Euphorbiaceae plant active substance for restraining growth of cancer and/or tumor and application thereof
An active substance and tumor cell technology, applied in the field of Euphorbiaceae plant active substance in the field of animal health, can solve the problems of tumor recurrence or metastasis, cost considerations, etc., and achieve the goal of inhibiting the formation of tumor cell colonies, inhibiting the ability to proliferate, and inhibiting the ability to migrate Effect
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Embodiment 1
[0045] The preparation of embodiment one Euphorbiaceae plant active substance
[0046] 1. Active substances extracted from ethanol (Ethanol)
[0047] Euphorbia neriifolia was collected from Yilan, Taiwan. Firstly, wash the stems and leaves of the collected vajras with water, let them dry, weigh them and cut them into slices, then put the stems and leaves of vajras in a brown glass bottle that can be protected from light, and add 95% ethanol to make them dry. The stems and leaves of the diamondback are completely soaked in ethanol, and stand at room temperature for extraction. When the ethanol turns from transparent and colorless to dark green or dark brown (about 3 to 10 days), the ethanol extract is collected, and then concentrated under reduced pressure to remove Ethanol, in order to obtain the active substance extracted from Ethanol.
[0048] 2. Active substances extracted by n-hexane (Hexane)
[0049] Get the active substance 10g of above-mentioned vajra ethanol extract...
Embodiment 2
[0050] Example 2 Analysis of Euphorbiaceae Plant Active Substances Inhibiting Tumor Cell Proliferation
[0051] 1. Test method
[0052] In this embodiment, canine breast tumor cell lines, CMT-1 (canine mammary tumor-1) cell line and MPG cell line are used as test objects. CMT-1 cells or MPG cells were seeded in 96-well flat-bottom cell culture plates at a density of 3,000-5,000 cells per well, and cultured in DMEM containing 5-10% fetal bovine serum and 1% antibacterial and antifungal solution liquid culture at 37°C, 5% CO 2 Cultivate in the incubator for 24 hours. After confirming that the cells are attached to the bottom of the culture dish, replace the original cell culture medium with DMEM cell culture medium (2ml / well) containing 0.5% fetal bovine serum and 1% antibacterial and antifungal liquid. Add different concentrations (2.5 μg / ml, 5 μg / ml, 10 μg / ml, 20 μg / ml) of the adamantium ethanol-extracted active substance or adamantine-n-hexane extracted active substance obt...
Embodiment 3
[0060] Example 3 Analysis of Effects of Euphorbiaceae Plant Active Substances on Tumor Cell Survival
[0061] 1. Analysis of cell viability
[0062] CMT-1 cells or MPG cells were added to each well at 1x10 5 -4x10 5 The density of the single cell was inoculated in a 6-well flat-bottomed cell culture dish, and cultured in DMEM cell culture medium containing 5-10% fetal bovine serum and 1% antibacterial and antifungal liquid, at 37°C, 5% CO 2 Cultivate in the incubator for 24 hours. After confirming that the cells are attached to the bottom of the culture dish, replace the original cell culture medium with DMEM cell culture medium (2ml / well) containing 0.5% fetal bovine serum and 1% antibacterial and antifungal liquid. And add the active substance (10 μg / ml, 20 μg / ml) or the active substance (5 μg / ml, 10 μg / ml) of the adamantine ethanol extraction obtained by Example 1 or the active substance extracted by adamantium n-hexane in different concentrations. And on the third day o...
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