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A Chelator-Free Multifunctional [64Cu]CuS Nanoparticle Platform for Simultaneous Micro-PET/CT Imaging and Photothermal Ablation Therapy

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    A Chelator-Free Multifunctional [64Cu]CuS Nanoparticle Platform for Simultaneous Micro-PET/CT Imaging and Photothermal Ablation Therapy
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    Department of Experimental Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, United States, and Department of Pharmaceutical Sciences, Texas Southern University, Houston, Texas 77004, United States
    [email protected]
    †The University of Texas MD Anderson Cancer Center.
    ‡Texas Southern University.
    §On leave from the Department of Nuclear Medicine, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200127, P. R. China.
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    Cite this: J. Am. Chem. Soc. 2010, 132, 43, 15351–15358
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    https://doi.org/10.1021/ja106855m
    Published October 13, 2010
    Copyright © 2010 American Chemical Society
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    Abstract

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    We synthesized and evaluated a novel class of chelator-free [64Cu]CuS nanoparticles (NPs) suitable both for PET imaging and as photothermal coupling agents for photothermal ablation. These [64Cu]CuS NPs are simple to make, possess excellent stability, and allow robust noninvasive micro-PET imaging. Furthermore, the CuS NPs display strong absorption in the near-infrared (NIR) region (peak at 930 nm); passive targeting prefers the tumor site, and mediated ablation of U87 tumor cells occurs upon exposure to NIR light both in vitro and in vivo after either intratumoral or intravenous injection. The combination of small diameter (∼11 nm), strong NIR absorption, and integration of 64Cu as a structural component makes these [64Cu]CuS NPs ideally suited for multifunctional molecular imaging and therapy.

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    Complete refs 17 and 31; NMR, XRD, HRTEM, and DLS characterization data for CuS NPs; stability and radiolabeling efficiency of CuS NPs; and results of in vitro PTA therapy studies. This material is available free of charge via the Internet at http://pubs.acs.org.

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    Cite this: J. Am. Chem. Soc. 2010, 132, 43, 15351–15358
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