In Vivo Combined Photoacoustic Imaging and Photothermal Treatment of HPV‐Negative Head and Neck Carcinoma with NIR‐Responsive Non‐Persistent Plasmon Nano‐Architectures

Author:

Frusca Valentina12,Cavallini Chiara3,Zamborlin Agata14,Drava Giuliana5,Barone Virginia6,Gherardini Lisa7,Chiariello Mario7,Armanetti Paolo3,Ermini Maria Laura1,Menichetti Luca3,Voliani Valerio15ORCID

Affiliation:

1. Center for Nanotechnology Innovation@NEST Istituto Italiano di Tecnologia Piazza San Silvestro 12 Pisa 56127 Italy

2. Scuola Superiore Sant'Anna Piazza Martiri della Libertà 33 Pisa 56127 Italy

3. Institute of Clinical Physiology Italian National Research Council via Giuseppe Moruzzi 1 Pisa 56124 Italy

4. NEST‐Scuola Normale Superiore Piazza San Silvestro 12 Pisa 56127 Italy

5. Department of Pharmacy, School of Medical and Pharmaceutical Sciences University of Genoa Viale Cembrano 4 Genoa 16148 Italy

6. Department of Molecular and Developmental Medicine University of Siena Via Aldo Moro 2 Siena 53100 Italy

7. Institute of Clinical Physiology Italian National Research Council and Core Research Laboratory (CRL) Istituto per lo Studio la Prevenzione e la Rete Oncologica (ISPRO) Via Fiorentina 1 Siena 53100 Italy

Abstract

AbstractThe combination of photoacoustic imaging (PAI) and photothermal therapy (PTT) is an attractive approach in cancer management due to the non‐invasive features combined with real‐time imaging and selective tissue damage by non‐ionizing radiation. This approach is especially appealing for Head and Neck Squamous Cell Carcinoma (HNSCC) management, where up to 40% of patients require modifications of the treatment regimen. On the other hand, most of the agents developed for PAI/PTT suffer from persistence or re‐shaping issues. Here, a unique non‐persistent plasmon nano‐architecture (tNAs‐IRDye) is presented that simultaneously acts as a contrast agent for PAI and as a photothermal transducer for PTT. The tNAs‐IRDye are fully characterized and evaluated in vitro and ex vivo, and their performance as theranostic agents is assessed in HPV‐negative HNSCC murine models. A significant modulation of tumor growth is obtained in vivo upon intratumoral injection of tNAs‐IRDye and subsequent NIR irradiation compared to the solely irradiated control. The outcomes of this study exhibit a noteworthy potential to foster the development of innovative clinical strategies for the management of HPV‐negative head and neck carcinoma.

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

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