Preparation method of ginger extract with detoxifying effect on exogenous carcinogens and product
A technology of ginger extract and detoxification, applied in the field of ginger deep processing, can solve the problems of low comprehensive utilization rate, low technical added value, backward ginger deep processing technology, etc., and achieve the effect of simple preparation process
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Embodiment 1
[0011] Embodiment 1: the preparation of ginger extract
[0012] 2.21kg fresh ginger (Zingiber officinale Rosc.) was purchased in a local supermarket in April 2009. After being selected, wash and remove mud, freeze-dry, and then pulverize, extract the above-mentioned ginger powder with 95% ethanol solution (1:10, m / v) at 70 ° C for 4 hours, filter and take the extract to concentrate in vacuum rotation . Dissolve the alcoholic extract of ginger in 500mL of water, then add an equal volume of ethyl acetate, let stand to separate layers, collect the ethyl acetate layer, extract repeatedly 5-6 times, combine the extracts and concentrate and dry; take 10g of ginger ethyl acetate extract Mix with 3 times the mass of silica gel, use a 5.5cm×60cm glass column for silica gel column chromatography, and perform isocratic elution with ethyl acetate / n-hexane (0-100% ethyl acetate, v / v) system, Collect 30%-70% ethyl acetate eluate elution fraction, concentrate in vacuum rotation, evaporate...
Embodiment 2
[0013] Example 2: Determination of Phase II Enzyme Activity Induced by Ginger Extract
[0014] 2.1 Principle: quinone oxidoreductase (QR) is an important phase II detoxification enzyme. It has the advantages of easy synergy with other phase II enzymes, good responsiveness to elicitors, and convenient measurement, and is widely used as a biomarker for the determination of phase II enzymes; while the expression of QR in the mouse liver cancer Hepa 1c1c7 cell line is stable and reproducible The good performance makes this cell line gradually become a fast and reliable model for the determination of QR enzyme activity.
[0015] 2.2 Cell line: mouse liver cancer hepa1c1c7 cells, purchased from American Type Culture Collection (ATCC).
[0016] 2.3 Determination method: Hepa1c1c7 cells with a confluence of 80% were inoculated in a 96-well plate at 5000 / well, and cultured in an incubator at 37°C and 5% CO2 for 24 hours. Then add 200 μL of fresh culture solution containing ginger e...
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