Method for preparing high-purity astaxanthin extract
An astaxanthin and extract technology, which is applied in the field of preparing high-purity astaxanthin extract, can solve problems such as inability to realize industrialized production, and achieve the effects of good promotion and application prospect, good health care function, and high development value.
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[0036] Example 1. A method for preparing a high-purity astaxanthin extract, followed by the following steps:
[0037] 1) Take 1mL of natural astaxanthin oil produced by Ningbo Honglong Biotechnology Co., Ltd. and dilute it with 5mL of absolute ethanol to obtain the diluted astaxanthin crude extract;
[0038] Take 1mL of the diluted crude astaxanthin extract and add 4mL12mmol / L NaOH-anhydrous ethanol solution, mix well and place in a dark place at room temperature (25℃) to saponify for 1h to obtain a saponification solution;
[0039] 2). Add the saponification liquid obtained in step 1) to a dichloromethane-water solution (obtained by mixing 5 mL of dichloromethane + 5 mL of water), mix well, stand still for layering, and discard the upper liquid. The lower liquid was concentrated at 45°C under vacuum (0.09MPa) to obtain an extract (about 200mg);
[0040] 3). Dissolve the extract obtained in step 2) in 1 mL of n-hexane: acetone=4:1 (volume ratio) solution, and load all samples onto a 2...
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[0062] Example 2. A method for preparing a high-purity astaxanthin extract, followed by the following steps:
[0063] 1) Take 0.1 mL of the natural astaxanthin oil produced by Ningbo Honglong Biotechnology Co., Ltd. and dilute it with 0.5 mL of absolute ethanol to obtain the diluted astaxanthin crude extract;
[0064] Take 0.1mL of diluted astaxanthin crude extract and add 0.4mL6mmol / L NaOH-anhydrous ethanol solution, mix well and place in a dark place at room temperature (30℃) for 0.5h saponification to obtain saponification liquid;
[0065] 2). Add the saponification liquid obtained in step 1) to a dichloromethane-water (2mL+1mL) solution, mix well and then stand still for layering, and discard the upper liquid. The lower liquid was concentrated under vacuum at 40°C to obtain the extract;
[0066] 3). Dissolve the extract obtained in step 2) in 1 mL of n-hexane:acetone=4:1 (volume ratio) solution, and load all the samples onto a 2.5cm×40cm silica gel column. The silica gel column u...
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