Phase-change ultrasound contrast agents for proton range verification: towards an in vivo application

<i>Objective.</i>In proton therapy, range uncertainties prevent optimal benefit from the superior depth-dose characteristics of proton beams over conventional photon-based radiotherapy. To reduce these uncertainties we recently proposed the use of phase-change ultrasound contrast agents as an affordable and effective range verification tool. In particular, superheated nanodroplets can convert into echogenic microbubbles upon proton irradiation, whereby the resulting ultrasound contrast relates to the proton range with high reproducibility. Here, we provide a first<i>in vivo</i>proof-of-concept of this technology.<i>Approach.</i>First, the<i>in vitro</i>biocompatibility of radiation-sensitive poly(vinyl alcohol) perfluorobutane nanodroplets was investigated using several colorimetric assays. Then,<i>in vivo</i>ultrasound contrast was characterized using acoustic droplet vaporization (ADV) and later using proton beam irradiations at varying energies (49.7 MeV and 62 MeV) in healthy Sprague Dawley rats. A preliminary evaluation of the<i>in vivo</i>biocompatibility was performed using ADV and a combination of physiology monitoring and histology.<i>Main results.</i>Nanodroplets were non-toxic over a wide concentration range (<1 mM). In healthy rats, intravenously injected nanodroplets primarily accumulated in the organs of the reticuloendothelial system, where the lifetime of the generated ultrasound contrast (<30 min) was compatible with a typical radiotherapy fraction (<5 min). Spontaneous droplet vaporization did not result in significant background signals. Online ultrasound imaging of the liver of droplet-injected rats demonstrated an energy-dependent proton response, which can be tuned by varying the nanodroplet concentration. However, caution is warranted when deciding on the exact nanodroplet dose regimen as a mild physiological response (drop in cardiac rate, granuloma formation) was observed after ADV.<i>Significance.</i>These findings underline the potential of phase-change ultrasound contrast agents for<i>in vivo</i>proton range verification and provide the next step towards eventual clinical applications.

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Publication Details

Journal
Physics in Medicine and Biology
Published
2024-09-23
DOI
https://doi.org/10.1088/1361-6560/ad7e76
Citations
2
Primary Topic
Electron Spin Resonance Studies
Type
article
Field-Weighted Citation Impact
1.32

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article

Phase-change ultrasound contrast agents for proton range verification: towards an in vivo application

Edmond Sterpin, Marcus Ingram, Uwe Himmelreich, Gonzalo Collado‐Lara et al.
2 citations
Physics in Medicine and Biology
Electron Spin Resonance Studies
1.32
article

Phase-change ultrasound contrast agents for proton range verification: towards an in vivo application

Edmond Sterpin, Marcus Ingram, Uwe Himmelreich, Gonzalo Collado‐Lara, Gaio Paradossi, Bram Carlier, Hendrik J. Vos, Koen Van Den Abeele, Jan D’hooge, Tania Roskams, Sophie V. Heymans, Yosra Toumia, Luigi Musetta
article en
2 citations

Abstract

<i>Objective.</i>In proton therapy, range uncertainties prevent optimal benefit from the superior depth-dose characteristics of proton beams over conventional photon-based radiotherapy. To reduce these uncertainties we recently proposed the use of phase-change ultrasound contrast agents as an affordable and effective range verification tool. In particular, superheated nanodroplets can convert into echogenic microbubbles upon proton irradiation, whereby the resulting ultrasound contrast relates to the proton range with high reproducibility. Here, we provide a first<i>in vivo</i>proof-of-concept of this technology.<i>Approach.</i>First, the<i>in vitro</i>biocompatibility of radiation-sensitive poly(vinyl alcohol) perfluorobutane nanodroplets was investigated using several colorimetric assays. Then,<i>in vivo</i>ultrasound contrast was characterized using acoustic droplet vaporization (ADV) and later using proton beam irradiations at varying energies (49.7 MeV and 62 MeV) in healthy Sprague Dawley rats. A preliminary evaluation of the<i>in vivo</i>biocompatibility was performed using ADV and a combination of physiology monitoring and histology.<i>Main results.</i>Nanodroplets were non-toxic over a wide concentration range (<1 mM). In healthy rats, intravenously injected nanodroplets primarily accumulated in the organs of the reticuloendothelial system, where the lifetime of the generated ultrasound contrast (<30 min) was compatible with a typical radiotherapy fraction (<5 min). Spontaneous droplet vaporization did not result in significant background signals. Online ultrasound imaging of the liver of droplet-injected rats demonstrated an energy-dependent proton response, which can be tuned by varying the nanodroplet concentration. However, caution is warranted when deciding on the exact nanodroplet dose regimen as a mild physiological response (drop in cardiac rate, granuloma formation) was observed after ADV.<i>Significance.</i>These findings underline the potential of phase-change ultrasound contrast agents for<i>in vivo</i>proton range verification and provide the next step towards eventual clinical applications.

Physics in Medicine and BiologyVol. 69(20)
University of Rome Tor Vergata (IT), University College West Flanders (BE), Istituto Nazionale di Fisica Nucleare (IT), Erasmus MC (NL), Institute of Particle Physics (CA), Istituto Nazionale di Fisica Nucleare, Roma Tor Vergata (IT), Vlakwa (BE), Erasmus University Rotterdam (NL), KU Leuven (BE)
Université Catholique de Louvain, European Commission, Fonds Wetenschappelijk Onderzoek, KU Leuven, Vlaamse regering, H2020 Excellent Science
Openalex Percentile: Top 15%
Electron Spin Resonance Studies
1.32
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