Composition for preventing or treating nicotine addiction, which contains liriope latifolia extract as active ingredient
A technology of Ophiopogon japonicus extract and M. broadleaf, which is applied in the field of drugs for preventing or treating nicotine addiction, can solve the problem that there is no literature report of Ophiopogon japonicus, and there is no composition for preventing or treating symptoms of nicotine addiction. Healthy functional food And other issues
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Embodiment 1
[0095] Embodiment 1: Preparation of the hot water extract of Ophiopogon japonicus
[0096] The root of Ophiopogon japonicus was dried, and 2.1 L of water was added to 300 g of dried Ophiopogon japonicus root, which was then extracted twice in a reflux device at 80° C. for 4 hours. After reflux and filtration, the extract was freeze-dried under reduced pressure. The results showed that 197g of the hot water extract of Ophiopogon japonicus was obtained, and the yield was 65%.
Embodiment 2
[0097] Embodiment 2: the preparation of the ethanol extract of Ophiopogon japonicus broadleaf
[0098] Preparation of 30% ethanol extract of Ophiopogon japonicus
[0099] The root of Ophiopogon japonicus was dried, and 2.1 L of 30% ethanol (v / v) was added to 300 g of dried Ophiopogon japonicus root, and it was extracted twice in a reflux device at 70° C. for 4 hours. After reflux and filtration, the extract was freeze-dried under reduced pressure. The results showed that 191g of the 30% ethanol extract of Ophiopogon japonicus was obtained, and the yield was 63%.
[0100] Preparation of 50% ethanol extract of Ophiopogon japonicus
[0101] Dry the root of Radix Ophiopogon japonicus, and add 2.1 L of 50% ethanol (v / v) to 300 g of the dried root of Ophiopogon japonicus, and extract it twice in a reflux device at 60° C. for 4 hours . After reflux and filtration, the extract was freeze-dried under reduced pressure. The results showed that 171 g of the 50% ethanol extrac...
experiment example 1
[0102] Experimental Example 1: Measuring the concentration of neuronal cell line (PC-12 cells) cell activity in
[0103] The cell viability of the neuronal cell line (PC-12 cell line) according to the treatment concentrations of nicotine and Ophiopogon japonicus extract was determined by MTT assay.
[0104] Specifically, PC-12 cells were cultured in DMEM medium (Dulbecco's modified Eagle's medium) supplemented with 10% fetal bovine serum (FBS), 5% horse serum and 1% antibiotics (Thermo fisher company, Cat. No. 15140122) at 37 °C, 5% CO 2 cultured in an incubator. Distribute the cultured PC-12 cells in 1 x 10 4 Cells / well density in 96-well plates and further cultured in the same medium and conditions for 24 hr. Then, PC-12 cells were treated with the nicotine (1, 10, 100 and 1000 μM / ml) and the extract of Ophiopogon japonicus (1, 10, 100 and 1000 μg / ml) of Example 1 for 24 hours, respectively. Then, 20 μl of the dye solution (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyme...
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