Novel method for drug loading system constructed by means of sensitization blood platelets for treating immune thrombocytopenia
A technology for thrombocytopenia and sensitive platelets, applied in pharmaceutical formulations, allergic diseases, blood diseases, etc., can solve the problems of short curative effect and high price, and achieve the advantages of prolonged circulation time, good biocompatibility, and avoidance of toxic and side effects. Effect
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Embodiment 1
[0033] A new method of a drug-loading system for treating immune thrombocytopenia constructed based on sensitized platelets carrying vincristine, the method comprising the following steps:
[0034] Step 1: Add 3.2% sodium citrate solution by weight to the obtained whole blood at room temperature of 20±5°C for anticoagulation, and the volume ratio of whole blood to sodium citrate solution is 9:1 After centrifugation at 1200rpm for 5min, platelet-rich plasma was obtained;
[0035] Step 2: Platelet-rich plasma was centrifuged at 3500rpm for 10min, and washed three times with PBS buffer to make it no longer contain plasma and other blood components, and the supernatant was discarded to obtain washed platelets, and the platelet count was controlled to be (5-10)×10 6 / ul.
[0036] Step 3: Incubate 500 μl of the resuspension of washed platelets with 2.5 μl of CD41 antibody in an environment of 25±0.5° C. for 15 minutes with shaking, and centrifuge at 3500 rpm for 2 times for 5 minut...
Embodiment 2
[0045] A new method of a drug-loading system for treating immune thrombocytopenia constructed by carrying modified vindesine on sensitized platelets, the method comprises the following steps:
[0046] Step 1: Add 4% sodium citrate solution by weight to the obtained whole blood at room temperature of 20±5°C for anticoagulation, and the volume ratio of whole blood to sodium citrate solution is 10:1 After centrifugation at 1200rpm for 5min, platelet-rich plasma was obtained;
[0047] Step 2: Platelet-rich plasma was centrifuged at 3500rpm for 5min, and washed three times with PBS buffer to make it no longer contain plasma and other blood components, and the supernatant was discarded to obtain washed platelets, and the platelet count was controlled to be (5-10)×10 6 / ul.
[0048] Step 3: Incubate 400 μl of the resuspension of the washed platelets with 2 μl of CD41 antibody in an environment of 25±0.5° C. for 30 minutes with shaking, and centrifuge at 3500 rpm for 3 times for 10 m...
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