Federica Fiorini
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Federica Fiorini has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Ariadna Lázaro
Institute of Functional Interfaces (IFG) Karlsruhe Institute of Technology (KIT) Karlsruhe Germany
1 shared publication - Daria Di Prisco
Department of Biochemistry Istituto di Ricerche Farmacologiche Mario Negri IRCCS Milan 20156 Italy
1 shared publication - Elena Longhi
Institut de Science et d'Ingénierie Supramoléculaires (I.S.I.S.) Université de Strasbourg 8 allée Gas-pard Monge Strasbourg 67000 France
1 shared publication - Giulia Tamboia
Department of Biochemistry and Molecular Pharmacology
1 shared publication - Giuseppe Alonci
Department of Research and Development, Matex Lab Switzerland SA, 1228 Geneve, Switzerland
1 shared publication - Luigi Menduti
Dipartimento di Scienze Farmaceutiche, Università degli Studi di Milano, via C. Golgi 19, 20133 Milano, Italy
1 shared publication
Latest Publications
- Open Access
- 6 March 2025
- Published by Wiley in Chemistry – A European Journal
- Vol. 31 (19) , e202404572
Label‐Free 3D Cell Imaging Using Hydrogels Functionalized with Switchable Iridium Complexes
The use of fluorescent labels is the most common tool to visualize cells. However, the internalization of dye molecules often modifies the cell behavior. In this paper we demonstrate that it is possible to transiently label cells using a 3D scaffold, a hydrogel, covalently functionalized with luminescent cyclometalated iridium(III) complexes. The unique feature of our design is that the complexes are emissive only when they interact with the cell membrane while their emission is quenched in water. We exploited this feature to perform real‐time and staining‐free cell visualization and imaging. Iridium functionalized hydrogels are very weakly luminescent when immerged in culture media. When cells are added to them, they interact with the iridium complexes, covalently linked to the gel, and their lipophilic membrane “switches on” the luminescence enabling a clear and dynamic, real‐time 3D visualization of cell proliferation. A complete photophysical and biological study of the materials is presented which demonstrates the potential of our methodology for 3D‐realtime cell tracking.
- 6 March 2025
- Published by Wiley in Chemistry – A European Journal
- Vol. 31 (19) , e202404572
Open AccessLabel‐Free 3D Cell Imaging Using Hydrogels Functionalized with Switchable Iridium Complexes
The use of fluorescent labels is the most common tool to visualize cells. However, the internalization of dye molecules often modifies the cell behavior. In this paper we demonstrate that it is possible to transiently label cells using a 3D scaffold, a hydrogel, covalently functionalized with luminescent cyclometalated iridium(III) complexes. The unique feature of our design is that the complexes are emissive only when they interact with the cell membrane while their emission is quenched in water. We exploited this feature to perform real‐time and staining‐free cell visualization and imaging. Iridium functionalized hydrogels are very weakly luminescent when immerged in culture media. When cells are added to them, they interact with the iridium complexes, covalently linked to the gel, and their lipophilic membrane “switches on” the luminescence enabling a clear and dynamic, real‐time 3D visualization of cell proliferation. A complete photophysical and biological study of the materials is presented which demonstrates the potential of our methodology for 3D‐realtime cell tracking.