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本文引用的文献

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Reduction-responsive fluorescence off-on BODIPY-camptothecin conjugates for self-reporting drug release.用于自报告药物释放的还原响应型荧光开-关硼二吡咯-喜树碱共轭物
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Dual-channel NIR activatable theranostic prodrug for spatiotemporal tracking thiol-triggered chemotherapy.用于时空追踪硫醇触发化疗的双通道近红外可激活治疗诊断前药
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Chemical Modulation of Macrophage Function with Subpopulation-Specific Fluorescent Prodrug Conjugates.用亚群特异性荧光前药缀合物对巨噬细胞功能进行化学调控
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Visualization of drug delivery processes using AIEgens.使用聚集诱导发光(AIE)gens可视化药物递送过程。
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Fluorescent bioimaging of pH: from design to applications.荧光生物成像 pH 值:从设计到应用。
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Development of a novel near-infrared fluorescent theranostic combretastain A-4 analogue, YK-5-252, to target triple negative breast cancer.开发一种新型近红外荧光诊疗用癌光啉A-4类似物YK-5-252,用于靶向三阴性乳腺癌。
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Targeted combinational therapy inducing mitochondrial dysfunction.诱导线粒体功能障碍的靶向联合疗法。
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A theranostic prodrug based on FRET for real-time drug release monitoring in response to biothiols.一种基于荧光共振能量转移(FRET)的诊疗前体药物,用于响应生物硫醇时的实时药物释放监测。
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Reconsidering azobenzene as a component of small-molecule hypoxia-mediated cancer drugs: A theranostic case study.重新考虑偶氮苯作为小分子缺氧介导的癌症药物的组成部分:治疗诊断案例研究。
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基于荧光反应的前药缀合物作为靶向癌症诊疗试剂

Fluorogenic reaction-based prodrug conjugates as targeted cancer theranostics.

作者信息

Lee Min Hee, Sharma Amit, Chang Min Jung, Lee Jinju, Son Subin, Sessler Jonathan L, Kang Chulhun, Kim Jong Seung

机构信息

Department of Chemistry, Sookmyung Women's University, Seoul 04310, Korea.

出版信息

Chem Soc Rev. 2018 Jan 2;47(1):28-52. doi: 10.1039/c7cs00557a.

DOI:10.1039/c7cs00557a
PMID:29057403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5750141/
Abstract

Theranostic systems are receiving ever-increasing attention due to their potential therapeutic utility, imaging enhancement capability, and promise for advancing the field of personalized medicine, particularly as it relates to the diagnosis, staging, and treatment of cancer. In this Tutorial Review, we provide an introduction to the concepts of theranostic drug delivery effected via use of conjugates that are able to target cancer cells selectively, provide cytotoxic chemotherapeutics, and produce readily monitored imaging signals in vitro and in vivo. The underlying design concepts, requiring the synthesis of conjugates composed of imaging reporters, masked chemotherapeutic drugs, cleavable linkers, and cancer targeting ligands, are discussed. Particular emphasis is placed on highlighting the potential benefits of fluorogenic reaction-based targeted systems that are activated for both imaging and therapy by cellular entities, e.g., thiols, reactive oxygen species and enzymes, which are present at relatively elevated levels in tumour environments, physiological characteristics of cancer, e.g., hypoxia and acidic pH. Also discussed are systems activated by an external stimulus, such as light. The work summarized in this Tutorial Review will help define the role fluorogenic reaction-based, cancer-targeting theranostics may have in advancing drug discovery efforts, as well as improving our understanding of cellular uptake and drug release mechanisms.

摘要

由于其潜在的治疗效用、成像增强能力以及在推进个性化医疗领域(特别是与癌症的诊断、分期和治疗相关)的前景,治疗诊断系统正受到越来越多的关注。在本教程综述中,我们介绍了通过使用能够选择性靶向癌细胞、提供细胞毒性化疗药物并在体外和体内产生易于监测的成像信号的缀合物来实现治疗诊断药物递送的概念。讨论了其潜在的设计理念,这需要合成由成像报告分子、掩蔽化疗药物、可裂解连接子和癌症靶向配体组成的缀合物。特别强调突出基于荧光反应的靶向系统的潜在益处,这些系统可被细胞实体(如硫醇、活性氧和酶)激活用于成像和治疗,这些细胞实体在肿瘤环境中相对较高水平存在,同时也强调癌症的生理特征(如缺氧和酸性pH)。还讨论了由外部刺激(如光)激活的系统。本教程综述中总结的工作将有助于确定基于荧光反应的癌症靶向治疗诊断在推进药物发现工作以及增进我们对细胞摄取和药物释放机制理解方面可能发挥的作用。