Method for extracting undenatured type II collagen from squid cartilage
A squid cartilage and collagen technology, which is applied in the field of type II collagen extraction, can solve problems such as failure to make good use of type II collagen, and achieve the effects of complete deashing, subsequent operations, and improved extraction purity.
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Embodiment 1
[0036] A method for extracting non-denatured type II collagen from squid cartilage, comprising:
[0037] (1) Take the fresh squid to peel off the cartilage, remove the attached muscles, and freeze-dry it under vacuum at -40°C;
[0038] (2) the freeze-dried squid cartilage is pulverized into 100 mesh particle diameter cartilage powder;
[0039] (3) Weigh 100g squid cartilage powder, suspend with 3000mL pH2.0HCl solution, stir slowly at 4°C for 24h, centrifuge at 10000r / min for 30min at 4°C, and remove the supernatant;
[0040] (4) The precipitate was fully washed with deionized water at 4°C, centrifuged at 4°C and 10000r / min, and the precipitate was retained;
[0041] (5) Suspend the precipitate with 3000mL0.5 MEDTA solution (pH8.0), stir slowly at 4°C for 24h, centrifuge at 10000r / min at 4°C for 30min, and remove the supernatant;
[0042] (6) The precipitate was fully washed with deionized water at 4°C, centrifuged at 4°C and 10000r / min, and the precipitate was retained;
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Embodiment 2
[0051] A method for extracting non-denatured type II collagen from squid cartilage, comprising:
[0052] (1) Take the fresh squid to peel off the cartilage, remove the attached muscles, and freeze-dry it under vacuum at -20°C;
[0053] (2) the freeze-dried squid cartilage is pulverized into 200 mesh particle diameter cartilage powder;
[0054] (3) Weigh 100g of squid cartilage powder, suspend in 5000mL of pH3.0HCl solution, stir slowly at 4°C for 24h, centrifuge at 10,000r / min at 4°C for 30 minutes, and remove the supernatant;
[0055] (4) The precipitate was fully washed with deionized water at 4°C, centrifuged at 4°C and 10000r / min, and the precipitate was retained;
[0056] (5) Suspend the precipitate with 5,000 mL of 1.0 MEDTA solution (pH 8.0), stir slowly at 4°C for 24 hours, centrifuge at 10,000 r / min for 30 minutes at 4°C, and remove the supernatant;
[0057] (6) The precipitate was fully washed with deionized water at 4°C, centrifuged at 4°C and 10000r / min, and the ...
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