A method for separating heparan sulfate and dermatan sulfate in heparin
A technology of heparan sulfate and dermatan sulfate, which is applied in the field of medicine, can solve problems such as the inability to separate heparan sulfate and dermatan sulfate in heparan or precise quantitative control, and achieve the effect of easy amplification, avoiding loss, and simple process
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Embodiment 1
[0021] This embodiment provides a method for separating heparan sulfate and dermatan sulfate in heparan, which comprises the following steps:
[0022] (a) 40 g of heparinoid (specific optical rotation +5°, anticoagulant factor Xa activity 15 IU / mg) was dissolved in 400 ml of deionized water to prepare a 10% heparinoid solution;
[0023] (b) Inject the heparinoid solution into a polyacrylate anion exchange column with a column volume of 4 L for adsorption;
[0024] (c) Use 0~1mol / L sodium chloride solution for gradient elution (that is, linear gradient elution), the elution time is 100 minutes, and collect the eluent of each component; track with an ultraviolet detector (210nm ) to get as figure 1 The spectrogram shown;
[0025] (d) Concentrate the eluent of each component respectively (concentrate the eluent of each component to a sodium chloride concentration of 3~4wt%), add ethanol precipitation (so that each component elutes the ethanol in the mixed solution The concentr...
Embodiment 2
[0028] This example provides a method for separating heparan sulfate and dermatan sulfate in heparan, which is basically the same as the method in Example 1, except that: in step (a), a 5% heparan solution is prepared; finally 17 g of heparan sulfate and 17.5 g of dermatan sulfate were obtained.
Embodiment 3
[0030] This example provides a method for separating heparan sulfate and dermatan sulfate in heparan, which is basically the same as the method in Example 1, except that: in step (a), an 8% heparan solution is prepared; finally 17.2 g of heparan sulfate and 18.1 g of dermatan sulfate were obtained.
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