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用于病理诊断和治疗评估的可激活荧光-光声集成探针,具有深组织穿透性,可用于急性炎症的小鼠模型。

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

机构信息

Guangxi Key Laboratory of Electrochemical Energy Materials, Institute of Optical Materials and Chemical Biology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China.

出版信息

Anal Chem. 2022 Jun 7;94(22):7996-8004. doi: 10.1021/acs.analchem.2c01048. Epub 2022 May 23.

DOI:10.1021/acs.analchem.2c01048
PMID:35604398
Abstract

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 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 for noninvasive and sensitive visualization of CO levels in deep inflammatory lesions in vivo. The novel probe exhibited rapid and sensitive NIRF/PA dual activation responses toward CO. In addition, the CO-activated probe was successfully used for the diagnosis of inflammation and evaluation of anti-inflammation drug efficacy in living mice though the NIRF/PA dual-mode imaging technology for the first time. More importantly, the probe could accurately locate the deep inflammatory lesion tissues (≈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 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.

摘要

炎症与许多疾病有关,因此开发一种出色的近红外荧光(NIRF)和光声(PA)双模探针对于炎症的准确诊断和疗效评估至关重要。然而,目前大多数 NIRF/PA 支架都是基于重新利用现有的荧光染料平台,这些平台在 NIRF 和 PA 信号输出方面都不是最佳的。在此,我们通过优化经典半花菁染料的 NIRF 和 PA 信号来开发一种新型染料支架。基于这种优化的染料,我们开发了第一个 NIRF/PA 双模一氧化碳(CO)探针,用于非侵入性和敏感地可视化体内深部炎症病变中的 CO 水平。新型探针对 CO 表现出快速和敏感的 NIRF/PA 双激活响应。此外,该 CO 激活探针还成功地通过 NIRF/PA 双模成像技术首次用于活体小鼠的炎症诊断和抗炎药物疗效评估。更重要的是,该探针可以准确地定位小鼠深部炎症病变组织(≈1cm),并获得具有深穿透深度和空间分辨率的 3D PA 诊断图像。因此,新型 NIRF/PA 双模探针具有在体内对 CO 进行深部组织诊断成像的巨大潜力。这些发现可能为 CO 相关疾病的未来研究和诊断提供新的工具和方法。

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