Copper-doxorubicin as a nanoparticle cargo retains efficacy with minimal toxicity.

ABSTRACT: Repeated administration of chemotherapeutics is typically required for the effective treatment of highly aggressive tumors and often results in systemic toxicity. We have created a copper-doxorubicin complex within the core of liposomes and applied the resulting particle in multidose therapy. Copper and doxorubicin concentrations in the blood pool were similar at 24 h (∼40% of the injected dose), indicating stable circulation of the complex. Highly quenched doxorubicin fluorescence remained in the blood pool over tens of hours, with fluorescence increasing only with the combination of liposome disruption and copper trans-chelation. At 48 h after injection, doxorubicin fluorescence within the heart and skin was one-fifth and one-half, respectively, of fluorescence observed with ammonium sul

SUBMITTER: Kheirolomoom A 

PROVIDER: S-EPMC3037269 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature