Toad venom extract and preparation thereof
An extract and toad venom technology, applied in the field of venom venom extract and preparation thereof, can solve the problems of complicated gradient elution operation, time-consuming and the like, and achieve the effects of improving safety and effectiveness, shortening time-consuming, and reducing toxic and side effects
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Embodiment 1
[0019] Take 1 gram of toad venom medicinal material, add 10ml of absolute ethanol, heat and reflux for 40min, and extract twice under the above conditions. The extract was filtered while it was hot, concentrated by rotary evaporation, and then 0.9 g of silica gel was added to mix the sample to obtain the mixed sample silica gel. Take 20 grams of silica gel soaked in petroleum ether: acetone (volume ratio 5: 1) and then wet-pack the column, add sample-mixed silica gel, and perform isocratic elution with petroleum ether: acetone (volume ratio 5: 1) eluent. Identification by HPLC (e.g. figure 1 As shown, the retention time is 7.184min for bufalin, 8.886min for cinobufagin, and 9.549min for bufafagenin), collect the eluate containing these three fat-soluble components, evaporate to dryness, That is to say, the toad venom extract of the present invention is obtained, wherein the mixture of three kinds of bufoligin accounts for 98.01% by weight of the whole extract.
Embodiment 2
[0021] Take 2 grams of toad venom medicinal material, add 25ml of absolute ethanol, heat and reflux for 40min, and extract twice under the above conditions. The extract was filtered while it was hot, concentrated by rotary evaporation, and then 1.8 g of silica gel was added to mix the sample to obtain the mixed sample silica gel. Take 22 grams of silica gel soaked in petroleum ether: acetone (volume ratio 5:1) and then wet-pack the column, add sample silica gel, and perform isocratic elution with petroleum ether: acetone (volume ratio 5:1) eluent. Through HPLC identification, collect the eluate containing the three fat-soluble components of bufagenin, cinobufagenin, and bufafalin, and evaporate to dryness to obtain the toad venom extract of the present invention, wherein the three kinds of bufabugenin mixtures The content is 97.94%.
Embodiment 3
[0023] Take 3 grams of toad venom medicinal material, add 35ml of absolute ethanol, heat and reflux for 40min, and extract twice under the above conditions. Filter the extract while it is hot, concentrate by rotary evaporation, add 3 grams of silica gel to mix the sample, and obtain the mixed sample silica gel. Take 22 grams of silica gel soaked in petroleum ether: acetone (volume ratio 5:1) and then wet-pack the column, add sample silica gel, and perform isocratic elution with petroleum ether: acetone (volume ratio 5:1) eluent. Through HPLC identification, collect the eluate containing the three fat-soluble components of bufagenin, cinobufagenin, and bufafalin, and evaporate to dryness to obtain the toad venom extract of the present invention, wherein the three kinds of bufabugenin mixtures The content is 99.08%.
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