PSMA-targeted fluorescent probe for NIR-II imaging in prostate cancer intraoperative navigation and tumor margin mapping

前列腺癌 医学 边距(机器学习) 放射科 荧光 手术切缘 荧光寿命成像显微镜 前列腺 病理 癌症研究 分子成像 癌症
作者
Zhongji Jiang,Haozhe Tan,Bo Wu,Lin Zhang,Gaohaer Kadeerhan,Jin Zhang,Jiali Jin,Zikuan Zhang,Hong Guo,Wenmin Guo,Jiedong Jia,Jun Tian,Ben Zhong Tang,Dongwen Wang
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:16 (9): 4551-4565
标识
DOI:10.7150/thno.117540
摘要

Accurate delineation of tumor margins during prostate cancer surgery remains challenging due to limited intraoperative visualization and insufficient molecular specificity.Here, we developed a PSMA-targeted near-infrared fluorescent probe, PSMA-12-IRDye800CW, that leverages the clinically used IRDye800CW scaffold and its extended emission tail beyond 1000 nm to support NIR-II fluorescence imaging for intraoperative navigation and histopathological margin mapping.Methods: PSMA-12-IRDye800CW integrates a PSMA-targeting ligand with an albumin-binding linker to enable active targeting and circulation-assisted tumor accumulation.Optical properties, targeting specificity, imaging performance, and biosafety were evaluated in vitro, in prostate cancer xenograft models with direct comparison to indocyanine green (ICG) across defined time points, and in clinical formalin-fixed paraffin-embedded (FFPE) prostate specimens with matched histopathology and PSMA immunohistochemistry. Results: In 22Rv1 (PSMA) xenografts, PSMA-12-IRDye800CW achieved significantly higher tumor-to-background ratios than ICG at key surgical-relevant time points, including 24 h (4.31 0.17 vs. 2.65 0.15), providing a practical imaging window for fluorescence-guided resection.Ex vivo tissue analyses further confirmed significantly higher fluorescence in tumors than in muscle and skin.In human FFPE specimens, fluorescence showed pathology-aligned spatial correspondence with PSMA immunohistochemistry, and fluorescence intensity correlated strongly with PSMA H-scores (R = 0.8616, P < 0.0001), enabling micron-scale histopathological margin mapping.Multimodal biosafety assessments indicated favorable biocompatibility with no evident acute toxicity and low immunogenic potential.Conclusions: PSMA-12-IRDye800CW enables NIR-II fluorescence imaging-assisted intraoperative navigation and provides a quantitative, pathology-anchored readout for histopathological margin mapping in prostate cancer, supporting further clinical validation of this PSMA-targeted strategy for fluorescence-guided surgery and margin assessment.
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