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Nano-palladium is a cellular catalyst for in vivo chemistry

Author

Listed:
  • Miles A. Miller

    (Center for Systems Biology, Massachusetts General Hospital)

  • Bjorn Askevold

    (Center for Systems Biology, Massachusetts General Hospital)

  • Hannes Mikula

    (Center for Systems Biology, Massachusetts General Hospital)

  • Rainer H. Kohler

    (Center for Systems Biology, Massachusetts General Hospital)

  • David Pirovich

    (Center for Systems Biology, Massachusetts General Hospital)

  • Ralph Weissleder

    (Center for Systems Biology, Massachusetts General Hospital
    Harvard Medical School)

Abstract

Palladium catalysts have been widely adopted for organic synthesis and diverse industrial applications given their efficacy and safety, yet their biological in vivo use has been limited to date. Here we show that nanoencapsulated palladium is an effective means to target and treat disease through in vivo catalysis. Palladium nanoparticles (Pd-NPs) were created by screening different Pd compounds and then encapsulating bis[tri(2-furyl)phosphine]palladium(II) dichloride in a biocompatible poly(lactic-co-glycolic acid)-b-polyethyleneglycol platform. Using mouse models of cancer, the NPs efficiently accumulated in tumours, where the Pd-NP activated different model prodrugs. Longitudinal studies confirmed that prodrug activation by Pd-NP inhibits tumour growth, extends survival in tumour-bearing mice and mitigates toxicity compared to standard doxorubicin formulations. Thus, here we demonstrate safe and efficacious in vivo catalytic activity of a Pd compound in mammals.

Suggested Citation

  • Miles A. Miller & Bjorn Askevold & Hannes Mikula & Rainer H. Kohler & David Pirovich & Ralph Weissleder, 2017. "Nano-palladium is a cellular catalyst for in vivo chemistry," Nature Communications, Nature, vol. 8(1), pages 1-13, August.
    • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15906
    DOI: 10.1038/ncomms15906
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    Cited by:

    1. Qing Wang & Yikang Song & Shuowei Yuan & Yaoji Zhu & Wenjing Wang & Ling Chu, 2024. "Prodrug activation by 4,4’-bipyridine-mediated aromatic nitro reduction," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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