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Discover Supplement-Drug Interactions

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Last Updated: 3 years ago

Possible Interaction: Doxorubicin Hydrochloride and Polypeptides

Research Papers that Mention the Interaction

Haemolysis assays demonstrated that the polypeptide was haemocompatible, and the polypeptide drug carrier significantly reduced the haemolysis ratio of DOX·HCl.
Journal of colloid and interface science  •  2016  |  View Paper
In vitro cytotoxicity and hemolysis assays demonstrated that the block copolypeptide was cytocompatible and hemocompatible, and the presence of copolypeptide carrier could reduce the hemolysis ratio of DOX·HCl significantly.
ACS applied materials & interfaces  •  2013  |  View Paper
The spontaneous formation of polymersomes with uniform size is found to occur in aqueous medium via electrostatic interaction between the anionic polypeptide and cationic doxorubicin hydrochloride (DOX·HCl).
Macromolecular bioscience  •  2013  |  View Paper
Doxorubicin intercalates into mitochondrial DNA (mtDNA) and disrupts genes encoding for polypeptides that make adenosine triphosphate.
Cancer  •  2016  |  View Paper
Inhibition of c-Myc and Max dimerization by this polypeptide leads to as much as a 2-fold reduction in the doxorubicin and etoposide IC(50) in three different cell lines tested.
This report demonstrates that pretreatment of cells with a polypeptide , which inhibits c-Myc transcriptional function causes cells to be more susceptible to the topoisomerase II inhibitors doxorubicin and etoposide.
Biochemical pharmacology  •  2006  |  View Paper
Two co-regulated polypeptides around 64 kDa (termed p64) were induced 10-30-fold in response to adriamycin and some other drugs at the IC50 (the concentration inhibiting cell growth by 50%).
Mutation research  •  1995  |  View Paper