Method for detecting content of alpha-homonojirimycin in suregade glomerulata medicinal material
A technology of konojirimycin and a detection method is applied in the field of content detection of α-konojirimycin in white tree medicinal materials, and can solve the problems of high risk, insufficient resolution, cumbersome reaction procedures, etc. The effect of good system suitability
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Embodiment 1
[0059] A method for detecting the content of α-konojirimycin in Radix Radix Medicae, the specific operations are as follows:
[0060] (1) Preparation of reference substance solution: take 150 mg of α-konojirimycin reference substance, accurately weigh it, transfer it to a 50mL volumetric flask, add ethanol solution with a volume concentration of 60% to dissolve, and constant volume to obtain a stock solution. Dilute to a concentration of 3 μg / mL, and filter through a 0.22 μm organic filter membrane to obtain the reference substance solution;
[0061] (2) Preparation of the test solution: take 1.0 g of the white tree medicinal material powder to be tested (passed through a No. 4 sieve), accurately weigh it, place it in a stoppered conical flask, and accurately transfer it into 100 mL of ethanol solution with a volume concentration of 60%. Ultrasonic extraction at 50°C for 50 minutes, let it cool, supplement the lost weight with ethanol solution with a volume concentration of 60...
Embodiment 2
[0075] A method for detecting the content of α-takanojirimycin in the Radix Gelvinia medicinal material, the specific operation is the same as that in Example 1, the difference is that in step (2): the extraction solvent is ultrapure water, and Gelbelina is added before the ultrasonic extraction The mass volume ratio of medicinal material powder to extraction solvent is 0.5:100g / mL, and the ultrasonic extraction condition is ultrasonic extraction at 40°C for 50min; in liquid chromatography conditions, column temperature: 20°C.
Embodiment 3
[0077] A method for detecting the content of α-konojirimycin in Radix Radix Medicinae, the specific operation is the same as in Example 1, the difference is that in step (2): the extraction solvent is an ethanol solution with a volume concentration of 20%, and ultrasonic extraction The conditions are ultrasonic extraction at 60°C for 50min; in liquid chromatography conditions, flow rate: 0.5mL / min, column temperature: 50°C.
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