Multibranched-Based Fluorinated Materials: Tailor-Made Design of ¹⁹F-MRI Probes

Beatrice Bona, Dr. Cristina Chirizzi, Prof. Valentina Dichiarante, Prof. Pierangelo Metrangolo, Prof. Francesca Baldelli Bombelli and others have recently published an article on Accounts of Materials Research about "Multibranched-Based Fluorinated Materials: Tailor-Made Design of 19F-MRI Probes".

The full paper can be found at the following link: Multibranched-Based Fluorinated Materials: Tailor-Made Design of 19F-MRI Probes.

Abstract. Future medicine is primarily aiming at the development of novel approaches for an early diagnosis of diseases and a personalized therapy for patients. For achieving these objectives, a key role is played by medical imaging. Among available noninvasive imaging techniques, Fluorine-19 (19F) Magnetic Resonance Imaging (MRI) is emerging as a powerful quantitative detection modality for clinical use both for molecular imaging and for cell tracking. The strength of using 19F-MRI is mainly related to the lack of endogenous organic fluorine in tissues, with no background, enabling the visualization of fluorinated tracers as hot-spot images, adding secondary independent information to the anatomical features provided by the grayscale 1H-MRI. The main challenge for 19F-MRI clinical application is the intrinsic reduced sensitivity of MRI. To improve sensitivity, undoubtedly the use of a high field MRI scanner and cryogenic radiofrequency probes is advantageous, but there is a clear need of developing increasingly effective fluorinated tracers. The ideal tracer should bear as many as possible magnetically equivalent fluorine atoms and show optimal magnetic resonance relaxivity properties (i.e., T1 and T2), which enable reduced acquisition time with the possibility to apply fast imaging methods. Moreover, it should be biocompatible with reduced tendency to bioaccumulate in tissues, which is one of the main drawbacks in using perfluorocarbons (PFCs), together with their difficulty to be chemically modified with functional groups. In fact, PFCs such as perfluorooctyl bromide (PFOB), perfluoro-15-crown-5-ether (PFCE), and linear perfluoropolyethers (PFPE) are currently the most used tracers in 19F-MRI preclinical and clinical studies, with the above-mentioned limitations. In this regard, molecules bearing short branched fluorinated chains gained a lot of attention for their high number of equivalent fluorines and expected capability of reducing bioaccumulation concerns. A valuable building block for branched fluorinated tracers is perfluoro-tert-butanol (PFTB), with nine magnetically equivalent fluorines and easy availability and modification. In this Account we will discuss the main challenges that 19F-MRI has to overcome for increasing its clinical use, highlighting on one hand the need of developing customized fluorinated materials for increasing sensitivity and enabling multimodal properties, and on the other hand, the importance of the ultrastructure of the final formulation for the final biological response (i.e., clearance). In this context, our group has been focusing on the synthesis and development of branched fluorinated tracers, for which the originator is a molecule called PERFECTA (from suPERFluorinatEdContrasT Agent), bearing 36 equiv 19F atoms, which showed not only optimal relaxometry properties but also a very specific and intense Raman signal. Thus, PERFECTA and its derivatives represent a new family of multimodal tracers enabling multiscale analysis, from whole body imaging (19F-MRI) to microscopic detection at the cellular/tissue level (Raman microscopy). We believe that our proposed PFTB strategy can strongly promote the production of increasingly effective 19F-MRI materials with additional functionalities, facilitating the clinical translation of this imaging modality.

 

How to cite:
Beatrice Lucia Bona, Olga Koshkina, Cristina Chirizzi, Valentina Dichiarante, Pierangelo Metrangolo and Francesca Baldelli Bombelli, Multibranched-Based Fluorinated Materials: Tailor-Made Design of 19F-MRI Probes, Acc. Mater. Res., 2022, 4, 1, 71-85
DOI: https://doi.org/10.1021/accountsmr.2c00203

 

Optimization of superfluorinated PLGA nanoparticles for enhanced cell labelling and detection by ¹⁹F-MRI

Dr. Cristina Chirizzi, Prof. Pierangelo Metrangolo, Prof. Francesca Baldelli Bombelli and others have recently published an article on Colloids and Surfaces B: Biointerfaces about the "Optimization of superfluorinated PLGA nanoparticles for enhanced cell labelling and detection by 19F-MRI".

The full paper can be found at the following link: Optimization of superfluorinated PLGA nanoparticles for enhanced cell labelling and detection by 19F-MRI.

Abstract. Fluorine-19 (19F) Magnetic Resonance Imaging (MRI) is an emergent imaging technique for molecular imaging and cell tracking. Lack of intrinsic 19F signals in tissues allows unambiguous in vivo detection of exogenous fluorinated probes, complementary to the anatomical and multiparametric information obtained by standard 1H-MRI. However, the intrinsic low sensitivity of MRI technique requires the need of designing increasingly effective fluorinated tracers. PERFECTA, with its 36 magnetically equivalent 19F atoms and a designed branched molecular structure, represents an excellent superfluorinated tracer. In this paper, we report the development of PERFECTA loaded PLGA NPs stabilized by different coatings as promising 19F-MRI probes. The results clearly show the optimal cellular uptake of the produced colloidally stable PERFECTA loaded PLGA NPs without impact on cells viability. Importantly, NPs stabilization with the anionic surfactant sodium cholate (NaC) clearly enhances NPs internalization within cells with respect to PVA-coated NPs. Moreover, the optimized NPs are characterized by shorter T1 relaxation times with respect to other PERFECTA formulations that would allow the increase of 19F-MRI sensitivity with fast imaging acquisitions.

 

How to cite:
Cristina Chirizzi, Lodovico Gatti, María Sancho-Albero, Victor Sebastian, Manuel Arruebo, Laura Uson, Giulia Neri, Jesus Santamaria, Pierangelo Metrangolo, Linda Chaabane, Francesca Baldelli Bombelli, Optimization of superfluorinated PLGA nanoparticles for enhanced cell labelling and detection by 19F-MRI, Colloids Surf. B, 2022, 112932
DOI: https://doi.org/10.1016/j.colsurfb.2022.112932

 

Emergence of Elastic Properties in a Minimalist Resilin-Derived Heptapeptide upon Bromination

Dr. Andrea Pizzi, Lorenzo Sori, Dr. Claudia Pigliacelli, Prof. Francesca Baldelli Bombelli, Prof. Pierangelo Metrangolo and others have recently published an article on Small about the "Emergence of Elastic Properties in a Minimalist Resilin-Derived Heptapeptide upon Bromination".

The full paper can be found at the following link: Emergence of Elastic Properties in a Minimalist Resilin-Derived Heptapeptide upon Bromination.

Abstract. Bromination is herein exploited to promote the emergence of elastic behavior in a short peptide—SDSYGAP—derived from resilin, a rubber-like protein exerting its role in the jumping and flight systems of insects. Elastic and resilient hydrogels are obtained, which also show self-healing behavior, thanks to the promoted non-covalent interactions that limit deformations and contribute to the structural recovery of the peptide-based hydrogel. In particular, halogen bonds may stabilize the β-sheet organization working as non-covalent cross-links between nearby peptide strands. Importantly, the unmodified peptide (i.e., wild type) does not show such properties. Thus, SDSY(3,5-Br)GAP is a novel minimalist peptide elastomer.

 

How to cite:
Andrea Pizzi, Lorenzo Sori, Claudia Pigliacelli, Alfonso Gautieri, Clara Andolina, Greta Bergamaschi, Alessandro Gori, Pierre Panine, Antonio Mattia Grande, Markus B. Linder, Francesca Baldelli Bombelli, Monica Soncini and Pierangelo Metrangolo, Emergence of Elastic Properties in a Minimalist Resilin-Derived Heptapeptide upon Bromination, Small, 2022, 2200807
DOI: https://doi.org/10.1002/smll.202200807

 

Hydrogen and halogen bond synergy in the self-assembly of 3,5-dihalo-tyrosines: structural and theoretical insights

Lorenzo Sori, Dr. Andrea Pizzi, Prof. Giancarlo Terraneo, Prof. Pierangelo Metrangolo and others have recently published an article on CrystEngComm about "Hydrogen and halogen bond synergy in the self-assembly of 3,5-dihalo-tyrosines: structural and theoretical insights".

The full paper can be found at the following link: Hydrogen and halogen bond synergy in the self-assembly of 3,5-dihalo-tyrosines: structural and theoretical insights.

Abstract. Halogenation, generally introduced on aromatic amino acids, is becoming a key supramolecular tool in peptides. Herein, we report the crystal structures and DFT study of two bis-halogenated tyrosines showing the subtle relationship between hydrogen and halogen bonds in promoting their supramolecular self-assembly.

 

How to cite:
Lorenzo Sori, Andrea Pizzi, Nicola Demitri, Giancarlo Terraneo, Antonio Frontera and Pierangelo Metrangolo, Hydrogen and halogen bond synergy in the self-assembly of 3,5-dihalo-tyrosines: structural and theoretical insights, CrystEngComm, 2022, d2ce00670g
DOI: https://doi.org/10.1039/D2CE00670G

 

Online Participation to the 1st School of Supramolecular and Bio-Nanomaterials

Do not miss the chance to participate online to the 1st School of Supramolecular and Bio-Nanomaterials

Registration is still open at the following link: https://sbn.lakecomoschool.org/registration/.

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School website: https://sbn.lakecomoschool.org.

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