Activatable Fluorescent-Photoacoustic Integrated Probes with Deep Tissue Penetration for Pathological Diagnosis and Therapeutic Evaluation of Acute Inflammation in Mice

被引:19
作者
Li, Wenxiu [1 ]
Li, Rong [1 ]
Chen, Rui [1 ]
Ai, Sixin [1 ]
Zhu, Huayong [1 ]
Huang, Ling [1 ]
Lin, Weiying [1 ]
机构
[1] Guangxi Univ, Inst Opt Mat & Chem Biol, Sch Chem & Chem Engn, Guangxi Key Lab Electchem & Energy Mat, Nanning 530004, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
ENDOGENOUS CARBON-MONOXIDE; DESIGN; STRATEGIES; AGENTS;
D O I
10.1021/acs.analchem.2c01048
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Inflammation is associated with many diseases, so the development of an excellent near infrared fluorescent (NIRF) and photoacoustic (PA) dual-modality probe is crucial for the accurate diagnosis and efficacy evaluation of inflammation. However, most of the current NIRF/PA scaffolds are based on repurposing existing fluorescent dye platforms that exhibit non-optimal properties for both NIRF and PA signal outputs. Herein, we developed a novel dye scaffold QL-OH by optimizing the NIRF and PA signal of classical hemicyanine dyes. Based on this optimized dye, we developed the first NIRF/ PA dual-mode carbon monoxide (CO) probe QL-CO for noninvasive and sensitive visualization of CO levels in deep inflammatory lesions in vivo. The novel probe QL-CO exhibited rapid and sensitive NIRF775/PA(730) dual activation responses toward CO. In addition, the CO-activated probe QL-CO was successfully used for the diagnosis of inflammation and evaluation of antiinflammation drug efficacy in living mice though the NIRF/PA dual-mode imaging technology for the first time. More importantly, the probe QL-CO could accurately locate the deep inflammatory lesion tissues (approximate to 1 cm) in mice and obtain 3D PA diagnostic images with deep penetration depth and spatial resolution. Therefore, the new NIRF/PA dual-mode probe QL-CO has high potential for deep-tissue diagnosis imaging of CO in vivo. These findings may provide a new tool and approach for future research and diagnosis of CO-associated diseases.
引用
收藏
页码:7996 / 8004
页数:9
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