Detection method of nafil medicines and detection kit
A detection method and drug technology, which are used in material analysis by observing the influence of chemical indicators, and analysis by chemical reaction of materials, etc., can solve the problem of chromatographic columns being easily contaminated, high analysis costs, and expensive instruments. problems, to achieve the effect of strong anti-interference ability of coexisting substances, obvious experimental phenomena, and reduced analysis costs
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Embodiment 1
[0033] Example 1 Detection of Libu Jinqiu Capsules (capsules, the marked dosage is 2 capsules each time, and the results of HPLC determination of this product contain 58mg of nafil drug)
[0034] Take 0.5 grains of the contents, grind them evenly, put them in a 50mL beaker, add 25mL of 0.05mol / L dilute hydrochloric acid, mix well, shake for two minutes, let stand for four minutes, filter, and collect the filtrate. Transfer the filtrate to a 125mL separatory funnel, add 5mL chloroform, shake for two minutes, and let stand for one minute. The extract was transferred to a 50mL beaker, the aqueous phase was continuously extracted with 5mL chloroform, and the extracts were combined. Add 3mL sodium acetate-acetic acid buffer solution with pH=2.0 and 2.5mL bromocresol green color developer to the extract, and the solution will immediately turn yellow, so it can be judged that the sample contains nafils.
Embodiment 2
[0035] Example 2 Detection of Zangbianba pills (big honey pills, the specification is 10g per pill, and the indicated dosage is 1 pill per day, as determined by high performance liquid chromatography, each pill of this product contains 176mg of nafil drug)
[0036] Cut the sample into rice grain size, take a sample of 0.6g, put it in a 50mL beaker, add 25mL of 0.01mol / L dilute sulfuric acid, mix well, shake for two minutes (mashing with a glass rod if necessary), let stand for four minutes, and collect by filtration filtrate. Transfer the filtrate to a 125mL separatory funnel, add 5mL carbon tetrachloride, shake for two minutes, and let stand for one minute. The extract was transferred to a 50mL beaker, the aqueous phase was continuously extracted with 5mL carbon tetrachloride, and the extracts were combined. Add 3 mL of sodium citrate-hydrochloric acid buffer solution with pH=2.5 and 2.5 mL of bromocresol green color developer to the extract, and the solution will immediatel...
Embodiment 3
[0038] Example 3 Detection of Jiubian Pills (blue coated tablet, white tablet core; the indicated dosage is 1 tablet each time; the results of HPLC determination of this product contains 72 mg of nafil in each tablet)
[0039]Take 0.5 pieces of the sample, put it in a 50mL beaker, add 25mL of 0.1mol / L dilute phosphoric acid, smash it with a glass rod, mix well, shake for two minutes, let stand for four minutes, filter and collect the filtrate. Transfer the filtrate to a 125mL separatory funnel, add 5mL of dichloromethane, shake for two minutes, and let stand for one minute. The extract was transferred to a 50mL beaker, and the aqueous phase was continuously extracted with 5mL of dichloromethane, and the extracts were combined. Add 3 mL of glycine-hydrochloric acid buffer solution with pH=1.5 and 2.5 mL of bromocresol green color developer to the extract, and the solution will immediately turn yellow, so it can be judged that the sample contains nafils.
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