Technology for extracting heparin sulfate from duodena
A technology of heparan sulfate and duodenum, applied in the field of biomedicine, can solve the problems of uncontrollable product quality of heparan sulfate, inability to effectively improve yield, low chemical purity, etc., and achieve controllable product quality and suitable for large-scale production. Production, the effect of high chemical purity
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[0061] Option One:
[0062] ⑴ Thaw 1Kg pig duodenum, remove excess fat, wash and mince to obtain intestinal paste.
[0063] ⑵. Add 3000mL of water under stirring, adjust the temperature to 60℃, pH10.0, add 30g of Novozymes protease, and enzymatically hydrolyze for 8 hours.
[0064] (3) Adjust the pH to 7.0, raise the temperature to 90°C, and heat for 10 minutes.
[0065] ⑷. Cool the material liquid to room temperature, centrifuge, and collect the centrifugal liquid.
[0066] ⑸. Add 300mL of A98 resin, and absorb in a 60℃ water bath for 5 hours.
[0067] ⑹. Clean the adsorbed resin, add 900 mL of 2.5% sodium chloride solution, add in three times, stir for 30 minutes each time, and collect the eluent. Then add 900 mL of 6% sodium chloride solution, add in three times, stir for 60 minutes each time, and collect the eluent.
[0068] ⑺. Add 45 g of sodium chloride to the collected 6% eluate, and add 1300 mL of medicinal ethanol for precipitation.
[0069] ⑻ Dissolve the precipitate into 500 mL...
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