A preparation method of Platycodon grandiflora secondary saponins capable of improving cell membrane permeability
A technology of permeability and cell membrane is applied in the field of preparation of secondary saponins from Platycodon grandiflorum, and can solve the problems that do not involve the preparation process and method of secondary saponins from Platycodon grandiflorum, the medicinal component of Platycodon grandiflorum saponins.
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Embodiment 1
[0029] Embodiment 1: Separation and preparation of Platycodon grandiflorum total saponins
[0030] Take 2.5 kg of Platycodon grandiflora decoction pieces (purchased from Xi'an Tianrui Biotechnology Co., Ltd., batch number TR-170810), add 25 liters of 10 times the amount of distilled water, and heat and reflux for extraction for 2 hours. Filtrate while hot, and concentrate the filtrate under reduced pressure to about 500 ml. After cooling, add absolute ethanol to 1500 ml to make the ethanol ratio reach 70%, mix well and let stand overnight. The supernatant was collected by filtration, concentrated under reduced pressure to obtain 210 grams of platycodon saponin crude extract. Take 200 grams of it and add 20 liters of distilled water to dissolve it, configure it into a 1% solution, and load it on AB-8 macroporous adsorption resin (diameter: 5.5 cm; column height: 30 cm), and use ethanol solutions of different concentrations (0 % → 30% → 70% → 100% ethanol) gradient elution, ea...
Embodiment 2
[0033] Embodiment 2: Analysis of Platycodon grandiflorum total saponins
[0034] Platycodon saponins are mainly pentacyclic triterpenoid saponins, which mainly include platycodon saponin and platycodon acid saponin. Adopt UPLC-Q / TOF to analyze the platycodon total saponins of embodiment 1 and find that it mainly contains 10 platycodon saponins (see figure 2 ). It is speculated that the secondary saponins platycodon saponin 682 and platycodon saponin 696 that enter the blood are derived from the in vivo metabolites of platycodon saponins and platycodon acid saponins, respectively.
[0035] UPLC-Q / TOF experimental conditions:
[0036] 1) Liquid chromatography conditions:
[0037] ColumnWaters ACQUITY BEH C18 chromatographic column (2.1×100mm, 1.7μm); flow rate 0.4ml / min; PDA detector, detection wavelength 210nm; sample injection volume: 5.0μl; column temperature 30℃; mobile phase: A is 0.1% formic acid- Aqueous solution, B is acetonitrile; binary gradient elution: 0~2 min...
Embodiment 3
[0044] Embodiment 3: the investigation of the hydrolysis condition of Platycodon grandiflora secondary saponin
[0045] Using platycodon saponin D (Shanghai Boka Chemical Technology Co., Ltd., batch number: J-013-161216) as the reaction substrate (1 mg / ml), the hydrolysis conditions were investigated in a water bath at 85°C. The effects of acid (pH=1) and alkali (pH=14) on the hydrolysis efficiency were discussed respectively. And by the HPLC method of Example 1, the formation of Platycodon grandiflora secondary saponins 682 and 696 was investigated. The result is as image 3 As shown, the yield of secondary saponin 682 by alkali hydrolysis is significantly better than the effect of acid hydrolysis, so it is determined to use the method of alkali hydrolysis to optimize the hydrolysis conditions in the next step.
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