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Last Updated: 3 years ago

Possible Interaction: Cannabidiol and Doxorubicin Hydrochloride

Research Papers that Mention the Interaction

At concentrations ranging from 5 to 100 μM, CBD robustly enhanced the intracellular accumulation of known P-gp substrates rhodamine 123 and doxorubicin in a concentration-dependent manner in Caco-2 and LLC-PK1/MDR1 cells.
Journal of Pharmacology and Experimental Therapeutics  •  2006  |  View Paper
CBD EVs and DOX combination significantly reduced tumor burden (***P<0.001) in MDA-MB-231 xenograft tumor model.
CBD EVs and DOX combination will have profound clinical significance in not only decreasing the side effects but also increasing the therapeutic efficacy of DOX in TNBC.
Western blotting and immunocytochemical analysis demonstrated that CBD EVs and DOX combination decreased the expression of proteins involved in inflammation, metastasis and increased the expression of proteins involved in apoptosis.
International journal of pharmaceutics  •  2021  |  View Paper
CBDsol , previously administered at suboptimal concentrations (cell death <10%), enhanced the PTX and DOX effect in both breast cancer cells.
The co-administration of CBDsol and PTX or DOX showed a synergistic effect.
International journal of pharmaceutics  •  2019  |  View Paper
Immunohistochemical analysis revealed that cannabidiol significantly reduced the expression of inducible nitric oxide synthase, nuclear factor-κB, Fas ligand and caspase-3, and increased the expression of survivin in cardiac tissue of doxorubicin-treated rats.
These results indicate that cannabidiol represents a potential protective agent against doxorubicin cardiac injury.
Environmental toxicology and pharmacology  •  2013  |  View Paper
Moreover, we demonstrate that sub-effective doses of doxorubicin when co-applied with either 2-APB or CBD lead to a significant decrease in the number of living BNL1 ME cell and BNL1 ME cell colonies in comparison to application of doxorubicin alone.
We show that co-application of either cannabidiol (CBD) or 2-APB, the activators of TRPV2 channels, together with doxorubicin leads to significantly higher accumulation of doxorubicin in BNL1 ME cells than in BNL1 ME cells that were exposed to doxorubicin alone.
Front. Pharmacol.  •  2019  |  View Paper