Blood glucose reducing and islet protecting activity test method for horseradish tree leaf flavonoids extract and application thereof
A technology for testing the flavonoids and activity of the leaves, which is applied in the field of biomedicine to achieve the effects of reducing glucose tolerance, saving costs, and high extraction efficiency
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Embodiment 1
[0046] The hypoglycemic and islet protective activity test method of Moringa oleifera flavonoids extract comprises the following steps:
[0047] S1. Preparation of flavonoid extract: Weigh 100mg of flavonoid powder from Moringa oleifera leaves, dilute to 1mL, mix well, filter through a 0.22um filter, divide into 5 equal samples, and set aside;
[0048] S2. Glucose uptake test: Digest the HepG2 cell solution for the test with 0.25% trypsin solution, inoculate it on a culture plate, and place it together in CO 2 cultured in an incubator, wherein the cell concentration of the HepG2 cell solution was 1.0×10 5 cells / mL, after the cells adhered to the wall, the original culture solution was discarded, and the initial glucose concentration in the culture solution of each well was measured with a glucose kit, calculated as G 1 , change the serum-free culture medium, starve for 10 h, add 180 μL of DMEM high-glucose culture medium, and then add 30 μL of samples respectively, after incu...
Embodiment 2
[0057] The hypoglycemic and islet protective activity test method of Moringa oleifera flavonoids extract comprises the following steps:
[0058] S1. Preparation of flavonoids extract: Weigh 80 mg of flavonoids powder from Moringa oleifera leaves, dilute to 1 mL, mix well, filter through a 0.22um filter, divide into 5 equal samples, and set aside;
[0059] S2. Glucose uptake test: Digest the HepG2 cell solution for the test with 0.25% trypsin solution, inoculate it on a culture plate, and place it together in CO 2 cultured in an incubator, wherein the cell concentration of the HepG2 cell solution was 0.8×10 5 cells / mL, after the cells adhered to the wall, the original culture solution was discarded, and the initial glucose concentration in the culture solution of each well was measured with a glucose kit, calculated as G 1 , change the serum-free culture medium, starve for 12 hours, add 160 μL of DMEM high-glucose culture solution, and then add 20 μL of samples respectively, a...
Embodiment 3
[0067] The hypoglycemic and islet protective activity test method of Moringa oleifera flavonoids extract comprises the following steps:
[0068] S1. Preparation of flavonoids extract: Weigh 90 mg of flavonoids powder from Moringa oleifera leaves, dilute to 1 mL, mix well, filter through a 0.22um filter, divide into 5 equal samples, and set aside;
[0069] S2. Glucose uptake test: Digest the HepG2 cell solution for the test with 0.25% trypsin solution, inoculate it on a culture plate, and place it together in CO 2 cultured in an incubator, wherein the cell concentration of the HepG2 cell solution was 1.5×10 5 cells / mL, after the cells adhered to the wall, the original culture solution was discarded, and the initial glucose concentration in the culture solution of each well was measured with a glucose kit, calculated as G 1 , change the serum-free culture medium, starve for 12 hours, add 200 μL of DMEM high-glucose culture medium, and then add 50 μL of samples respectively, aft...
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