°C after maintaining for 2 hours. After maintaining for 3 hours, the vacuum degree does not change, and then it is out of the box, capped, inspected, and packaged. Product moisture is not more than 1%.
Embodiment 2
[0036] Example 2 Preparation of freeze-dried oral powder
[0037] Weigh 0.25g of pregeniposide, 1.7g of baicalin, 0.005g of p-hydroxyacetophenone, and 0.13g of chlorogenic acid, dissolve them in 800ml of purified water, adjust the pH value to 7.0 with 10% NaOH, and then add purified water to 1000ml. Filter and distribute to vials, 1ml per bottle. Move the vials to a vacuum freeze dryer for freeze drying. The temperature drops to -40°C within 1 hour, after 2 hours of heat preservation, the vacuum pump is turned on, the vacuum degree is maintained at 300 Pa, and the temperature is gradually raised to -5°C within 10 hours, the vacuum degree is reduced to 10 Pa, and the temperature is raised to +35°C after maintaining for 2 hours. After maintaining for 3 hours, the vacuum degree does not change, and then it is out of the box, capped, inspected, and packaged. Product moisture is not more than 1%.
Embodiment 3
[0038] Example 3 Preparation of freeze-dried oral powder
[0039] Weigh 0.7g of geniposide, 8.0g of baicalin, 0.02g of p-hydroxyacetophenone, and 0.7g of chlorogenic acid, dissolve them in 800ml of purified water, adjust the pH value to 7.0 with 10% NaOH, add purified water to 1000ml, and filter , Packed into vials, 1ml per bottle. Move the vials to a vacuum freeze dryer for freeze drying. The temperature drops to -40°C within 1 hour, after 2 hours of heat preservation, the vacuum pump is turned on, the vacuum degree is maintained at 300 Pa, and the temperature is gradually raised to -5°C within 10 hours, the vacuum degree is reduced to 10 Pa, and the temperature is raised to +35°C after maintaining for 2 hours. After maintaining for 3 hours, the vacuum degree does not change, and then it is out of the box, capped, inspected, and packaged. Product moisture is not more than 1%.
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