Application of sea cucumber enzymatic hydrolysate in preparation of medicine for improving phlebothrombosis
A technology of venous thrombosis and enzymatic hydrolysis solution, which is applied in the field of medicine, can solve the problems of biological activity destruction of active substances, achieve the effects of improving venous thrombosis, protecting the fibrinolytic system, and protecting from damage
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Embodiment 1
[0045] This example is an example of thrombolysis in vivo.
[0046] (1) Experimental grouping and processing
[0047] 84 mice were randomly divided into 5 groups after routine feeding for one week: blank control group (n=16), model control group (n=20), high-dose group (n=16), middle-dose group (n=16) , low dose group (n=16). All groups were administered by intragastric administration, and administered at a dosage of 0.1mL / 10g.bw. Feed for 30 days with weighing every 5 days. The grouping and processing methods are shown in Table 1.
[0048] Table 1 Grouping and processing methods
[0049]
[0050] (2) Preparation of mouse venous thrombosis model
[0051] Modeling was started on the 30th day, and the carrageenan was accurately weighed, and the mass concentration of 0.2% was prepared with physiological saline; after the mice were weighed, the mice were administered by intraperitoneal injection. The injection dose is 0.1mL / 10g.bw. The blank control group was injected wi...
Embodiment 2
[0069] This example is an example of antithrombotic in vitro.
[0070] (1) Antithrombotic model experiment in vitro
[0071] Take fresh New Zealand white rabbit blood, coagulate into clots in the natural state, and divide the blood clots into five equal parts, 0.5g each, and put them in centrifuge tubes. The high-dose group is 800mg / kg, the middle-dose group is 400mg / kg, and the low-dose group is 200mg / kg. Do 6 parallels for each set. Then 1 mL of the corresponding solution was added to the centrifuge tube, and incubated on a constant temperature shaker at 37° C. for 5 h. Finally, take out the remaining plug and weigh it quickly.
[0072] Thrombolysis rate = (weight before thrombolysis - weight after thrombolysis) / weight before thrombolysis × 100%
[0073] (2) Fibrin plate method to measure the in vitro fibrinolytic activity of sea cucumber enzymatic hydrolyzate
[0074] Solution preparation:
[0075] ② Accurately weigh 0.075g of fibrinogen into a conical flask filled ...
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