Magnetic resonance imaging (MRI) and optical imaging (OI) are attractive for constructing bimodal probes due to their complementary imaging characteristics. The combination of these two techniques could be a useful tool to simultaneously obtain both anatomical and molecular information as well as to significantly improve the accuracy of detection. In this study, we found that β-diketonate-lanthanide complexes, BHHBCB-Ln, could covalently bind to proteins to exhibit long-lived and intense luminescence (Ln = Eu, τ = 0.52 ms, Φ = 0.40) and remarkably high relaxivity (Ln = Gd, r = 35.67 mM s, r = 43.25 mM s) with excellent water solubility, stability and biocompatibility. Hence, we conjugated BHHBCB-Ln with a tumor-targetable biomacromolecule, transferrin (Tf), to construct the probes, Tf-BHHBCB-Ln, for time-gated luminescence (TGL, Ln = Eu) and MR (Ln = Gd) imaging of cancerous cells in vitro and in vivo. As expected, the as-prepared probes showed high specificity to bind with the transferrin receptor-overexpressed cancerous cells, to enable the probe molecules to be accumulated in these cells. Using Tf-BHHBCB-Ln as probes, the cultured cancerous cells and the tumors in tumor-bearing mice have been clearly visualized by background-free TGL and in vivo MR imaging. The research outcomes suggested the potential of β-diketonate-lanthanide complexes for use in constructing bimodal TGL/MR imaging bioprobes.
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http://dx.doi.org/10.1039/d1tb00144b | DOI Listing |
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