Extraction method of cucurbitane type triterpene compound and medical application in resisting Alzheimer's disease
A triterpene compound and cucurbitane-type technology, which is applied in the field of drug extraction, can solve the problems of side effects and reduced drug efficacy, and achieve the effect of low price, simple method and wide source
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Embodiment 1
[0041] Embodiment 1: Extract cucurbitane type triterpenoids in bitter melon fruit
[0042] A method for extracting cucurbitane-type triterpenoids from balsam pear fruits, comprising the following steps:
[0043] (1) After pulverizing 1.5kg (dry weight) of bitter gourd (Momordica charantia), extract it with 5L industrial grade methanol, place it in a shaker for 3 days with shaking at room temperature, vacuum filter, take the filtrate, and concentrate under reduced pressure to obtain Methanol extract 224g.
[0044] (2) Alternately use ethyl acetate and water to dissolve the sample of the methanol extract obtained in (1) and transfer it to a separatory funnel for distribution. After standing overnight, spin the ethyl acetate layer and the water layer to obtain ethyl acetate Layer sample 30g, water layer sample 170g.
[0045] (3) The sample of the ethyl acetate layer is separated by a silica gel open column (silica gel 200-300 mesh), and the elution system is n-hexane:acetone=99...
Embodiment 2
[0069] Embodiment 2: the biological activity analysis of compound 1-11
[0070] Studies have found that NGF can promote nerve growth and neuroprotection, can prevent or reduce neuronal degeneration, and to a certain extent can prevent the progression of AD. Because PC12 cells have the general characteristics of nerve cells, under the action of NGF, they will stop dividing, grow protrusions, and transform into neuron-like cells. Therefore, using PC 12 cells as an effective in vitro biological activity identification system to screen compounds with neuromimetic activity may become an effective drug for the treatment of Alzheimer's disease.
[0071] The analytical method includes the following steps:
[0072] (1) Culture of PC 12 cells (rat adrenal pheochromoma cell line): In a 100mm culture dish, add 10mL containing 20×10 4 The DMEM medium (containing 10% horse serum and 5% fetal calf serum) of each PC 12 cell was replaced after two days, and subcultured three days later. Whe...
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