Lignin-derived tyrosinase inhibitor and preparation method thereof
A technology of tyrosinase and lignin, which is applied in the field of high-value lignin utilization, and can solve problems such as high dispersion, uneven structure, and uneven lignin activity
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Embodiment 1
[0012] The air-dried corn stalks were pulverized, and 50% ethanol aqueous solution (v / v) was added to cook at 150° C. for 1 h according to the solid-to-liquid ratio of 1:12 (m / v). After the cooking liquor was obtained by suction filtration, ethanol was removed by rotary evaporation and lignin was precipitated. The precipitated lignin is washed with water and centrifuged to remove water-soluble impurities, and freeze-dried to obtain ethanol lignin. After mixing corn stalk ethanol lignin and dichloromethane at a solid-to-liquid ratio of 1:40 (m / v), the lignin raw material was fully dissolved in dichloromethane by ultrasonication for 0.5 h, and the supernatant was obtained by centrifugation. The supernatant was rotary evaporated to remove dichloromethane to obtain low molecular weight lignin. The obtained low molecular weight lignin was analyzed for tyrosinase inhibitory activity, and at a concentration of 0.4 mg / ml, the inhibitory rate of tyrosinase activity was 70.56%.
Embodiment 2
[0014] The air-dried corn stalks were crushed, and 60% ethanol aqueous solution (v / v) was added to cook at 160° C. for 2 hours according to the solid-to-liquid ratio of 1:10 (m / v). After the cooking liquor was obtained by suction filtration, ethanol was removed by rotary evaporation and lignin was precipitated. The precipitated lignin is washed with water and centrifuged to remove water-soluble impurities, and freeze-dried to obtain ethanol lignin. After mixing corn stalk ethanol lignin and dichloromethane at a solid-to-liquid ratio of 1:45 (m / v), the lignin raw material was fully dissolved in dichloromethane by ultrasonication for 1 h, and the supernatant was obtained by centrifugation. The clear liquid was removed by rotary evaporation to remove dichloromethane to obtain low molecular weight lignin. The obtained small molecular weight lignin was analyzed for tyrosinase inhibitory activity, and at a concentration of 0.4 mg / ml, the inhibitory rate of tyrosinase activity was 7...
Embodiment 3
[0016] The air-dried corn stalks were crushed, and 80% ethanol aqueous solution (v / v) was added to cook at 160° C. for 2 hours according to the solid-to-liquid ratio of 1:15 (m / v). After the cooking liquor was obtained by suction filtration, ethanol was removed by rotary evaporation and lignin was precipitated. The precipitated lignin is washed with water and centrifuged to remove water-soluble impurities, and freeze-dried to obtain ethanol lignin. After mixing corn stalk ethanol lignin and dichloromethane at a solid-to-liquid ratio of 1:50 (m / v), the lignin raw material was fully dissolved in dichloromethane by ultrasonication for 0.5 h, and the supernatant was obtained by centrifugation. The supernatant was rotary evaporated to remove dichloromethane to obtain low molecular weight lignin. The obtained low molecular weight lignin was analyzed for tyrosinase inhibitory activity, and at a concentration of 0.4 mg / ml, the inhibitory rate of tyrosinase activity was 73.12%.
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