Application of salvianolic acid A in preparation of medicine for resisting tunica intima thickening, post-angioplasty restenosis and/or in-stent restenosis
An angioplasty and vascular intima technology is applied in the application field of salvianolic acid A in the preparation of anti-intimal thickening, anti-angioplasty and/or in-stent restenosis drugs, and can solve the problem of unseen dandruff. Phenolic acid A application reports and other issues, to achieve significant vascular intimal thickening and lumen restenosis, reduce restenosis rate, anti-intimal thickening and lumen restenosis effect
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Embodiment 1
[0037] Example 1. SAA inhibits the proliferation of human umbilical artery smooth muscle cells induced by PDGF-BB
[0038] Experimental Materials:
[0039] Human umbilical artery smooth muscle cells (hUASMCs) were purchased from ScienCell (Carlsbad, Calif). Smooth muscle cell culture medium: ScienCell (Carlsbad, Calif), fetal bovine serum FBS (Gibco). PDGF-BB was purchased from R&D Company. SAA was dissolved in DMSO into a 20mM stock solution, and the final concentration of DMSO was less than 0.1%, which had no effect on the growth of smooth muscle cells. The stock solution was aliquoted and stored in a -20°C refrigerator in the dark.
[0040] human umbilical artery smooth muscle cells 4 The density of each well was planted in a 96-well plate until 50% confluence, the serum was withdrawn and incubated for 48 hours, then according to the experimental design, 0, 0.1, 0.3 and 1 μM SAA were added for pre-incubation for 24 hours, and then 20ng / ml PDGF-BB were respectively conti...
Embodiment 2
[0044] Example 2. SAA inhibits the cell cycle of human umbilical artery smooth muscle cells
[0045] Cell culture method is the same as embodiment 1. smooth muscle cells at 5×10 6 The density was planted in a 100mm petri dish until it was 50% confluent, and cultured in serum-free DMEM medium for 48h. Give different concentrations of SAA for pre-incubation for 24 hours, then give 20ng / ml PDGF-BB stimulation, and continue to incubate for 48 hours; collect the cell supernatant, digest the cells with 0.25% trypsin, collect the cell suspension, centrifuge at 1000r / min×5min, discard supernatant. Fix with 70% cold ethanol pre-cooled at 4°C for 18h, then adjust the cell concentration to 10 6 / ml, stained with propidium iodide (PI) and incubated at 37°C for 30 min, followed by flow cytometry analysis, and the percentage of cells in each phase of the cell cycle was analyzed by using ModFitLT3.0 software; the cell proliferation index (PI) was calculated, PI = (S+G2 / M) / (G0 / G1+S+G2 / M)....
Embodiment 3
[0050] Example 3. Experimental study of SAA against restenosis after balloon-injured common carotid artery in rats
[0051] The restenosis model of rat common carotid artery balloon injury is an internationally recognized classic animal model of restenosis after PTA and in-stent restenosis.
[0052] Experimental materials: salvianolic acid A (purity ≥ 98%), made into 0.01mg / mL with triple distilled water; male SD rats with a body weight of 300-350g (purchased from Beijing Weitong Lihua Experimental Animal Technology Co., Ltd.) .
[0053] Experimental method: the rats were randomly divided into 3 groups, namely the sham operation group, the model group and the salvianolic acid A group; after intraperitoneal anesthesia with 30% chloral hydrate 0.1mL / 100g. The skin and subcutaneous tissue were incised in the front of the neck, the common carotid artery and the internal carotid artery were clamped with arterial clips, a wedge-shaped incision was made in the external carotid arter...
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