Application of a flavonoid compound in snow chrysanthemum and its pharmaceutical composition in the preparation of medicines for treating acute pancreatitis
A kind of acute pancreatitis, compound technology, application in snow chrysanthemum flavonoid compound and its pharmaceutical composition in the preparation of acute pancreatitis medicine application field
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Embodiment 1
[0049] Preparation and Identification of Flavonoids in Example 1 Snow Chrysanthemum
[0050] 1. Weigh 5 kg of dried snow chrysanthemum, add 25 L of 95% ethanol, and extract under reflux for 3 times at 80° C. for 3 hours each time. The extract is concentrated under reduced pressure to obtain 580 g of extract.
[0051] 2. Mix the 580g extract obtained in step 1 with 580g polyamide, carry out column chromatography through a polyamide column, and use water, 35% ethanol and 65% ethanol as mobile phases to elute successively, as shown in Table 1 As shown, the eluate XP2 obtained by elution with 35% ethanol was concentrated to obtain a 35% ethanol extraction fraction (60.5 g, XP2).
[0052] The elution condition of table 1 polyamide chromatographic column (eluent is 4-5 retention volumes)
[0053] eluent Elution volume eluent water 20L XP1 35% ethanol 20L XP2 65% ethanol 20L XP3
[0054] 3. The 35% ethanol extraction fraction (60.5 g, XP2) ob...
Embodiment 2
[0063] Example 2 Protective effect of flavonoids on pancreatic acinar cell necrosis induced by sodium thiocholate in vitro
[0064] After the male Balb / c (20-25g) mice were killed by dislocation, the pancreatic tissue was taken, washed twice with HEPES solution, and collagenase was injected into the pancreatic tissue along the pancreatic duct with a syringe. Put the pancreatic tissue into 1mL of collagenase, place it in a water bath at 37°C for 18-20min, suck out the pancreas, put it into 4mL HEPES solution, pipette, suck out and filter, then pipette in turn, filter with a 100μM filter, and centrifuge at 700rpm After 2 minutes, pour out the upper liquid completely, add 4-6ml HEPES solution to resuspend, and mix well to obtain the experimental cells. The cells were equally divided into blank group, model group and different dosage administration groups, 1 mL in each group.
[0065] The drug is directly prepared with normal saline, and diluted with freshly prepared HEPES before...
Embodiment 3
[0067] Example 3 Improvement of local and systemic symptoms of cerulein-induced acute pancreatitis mouse model by flavonoids.
[0068] 1) Model establishment
[0069] Male Blab / C mice were randomly divided into groups, and fasted for 12 hours before the experiment. Intraperitoneal injection of cerulein 50μg / kg, 7 consecutive injections, each interval of 1h.
[0070] 2) Animal grouping and handling
[0071] Thirty male Blab / C mice were randomly divided into five groups (N=6): normal control group, acute pancreatitis group, and three dose groups of compound 1 (12.5, 25 and 50 mg / kg).
[0072] Normal control group: intraperitoneal injection of normal saline at the same dose as cerulein solution, 7 consecutive injections with an interval of 1 hour between each injection. The first injection of cerulein was recorded as 0h, and the same amount of solvent as the test drug was injected at 0, 4 and 8h.
[0073] Acute pancreatitis group: intraperitoneal injection of cerulein, 7 cons...
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