Method for extracting astaxanthin from haematococcus pluvialis
A technology of Haematococcus pluvialis and astaxanthin, which is applied in the field of biological and chemical processes, can solve the problems of fast wear of high-pressure homogenizers and increased production costs, and achieve the goals of low environmental pollution, low production costs, and improved extraction quality Effect
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Embodiment 1
[0028] Step 1: High pressure extraction to break the algae
[0029] Broken algae: Weigh 10g algae, add 100mL soybean oil to the algae, pump it into a high-pressure vessel at a flow rate of 345mL / min, and perform wall-breaking treatment at a pressure of 100Mpa and a temperature of 4℃. Centrifugal separation to obtain astaxanthin extract and algae residue;
[0030] Step 2: Fast separation of astaxanthin
[0031] Extraction: Mix the astaxanthin extract and algae residue with silica gel at a weight ratio of 2:1, then add 5 mL ethanol and 15 mL ethyl acetate, stir and extract for 1 hour, then load the extraction mixture into the chromatography column;
[0032] Elution: Elute with ethanol and collect the red effluent part;
[0033] Concentration: Distill the red effluent 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 potassium hydroxide-ethanol ...
Embodiment 2
[0041] Step 1: High pressure extraction to break the algae
[0042] Broken algae: Weigh 10g of algae, add 100mL soybean oil to the algae, pump it into a high-pressure vessel at a flow rate of 345mL / min, and perform wall-breaking treatment at a pressure of 200Mpa and a temperature of 4℃. Centrifugal separation to obtain astaxanthin extract and algae residue;
[0043] Step 2: Fast separation of astaxanthin
[0044] Extraction: Mix the astaxanthin extract and the algae residue with silica gel at a weight ratio of 3:1, then add 8mL ethanol and 18mL ethyl acetate, stir and extract for 2h, then load the extraction mixture into the chromatography column;
[0045] Elution: Elute with ethanol and collect the red effluent part;
[0046] Concentration: Distill the red effluent 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 potassium hydroxide-ethanol...
Embodiment 3
[0054] Step 1: High pressure extraction to break the algae
[0055] Broken algae: Weigh 10g algae, add 100mL soybean oil to the algae, pump it into a high-pressure container at a flow rate of 345mL / min, and perform wall-breaking treatment at a pressure of 300Mpa and a temperature of 4℃. Centrifugal separation to obtain astaxanthin extract and algae residue;
[0056] Step 2: Fast separation of astaxanthin
[0057] Extraction: Mix the astaxanthin extract and algae residue with silica gel at a weight ratio of 3:1, then add 10mL ethanol and 20mL ethyl acetate, stir and extract for 3h, then load the extraction mixture into the chromatography column;
[0058] Elution: Elute with ethanol and collect the red effluent part;
[0059] Concentration: Distill the red effluent 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 / L potassium hydroxide-ethanol so...
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