Application of cannabidiol in preparation of medicine for treating non-Hodgkin lymphoma
A non-Hodgkin and cannabidiol technology, applied in the field of biomedicine, can solve the problems affecting the curative effect and disease outcome, poor prognosis and toxic effects of relapsed or refractory non-Hodgkin's lymphoma patients
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Embodiment 1
[0029] Example 1. The inhibitory effect of cannabidiol (CBD) on the survival of human non-Hodgkin's lymphoma cell line Jeko-1 in vitro
[0030] 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 desired concentration before use, and the DMSO concentration was determined to be less than 0.001%. The human non-Hodgkin's lymphoma cell Jeko-1 used in this experiment was used as the test cell. The cells were cultured at 37°C in a humidified atmosphere of 5% CO2 and 95% air in RPMI-1640 containing 10% heat-inactivated fetal bovine serum. The survival of human non-Hodgkin's lymphoma cells Jeko-1 was tested at different concentrations of cannabidiol (CBD).
[0031] result: figure 1 The survival of human non-Hodgkin's lymphoma cells Jeko-1 when administered with cannabidiol (CBD) is described. It can be seen that as the dose of cannabidiol (CBD) increased, the survival rate of the lymphoma c...
Embodiment 2
[0032] Example 2. The inhibitory effect of cannabidiol (CBD) on the survival of human non-Hodgkin's lymphoma cells REC1 in vitro
[0033]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 desired concentration before use, and the DMSO concentration was determined to be less than 0.001%. The human non-Hodgkin's lymphoma cell REC1 used in this experiment was used as the test cell. The cells were cultured at 37°C in a humidified atmosphere of 5% CO2 and 95% air in RPMI-1640 containing 10% heat-inactivated fetal bovine serum. The survival of human non-Hodgkin's lymphoma cells REC1 was tested at various concentrations of cannabidiol (CBD).
[0034] result: figure 2 Survival of human non-Hodgkin's lymphoma cells REC1 in response to cannabidiol (CBD) administration is described. It can be seen that as the dose of cannabidiol (CBD) increased, the survival rate of the lymphoma cells decrea...
Embodiment 3
[0035] Example 3. Cytotoxicity of cannabidiol (CBD) on monocytes isolated and cultured from healthy human peripheral blood and human non-Hodgkin's lymphoma cells (Jeko-1, REC1) in vitro
[0036] The concentration of cannabidiol (CBD) used in this example was 20 μM. In this experimental example, different human non-Hodgkin's lymphoma cells (Jeko-1, REC1) and monocytes isolated and cultured from peripheral blood of healthy people were used as test cells. The specific operation steps for extracting mononuclear cells from peripheral blood collected from normal volunteers are as follows: (1) Dilute the collected anticoagulated blood with an equal amount of normal saline; (2) Add Lymphoprep lymphocytes equal to the volume of blood in a 15ml centrifuge tube Cell separation solution, and add diluted blood, the separation solution should be in the lower layer to avoid mixing of blood and separation solution; (3) Centrifuge at 800 × g in a horizontal rotor for 20 minutes at room tempera...
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