Pharmaceutical composition for treating mantle cell lymphoma
A kind of technology of mantle cell lymphoma and composition, applied in the field of pharmaceutical composition for treating mantle cell lymphoma
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Embodiment 1
[0021] Example 1. Effect of Ibrutinib on the proliferation of mantle cell lymphoma Jeko-1
[0022] 1. Ibrutinib drug treatment: 10 mM Ibrutinib was diluted into different concentrations in gradients with DMSO, and 3 replicate wells were set for each concentration.
[0023] 2. Collect and culture healthy Jeko-1 cells, centrifuge at 300 g for 5 min, resuspend the culture medium, use a cell counting plate for cell counting, use a 24-well plate, and resuspend 600 μL of the culture medium according to the cell growth characteristics, each well contains 5×10 4 cells.
[0024] 3. Add different concentrations of Ibrutinib to each well, and put it in 37 ℃, 5% CO 2 They were cultured in a constant temperature incubator for 72 h and divided into experimental group and blank control group.
[0025] 4. Use the MTT method for cell proliferation detection: add 60 μL of 5 mg / mL MTT solution to each well, incubate in the incubator for 1.5 h, observe blue-purple formazan crystals under the m...
Embodiment 2
[0028] Example 2. Effect of Ibrutinib on the proliferation of mantle cell lymphoma Granta-519
[0029] 1. Ibrutinib drug treatment: 10 mM Ibrutinib was diluted into different concentrations in gradients with DMSO, and 3 replicate wells were set for each concentration.
[0030] 2. Collect and cultivate healthy Granta-519 cells, centrifuge at 300 g for 5 min, resuspend the medium, and use a cell counting plate for cell counting. Use a 24-well plate. According to the characteristics of cell growth, resuspend 600 μL of the medium, and each well contains 10×10 4 cells.
[0031] 3. Add different concentrations of Ibrutinib to each well, and put it in 37 ℃, 5% CO 2 They were cultured in a constant temperature incubator for 72 h and divided into experimental group and blank control group.
[0032]4. Use the MTT method for cell proliferation detection: add 60 μL of 5 mg / mL MTT solution to each well, incubate in the incubator for 1.5 h, observe blue-purple formazan crystals under the...
Embodiment 3
[0035] Example 3. Effect of Ganetespib on the proliferation of mantle cell lymphoma Jeko-1
[0036] 1. Ganetespib drug treatment: Dilute 10 mM Ganetespib with DMSO to different concentrations according to the gradient, and set 3 replicate wells for each concentration.
[0037] 2. Collect and cultivate healthy Jeko-1 cells, centrifuge at 300 g for 5 min, resuspend the medium, and use a cell counting plate for cell counting. Use a 24-well plate. According to the cell growth characteristics, resuspend 600 μL of the medium, and each well contains 5×10 4 cells.
[0038] 3. Add different concentrations of Ganetespib to each well, and put in 37 ℃, 5% CO 2 They were cultured in a constant temperature incubator for 72 h and divided into experimental group and blank control group.
[0039] 4. Use the MTT method for cell proliferation detection: add 60 μL of 5 mg / mL MTT solution to each well, incubate in the incubator for 1.5 h, observe blue-purple formazan crystals under the microsco...
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