Efficient preparation method of active ingredients of honeysuckle leaves and antiviral application of active ingredients
A technology of active ingredient and honeysuckle leaves, applied in the field of separation of honeysuckle leaf extracts, which can solve problems such as waste of resources
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Embodiment 1
[0066] 1. Preparation of Crude Samples
[0067] Pick the purchased dry honeysuckle leaves and discard the mixed honeysuckle and honeysuckle vines. Weigh 1 kg of selected dried honeysuckle leaves, put them into a round bottom flask after crushing, add 10 L of 95% ethanol according to the ratio of solid to liquid of 1:10, heat and reflux for extraction three times, each time for 2 hours. The ethanol crude extract of honeysuckle leaves obtained by extraction was suction-filtered and concentrated under reduced pressure to obtain 386 g of brown viscous ethanol extract.
[0068] The ethanol extract was made into a suspension with distilled water, and then distributed and extracted three times with equal volumes of petroleum ether, ethyl acetate, and n-butanol, concentrated under reduced pressure, and freeze-dried to obtain honeysuckle leaf petroleum ether extract, honeysuckle leaf ethyl acetate Ester extract, honeysuckle leaf n-butanol extract 22g, 19g, 135g, the extraction rate is...
Embodiment 2
[0115] 1.1 Concentration gradient preparation of the test sample solution
[0116] The various parts obtained by separating the ethyl acetate extract and n-butanol extract of honeysuckle leaves from LGCCC, ethanol extract of honeysuckle leaves, petroleum ether extract of honeysuckle leaves, ethyl acetate extract of honeysuckle leaves, n-butanol extract of honeysuckle leaves, honeysuckle leaves The remaining water-soluble matter was dissolved in 50% ethanol aqueous solution to prepare a 1 mg / mL test sample solution, and the 1 mg / mL test sample solution was serially diluted 2 times with 50% ethanol aqueous solution for a total of 9 times, and a total of 10 different samples were obtained. Concentrations and adjacent concentrations are 2-fold diluted test sample solutions.
[0117] Zanamivir was selected as the positive control group of the experiment, and chlorogenic acid was selected as the positive control group of natural components of the experiment, and a 0.005 mg / mL zanami...
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