Application of cannabidiol in preparation of medicine for treating acute B lymphocytic leukemia
A technology of B lymphocytes and cannabidiol, which is applied in the field of biomedicine and can solve the problems that cannot be used to predict efficacy and the like
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Embodiment 1
[0033]Embodiment 1, the inhibitory effect of cannabidiol (CBD) on the survival of human acute lymphoblastic leukemia cell Nalm-6 in vitro
[0034] Cannabidiol (CBD) was dissolved in DMSO to a concentration of 50 μM and stored at -20°C until use. Cannabidiol (CBD) was further diluted to the required concentration before use, and the DMSO concentration was determined to be less than 0.001%. The human acute B-lymphoblastic leukemia cell Nalm-6 used in this experiment was used as the test cell. The cells were cultured at 37°C in a humid atmosphere with 5% CO2 and 95% air, and the culture medium was RPMI-1640 containing 10% heat-inactivated fetal bovine serum. The survival rate of human acute B-lymphoblastic leukemia cells Nalm-6 at different concentrations of cannabidiol (CBD) was tested.
[0035] result: figure 1 Describes the survival of Nalm-6 human acute lymphoblastic leukemia cells when cannabidiol (CBD) is administered. It can be seen that as the dose of cannabidiol (CBD...
Embodiment 2
[0036] Embodiment 2, cannabidiol (CBD) is to the inhibitory effect of human acute lymphoblastic leukemia cell Reh survival in vitro
[0037] Cannabidiol (CBD) was dissolved in DMSO to a concentration of 50 μM and stored at -20°C until use. Cannabidiol (CBD) was further diluted to the required concentration before use, and the DMSO concentration was determined to be less than 0.001%. The human acute B-lymphoblastic leukemia cell line Reh used in this experiment was used as the test cell. The cells were cultured at 37°C in a humid atmosphere with 5% CO2 and 95% air, and the culture medium was RPMI-1640 containing 10% heat-inactivated fetal bovine serum. The survival of human acute B-lymphoblastic leukemia cells Reh was tested at various concentrations of cannabidiol (CBD).
[0038] result: figure 2 The survival of human acute B-lymphoblastic leukemia cells Reh in response to cannabidiol (CBD) administration is described. It can be seen that as the dose of cannabidiol (CBD) ...
Embodiment 3
[0039] Embodiment 3, cannabidiol (CBD) is to human acute lymphoblastic leukemia cell RS4 in vitro; 11 survival inhibitory effect
[0040] Cannabidiol (CBD) was dissolved in DMSO to a concentration of 50 μM and stored at -20°C until use. Cannabidiol (CBD) was further diluted to the required concentration before use, and the DMSO concentration was determined to be less than 0.001%. The human acute lymphoblastic leukemia cell line RS4;11 used in this experiment was used as the test cell. The cells were cultured at 37°C in a humid atmosphere with 5% CO2 and 95% air, and the culture medium was RPMI-1640 containing 10% heat-inactivated fetal bovine serum. The survival of human acute B-lymphoblastic leukemia cells RS4;11 was tested at various cannabidiol (CBD) concentrations.
[0041] result: image 3 The viability of human acute B-lymphoblastic leukemia cells RS4;11 in response to cannabidiol (CBD) administration is described. It can be seen that as the dose of cannabidiol (CBD)...
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