Hydrazone-based molecular
switches serve as efficient ratiometric
pH-sensitive agents that can be tracked with 19F NMR/MRI
and 1H NMR. Structural changes induced between pH 3 and
4 lead to signal appearance and disappearance at 1H and 19F NMR spectra allowing ratiometric pH measurements. The most
pronounced are resonances of the CF3 group shifted by 1.8
ppm with 19F NMR and a hydrazone proton shifted by 2 ppm
with 1H NMR.
Magnetic resonance imaging (MRI) is one of the most powerful imaging tools today, capable of displaying superior soft‐tissue contrast. This review discusses developments in the field of 19F MRI multimodal probes in combination with optical fluorescence imaging (OFI), 1H MRI, chemical exchange saturation transfer (CEST) MRI, ultrasonography (USG), X‐ray computed tomography (CT), single photon emission tomography (SPECT), positron emission tomography (PET), and photoacoustic imaging (PAI). In each case, multimodal 19F MRI probes compensate for the deficiency of individual techniques and offer improved sensitivity or accuracy of detection over unimodal counterparts. Strategies for designing 19F MRI multimodal probes are described with respect to their structure, physicochemical properties, biocompatibility, and the quality of images.
19 F magnetic resonance imaging (MRI) is a promising tool in medical diagnostics. An important class of 19 F MRI contrast agents is based on paramagnetic resonance enhancement. This effect allows an improvement in sensitivity by increasing the number of scans per unit of time or facilitates the development of responsive contrast agents that are based on changes in relaxation rates as a detection principle. In this work, Bloch− Redfield−Wangsness relaxation theory was used to predict the relaxation properties of existing lanthanoid and transition metal complexes of fluoroorganic ligands and to evaluate several design strategies for responsive contrast agents. Electron−nucleus dipole−dipole, Curie relaxation, and contact interactions were included in the model. Potential significance of chemical shift anisotropy−anisotropic dipolar shielding cross-correlation was discussed. The calculated and experimental results were well aligned. The presented model, along with the optimized field-dependent values of electronic relaxation times, could be used for the preliminary selection of the optimal metal ion for applications in 19 F MRI. The results indicate potential advantages of other metal ions in addition to Gd 3+ particularly Cu 2+ , Mn 2+ , Ni 2+ , Fe 3+ , and other lanthanoids as a part of 19 F contrast agents.
This review focuses on multimodal imaging encompassing 19F MRI (magnetic resonance imaging) as one of the modalities. Structure of the probes and example applications in optical fluorescence imaging (OFI), 1H MRI, chemical exchange saturation transfer (CEST), MRI, ultrasonography (USG), X‐ray computed tomography (CT), single‐photon emission tomography (SPECT), positron emission tomography (PET), and photoacoustic imaging (PAI) as well as other less popular techniques were discussed. For more information, see the Review by D. Janasik and T. Krawczyk on page 4–35.
19F MRI is a promising method of diagnosis that can complement the commonly used 1H MRI with gadolinium contrast agents. Copolymers containing fluoroorganic groups demonstrate many advantages as potential 19F MRI contrast agents. In this work, a series of copolymers based on 2,2,2‐trifluoroethyl methacrylate (TFEMA), 1,1,1,3,3,3‐hexafluoroisopropyl methacrylate (HFiPMA), 2‐(dimethylamino)ethyl methacrylate (DMAEMA), or 2‐hydroxyethyl methacrylate (HEMA) units are prepared using atom transfer radical polymerization. The highest S/N values in a 19F NMR spectra is achieved with a copolymer containing 15–25 wt% TFEMA or 18–22 wt% HFiPMA. Copolymers of HFiPMA show a strong effect of pH on T1 and T2 relaxation times while only T2 is significantly affected for the TFEMA copolymers. DFT calculations reveal that the phenomenon is most likely caused by the pH‐induced changes in the distance of fluoroorganic groups within a polymer chain.
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