Seminari - Dipartimento Biotecnologie validi dal 05.04.2026 al 05.04.2027. https://www.dbt.univr.it/?ent=seminario&rss=0 https://www.dbt.univr.it/?ent=seminario&rss=0&id=6972 Relatore: Prof. Dr. Silvia Giordani; Provenienza: School of Chemical Sciences, Dublin City University; Data inizio: 2026-04-17; Ora inizio: 15.00; Note orario: Room T.02b -Ca' Vignal3 Borgo Roma; Referente interno: Roberto Fiammengo; Riassunto: Carbon nano-onions (CNOs) are multi-layered fullerenes composed of concentric spsup2;-hybridized carbon shells. Owing to their small size, high surface area, tunable surface chemistry, and excellent biocompatibility, they are emerging as versatile nanocarriers for targeted drug delivery. We established a reliable synthetic strategy to produce pure, monodisperse CNOs and engineered their surfaces with targeting and imaging functionalities. These nanomaterials exhibit strong photostability in aqueous environments, selective uptake by cancer cells, and minimal cytotoxicity. For tumor-specific targeting, supramolecular functionalization with a hyaluronic acidndash;phospholipid conjugate (HA-DMPE) enabled selective recognition of CD44-overexpressing cancer cells. HA-DMPEndash;CNOs demonstrated enhanced uptake in CD44⁺ breast cancer cells compared to CD44⁻ ovarian cells, while zebrafish studies confirmed in vivo biocompatibility. Boron nitridendash;doped CNOs further enabled pH-responsive doxorubicin release, resulting in improved cellular uptake and anticancer activity in breast cancer cell lines (MDA-MB-231, MDA-MB-468, MCF-7) compared to free DOX and Caelyxreg;, with reduced cardiotoxicity in AC16 cardiomyocytes. Additionally, gemcitabine-loaded HA-CNOs showed strong activity against pancreatic cancer cells, and folic acidndash;modified CNOs achieved receptor-mediated targeting with controlled drug release. Overall, these findings establish CNOs as safe, adaptable, and highly effective platforms for precision cancer nanotherapy. Fri, 17 Apr 2026 15:00:00 +0200 https://www.dbt.univr.it/?ent=seminario&rss=0&id=6972