Nano Letters · 2024 · 15 citations · 67 references
MedicineMolecular BiologyOncologyBiomedical ImagingDiagnostic ImagingMolecular ImagingBreast Cancer ImagingFluorescence ImagingFluorescence MicroscopyMedical ImagingMolecular Imaging In OncologyTumor ImagingAutofluorescenceAutofluorescence ImagingCancer ImagingCancer MisdiagnosisMolecular Imaging Of CancerNear-infrared Fluorescence ImagingSignal-to-background RatioTissue Autofluorescence
Breast cancer (BC) is the most common tumor worldwide and requires crucial molecular typing for treatment and prognosis assessment. Currently, approaches like pathological staining, immunohistochemistry (IHC), and immunofluorescence (IF) face limitations due to the low signal-to-background ratio (SBR) and high tumor heterogeneity, resulting in a high misdiagnosis rate. Fluorescent assay in the second near-infrared region (NIR-II, 1000–1700 nm) exhibits ultrahigh SBR owing to diminished scattering and tissue autofluorescence. Here, we present a NIR-II strategy for accurate BC molecular typing and three-dimensional (3D) visualization based on the atomically precise fluorescent Au 24 Pr 1 clusters. Single-atom Pr doping results in 3.9-fold fluorescence enhancement and long-term photostability. The Au 24 Pr 1 clusters possess high fluorescence centered at ∼1100 nm and the SBR on pathological section diagnosis was 4 times higher than that of NIR-I imaging. This enables high spatial resolution 3D visualization of biopsy specimens, which can surmount tissue heterogeneity for clinical diagnosis of BC.
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