Quality standard and test method of hoove pill and detection method
A technology of preparation and standard curve, which is applied in the field of quality standards and testing of Fuzheng Pills and its preparations, can solve the problems of no content determination indicators, few detection indicators, poor specificity, etc.
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Embodiment 1
[0076] Embodiment 1: the identification method and content determination method of pharmaceutical composition pill of the present invention
[0077] Identification: A. Get 8g of pharmaceutical composition pills of the present invention, grind finely, add methanol 70ml, sonicate for 20 minutes, filter, evaporate the filtrate to dryness, add water 35ml to dissolve the residue, extract three times with n-butanol, each time the solvent is 15ml, and combine the extracts , evaporated to dryness, the residue was dissolved in 1ml of methanol, and used as the test solution; another 7 g of Kansui control medicinal material was added, 35 ml of methanol was added, ultrasonic treatment was performed for 50 minutes, filtered, the filtrate was evaporated to dryness, and the residue was dissolved in 1 ml of methanol, as a control Medicinal material solution; according to the Chinese Pharmacopoeia 2005 edition one appendix VIB thin-layer chromatography test, absorb 0.006ml of the test product ...
Embodiment 2
[0084] Embodiment 2: the identification method and assay method of pharmaceutical composition tablet of the present invention
[0085]A. Take 20g of the tablet of the pharmaceutical composition of the present invention, grind it finely, add 60ml of ethyl acetate, extract under heat reflux for 40 minutes, filter, evaporate the filtrate to dryness, add 30ml of water to the residue to dissolve, extract three times with ethyl acetate, each solvent is 20ml , combine the extracts, evaporate to dryness, add 1ml of ethanol to the residue to dissolve, and use it as the test solution; take 3g of Gansui reference medicinal material, add 40ml of ethyl acetate, extract under reflux for 40 minutes, filter, evaporate the filtrate to dryness, add Dissolve 1ml of ethyl acetate as the reference medicinal material solution; according to the Chinese Pharmacopoeia 2005 edition, appendix VIB thin-layer chromatography test, absorb 0.01ml of the test solution and 0.005ml of the reference medicinal so...
Embodiment 3
[0091] Embodiment 3: the identification method of pharmaceutical composition oral liquid preparation of the present invention:
[0092] Take 25ml of the oral liquid preparation of the pharmaceutical composition of the present invention, add 50ml of petroleum ether with a boiling range of 60 to 90°C, extract by cold soaking for 40 minutes, filter, evaporate the filtrate to dryness, add 1ml of n-butanol to the residue to dissolve, and use it as the test solution Take another 3 g of Muxiang reference medicinal material, add 10 ml of methanol, soak in cold for 40 minutes, filter, evaporate the filtrate to dryness, add 1 ml of ethanol to the medicinal residue to dissolve, and use it as the reference medicinal material solution; Method test, draw 0.01ml of each of the above two solutions, point them on the same silica gel G thin-layer plate, use cyclohexane: acetone = 9:2 solution as developing agent, develop, take out, dry in the air, spray with 10% Sulfuric acid ethanol solution u...
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