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SPECT/CT Imaging of 111Ag for the Preclinical Evaluation of Silver-Based Antimicrobial Nanomedicines

  • Colin Blackadar
  • , Ka Yee Grace Choi
  • , Mary F. Embree
  • , Heather M. Hennkens
  • , Cristina Rodríguez-Rodríguez
  • , Robert E.W. Hancock
  • , Katayoun Saatchi*
  • , Urs O. Häfeli
  • *Corresponding author af dette arbejde

    Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

    Abstract

    With the growing interest in developing silver-based antimicrobials, there is a need to better understand the behavior of silver within biological systems. To address this, we showed that single-photon emission computed tomography (SPECT) is a suitable method to noninvasively image 111Ag-labeled compounds in mice. Formed by neutron irradiation of palladium foil, 111Ag can be rapidly isolated with a high degree of purity and stably incorporated into antimicrobial silver nanoparticles. The imaging showed that nanoparticles are retained in the lungs for up to 48 h following intratracheal instillation, with limited uptake into the systemic circulation or organs of the reticuloendothelial system. Furthermore, in a mouse model of pulmonary Pseudomonas aeruginosa infection, the nanoparticles reduced the bacterial burden by 11.6-fold without inducing the production of pro-inflammatory mediators. Overall, SPECT imaging with 111Ag is a useful tool for noninvasively visualizing the biodistribution of silver-containing compounds in rodents. This knowledge of how silver nanoparticles distribute in vivo can be used to predict their therapeutic efficacy.

    OriginalsprogEngelsk
    TidsskriftACS Applied Materials and Interfaces
    Vol/bind14
    Udgave nummer23
    Sider (fra-til)26382-26393
    ISSN1944-8244
    DOI
    StatusUdgivet - 2022

    Bibliografisk note

    Publisher Copyright:
    © 2022 American Chemical Society. All rights reserved.

    Finansiering

    K.S. and U.O.H. conceptualized the project. U.O.H. and R.E.W.H. provided financial support. C.B. synthesized and characterized the AgNPs. M.E. and H.H. prepared Ag. C.B. and C.R.R performed SPECT/CT and biodistribution experiments. K.G.C. performed in vitro and in vivo characterizations of the AgNP antimicrobial activities. C.B. drafted the manuscript. All authors contributed to the manuscript revisions. 111

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