Preparation method and application of total saponins from flos hosta ventricosa
A technology of total saponins and purple hosta, which is applied in the field of medicine, can solve the problems of low purity and low yield of saponins, and achieve the effect of simple process, simple method and accelerated fracture
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specific Embodiment approach 1
[0018] Specific embodiment one: the preparation method of the total saponins of Jaspa japonica in this embodiment is carried out according to the following steps:
[0019] Step 1. Take fresh Japa japonica, wash it and put it in a refiner, add ethanol with a volume fraction greater than or equal to 85% according to the mass ratio of Japa jasmine and ethanol at a ratio of 1:10 to 15, and heat up to 50°C for grinding 10min-15min, then filter or centrifuge, extract 3 times, combine the ethanol extracts, concentrate to obtain the extract. The extract is dispersed into a real solution with hot water, and then extracted with 1 to 3 times of water-saturated n-butanol for 5 to 8 times, combined with the n-butanol extract, and concentrated to obtain the n-butanol extract.
[0020] Step 2. Pretreat the AB8 macroporous resin, and then load it into a resin column. The n-butanol extract obtained in step 1 is dispersed into a true solution with hot water and loaded on the sample. First, it i...
specific Embodiment approach 2
[0034] Embodiment 2: This embodiment differs from Embodiment 1 in that: the AB8 macroporous resin described in step 2 is replaced with HPD826 macroporous resin. Other steps and parameters are the same as in the first embodiment.
specific Embodiment approach 3
[0035] Embodiment 3: This embodiment differs from Embodiment 1 in that: the AB8 macroporous resin described in step 2 is replaced with D101 macroporous resin. Other steps and parameters are the same as in the first embodiment.
[0036] Adopt following experiment verification invention effect
[0037] Weigh each 15g of pretreated macroporous adsorption resins of AB-8, D101, HPD100, H103, HPD826, and NKA-96 types, put them in a 100mL beaker, and add 40mL of total saponins solution (total saponins content of 6.26mg / mL), put it in a shaker and vibrate for 8 hours, then filter with suction, collect the filtrate, and measure the quality of saponin in the filtrate with ultraviolet light, which is M residue. Then put the resin into a chromatographic column (with an inner diameter of 1.5cm and a height of 20cm), with a diameter-to-height ratio of 1:9, and remove impurities with 3BV distilled water at a flow rate of 2-3BV / h, collect the water, and measure the saponin quality, which is ...
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