Process for extracting rhynchophylline monomers from uncaria rhynchophylla
An extraction process, the technology of rhynchophylline, applied in the field of extraction process for extracting rhynchophylline monomer, can solve the problems of difficult repetition, complicated steps, cumbersome operation, etc., and achieve the effect of easy operation, simple preparation method and good repeatability
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Embodiment 1
[0042] Example 1 Preparation of crude extract of Uncaria medicinal materials
[0043] Take dried Uncaria with hooked stems and branches (Hunan Uncaria), pulverize with a pulverizer, pass through a 40-mesh sieve, weigh 1kg into a large beaker, add 5L of 80% ethanol aqueous solution, mix well, seal with plastic wrap and store in In the refrigerator at 4℃; after 12 hours, take out the cold soaking liquid of medicinal materials, ultrasonic for 30min at room temperature and frequency of 50kHz, and shake every 10min during this period to ensure that the solution and medicinal powder are fully effected; after the end of ultrasonic, let it stand for 10min, first with gauze The medicinal residues are filtered off, the filtrate is collected and then filtered through filter paper to obtain the preliminary extract, which is light brown in color; the preliminary extract is divided into 3 times in a rotary evaporator and evaporated to dryness under reduced pressure, each time the temperature is...
Embodiment 2
[0044] Example 2 The crude extract of Uncaria is separated by column chromatography
[0045] The eluent of column chromatography is acetone: petroleum ether: ammonia (1: 2: 0.2). After installing the atmospheric chromatography column (column specification: 5×100cm), add a small amount of eluent and fill a small amount of crude silica gel at the bottom. (80~100 mesh), about 3cm high, always keep the liquid level above the silica gel layer, settling naturally for 15 minutes, add the eluent at any time with a peristaltic pump; weigh 600g of fine silica gel (200~300 mesh) for column chromatography , Add 1500mL eluent, stir well and pour it into the column at one time, settling naturally for 6 hours, the flow rate at the lower end is about 500mL / h, the eluent flowing out is reused, and the silica gel layer is about 70cm high after the sedimentation, which is higher than the fine silica gel layer. Spread a layer of crude silica gel as the sample layer, about 2cm high, and continue to s...
Embodiment 3
[0046] Example 3 Purification and preparation of rhynchophylline monomer
[0047] Transfer 500 mL of the rhynchophylline fraction separated by column chromatography into a 1L separatory funnel, add 4 mL of 2% HCl, shake vigorously for 3 min, let stand for 15 min, collect the lower acid solution, add 2% HCl 4 mL again, repeat the extraction 3 times, and combine The acid solution was transferred to a 100mL separatory funnel; 2mL of chloroform was added to the acid solution and shaken well for 3 minutes to extract impurities and organic phase in the acid solution. After standing for 30 minutes, the lower organic phase was removed, and 2mL of chloroform was added again, and the extraction was repeated 3 times; Add ammonia water dropwise to the acid solution after extraction, adjust the pH to 8-9, and a light yellow precipitate can be seen. Centrifuge at 3000r / min for 10min, discard the supernatant, add 2mL of ultrapure water to the precipitate, mix and shake for 1min to elute Uncaria ...
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