Oral Contributed Presentation
RAM
Renzo Vanna, PhD
PhD, senior scientist
Consiglio Nazionale delle Ricerche - Istituto di Fotonica e Nanotecnologie
Milano, Lombardia, Italy
Benedetta Gavazzoni
Consiglio Nazionale delle Ricerche - Istituto di Fotonica e Nanotecnologie
Milano, Lombardia, Italy
Francesco Manna
Physics Department, Politecnico di Milano
Milano, Lombardia, Italy
Beatrice Lucia Bona
Department of Chemistry, Materials, and Chemical Engineering, Politecnico di Milano
Milano, Lombardia, Italy
Francesca Garello
Department of Molecular Biotechnology and Health Sciences, University of Turin
Turin, Piemonte, Italy
Cristina Chirizzi
IRCCS Istituto Neurologico Carlo Besta
Milan, Lombardia, Italy
Alberto Lux
CNR-ISPC, Sapienza University of Rome
Milano, Lombardia, Italy
Dario Polli, PhD
Professor of Physics
Politecnico di Milano, Department of Physics//CNR-Institute for Photonics and Nanotechnologies
Milan, Lombardia, Italy
Giuseppe Digilio
Università del Piemonte Orientale
Alessandria, Piemonte, Italy
Claudia Conti, PhD
Senior Researcher
CNR-ISPC
Milano, Lombardia, Italy
Francesca Baldelli Bombelli
Department of Chemistry, Materials, and Chemical Engineering, Politecnico di Milano
Milano, Lombardia, Italy
Accurate intraoperative evaluation of tumor-free margins is critical for reducing recurrence rates and improving surgical outcomes. Current gold-standard histopathological analysis is time-consuming, requires extensive sample handling, and may miss residual tumor cells due to sampling limitations. There is thus a strong need for real-time, reliable tools to assess surgical margins directly in situ.
We present a multimodal approach based on fluorinated nanoparticles—PLGA nanocarriers loaded with PERFECTA, a superfluorinated molecular probe with exceptional 19F MRI sensitivity and distinct Raman signatures (1, 2). Nanoparticles were stabilized with either polyvinyl alcohol (PVA) or sodium cholate (NaC) and are amenable to future surface functionalization for tumor targeting.
We first characterized their Raman fingerprints and investigated cellular uptake in NIH3T3 fibroblasts using a custom-built 660 nm inverted Raman microscope equipped for live-cell imaging, revealing time-dependent internalization of both the fluorinated core and the PLGA shell. In vivo studies were performed in BALB/c mice bearing orthotopic mammary tumors. After nanoparticle administration (intratumoral or intravenous), 19F MRI confirmed tumor localization. Raman detection was then performed ex vivo on intact tumors, limbs and whole mice using both a 660 nm microscope and two additional 785 nm systems configured for SORS and micro-SORS. Signals from PERFECTA were consistently detected at tumor surfaces. Adjacent histological sections were further analyzed to confirm tissue-level localization.
This multimodal workflow demonstrates the feasibility of using a single probe for MRI-based tumor localization and in situ Raman-based detection at the surgical level, paving the way for intraoperative assessment of tumor margins in a label-free, histology-independent manner.
1) J. Am. Chem. Soc. 2014, 136, 8524;
2) J. Am. Chem. Soc. 2021, 143, 12253.