HPLC fingerprint spectrum detection method for Tibetan codonopsis pilosula
A technology of fingerprints and detection methods, which is applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problem of chemical identification method research on the distinction between Tibetan Codonopsis pilosula and Tibetan Codonopsis pilosula, and the distinction between gray-haired Codonopsis pilosula and veined Codonopsis pilosula in Tibetan Codonopsis pilosula And other issues
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Embodiment 1
[0037] Example 1 Fingerprint detection of Codonopsis pilosula of the present invention
[0038] 1) Preparation of reference solution
[0039] Take chlorogenic acid, luteolin, luteolin and apigenin reference substances, weigh them accurately, add 50% ethanol to make a mixed reference solution with a mass concentration of each component of 0.1 mg / mL.
[0040] 2) Preparation of the test solution
[0041] Weigh 1 g of the aerial part of Codonopsis pilosula (passed through a No. 4 sieve), weigh it accurately, put it in a stoppered Erlenmeyer flask, add 25 mL of 50% ethanol accurately, weigh it, and ultrasonically treat it (power 100W, frequency 45kHz) for 45min , then weigh the mass, make up the lost mass with 50% ethanol, shake well, filter, and take the filtrate to obtain the final product.
[0042] 3) Accurately draw 10 μl each of the reference substance solution and the test solution, inject them into the liquid chromatograph, and record the chromatograms. The chromatographi...
Embodiment 2
[0046] Embodiment 2 Fingerprint detection of Codonopsis pilosula of the present invention
[0047] 1) Preparation of reference solution
[0048] Take chlorogenic acid, luteolin, luteolin and apigenin reference substances, weigh them accurately, add 50% ethanol to make a mixed reference solution with a mass concentration of each component of 0.2 mg / mL.
[0049] 2) Preparation of the test solution
[0050] Weigh 2 g of the medicinal material powder of Codonopsis pilosula (through No. 4 sieve), accurately weigh it, put it in a stoppered Erlenmeyer flask, accurately add 80 mL of 50% ethanol, weigh it, and ultrasonically treat it (power 100W, frequency 45kHz) for 45min , then weigh the mass, make up the lost mass with 50% ethanol, shake well, filter, and take the filtrate to obtain the final product.
[0051] 3) Accurately draw 10 μl each of the reference substance solution and the test solution, inject them into the liquid chromatograph, and record the chromatograms. The chroma...
experiment example 1
[0057] 1 material
[0058] 1.1 Instrument
[0059] UItiMate3000 high performance liquid chromatograph (Thermo Fisher Scientific China Co., Ltd.); BP121S 1 / 100,000 electronic analytical balance (company); Milli-Q ultrapure water machine; KQ-500VDE dual-frequency numerical control ultrasonic cleaner (Kunshan City Ultrasonic Instrument Co., Ltd.); DZKW-4 electronic constant temperature water bath (Beijing Zhongxing Weiye Instrument Co., Ltd.).
[0060] 1.2 Reagent
[0061] Reference substances chlorogenic acid (batch number MUST-21030304), luteolin (batch number MUST-20062810), luteolin (batch number MUST-20102418), apigenin (batch number MUST-21030615) were purchased from Chengdu Master Biotechnology Co., Ltd. company, the mass fraction is greater than 98%; acetonitrile is chromatographically pure; water is ultrapure water; others are analytically pure.
[0062] 18 batches of gray and hairy Codonopsis, 17 batches of Maihua Codonopsis, 2 batches of Codonopsis pilosula, 1 batch...
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