纳米探针
化学
荧光团
生物医学中的光声成像
荧光
纳米颗粒
纳米技术
光热治疗
分子成像
量子点
荧光寿命成像显微镜
自体荧光
两亲性
量子产额
生物相容性
共轭体系
作者
Siyu Lu,Jing Wu,Shuxin Lyu,Yifeng Yu,Jong Seung Kim,Ruiping Zhang,Yuling Xiao,Xuechuan Hong,Xiaodong Zeng,Siyu Lu,Jing Wu,Shuxin Lyu,Yifeng Yu,Jong Seung Kim,Ruiping Zhang,Yuling Xiao,Xuechuan Hong,Xiaodong Zeng
标识
DOI:10.1021/acs.analchem.5c05017
摘要
The integration of photoacoustic imaging (PAI) and near-infrared II (NIR-II) fluorescence imaging holds transformative potential for cancer diagnostics but faces challenges in developing high-performance dual-modal contrast agents. We report tH7@CT8, an organic nanoprobe engineered through fluorophore trimerization to address the photothermal conversion efficiency limitations of small-molecule agents. Trimerization of the [1,2,5]thiadiazolo[3,4-g]quinoxaline fluorophore derivative H7 induced aggregation, suppressing fluorescence quantum yield (0.11% vs 0.42% monomer) while amplifying PTCE to 43.1%. Encapsulation within an osteosarcoma-targeting amphiphilic matrix yielded nanoparticles (72 ± 19 nm) with 4-fold enhanced tumor uptake versus nontargeted controls. In orthotopic osteosarcoma models, tH7@CT8 enabled PAI detection and real-time NIR-II guidance with signal (tumor)-to-background ratios >12:1. This work establishes a molecular design strategy to reconcile depth-resolution trade-offs in oncology while advancing organic contrast agents toward clinical translation.
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