Application of panax notoginseng flos saponin in preparing medicine for promoting angiogenesis
A technology for angiogenesis and total saponins, which is applied in the field of medicine, can solve the problems of less flowers of Panax notoginseng and underutilized medicinal value.
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Embodiment 1 10
[0018] Example 1 Effect test of Panax notoginseng saponins on promoting angiogenesis in zebrafish model
[0019] 1. Materials and Methods
[0020] The animal transgenic zebrafish Tg(flila-EGFP)y1 was provided by Zebrafish International Resource Center (Oregon, PO), USA. Zebrafish were reared according to the zebrafish handbook method.
[0021] Drugs, reagents and instruments Panax notoginseng were provided by Yunnan Wenshan Science and Technology Innovation Center Co., Ltd. (origin: Wenshan, Yunnan). AB-8 macroporous adsorption resin (chemical plant of Nankai University, Tianjin) was selected, and the diameter-to-height ratio of the column was 1:10. Load 1.25g dry resin per gram of crude drug, and the sample concentration is 0.2g crude drug / ml. After fully adsorbed, wash with water until there is no Molish reaction, and then elute with 70% ethanol solution that is 3 times the volume of the resin. The adsorption and elution flow rate Both were 2 times the volume of the resin ...
Embodiment 2 10
[0031] Example 2 Effect experiment of Panax notoginseng saponins on the proliferation of human umbilical vein endothelial cells
[0032] Human umbilical vein endothelial cell culture: HUVECs were cultured in F-12K medium containing 10% inactivated newborn bovine serum, 1% penicillin-streptomycin, 100μg / ml heparin, 30μg / ml ECGS, 3-8 passages in logarithmic growth phase Cells are used for experiments, culture flasks for experiments, 24-well plates and 96-well plates are pre-coated with 0.1% gelatin;
[0033] Proliferation experiment of human umbilical vein endothelial cells: Seed human umbilical vein endothelial cells (HUVECs) in a 96-well plate at a density of 1×104 cells / well, culture for 24 hours, and replace with low-serum medium (0.5% FBS) The original culture medium (10% FBS), continue to culture for 24 hours to make the cells in a static state, and then replace the low Serum culture solution (culture solution containing 0.1% DMSO as blank control, 20ng / ml VEGF low serum ...
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