Oryzanol composition and preparation method thereof
A technology of oryzanol and its composition, which is applied in the field of medicine, can solve the problems of patient pain, poor compliance of muscle agglomeration, poor oral effect of oryzanol, and difficulty in controlling the particle size of emulsion, so as to prolong the time of drug effect, improve bioavailability and Therapeutic index, effect of enhancing bioavailability
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Embodiment 1
[0043] Oryzanol 10mg
[0044] Phosphatidylcholine 50mg
[0045] Ursodeoxycholic acid 50mg
[0046] Mannitol 50mg
[0047] Water for injection to 10ml
[0048] Oryzanol, phosphatidylcholine and ursodeoxycholic acid were dissolved in 2 ml of ethyl acetate, heated to 60°C and stirred until fully dissolved. The organic phase was obtained by distillation under reduced pressure. The water for injection in which mannitol has been dissolved is added to the full amount, and the injection solution of the present invention is obtained by fully stirring and mixing at 60°C. Adjust the pH to 7.0 with sodium hydroxide solution, add 0.05% activated carbon for injection and stir for 30 minutes, after decarburization and filtration, carry out fine filtration with 0.22um microporous membrane, and then pack it into vials.
Embodiment 2
[0050] Oryzanol 2mg
[0051] Soy Lecithin 800mg
[0052] Phosphatidylcholine 200mg
[0053] Taurocholic acid 200mg
[0054] Lactose 80mg
[0055] Water for injection to 10ml
[0056] Oryzanol, taurocholic acid, soybean lecithin, and phosphatidylcholine were dissolved in 5 ml of ethanol, heated to 80° C. and stirred until fully dissolved. The organic phase was obtained by distillation under reduced pressure. Add water for injection to the full amount, and then add lactose at 60° C. and stir and mix well to obtain the injection of the present invention. Adjust the pH to 7.0 with sodium hydroxide solution, add 0.05% activated carbon for injection and stir for 30 minutes, after decarburization and filtration, carry out fine filtration with 0.22um microporous membrane, and then pack it into vials.
Embodiment 3
[0058] Oryzanol 10mg
[0059] Soybean sphingomyelin 60mg
[0060] Sodium Glycodeoxycholate 100mg
[0061] Propylene Glycol 10mg
[0062] Glycine 20mg
[0063] Water for injection to 10ml
[0064] Oryzanol, soybean sphingomyelin, sodium glycodeoxycholate, and propylene glycol were dissolved in 7 ml of dichloromethane, heated to 80° C. and stirred until fully dissolved. The organic phase was obtained by distillation under reduced pressure. The water for injection in which the glycine has been dissolved is added to the full amount, and the injection solution of the present invention is obtained by fully stirring and mixing at 65°C. Adjust the pH to 7.5 with sodium hydroxide solution, add 0.05% activated carbon for injection and stir for 30 minutes, after decarburization and filtration, carry out fine filtration with 0.22um microporous membrane, and then pack into vials.
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