Recently, extending single-atom catalysts from mono- to binary sites has been proved to be a promising way to realize more efficient chemical catalytic processes. In this work, atomically dispersed Fe, Pt dinuclear catalysts ((Fe, Pt)-N-C) with an . 2.38 Å distance for Fe (Fe-N) and Pt (Pt-N) could be precisely controlled via a novel secondary-doping strategy. In response to tumor microenvironments, the Fe-N/Pt-N moieties exhibited synergistic catalytic performance for tumor catalytic therapy. Due to its beneficial microstructure and abundant active sites, the Fe-N moiety effectively initiated the intratumoral Fenton-like reaction to release a large amount of toxic hydroxyl radicals (OH), which further induced tumor cell apoptosis. Meanwhile, the bonded Pt-N moiety could also enhance the Fenton-like activity of the Fe-N moiety up to 128.8% by modulating the 3 electronic orbitals of isolated Fe-N sites. In addition, the existence of amorphous carbon revealed high photothermal conversion efficiency when exposed to an 808 nm laser, which synergistically achieved an effective oncotherapy outcome. Therefore, the as-obtained (Fe, Pt)-N-C-FA-PEG has promising potential in the bio-nanomedicine field for inhibiting tumor cell growth and .
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http://dx.doi.org/10.1021/acsami.2c01683 | DOI Listing |
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