Extraction process of response surface process optimization uralla total flavonoids and anti-oxidization purpose thereof
A response surface method and the technology of Uralia sativa, which are applied to medical preparations containing active ingredients, anti-toxins, chemical process analysis/design, etc., can solve the problem of less flavonoids in Urastia sativa
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Embodiment 1
[0028] The preferred embodiments of the present invention will be described below in conjunction with the accompanying drawings. It should be understood that the preferred embodiments described here are only used to illustrate and explain the present invention, and are not intended to limit the present invention.
[0029] (1) Dry and pulverize Uralia ulata to obtain Urla ulati powder, which is passed through a 40-mesh pharmacopoeia sieve.
[0030] (2) Extract the Ulacao powder with ethanol, concentrate and dry the extract, and determine the total flavonoid content of the dry extract.
[0031] (3) Select the four factors of ethanol concentration, liquid-to-solid ratio, extraction time, and extraction temperature to conduct a single-factor experiment on step (2) to determine the optimal levels of ethanol concentration, liquid-to-solid ratio, extraction time, and extraction temperature. The optimal point of the experiment is centered, and one horizontal value is taken around the ...
Embodiment 2
[0062] LC-MS analysis of flavonoids from Uralia pratense
[0063] Preparation of the test solution
[0064] Precisely weigh the appropriate amount of flavonoids from Ulagrass flavonoids, dissolve it with a small amount of acetonitrile to prepare a certain concentration of the sample solution to be tested, and use it for later use. Substances are analyzed and identified.
[0065] Chromatography and mass spectrometry conditions
[0066] Liquid chromatography conditions: Symmetry® C18 (5μm, 4.6×250mm), injection volume 5μL, see Table 4 for mobile phase elution program.
[0067] Mass spectrometry conditions: the ESI source injection voltage was set to 4000 V, the source temperature (TEM) was 300 °C, the volume flow rate of the dry gas was 1 L / min, the pressure of the atomizing gas was 30 psi, the pressure of the auxiliary gas was 60 psi, and the interface was continuously heated. Time-of-flight mass spectrometry detector.
Embodiment 3
[0073] Antioxidant research on total flavonoids of Uralia pratense under optimal extraction parameters
[0074] Take the total flavonoids extract of Uralia sativa extracted under the optimal conditions, measure its flavonoid content as the stock solution of 0.069 mg / mL, configure it as a stock solution of 0.05 mg / mL, and then divide the stock solution every 0.1 mg / mL (remove hydroxyl free Radicals and scavenging ABTS free radicals) and 0.01 mg / mL (scavenging DPPH free radicals) as a gradient, which were successively diluted into 5 concentrations for later use. Take the VC test sample and make it into 0.1 mg / mL VC stock solution, and then dilute the stock solution into 5 concentrations at intervals of 0.2 mg / mL and 0.02 mg / mL as a gradient. Experiments were repeated three times.
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