{"title":"Single- and multi-modal molecular probes with second near-infrared activatable optical signals for disease diagnosis and theranostics","authors":"Minghui Wang, Shuaige Bai, Yan Zhang","doi":"10.1039/d5cs00502g","DOIUrl":null,"url":null,"abstract":"Optical imaging in the second near-infrared window (NIR-II, 1000–1700 nm) enables real-time visualization of deep tissues with a higher signal-to-noise ratio than that enabled by visible and first NIR (NIR-I, 700–1000 nm) imaging owing to reduced tissue scattering and lower tissue autofluorescence. Its imaging capability can be further enhanced by integrating other imaging modalities, providing complementary biological information in living subjects. In parallel, activatable molecular probes have been designed to change signals only in the presence of biomarkers of interest, offering higher detection sensitivity and specificity than traditional “always-on” probes. These probes can also act as delivery vehicles for therapeutics, providing opportunities for precise imaging-guided therapy. This review highlights the recent advances in the development of single- and multi-modal molecular probes with NIR-II activatable optical signals for disease detection and theranostics. We begin by introducing the probe's design strategies, focusing on molecular mechanisms that enable activatable NIR-II optical signal output and biomarker specificity. Next, strategies to optimize the probe's performance in terms of improving its optical properties and overcoming biological barriers are discussed. Subsequently, the diagnostic and theranostic applications of these probes are detailed with representative examples across various <em>in vivo</em> disease models and <em>in vitro</em> tissue biopsy. Finally, we discuss the challenges and future perspectives for improving their diagnostic accuracy and precision theranostic capabilities in this emerging field.","PeriodicalId":68,"journal":{"name":"Chemical Society Reviews","volume":"20 1","pages":""},"PeriodicalIF":40.4000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Society Reviews","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cs00502g","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Optical imaging in the second near-infrared window (NIR-II, 1000–1700 nm) enables real-time visualization of deep tissues with a higher signal-to-noise ratio than that enabled by visible and first NIR (NIR-I, 700–1000 nm) imaging owing to reduced tissue scattering and lower tissue autofluorescence. Its imaging capability can be further enhanced by integrating other imaging modalities, providing complementary biological information in living subjects. In parallel, activatable molecular probes have been designed to change signals only in the presence of biomarkers of interest, offering higher detection sensitivity and specificity than traditional “always-on” probes. These probes can also act as delivery vehicles for therapeutics, providing opportunities for precise imaging-guided therapy. This review highlights the recent advances in the development of single- and multi-modal molecular probes with NIR-II activatable optical signals for disease detection and theranostics. We begin by introducing the probe's design strategies, focusing on molecular mechanisms that enable activatable NIR-II optical signal output and biomarker specificity. Next, strategies to optimize the probe's performance in terms of improving its optical properties and overcoming biological barriers are discussed. Subsequently, the diagnostic and theranostic applications of these probes are detailed with representative examples across various in vivo disease models and in vitro tissue biopsy. Finally, we discuss the challenges and future perspectives for improving their diagnostic accuracy and precision theranostic capabilities in this emerging field.
第二个近红外窗口(NIR- ii, 1000-1700 nm)的光学成像由于减少了组织散射和较低的组织自身荧光,因此比可见光和第一近红外窗口(NIR- i, 700-1000 nm)成像具有更高的信噪比,能够实时可视化深部组织。它的成像能力可以通过整合其他成像方式进一步增强,为活体提供补充的生物信息。与此同时,可激活的分子探针被设计为仅在感兴趣的生物标志物存在时改变信号,比传统的“永远在线”探针提供更高的检测灵敏度和特异性。这些探针还可以作为治疗药物的运载工具,为精确的成像引导治疗提供机会。本文综述了具有NIR-II可激活光信号的单模态和多模态分子探针在疾病检测和治疗方面的最新进展。我们首先介绍了探针的设计策略,重点介绍了激活NIR-II光信号输出和生物标志物特异性的分子机制。接下来,从改善其光学特性和克服生物屏障方面对探针性能进行了优化。随后,通过各种体内疾病模型和体外组织活检的代表性例子,详细介绍了这些探针的诊断和治疗应用。最后,我们讨论了在这一新兴领域提高其诊断准确性和精确治疗能力的挑战和未来前景。
期刊介绍:
Chemical Society Reviews is published by: Royal Society of Chemistry.
Focus: Review articles on topics of current interest in chemistry;
Predecessors: Quarterly Reviews, Chemical Society (1947–1971);
Current title: Since 1971;
Impact factor: 60.615 (2021);
Themed issues: Occasional themed issues on new and emerging areas of research in the chemical sciences