Method for extracting total flavonoid extract from desmodium styracifolium and method for measuring content of effective components in desmodium styracifolium
A technology of Guangshencao and active ingredients, which is applied in the field of biomedicine and can solve problems that need to be improved
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Embodiment 1
[0042] Example 1 Instruments and reagents
[0043] WatersUPLCH-class ultra-performance liquid chromatograph; WatersACQUITYBEHC 18 (2.1mm×100mm, 1.7 microns); Shiseido CapellcoreC 18 (2.1mm×100mm, 2.7μm); Shimadzu Shim-packXR-ODSII (2.0mm×75mm, 2.2μm), CQ250 Ultrasonic Instrument (Shanghai Ultrasonic Instrument Factory); METTLER-Toronto XP205 Analytical Balance; Mettler - Toronto XS204 analytical balance; 9 controls are shown in Table 1 below.
[0044] Table 1 Reference substance information
[0045]
[0046]
[0047] All self-made reference substances were obtained from the liquid phase prepared by Waters, and phosphorus pentoxide was dried under reduced pressure for 12 hours before use; methanol was chromatographically pure, water was Millipore ultrapure water, and the rest of the reagents were of analytical grade.
Embodiment 2
[0048] Example 2 Sample
[0049] Ten different origins of Radix Radix are collected, respectively, to prepare 10 batches of total flavonoid extracts from Radix Radix. The information is shown in Table 2 below.
[0050] Table 2 Ten batches of total flavonoids extracts from Chlorella chinensis and their origins
[0051]
Embodiment 3
[0052] The investigation of embodiment 3 chromatographic conditions
[0053] 3.1 Selection of detection wavelength: Take appropriate amounts of the total flavonoids extract, Schifftanoside and the other eight self-made reference substances, dissolve them in 75% ethanol with ultrasonic waves, perform full-wavelength UV scanning at 210-400 nm, and conduct UV scanning at 270 nm and 270 nm. There is a maximum absorption at 330nm, but by comparing the chromatograms of the test product at these two wavelengths, it is found that the interference of impurities at 330nm is less, so 330nm is selected as the detection wavelength. UV scanning chromatogram see figure 1 , see the superimposed chromatograms of the test solution at 272nm and 330nm figure 2 .
[0054] of which in figure 1 Among them, 1 is the full-wavelength scanning chromatogram of DS-1, 2 is the full-wavelength scanning chromatogram of DS-3, 3 is the full-wavelength scanning chromatogram of DS-4, 4 is the full-wavelength...
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