Method for preparing safflower extract through eutectic solvent
A technology of deep eutectic solvent and safflower extract, which is applied to medical preparations containing active ingredients, pharmaceutical formulas, plant raw materials, etc., can solve problems such as difficult quality control, low efficiency, and easy deterioration, and avoid extraction time long effect
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Embodiment 1
[0027] Embodiment 1.DES-17 is a solvent
[0028] Mix L-proline (1.15g), acetamide (0.59g), and deionized water (36μL) at a molar ratio of 1:1:2, heat and stir at 80°C for 1 hour to form a clear and uniform low-ethanol Melt solvent, recorded as DES-17. Mix 750μL of DES-17 and 250μL of water evenly, add it to a 1.5mL centrifuge tube, then accurately weigh 200.0mg of safflower powder and add it, and extract by ultrasonic at 50°C for 30min with an ultrasonic power of 200W. After ultrasonic extraction, centrifuge at 13300r / min for 10min, and take the supernatant, which is the safflower extract. The supernatant was diluted 10 times with volume concentration 50% aqueous methanol solution and then detected by high performance liquid chromatography ( figure 1 ), according to the compound (hydroxysafflower yellow A and hydroxysafflower yellow A) standard curve, obtain the type and content of the compound contained in the safflower extract, and calculate the extraction with the extract...
Embodiment 2D
[0030] Embodiment 2DES-21 is solvent
[0031] Choline chloride (1.40g), acetamide (0.59g), and deionized water (18μL) were mixed at a molar ratio of 1:1:1, heated and stirred at 80°C for 1 hour to form a clear and uniform eutectic Solvent, recorded as DES-21. Mix 750 μL of DES-21 and 250 μL of water evenly, add it to a 1.5 mL centrifuge tube, then accurately weigh 200.0 mg of safflower powder and add it to it, and perform ultrasonic extraction at 50°C for 30 min with an ultrasonic power of 200W. After ultrasonic extraction, centrifuge at 13300r / min for 10min, and take the supernatant, which is the safflower extract. After the supernatant is diluted 10 times with volume concentration 50% aqueous methanol solution, it is detected by high-performance liquid chromatography described in Example 1 ( figure 2 ), the measured extract contains: hydroxy safflower yellow A, 29.6mg / g; dehydrated safflower yellow B, 13.7mg / g.
Embodiment 3
[0032] Embodiment 3.DES-10 is solvent
[0033] Mix L-proline (1.15g) and lactic acid (1.80g) at a molar ratio of 1:1, heat and stir at 80°C for 1 hour to form a clear and uniform deep eutectic solvent, which is designated as DES-10. Mix 750 μL of DES-10 and 250 μL of water evenly, add it to a 1.5 mL centrifuge tube, then accurately weigh 200.0 mg of safflower powder and add it, and extract it by ultrasonic at 50°C for 30 min, with an ultrasonic power of 200W. After ultrasonic extraction, centrifuge at 13300r / min for 10min, and take the supernatant, which is the safflower extract. After the supernatant is diluted 10 times with volume concentration 50% aqueous methanol solution, it is detected by high-performance liquid chromatography described in Example 1 ( image 3 ), the measured extract contains: hydroxy safflower yellow A, 30.3mg / g; dehydrated safflower yellow B, 13.5mg / g.
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