A method for extracting astaxanthin from Haematococcus pluvialis
A technology of Haematococcus pluvialis and astaxanthin is applied in the fields of biology and chemical technology, which can solve the problems of high-pressure homogenizers wearing fast, increasing production costs, and achieving the effects of less environmental pollution, low production costs, and less impurities.
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Embodiment 1
[0028] Step 1: High-pressure extraction to break the algal wall
[0029] Algae body wall breaking: Weigh 10g algae body, add 100mL soybean oil to the algae body, pump it into a high-pressure container at a flow rate of 345mL / min, and carry out wall breaking treatment at a pressure of 100Mpa and a temperature of 4°C. centrifuged to obtain astaxanthin extract and algae residue;
[0030] Step 2: Rapid separation of astaxanthin
[0031] Extraction: Mix astaxanthin extract, algae residue and silica gel at a weight ratio of 2:1, then add 5mL of ethanol and 15mL of ethyl acetate, stir and extract for 1 hour, then put the extraction mixture into a chromatography column;
[0032] Elution: elute with ethanol, collect the red effluent;
[0033] Concentration: The red effluent was distilled under reduced pressure to obtain a dark red astaxanthin oily liquid.
[0034] Step 3: Crude extraction of astaxanthin oily liquid
[0035] Saponification: Mix astaxanthin oily liquid with 0.06mol / L...
Embodiment 2
[0041] Step 1: High-pressure extraction to break the algal wall
[0042] Algae body wall breaking: Weigh 10g algae body, add 100mL soybean oil to the algae body, pump it into a high-pressure container at a flow rate of 345mL / min, and carry out wall breaking treatment at a pressure of 200Mpa and a temperature of 4°C. centrifuged to obtain astaxanthin extract and algae residue;
[0043] Step 2: Rapid separation of astaxanthin
[0044] Extraction: Mix astaxanthin extract, algae residue and silica gel at a weight ratio of 3:1, then add 8mL of ethanol and 18mL of ethyl acetate, stir and extract for 2 hours, then put the extraction mixture into a chromatography column;
[0045] Elution: elute with ethanol, collect the red effluent;
[0046] Concentration: The red effluent was distilled under reduced pressure to obtain a dark red astaxanthin oily liquid.
[0047] Step 3: Crude extraction of astaxanthin oily liquid
[0048] Saponification: Mix astaxanthin oily liquid with 0.06mol / L ...
Embodiment 3
[0054] Step 1: High-pressure extraction to break the algal wall
[0055] Algae body wall breaking: Weigh 10g algae body, add 100mL soybean oil to the algae body, pump it into a high-pressure container at a flow rate of 345mL / min, and carry out wall breaking treatment at a pressure of 300Mpa and a temperature of 4°C. centrifuged to obtain astaxanthin extract and algae residue;
[0056] Step 2: Rapid separation of astaxanthin
[0057] Extraction: Mix astaxanthin extract, algae residue and silica gel at a weight ratio of 3:1, then add 10mL of ethanol and 20mL of ethyl acetate, stir and extract for 3 hours, then put the extraction mixture into a chromatography column;
[0058] Elution: elute with ethanol, collect the red effluent;
[0059] Concentration: The red effluent was distilled under reduced pressure to obtain a dark red astaxanthin oily liquid.
[0060] Step 3: Crude extraction of astaxanthin oily liquid
[0061] Saponification: Mix astaxanthin oily liquid with 0.06mol...
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