4.7 Article

Nanoscale Copper(II)-Diethyldithiocarbamate Coordination Polymer as a Drug Self-Delivery System for Highly Robust and Specific Cancer Therapy

Journal

MOLECULAR PHARMACEUTICS
Volume 17, Issue 8, Pages 2864-2873

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.0c00284

Keywords

disulfiram; drug repurposing; metal coordination; hyaluronic acid; breast cancer; targeted therapeutics

Funding

  1. Innovation-Driven Project of Central South University [20170030010004]
  2. National Natural Science Foundation of China [21804144, U1903125]
  3. Hunan Engineering Research Center for Optimization of Drug Formulation and Early Clinical Evaluation [2015TP2005]

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Disulfiram (DSF), an old alcohol-aversion drug, has been repurposed for cancer therapy, and mechanistic studies reveal that it needs to be metabolized to diethyldithiocarbamate (DTC) and subsequently coordinates with copper(II) to form the DTC-copper complex (CuET) for anticancer activation. Here, we utilized this mechanism to construct a CuET self-delivery nanosystem based on the metal coordination polymer for highly robust and selective cancer therapy. In our design, the nanoparticles were facilely prepared under mild conditions by virtue of the strong coordination between Cu2+ and DTC, yielding 100% CuET loading capacity and allowing for further hyaluronic acid (HA) modification (CuET@HA NPs). The CuET@HA NPs could selectively deliver into cancer cells and release the active component of CuET in response to both endo/lysosome acidic pH and intracellular abundant GSH, which induces strong cytotoxicity toward cancer cells over normal cells taking advantage of the p97 pathway interference mechanism. Upon intravenous injection, the self-assembled system could passively accumulate into a tumor and elicit potent tumor growth inhibition at a dose of 1 mg/kg without any noticeable side effects. Given the cost-effective and easily scaled-up preparation, our designed nanosystem provides a promising strategy to pave the way for clinical translation of DSF-based cancer chemotherapy.

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