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体内光学成像:聚焦儿科疾病,技术进展、当前临床前和临床应用及未来展望。

Optical imaging in vivo with a focus on paediatric disease: technical progress, current preclinical and clinical applications and future perspectives.

机构信息

Department of Molecular Biology of Neuronal Signals, Max-Planck-Institute for Experimental Medicine, Hermann-Rein-Str. 3, 37075, Göttingen, Germany.

出版信息

Pediatr Radiol. 2011 Feb;41(2):161-75. doi: 10.1007/s00247-010-1907-0. Epub 2011 Jan 11.

Abstract

To obtain information on the occurrence and location of molecular events as well as to track target-specific probes such as antibodies or peptides, drugs or even cells non-invasively over time, optical imaging (OI) technologies are increasingly applied. Although OI strongly contributes to the advances made in preclinical research, it is so far, with the exception of optical coherence tomography (OCT), only very sparingly applied in clinical settings. Nevertheless, as OI technologies evolve and improve continuously and represent relatively inexpensive and harmful methods, their implementation as clinical tools for the assessment of children disease is increasing. This review focuses on the current preclinical and clinical applications as well as on the future potential of OI in the clinical routine. Herein, we summarize the development of different fluorescence and bioluminescence imaging techniques for microscopic and macroscopic visualization of microstructures and biological processes. In addition, we discuss advantages and limitations of optical probes with distinct mechanisms of target-detection as well as of different bioluminescent reporter systems. Particular attention has been given to the use of near-infrared (NIR) fluorescent probes enabling observation of molecular events in deeper tissue.

摘要

为了获取有关分子事件发生和位置的信息,以及追踪特定靶点的探针(如抗体或肽、药物,甚至细胞)随时间推移的非侵入性变化,光学成像(OI)技术的应用越来越广泛。尽管 OI 为临床前研究的进展做出了巨大贡献,但除了光学相干断层扫描(OCT)外,它在临床环境中的应用非常有限。然而,随着 OI 技术的不断发展和改进,并且相对于其他方法来说具有较低的损伤性和相对低廉的成本,其作为评估儿童疾病的临床工具的应用正在不断增加。本文重点介绍了 OI 在临床常规中的目前的临床前和临床应用以及未来的潜力。在此,我们总结了不同荧光和生物发光成像技术的发展,用于微观和宏观的微结构和生物过程可视化。此外,我们还讨论了具有不同靶标检测机制的光学探针以及不同的生物发光报告系统的优缺点。特别关注了近红外(NIR)荧光探针的使用,因为它能够观察到更深组织中的分子事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c70/3032188/6746119b8020/247_2010_1907_Fig1_HTML.jpg

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