Development of Theranostic Nanoprobes Based on Gd-Doped CdSe QDs Radiolabeled with 177Lu
摘要
Hybrid imaging platforms integrating multiple modalities provide synergistic advantages by combining anatomical, functional, and molecular information. The aim of this study was to develop and evaluate a theranostic nanoprobe based on gadolinium-doped cadmium selenide quantum dots (Gd-CdSe QDs) modified with thioglycolic acid (TGA) and radiolabeled with 177Lu for potential biomedical applications.
MethodsGd-CdSe QDs were synthesized via a three-step aqueous-phase method and subsequently characterized for their structural and optical properties. The QDs were surface-modified with TGA and radiolabeled with 177Lu under mild, chelator-free conditions. Physicochemical characterization included particle size, fluorescence properties, and quantum yield. Cytotoxicity was evaluated in vitro, while biodistribution and imaging performance were studied in both normal and tumor-bearing mice using fluorescence imaging (FLI), magnetic resonance imaging (MRI), and single-photon emission computed tomography (SPECT).
ResultsThe Gd-CdSe QDs exhibited a narrow size distribution (~ 3.5 nm), strong fluorescence emission (λem ≈ 610 nm), high photostability, and a quantum yield (QY) of ~ 50%. Radiolabeling with 177Lu achieved > 99% radiochemical purity (RCP) without the need for chelators. Cytotoxicity assays indicated acceptable biocompatibility at low concentrations with dose-dependent effects. In vivo biodistribution revealed predominant hepatic uptake and notable tumor accumulation, attributed to retention effects. MRI and SPECT imaging confirmed dual-modality tumor visualization and accumulation of the nanoprobe at tumor sites.
ConclusionThe TGA-modified Gd-CdSe QDs radiolabeled with 177Lu demonstrated favorable physicochemical properties, biocompatibility, and multimodal imaging capabilities. This multifunctional trimodal platform (FLI/MRI/SPECT) with potential for therapy shows strong potential for preclinical applications in cancer diagnosis and image-guided therapy development.