Unprocessed rehmannia root identification platform and method for identifying unprocessed rehmannia root by using the same
A technology for identifying platforms and rehmannia glutinosa, applied in instruments, measuring devices, scientific instruments, etc., can solve the problems of no multi-dimensional data conversion, unclear adaptability of different sources, no actual spectrum of compounds, etc., to achieve improved applicability Effect
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Embodiment 1
[0115] Example 1 Establishment of Chinese Medicine Chromatography-Mass Spectrometry High Dimensional Image Database
[0116] 1. Preparation of known traditional Chinese medicine samples
[0117] The preparation methods of traditional Chinese medicine samples include but not limited to solvent extraction, including methods applicable to the preparation of all traditional Chinese medicine samples. The known Chinese medicine samples in the database of the present invention use 547 varieties of reference medicinal materials from China Food and Drug Research Institute (see Table 1). Take 100 mg of each kind of control medicinal material powder, add 0.5 ml of methanol with a volume concentration of 50% respectively, ultrasonically extract for 10 min, and centrifuge at 15,000 rpm for 10 min to get the supernatant, add 0.5 ml of methanol with a volume concentration of 50% to extract the supernatant for 10 min, and add 0.5 ml of methanol with a volume concentration of 15,000 RPM high-...
Embodiment 2
[0137] Example 2: Rapid identification of Rehmannia glutinosa samples
[0138] 1. Preparation of unknown samples
[0139] The preparation method of the unknown sample of the present invention is the same as the preparation method of the known traditional Chinese medicine sample. In this embodiment, the decoction pieces of Rehmannia glutinosa from the market are used as the unknown sample, which is named SS2-6520-006-0007. Take 100 mg of each unknown sample powder, add 0.5 ml of methanol with a volume concentration of 50% respectively, ultrasonically extract for 10 minutes, and centrifuge at a high speed of 15,000 rpm for 10 minutes to take the supernatant, add 0.5 ml of methanol with a volume concentration of 50% for ultrasonic extraction for 10 minutes Minutes, 15000 rpm high-speed centrifugation for 10 minutes to take the supernatant. The two supernatant extracts were combined.
[0140] 2. Raw data acquisition and data processing of unknown sample chromatography-mass spec...
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