Use of kudzu flower extract in prevention and treatment on oxidative damage
A kudzu flower extract and application technology, applied in medical preparations containing active ingredients, food science, drug combination, etc., can solve the problems of limiting oxidative damage disease treatment and prevention, lack of effective treatment of oxidative damage, etc.
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Embodiment 1
[0094] Preparation of Pueraria Alcohol Extract
[0095] After Pueraria pudica is crushed, add 5 times by weight of 95% (v / v) ethanol, heat and reflux for extraction for 10 hours, then filter, and the filtrate is concentrated and dried under reduced pressure to obtain a dry extract, i.e. Pueraria kudzu alcohol extract.
Embodiment 2
[0096] Example 2 investigates the improving effect of kudzu flower alcohol extract on oxidative damage
[0097] Pueraria ethanol extract: prepared in Example 1.
[0098] Statistical analysis: M±SD was used for measurement, data analysis was carried out by SPSS software, and t test was used for pairwise comparison, and p<0.05 was considered statistically significant.
[0099] experimental method:
[0100] ARPE-19 cells (human retinal pigment epithelial cells) were seeded in 96-well plates, 1x10 per well 6 Add 100 μL of DME / F12 medium containing 10% FBS to the cells, and after incubation for 24 hours, divide them into blank control group, hydrogen peroxide control group, low-dose group of kudzu flower alcohol extract, medium-dose group of kudzu flower alcohol extract, kudzu flower alcohol extract group, and kudzu flower alcohol extract group. Alcohol extract high dose group, vitamin C group and kudzu flower alcohol extract+vitamin C group, among them, the blank control group a...
Embodiment 3
[0107] Example 3 investigates the inhibitory effect of kudzu flower alcohol extract on the ROS produced by oxidative stress
[0108] Pueraria ethanol extract: prepared in Example 1.
[0109] Statistical analysis: M±SD was used for measurement, data analysis was carried out by SPSS software, and t test was used for pairwise comparison, and p<0.05 was considered statistically significant.
[0110] experimental method:
[0111] ARPE-19 cells (human retinal pigment epithelial cells) were seeded in 96-well plates, 1x10 per well 6 Add 100 μL of DME / F12 medium containing 10% FBS to the cells, and after incubation for 24 hours, divide them into blank control group, hydrogen peroxide control group, low-dose group of kudzu flower alcohol extract, medium-dose group of kudzu flower alcohol extract, kudzu flower alcohol extract group, and kudzu flower alcohol extract group. Alcohol extract high dose group, vitamin C group and kudzu flower alcohol extract+vitamin C group, among them, the ...
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