Method for rapidly separating triterpenes and sterols in lucid ganoderma alcohol extract
A technology for Ganoderma lucidum alcohol and sterol, which is applied in the field of extraction and separation of natural medicines, can solve the problems of complicated process, difficult separation of Ganoderma lucidum triterpenes and sterols, and high production cost, and achieves the effects of high separation accuracy, low cost and easy operation.
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Embodiment 1
[0032] S1. Take an appropriate amount of polyamide resin (100-200 mesh), add ethanol to immerse, remove air bubbles by ultrasonication for 10 minutes, and let stand for 10 hours after stirring;
[0033] S2. Column packing: select a glass chromatography column with a column diameter of 2.6cm, fill it to a column height of 20cm, and a column diameter ratio of 1:7, and elute with deionized water until there is no alcohol smell;
[0034] S3. Take 1.0 g of the ethanol extract of Ganoderma lucidum fruiting body, mix the sample with the polyamide resin soaked in step S1 according to the mass ratio of 1:1, evaporate the ethanol in an evaporating dish, and then load the sample;
[0035] S4. First wash the column with 50% ethanol for 3 times the column volume to obtain eluent A; then wash the column with 90% ethanol for 3 times the column volume to obtain eluent B;
[0036] S5, carry out chromatographic detection to eluent A and eluent B, the result is as follows figure 1 shown, from ...
Embodiment 2
[0039] S1. Take an appropriate amount of polyamide resin (100-200 mesh), add ethanol to immerse, remove air bubbles by ultrasonication for 10 minutes, and let stand for 15 hours after stirring;
[0040] S2. Column packing: select a glass chromatography column with a column diameter of 5.5 cm, fill it to a column height of 30 cm, and a column diameter ratio of 1:5, and elute with deionized water until there is no alcohol smell;
[0041] S3. Take 5.0 g of the ethanol extract of Ganoderma lucidum fruiting body, mix the sample with the polyamide resin soaked in step S1 according to the mass ratio of 1:1.5, evaporate the ethanol to dryness in an evaporating dish, and then load the sample;
[0042] S4. First wash the column with 55% ethanol for 5 times the column volume to obtain eluent A; then wash the column with 85% ethanol for 5 times the column volume to obtain eluent B;
[0043] S5, carry out chromatographic detection to eluent A and eluent B, the result is as follows figure...
Embodiment 3
[0046] S1. Take an appropriate amount of polyamide resin (100-200 mesh), add ethanol to immerse, stir to remove air bubbles, and let stand for 12 hours after stirring;
[0047] S2. Column packing: select a glass chromatography column with a column diameter of 6cm, fill it to a column height of 36cm, and a column diameter ratio of 1:6, and elute with deionized water until there is no alcohol smell;
[0048] S3. Take 10.0 g of the ethanol extract of Ganoderma lucidum fruiting body, mix the sample with the polyamide resin soaked in step S1 according to the mass ratio of 1:1, evaporate the ethanol to dryness in an evaporating dish, and then load the sample;
[0049] S4. First wash the column with 45% ethanol for 3 times the column volume to obtain eluent A; then wash the column with 80% ethanol for 3 times the column volume to obtain eluent B;
[0050] S5, carry out chromatographic detection to eluent A and eluent B, the result is as follows image 3 shown, from image 3 It can be...
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