Abstract
(19)F magnetic resonance imaging ((19)F MRI), with zero background, high tissue penetration depth, excellent spatial resolution, and nonradioactive features, has attracted considerable attention but faces tough challenges due to the shortage of sensitive and selective targetable probes. Herein, we report a biocompatible and highly sensitive (19)F MRI probe with an adaptable tumor-targeting ability. The fluorine-grafted polymer (PIBMA-F(SON)) probes were rich with sulfoxide and carboxy groups, containing a high fluorine content (∼17 wt %). The probes exhibit superhydrophilicity, strong (19)F MRI signals (enhancement of ∼95-fold), long transverse relaxation time (T(2), 422 ms), and excellent (19)F MRI capability. Conjugation using a targeting peptide (Arg-Gly-Asp, RGD) afforded ultrasmall soft polymer probes (PIBMA-F(SON)-RGD) with superhydrophilicity and tumor-targeting ability suitable for the (19)F MRI of orthotopic bladder cancer. Amidification of 5% of the carboxylate units with oleylamine resulted in PIBMA(OAm)-F(SON) nanoprobes (NPs) via self-assembly, displaying different targeting toward subcutaneous tumors. Further grafting with near-infrared (NIR) dyes renders the probe suitable for NIR-fluorescence and (19)F MRI dual-modality imaging. This study provides a suitable approach for designing highly sensitive and zero-background (19)F MRI probes with a tunable tumor-targeting ability.