Application of total flavone of wild jujube leaves
A technology of total flavonoids and wild jujube leaves, applied in the field of memory damage prevention and protection, total flavonoids of wild jujube leaves, can solve problems such as memory damage
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Embodiment 1
[0017] Preparation of total flavonoids from jujube leaves (ZSSLF)
[0018] Weigh 1000g of spiny jujube leaves, add 12L of 50% ethanol to soak for 3h, reflux extraction twice, each time for 0.5h, extract and filter, combine the filtrate, evaporate the solvent to get the solid spiny jujube leaf extract, apply D101 macroporous resin, and load the sample Concentration 0.5g·mL -1 , pass through the resin column at a flow rate of 0.5BV / h, wash away impurities with distilled water, then elute with 50% ethanol at a flow rate of 1BV / h, collect the eluate and evaporate the solvent to obtain 92g of Jujube leaf flavonoid extract powder. The purity of total flavonoids in jujube leaves was determined to be 40.95% by ultraviolet spectrophotometry;
Embodiment 2
[0020] Drug efficacy experiment, the effect on the memory ability of aging rats
[0021] experimental method:
[0022] (1) Model establishment and administration
[0023] Take 60 SPF grade healthy male SD rats, weighing 180-200g, provided by Beijing Weitong Lihua Experimental Animal Technology Co., Ltd., divide them into cages according to 5 rats per cage, and feed them adaptively for 7 days, and then randomly Divided into 4 groups on average, 15 rats in each group, respectively blank control group Control, D-galactose model group Model, Suan jujube leaf total flavonoids low-dose group D-gal+ZSSLF (1g / kg), Suan jujube leaf total flavonoids high-dose group Group D-gal+ZSSLF (2g / kg). Except for the blank group, the rat aging model was prepared by intraperitoneal injection of D-galactose in the other 6 groups, that is, 300 mg / kg / bw D-galactose was injected intraperitoneally every day, and the blank group was replaced by normal saline for 36 consecutive days. At the same time a...
Embodiment 3
[0041] Drug efficacy experiment, the effect on biochemical indicators of aging rats
[0042] experimental method:
[0043]After the exploratory experiment, the rats were anesthetized by intraperitoneal injection of 10% chloral hydrate at a dose of 3.5 mL / kg, and blood was collected from the abdominal aorta into an EP tube. After resting, the whole blood was centrifuged at 3500r / min for 15min at 4°C, and the serum was collected and stored in a -80°C refrigerator for later use. The rats were dissected, the brain tissue was quickly taken out on ice and rinsed in ice saline, the blood was removed and dried with filter paper, after accurate weighing, 9 times the amount of ice saline was added, mechanically homogenized in an ice water bath, Finally, 10% brain tissue homogenate was obtained, and the obtained tissue homogenate was centrifuged at 3000r / min for 10min, and the tissue homogenate supernatant and serum were taken, and MDA, SOD, T-AOC, GSH, CAT content.
[0044] Statistic...
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