Detection method for flavonoids compounds in cotton rose general flavone
A flavonoid compound and detection method technology, which is applied in the field of detection of flavonoid compounds in total flavonoids of hibiscus hibiscus, can solve the problems of simultaneous qualitative and quantitative detection of flavonoid components and troublesome detection, and achieve easy mastery, high precision, and uniform variety Effect
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[0101] Preparation of the test solution:
[0102] Weigh 0.5g of the total flavonoids of Hibiscus hibiscus, add appropriate amount of distilled water after weighing accurately, and ultrasonically dissolve, the power is 200w, the frequency is 40kHz, and the time is 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, dissolve the residue with methanol, 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 detectio...
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 rutin, hyperin, and quercitrin reference substances, add methanol to make solutions containing 40.0 μg, 32.2 μg, and 28.0 μg per 1 mL, respectively.
[0160] A negative co...
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