Preparation method and application of guava leaf extract
A guava leaf and extract technology, which is applied in the field of preparation of guava leaf extract, can solve the problems of unreported anti-inflammatory activity, high quality requirements of medicinal materials, and many impurities in effective parts, and achieve broad market prospects and development value , solution penetration rate is fast, the effect of low cost
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Embodiment 1
[0029] After 3 kg of fresh guava leaves were dried in the sun, they were extracted twice with 10 times the amount of 70% ethanol, respectively, for 1 hour each time, and the 2 extracts were combined, filtered, and concentrated under reduced pressure to alcohol-free to obtain 3 L of concentrated solution; Extracted with petroleum ether for 1 time, then extracted with 0.5 times the amount of ethyl acetate for 3 times, combined the ethyl acetate fractions, and concentrated under reduced pressure to obtain 50 g of ethyl acetate fraction extract.
[0030] Take the ethyl acetate part extract prepared by the above method, mix it with silica gel neutral alumina according to the mass ratio of 1:3, vacuum dry and grind at 50 °C, and dry the sample for neutral alumina column chromatography. , eluted with 100% dichloromethane, dichloromethane:methanol 10:1, dichloromethane:methanol 10:2, dichloromethane:methanol 2:1, dichloromethane:methanol 1:1 , the amount of eluent for each gradient co...
Embodiment 2
[0047] 1) Cell lines and reagents: RAW264.7 (mouse macrophages). Fetal bovine serum, DMEM medium, and RPMI-1640 medium were purchased from Shanghai Haoran Biotechnology Co., Ltd. EDTA trypsin and PBS buffer were purchased from Shanghai Biyuntian Reagent Company, China. MTT reagent was purchased from Shanghai Enyi Biotechnology Co., Ltd. LPS (lipopolysaccharide) was purchased from Beijing Soleibo Technology Co., Ltd.
[0048] 2) Test drugs: the guava leaf extract prepared in Example 1 of the present invention; the guava leaf extract prepared in Comparative Examples 1-5. The positive control drug was hydrocortisone.
[0049] 3) Cell culture and drug effects: mouse macrophages RAW264.7 are adherent cells. After the cells are revived, use DMEM medium (containing 10% fetal bovine serum) in an incubator containing 5% carbon dioxide at 37°C. Culture the cells, take the cells in the logarithmic growth phase, digest with trypsin and adjust the suspension density to 5×10 5 cells / mL...
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