Extracts of panaxtriol saponins and preparation process thereof
A technology of notoginseng saponin and notoginseng triol group, which is applied in the field of extract notoginseng triol saponin extract of traditional Chinese medicine notoginseng and its preparation field, which can solve the problems of poor separation effect and achieve the reduction of hepatic microcirculation disturbance, The preparation method has the advantages of simple process and convenient operation
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Embodiment 1 10
[0062] The preparation of embodiment 1 notoginseng triol group saponins
[0063] Take notoginseng, crush it into coarse particles, add 6 times the amount of 70% ethanol to reflux and extract twice, the first time is 2.5 hours, and the second time is 2 hours to combine the extracts, and the extracts are concentrated under reduced pressure below 70°C to 1.5 times the medicinal materials , centrifuged at 4200r / min for 20min, the supernatant was loaded with D941 resin (resin and medicinal material 0.5~1:1g / g) at a flow rate of 0.8BV / h, 10 times the column volume, with a flow rate of 1BV / h, washed with water; liquid and water wash. Concentrate to dryness under reduced pressure, dissolve the dry paste with mobile phase, and use a particle size of 30-60 μmC 18 Reversed-phase silica gel packing column, for separation, sample and separation with C 18 Reverse phase silica gel ratio 1:200, wash with acetonitrile and water (23:77), thin layer chromatography (thin layer conditions: chlor...
Embodiment 3
[0077] Take notoginseng, crush it into coarse particles, add 6 times the amount of 70% ethanol to reflux and extract twice, the first time is 2.5 hours, and the second time is 2 hours to combine the extracts, and the extracts are concentrated under reduced pressure below 70°C to 1.5 times the medicinal materials , 300 mesh filter cloth, supernatant D941 resin (resin and medicinal materials 0.5 ~ 1: 1g / g) sample flow rate is 1BV / h, 8 times the column volume, flow rate 1.5BV / h, washed with water; liquid and water wash. Concentrate to dryness under reduced pressure, dissolve the dry paste with mobile phase, and use a particle size of 30-60 μmC 18 Reversed-phase silica gel packing column, for separation, sample and separation with C 18 The ratio of reversed-phase silica gel was 1:100, washed with acetonitrile and water (25:75), and the elution endpoint was judged by peak collection with an online ultraviolet detector. Collect according to the peak, and recover the organic solven...
Embodiment 4
[0079] The extraction steps are as follows:
[0080] a. take Radix Notoginseng, and crush it into coarse particles;
[0081] b. Add 4 times the amount of 45% ethanol to decoct twice, each time for 1 hour;
[0082] c. Combine the decoctions and concentrate under reduced pressure below 70°C to 1.5 times the volume of the medicinal materials;
[0083] d. Stand still to room temperature, centrifuge at 3500rpm for 20min, and separate the supernatant;
[0084] e. Put D941 resin on the supernatant, resin and medicinal material 0.5:1g / g, sample loading flow rate is 0.5BV / h, 5 times column volume, flow rate 1BV / h, wash with water; collect sample loading effluent and water washing solution.
[0085] f. Concentrate the sample loading effluent and washing solution under reduced pressure to dryness below 70°C;
[0086] g. The above dry paste is dissolved in the mobile phase and then applied to C 18 Reverse Phase Silica Column, C 18 Reverse filler particle size 30μm;
[0087] h. Eluti...
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