Cortex albiziae recognition platform and cortex albiziae recognition method using same
A recognition platform and technology of Albizia Julibrissin, applied in character and pattern recognition, drugs or prescriptions, instruments, etc., can solve the problems of no multi-dimensional data conversion, no actual spectrum of compounds, and unclear adaptability of different sources, etc., to achieve The effect of applicability improvement
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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 then add 0.5 ml of methanol with a volume concentration of 15,000 RPM ...
Embodiment 2
[0137] Embodiment 2: the rapid identification of the skin sample of Albizia juliensis
[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, 3 batches of Albizia juliensis skins from the market are used as unknown samples, named respectively as SS2-6520-007-0001 (SS2-LTQ-007-0001 is a different collection instrument for the same sample), SS2-6520-225004-03, SS2-6520-225142-03. Take 100mg of each unknown sample powder, add 0.5ml of methanol with a volume concentration of 50% respectively, ultrasonically extract for 10min, centrifuge at 15000 rpm for 10min to get the supernatant, add 0.5ml of methanol with a volume concentration of 50% for 10min, and extract the filter residue for 10min, 15000 RPM high-speed centrifugation for 10 min to take the supernatant. The two supernatant extracts were combined.
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