Detection method for flavonoids compounds in cotton rose general flavone
A technology for flavonoids and a detection method, which is applied in the field of detection of flavonoids in total flavonoids of Hibiscus chinensis, can solve the problems of troublesome detection, inability to qualitatively and quantitatively detect flavonoids at the same time, and achieves easy to master, good reproducibility, variety of uniform effect
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[0101] Preparation of the test solution:
[0102] Weigh 0.5g of total flavonoids from Hibiscus hibiscus, add appropriate amount of distilled water after weighing accurately, and dissolve by ultrasonication with power of 200w, frequency of 40kHz, and time of 10min; then dilute to 50ml with water, add petroleum ether (60°C-90°C) to extract three times, 50ml each time, discard the petroleum ether solution, add ethyl acetate to the aqueous solution for extraction three times, 50ml each time, combine the ethyl acetate solution and evaporate to dryness under reduced pressure, add methanol to dissolve the residue, dilute to 50ml, pass through 0.45μm micro Pore filter membrane, promptly needs testing solution;
[0103] Preparation of reference solution:
[0104] Accurately weigh the appropriate amount of rutin, hyperin and quercitrin reference substances, add methanol to make mixed solutions containing 40.0 μg, 32.2 μg, and 28.0 μg per 1 mL, respectively;
[0105] The detection in...
Embodiment 1
[0151] Preparation of the test solution: Weigh about 0.5g of hibiscus total flavonoids extract, place it in a stoppered Erlenmeyer flask after weighing accurately, add appropriate amount of distilled water, ultrasonically dissolve, power 200w, frequency 40kHz, time 10min, dilute with water to 50ml , then add petroleum ether (boiling point 60°C-90°C) for extraction three times, 50ml each time, discard the petroleum ether solution, add ethyl acetate to the aqueous solution for extraction three times, 50ml each time, combine the ethyl acetate solution and evaporate to dryness under reduced pressure, Add methanol to dissolve the residue, dilute to 50ml, and pass through a 0.45μm microporous membrane to obtain the product.
[0152] Preparation of reference substance solution: Accurately weigh appropriate amount of rutin, hyperin, and quercitrin reference substances, add methanol to make mixed solutions containing 40.0 μg, 32.2 μg, and 28.0 μg per 1 mL, respectively, to obtain the so...
Embodiment 2
[0158] Preparation of the test solution: Weigh about 0.5g of hibiscus total flavonoids extract, place it in a stoppered Erlenmeyer flask after weighing accurately, add appropriate amount of distilled water, ultrasonically dissolve, power 200w, frequency 40kHz, time 10min, dilute with water to 50ml , then add petroleum ether (boiling point 60°C-90°C) for extraction three times, 50ml each time, discard the petroleum ether solution, add ethyl acetate to the aqueous solution for extraction three times, 50ml each time, combine the ethyl acetate solution and evaporate to dryness under reduced pressure, Add methanol to dissolve the residue, dilute to 50ml, and pass through a 0.45μm microporous membrane to obtain the product.
[0159]Preparation of reference substance solution: Accurately weigh appropriate amount of reference substances of rutin, hyperin, and quercitrin, and add methanol to make solutions containing 40.0 μg, 32.2 μg, and 28.0 μg per 1 mL, respectively.
[0160] A nega...
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