Artocarpus hypargyreus hance extract and preparation method and application thereof
A technology of extract and white osmanthus, which is applied in the fields of medicine and food, can solve the problems of inducing skin diseases, cytotoxicity, and failing to meet the needs of the consumer market, and achieve the effect of protecting the skin and preventing skin aging
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Embodiment 1
[0037] After 20 kg of dry stems and branches of Osmanthus osmanthus were crushed, soaked in 100 liters of 95% (v / v) ethanol for 12 hours, then percolated, collected 400 liters of percolation liquid, concentrated and dried to obtain 1.8 kg of extract. Dissolve the extract in distilled water and then extract with chloroform and ethyl acetate respectively, take the ethyl acetate solvent extraction phase, recover the ethyl acetate solvent and concentrate to dryness to obtain 500 grams of Osmanthus osmanthus extract of the present invention. Measured by high-performance liquid chromatography, the chromatographic conditions are: the chromatographic column is a HyperClone BDS C18 (4.6mm × 250mm, 5 μm) column, the mobile phase is 70% (v / v) methanol-0.2% phosphoric acid aqueous solution, and the detection wavelength is 300nm. The sum of the contents of flavonoids artopetelin B, artonin A, artocarpin and brosimone I substituted by isopentenyl in the extract is 40% by weight.
Embodiment 2
[0039] After 20 kg of dried stems and branches of Osmanthus osmanthus were crushed, soaked in 100 liters of 70% (v / v) ethanol for 12 hours, then percolated, collected 400 liters of percolation liquid, concentrated and dried to obtain 1.5 kg of extract. Dissolve the extract in distilled water and then extract with chloroform and ethyl acetate respectively, take the ethyl acetate solvent extraction phase, recover the ethyl acetate solvent and concentrate to dryness to obtain 450 grams of Osmanthus osmanthus extract of the present invention. Determined by high performance liquid chromatography, the chromatographic conditions are: the chromatographic column is HyperClone BDS C 18 (4.6mm × 250mm, 5 μm) column, mobile phase is 70% (v / v) methanol-0.2% phosphoric acid aqueous solution, detection wavelength is 300nm, the flavonoids artopetelin B, artonin A that isopentenyl replaces in this extract The sum of the contents of , artocarpin and brosimone I is 34% by weight.
Embodiment 3
[0041] After 20 kg of dry stems and branches of Osmanthus osmanthus were crushed, soak them in 100 liters, 80 liters, and 60 liters of 80% (v / v) aqueous methanol at room temperature for three times, for 24 hours for the first time, and 12 hours for the second and third times respectively. hours, the combined extracts were concentrated and dried to obtain 1.2 kg of extract. Dissolve the extract in distilled water and then extract it with chloroform and ethyl acetate respectively, take the ethyl acetate solvent extraction phase, recover the ethyl acetate solvent and concentrate to dryness to obtain 420 grams of Osmanthus osmanthus extract of the present invention. Determined by high performance liquid chromatography, the chromatographic conditions are: the chromatographic column is HyperClone BDS C 18(4.6mm * 250mm, 5 μ m) column, mobile phase is 65% (v / v) acetonitrile-0.2% phosphoric acid aqueous solution, detection wavelength is 300nm, the flavonoid compound artopetelin B, art...
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