Method and application of identification of pharmacodynamic components of traditional Chinese medicine based on target component knockout
A technology with target components and efficacy, applied in the field of pharmaceutical technology and drug screening, it can solve the problems of high throughput and high precision, which are difficult to take into account the overall and systematic views of traditional Chinese medicine.
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Embodiment 1
[0040] 1. Preparation of Indigo Naturalis Extract Sample Powder
[0041] Accurately weigh six parts of Indigo Naturalis powder, 25 g each, and place them in a beaker. Measure 300 ml of N,N-dimethylformamide (DMF) and soak them for 30 minutes. The ultrasonic power is 700 W, the ultrasonic temperature is 50 °C, and the ultrasonic time is 60 minutes. , the ultrasonic extraction times were three times, collect the indigo naturalis extract, filter it, transfer it to a rotary evaporation bottle, and press the rotation speed of 140 r min. -1 , the heating temperature of the water bath is 65 ℃, and the cooling temperature is -4 ℃ to concentrate, and the indigo naturalis extract concentrate is placed in a vacuum oven to prepare powder.
[0042] The sample powder obtained from the experiment is about 2.2 g, and the calculated yield is about 1.47%.
[0043] 2. Preparation of knockout components of Qingdai extract
[0044] 1. Qualitative analysis by semi-preparative liquid chromatograph...
Embodiment 2
[0081] Preparation of Qingdai extract powder: ultrasonic extraction of chemical components in Qingdai, ultrasonic conditions: power 700 W, temperature 50 °C, time 60 min, times 3 times; the extract was concentrated, and the conditions were 140 r min. -1 , the heating temperature of the water bath is 65 °C, and the cooling temperature is -4 °C;
[0082] Preparation of knockout components of Qingdai extract: The target components indirubin, tryptamine and isorhamnetin were separated by semi-preparative liquid chromatography. Chromatographic conditions: Shim-pack GISS C18 column was used with a flow rate of 3 mL min -1 , the detection wavelength was 290 nm, and the sample volume was 4 mL; elution conditions: gradient elution was performed with 0.1% glacial acetic acid-methanol as the mobile phase. The elution procedure is shown in Table 1. like image 3 Indirubin, tryptamine, and isorhamnetin-free fractions (ABC-) were collected from 0.33 min to 57.5 min, 64.01 min to 75.0 min...
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