Gastrin-releasing peptide receptor-targeted gadolinium oxide-based multifunctional nanoparticles for dual magnetic resonance/fluorescent molecular imaging of prostate cancer

摘要

Bombesin (BBN), an analog of gastrin-releasing peptide (GRP), specifically binds to GRP receptors, which are overexpressed in human prostate cancer (PC). Here, we synthesized a BBN-modified gadolinium oxide (Gd₂O₃) nanoprobe containing fluorescein (Gd₂O₃-5(6)-carboxyfluorescein [FI]-polyethylene glycol [PEG]-BBN) for targeted magnetic resonance (MR)/optical dual-modality imaging of PC. The Gd₂O₃-FI-PEG-BBN nanoparticles exhibited a relatively uniform particle size with an average diameter of 52.3?nm and spherical morphology as depicted by transmission electron microscopy. The longitudinal relaxivity (r₁) of Gd₂O₃-FI-PEG-BBN (r₁ =4.23?mM–1s–1) is comparable to that of clinically used Magnevist (Gd-DTPA). Fluorescence microscopy and in vitro cellular MRI demonstrated GRP receptor-specific and enhanced cellular uptake of the Gd₂O₃-FI-PEG-BBN in PC-3 tumor cells. Moreover, Gd₂O₃-FI-PEG-BBN showed more remarkable contrast enhancement than the corresponding nontargeted Gd₂O₃-FI-PEG according to in vivo MRI and fluorescent imaging. Tumor immunohistochemical analysis further demonstrated improved accumulation of the targeted nanoprobe in tumors. BBN-conjugated Gd₂O₃ may be a promising nanoplatform for simultaneous GRP receptor-targeted molecular cancer diagnosis and antitumor drug delivery in future clinical applications.