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  3. Preclinical pharmacology of patient-derived extracellular vesicles for the intraoperative imaging of tumors.
 

Preclinical pharmacology of patient-derived extracellular vesicles for the intraoperative imaging of tumors.

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BORIS DOI
10.48620/70331
Date of Publication
September 2024
Publication Type
Article
Division/Institute

Department of Clinica...

Contributor
Villa, Alessandro
Crescenti, Daniela
De Mitri, Zemira
Crippa, Elisabetta
Rosa, Silvia
Rizzi, Nicoletta
Shojaei-Ghahrizjani, Fereshteh
Rebecchi, Monica
Vincenti, Simona
Department of Clinical Veterinary Medicine, Small Animal Clinic, Surgery
Department of Clinical Veterinary Medicine, Small Animal Clinic
Department of Clinical Veterinary Medicine
Selmin, Francesca
Brunialti, Electra
Simonotti, Nicolò
Maspero, Marianna
Dei Cas, Michele
Recordati, Camilla
Paltrinieri, Saverio
Giordano, Alessia
Paroni, Rita
Galassi, Margherita
Ladisa, Vito
Arienti, Flavio
Cilurzo, Francesco
Mazzaferro, Vincenzo
Ciana, Paolo
Series
Theranostics
ISSN or ISBN (if monograph)
1838-7640
Publisher
Ivyspring International Publisher
Language
English
Publisher DOI
10.7150/thno.98671
PubMed ID
39431003
Uncontrolled Keywords

Bench-to-bedside Tran...

EV Biodistribution Ki...

Intraoperative Imagin...

Toxicology

Description
Extracellular vesicles (EVs) derived from the plasma of oncological patients exhibit significant tumor-targeting properties, unlike those from healthy individuals. We have previously shown the feasibility of formulating the near-infrared (NIR) fluorescent dye indocyanine green (ICG) with patient-derived extracellular vesicles (PDEVs) for selective delivery to neoplastic tissue. This staining protocol holds promise for clinical application in intraoperative tumor margin imaging, enabling precise neoplastic tissue resection. To this end, we propose the ONCOGREEN protocol, involving PDEV isolation, ICG loading, and reinfusion into the same patients. : By in vivo studies on mice, we outlined key pharmacological parameters of PDEVs-ICG for intraoperative tumor imaging, PDEV biodistribution kinetics, and potential treatment-related toxicological effects. Additionally, we established a plasmapheresis-based protocol for isolating autologous PDEVs, ensuring the necessary large-scale dosage for human treatment. A potential lyophilization-based preservation method was also explored to facilitate the storage and transport of PDEVs. : The study identified the effective dose of PDEVs-ICG necessary for clear intraoperative tumor margin imaging. The biodistribution kinetics of PDEVs showed favorable targeting to neoplastic tissues, without off-target distribution. Toxicological assessments revealed no significant adverse effects associated with the treatment. The plasmapheresis-based isolation protocol successfully yielded a sufficient quantity of autologous PDEVs, and the lyophilization preservation method maintained the functional integrity of PDEVs for subsequent clinical application. : Our research lays the groundwork for the direct clinical application of autologous PDEVs, initially focusing on intraoperative imaging. Utilizing autologous PDEVs has the potential to accelerate the integration of EVs as a targeted delivery tool for anti-neoplastic agents to cancerous tissue. This approach promises to enhance the precision of neoplastic tissue resection and improve overall surgical outcomes for oncological patients.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/179987
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v14p6301.pdftextAdobe PDF2.71 MBpublishedOpen
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