Method for determining ginsenoside in rat plasma
A technology of ginsenosides and blood plasma, which is applied in the detection field of ginsenosides, can solve the problems of high instrument cost, and achieve the effects of high sensitivity, good standard addition recovery and good repeatability
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Embodiment 1
[0025] Take 100 μL of rat plasma, put it in a 2 mL centrifuge tube, add 200 μL methanol, vortex for 1 min, and centrifuge. Take the supernatant, put it into another clean 2 mL centrifuge tube, add 500 μL of dichloromethane, vortex for 1 min, and centrifuge. The above two centrifugation conditions were 1000 g, 3 min. The Oasis HLB column was activated sequentially with methanol, water, and dichloromethane, and the extracted supernatant was added, eluted with 3 mL of methanol, and the eluate was collected. The eluent was taken, blown with nitrogen gas to near dryness, and the residue was redissolved in methanol.
[0026] The chromatographic conditions are as follows: DB-35 MS, 30 m×0.25 mm, 0.25 μm; heating program: initial temperature is 60°C, rising to 160°C at a rate of 50°C / min, and then rising to 220°C at a rate of 20°C; Sample port temperature 250°C; carrier gas: nitrogen, purity ≥99.999%; flow rate 1.2 mL / min; injection volume 1 μL; splitless injection.
[0027] The de...
Embodiment 2
[0030] standard curve drawing
[0031] Add different volumes of ginsenoside reference solution in the centrifuge tube, after drying in a water bath, add blank plasma to form plasma samples containing different concentrations of ginsenoside, analyze using the pretreatment-analysis method of Example 1, and obtain a chromatogram Figure, record the peak area, take the peak area as the ordinate, and the concentration as the abscissa, draw the standard curve. The regression curves of ginsenosides Ra1, Rb1, Rh1, Re and Ro are as follows: y=0.057x+0.027, y=0.007x+0.215, y=0.098x-0.125, y=0.105x-0.024, y=0.0127x+ 0.114.
[0032] Method recovery
[0033] In order to verify the recovery rate of the method, the sample recovery experiment was carried out at three levels of high, medium and low respectively. The added material was then extracted and quantified. Three repetitions were performed for each of the three levels of high, middle and low. The results showed that the recoveries ...
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