New process for preparing cinnamon, Radix aconiti lateralis preparata and rehmannia root preparation
A technology of Guifu Rehmanniae and a new process is applied in the field of preparation of Guifu Rehmannia glutinosa preparations, which can solve the problems of capsule floating and difficulty in swallowing, and achieve the effect of improving the quality standard of finished products and ensuring product quality.
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Embodiment 1
[0030] The preparation of main medicine:
[0031] Preparation Process:
[0032] Raw material (unit: gram):
[0033] Cinnamon 155.54 Aconite (made) 155.54 Rehmannia glutinosa 1244.39 Wine cornus 622.16
[0034] Cortex Moutan 466.62 Yam 622.16 Poria 466.62 Alisma 466.62
[0035] operate:
[0036] Take 466.62g of Moutan cortex, add 15 times of water and 0.05 times of sodium chloride, soak for 24 hours, carry out steam distillation, collect 8 to 9 times of the distillate within 3 hours, put it in the refrigerator for 24 hours, and precipitate crystals , filtered, washed with cold water, dried at a low temperature below 40°C or with a cold air blower to obtain crystallization (I), and its medicinal residue (I) for subsequent use;
[0037] Get medicine dregs (I), wine cornus 622.16g, Rehmannia glutinosa 1244.39g, Alisma 466.62g, cinnamon 155.54g, aconite (made) 155.54g, add 5 times the amount of 80% ethanol to reflux and extract 3 times, each extraction 1.5 hours, the extracts ar...
Embodiment 2
[0042] The preparation of main medicine:
[0043] Preparation Process:
[0044] Raw material is with implementation example 1
[0045] Operation: Obtain crystallization (I) with embodiment 1, dissolve crystallization (I) in 95% ethanol for inclusion, inclusion material is β-cyclodextrin, dissolve 7 times of β-cyclodextrin in 9 times of purified water Carry out clathrate, complete clathrate, evaporate to dryness under reduced pressure, obtain dry substance, following operation is the same as embodiment 1, obtain dry substance, merge with above-mentioned dry substance, pulverize, sieve, mix and obtain final product;
Embodiment 3
[0046] Implementation example 3: drop pill preparation
[0047] Principal ingredient: prepared by implementation example 2
[0048] Preparation process operation:
[0049] Melt and mix the main drug and the base polyethylene glycol 4000 in a 1:1.5 ratio in a water bath at 85°C, and drop the mixture into the pre-cooled simethicone oil with a viscosity of 200 using a dropping pill machine, and the temperature of the coolant is 10 ~15℃, oil bath temperature 85~95℃, liquid medicine temperature 85℃, nozzle temperature 15~20℃, tube temperature 10~15℃, dripper air pressure 0.4MPa, dropper air pressure 0.02MPa, interval time 30 seconds , The dripping time is 0.03 seconds, the drop distance is 2-3cm, and the distance between 2 dripping pills is 3-5cm. Each pill weighs 200mg, 6 pills each time, 2 times a day.
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