Buddleja officinalis extract, and preparation method and application thereof
A technology of dense Mongolian flowers and extracts, applied in the field of medicine, can solve problems such as unresearched, complex chemical composition, and inability to know
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preparation Embodiment 1
[0094] Preparation Example 1: Extraction of active ingredients in Budisma japonica by water extraction and alcohol extraction
[0095] Weigh 100g of Mimenghua traditional Chinese medicine decoction pieces, add 1000ml of 95% ethanol, infiltrate for 0.5h, heat and reflux at 80°C for 1h, filter and collect the filtrate; add 1000ml of 95% ethanol to the filter residue, heat and reflux for 1h at 80°C, filter and combine twice The filtrate was concentrated under reduced pressure using a rotary evaporator to obtain a 95% extract concentrate of Budhimonica japonica, which was freeze-dried (19.6 g), and coded as MMH-95.
[0096] Add 1000ml of 50% ethanol to the filter residue after extraction with 95% ethanol, heat and reflux at 100°C for 1 hour, and collect the filtrate by filtration; Concentrate under pressure to obtain 50% Budisma japonica extract extract, and use a freeze dryer to freeze-dry to obtain a solid sample, numbered MMH-95-50 (11.3g).
[0097] Weigh 100g of Mimenghua tra...
preparation Embodiment 2
[0100] Preparation Example 2: Water Extraction-Solvent Extraction Separation of Active Components in Budisma Buddhisattva
[0101] Weigh 100g of Mimenghua traditional Chinese medicine decoction pieces, add 1000ml of distilled water, infiltrate for 0.5h, heat and reflux at 100°C for 1h, filter and collect the filtrate; Concentrate under reduced pressure with an evaporator to obtain 200ml of water-extracting concentrated solution of Budisma japonica, add 200ml of ethyl acetate solvent for extraction, let it stand until the layers are separated, collect the upper layer of ethyl acetate solution, perform the same extraction for 5 times, combine the ethyl acetate extract, and reduce Press and dry to obtain ethyl acetate extraction sample, number MMH-H 2 O-EA; add 200ml of n-butanol solvent to extract the remaining water layer, let it stand until the layers are separated, collect the n-butanol solution in the upper layer, perform the same extraction for 5 times, combine the n-butano...
preparation Embodiment 3
[0102] Preparation Example 3: Purification and Identification of Compounds I~V
[0103] Take by weighing the MMH-C-H obtained in Preparation Example 2 2 O sample 5g is added appropriate amount of distilled water heating ultrasonic dissolving, adopt macroporous resin (D101) to carry out column chromatography separation (500 * 60mm), first adopt distilled water 1000ml to wash, adopt 20% ethanol 1000ml to wash subsequently and collect eluate, this washing The deliquored liquid contains main characteristic peaks through HPLC analysis, and the purity is above 70%. It is concentrated and combined to obtain a sample eluted with 20% ethanol. The sample was purified again with ODS chromatography packing, eluted with distilled water and 10% methanol successively, concentrated and combined with 10% methanol eluate, and analyzed by HPLC, the purity was 94.14%. It was concentrated and dried under reduced pressure to obtain 86.2 mg of brown yellow solid powder, coded as Compound Ⅰ, which w...
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