Preparation method of lymphoma-targeted blood platelet targeting drug loading system carrying and loading anti-tumor drug and connecting CD22 monoclonal antibody
An anti-tumor drug, platelet technology, applied in anti-tumor drugs, drug combinations, pharmaceutical formulations and other directions, can solve the problem of high efficacy of tumor cells, achieve broad application prospects, reduce drug side effects, and have rich effects
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Embodiment 1
[0041] A preparation method of a platelet-targeted drug delivery system carrying daunorubicin linked to CD22 monoclonal antibody, the method comprising the following steps:
[0042] 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;
[0043] Step 2: The platelet-rich plasma was centrifuged at 3600rpm for 10min, and washed three times with PBS buffer to make it no longer contain plasma and other blood components, discard the supernatant to obtain washed platelets, and control the platelet count to (2.5-3.0)×10 5 / ul.
[0044] The third step: 500 μl of the resuspension of the washed platelets and 10 μl of MBS reagent were shaken and reacted in a light-proof environment at 37±0.5°C for 1 hour, and centrifuged at 3600rpm for 3 times, each time for 8 minutes,...
Embodiment 2
[0054] A preparation method of a platelet drug-loading system carrying cyclophosphamide linked to CD22 monoclonal antibody, the method comprising the following steps:
[0055] 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 8min, platelet-rich plasma was obtained;
[0056] Step 2: The platelet-rich plasma was centrifuged at 3600rpm for 12min, and washed three times with PBS buffer to make it no longer contain plasma and other blood components. The supernatant was discarded to obtain washed platelets, and the platelet count was controlled to be (2.5-3.0)×10 5 / ul.
[0057] The third step: 500 μl of the resuspension of the washed platelets and 10 μl of MBS reagent were shaken and reacted in a light-proof environment at 37±0.5°C for 1.5 hours, and centrifuged at 3600rpm for 2 times, each time ...
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