Method for establishing an HPLC (high performance liquid chromatography) fingerprint of rhizoma dioscoreae nipponicae, standard fingerprint of Dioscorea nipponica Makino and application of standard fingerprint
A high-performance liquid chromatography and standard fingerprint technology, which is applied in measuring devices, instruments, scientific instruments, etc., to achieve the effects of reliable stability, easy mastery and strong repeatability
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Embodiment 1
[0023] Example 1: Fingerprints of the same batch of Pangosia chinensis
[0024] 1. Test equipment: WATERS 2695 high performance liquid chromatograph; WATERS 2998PAD ultraviolet detector, including online vacuum degasser, high-pressure binary gradient pump, constant temperature autosampler, and column oven.
[0025] 2. Reagents: acetonitrile (chromatographically pure), ultrapure water.
[0026] 3. High performance liquid chromatography conditions: Chromatographic column: XBridge C18 (250mm×4.6mm, 5μm); flow rate is 1.0ml / min; injection volume is 10μl; detection wavelength is 208nm; column temperature is 30°C; mobile phase is acetonitrile (A)-Water (B), the method of gradient elution is 0~5min, 5%A; 5~15min, 5%~15%A; 15~55min, 15%~45%A; 55~65min, 45%~100%A; 65~80min, 100%A.
[0027] 4. Preparation of the test product solution: take the medicinal material of pangolinia, crush it and pass it through a 50-100 mesh sieve, accurately weigh 1g of the sieved pangolin powder, put it i...
Embodiment 2
[0045] Example 2: Fingerprints of 11 batches of Pangosia chinensis from different origins
[0046] (1) Determination of standard fingerprints: Take 11 batches of Pangosia chinensis medicinal materials from different origins such as Jilin, Anhui, Hebei, Liaoning, etc., and perform high-performance liquid chromatography analysis according to the detection conditions of Example 1, and obtain the HPLC fingerprints of 11 batches of samples, Such as figure 2 shown. Through the analysis and comparison of the HPLC fingerprints of 11 batches of pangolins from different origins, the similarity evaluation was carried out, and a total of 21 common characteristic peaks were determined. The chromatographic peak No. For the control peak, calculate the relative retention time of other 20 common characteristic peaks, which are as follows: the relative retention time of peak No. 1 is 0.591, the relative retention time of peak No. 2 is 0.649, the relative retention time of peak No. The retent...
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