Bionic cell membrane-inner core nanoparticle as well as preparation method and application thereof
A nanoparticle and cell membrane technology, applied in the direction of nanotechnology, nanotechnology, nanomedicine, etc., can solve the problems of high preparation cost and limited application, and achieve the effect of improving effectiveness, reducing drug concentration, and simple and efficient preparation method
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preparation example 1
[0068] (1) Take fresh blood from Balb / c mice, add anticoagulant (anticoagulant: blood=3:7, v / v), centrifuge at 216g for 11min, separate red blood cell layer, and obtain platelet-rich plasma;
[0069] (2) Add platelet extraction buffer (1:1, v / v) to the platelet-rich plasma obtained in step (1), and centrifuge at 850g for 5min to obtain platelet precipitate;
[0070] (3) Add platelet purification buffer (1:1, v / v) to the platelet precipitate obtained in step (2), centrifuge at 1000 g for 5 min after resuspension, and obtain purified platelets;
[0071] (4) The purified platelets obtained in step (3) were repeatedly frozen and thawed at -80° C. to 4° C. for three times, with an interval of 10 minutes between freezing and thawing, centrifuged at 10,000 g for 10 minutes, and resuspended to obtain platelet membranes.
preparation example 2
[0073] (1) Take fresh blood from Balb / c mice, add anticoagulant (anticoagulant: blood=1:5, v / v), centrifuge at 200g for 20min, separate red blood cell layer, and obtain platelet-rich plasma;
[0074] (2) Add platelet extraction buffer (2:1, v / v) to the platelet-rich plasma obtained in step (1), and centrifuge at 1200g for 2min to obtain platelet precipitates;
[0075] (3) Add platelet purification buffer (2:1, v / v) to the platelet precipitate obtained in step (2), and centrifuge at 800 g for 8 min after resuspending to obtain purified platelets;
[0076] (4) The purified platelets obtained in step (3) were repeatedly frozen and thawed four times at -80° C. to 4° C., with a freeze-thaw interval of 15 minutes, centrifuged at 5000 g for 20 minutes, and resuspended to obtain platelet membranes.
preparation example 3
[0078] (1) Take fresh blood from Balb / c mice, add anticoagulant (anticoagulant: blood=1:8, v / v), centrifuge at 230g for 5min, separate red blood cell layer, and obtain platelet-rich plasma;
[0079] (2) Add platelet extraction buffer (1:2, v / v) to the platelet-rich plasma obtained in step (1), and centrifuge at 600 g for 8 min to obtain platelet precipitates;
[0080] (3) Add platelet purification buffer (1:2, v / v) to the platelet precipitate obtained in step (2), centrifuge at 1500 g for 3 min after resuspension, and obtain purified platelets;
[0081] (4) The purified platelets obtained in step (3) were repeatedly frozen and thawed four times at -80° C. to 4° C., with a freeze-thaw interval of 15 minutes, centrifuged at 5000 g for 20 minutes, and resuspended to obtain platelet membranes.
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