Radix paeoniae rubrathe liver-protecting active component, and preparation method and purpose thereof
A technology of red peony root and effective components is applied in the application field of preparing liver-protecting drugs, can solve the problems of unclear liver-protecting effect and the like, and achieve the effects of good pharmacological activity and simple separation process
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Embodiment 1
[0014] Example 1 Preparation of effective components of Radix Paeoniae Rubra
[0015] After crushing 200 g of Radix Paeoniae Rubra, add 1 L of ethyl acetate, heat and reflux for extraction for 2 hours to obtain an extract, and concentrate the extract to dryness under reduced pressure to obtain 3.2 g of extract. Mix the extract with 50g of forward silica gel, separate it with a normal phase silica gel column (column height 15cm, diameter 4.65cm), and use petroleum ether (60-90°C) and chloroform with a volume ratio of 3:1 As mobile phase elution, the eluate of the first 3 column volumes was discarded, and the eluate of the fourth column volume was collected, concentrated under reduced pressure, and vacuum-dried to obtain 0.5 g of the effective component.
Embodiment 2
[0016] Example 2 Preparation of effective components of Radix Paeoniae Rubra
[0017] After crushing 500g of Radix Paeoniae Rubra, add 3L of absolute ethanol, heat and reflux for extraction for 2 hours to obtain an extract, and concentrate the extract to dryness under reduced pressure to obtain 70.2g of extract. Mix the extract with 250 g of forward silica gel, separate it with a normal phase silica gel column (column height 50 cm, diameter 7 cm), and use a volume ratio of 1:1 cyclohexane and ethyl acetate as the mobile phase for elution , remove the eluate of the first 3 column volumes, collect the eluate of the 4th column volume, concentrate it under reduced pressure, and vacuum dry to obtain 1.3 g of effective components.
Embodiment 3
[0018] The preparation of embodiment three Radix Paeoniae Rubra effective components
[0019] Take 250 g of Radix Paeoniae Rubra, crush it, add 1.5 L of ethyl acetate and ethanol solution with a volume ratio of 1:1, heat and reflux for 1 hour, extract twice, and combine the filtrates to obtain the extract. The extract was concentrated to dryness under reduced pressure to obtain 23.2 g of extract. Mix the extract and 100 g of silica gel, separate it with a normal-phase silica gel column (column height 25 cm, diameter 4.65 cm), use petroleum ether and ethyl acetate (volume ratio: 50:1) as mobile phase elution, discard The eluate of 3 column volumes was collected, and the eluate of the 4th column volume was collected, concentrated under reduced pressure, and vacuum-dried to obtain 0.7 g of the effective component.
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