A detection method for simultaneous determination of multiple active components in lung-clearing medicines
A determination method and technology for active ingredients, applied in the field of medicine, can solve the problems of single, inability to monitor the quality of prescriptions, and the detection of active ingredients is cumbersome, and achieve the effect of high precision and wide range of use.
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Embodiment 1
[0050] Example 1: Establish a method for determining the content of chlorogenic acid, caffeic acid, p-coumaric acid, scutellarin, rosmarinic acid, and apigenin (active components are chlorogenic acid, caffeic acid, p-coumaric acid, scutellarin fingerprints of glycosides, rosmarinic acid and apigenin)
[0051] 1.1 Preparation of reference stock solution
[0052] Precisely weighed chlorogenic acid and caffeic acid reference substances were 4.37 mg and 5.90 mg, respectively, and placed them in a 5ml volumetric flask. 5.71, 4.67, and 2.38 mg, respectively, were placed in 10 ml measuring bottles, dissolved in methanol and diluted to the mark, and shaken to obtain the concentrations of 0.874 mg / ml, 1.18 mg / ml, 0.626 mg / ml, and 0.571 mg / ml, respectively. , 0.467mg / ml, 0.238mg / ml of chlorogenic acid, caffeic acid, coumaric acid, scutellarin, rosmarinic acid, apigenin reference stock solution. Store in a refrigerator at 4°C for later use.
[0053] 1.2 Preparation of the test solutio...
Embodiment 2
[0091] Embodiment 2. Fritillin A, Fritillin B content assay method
[0092] Chromatographic conditions: Column: Kromasil C18, mobile phase: acetonitrile-water-diethylamine (70:30:0.03), flow rate: 0.7ml / min, column temperature: 30℃, evaporative light detector, drift tube temperature: 45 ℃, nitrogen flow rate 1.5L / min. Two-point determination method of external standard: Precisely draw 10 μl and 20 μl of the reference solution and 10 μl of the test solution, respectively, and inject them into the liquid chromatograph for determination. The contents of fritillin A and fritillin B were calculated by logarithmic equation. Preparation of the test solution: Rotary evaporation of the test solution in 1.2 at 80°C to 90ml to obtain a concentrated medicinal solution containing 2.5g crude drug per ml, accurately draw 10ml of the concentrated medicinal solution, place it in a flask, and add 0.8 of the concentrated ammonia test solution. ml soaked for 1.5 hours, accurately added 40ml of ...
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