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用于术中成像的近红外荧光小分子

NIR fluorescent small molecules for intraoperative imaging.

作者信息

Owens Eric A, Lee Stephanie, Choi JungMun, Henary Maged, Choi Hak Soo

机构信息

Department of Chemistry, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, GA, USA.

Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

出版信息

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2015 Nov-Dec;7(6):828-38. doi: 10.1002/wnan.1337. Epub 2015 Jan 30.

Abstract

Recent advances in bioimaging and nanomedicine have permitted the exploitation of molecular optical imaging in image-guided surgery; however, the parameters mediating optimum performance of contrast agents are not yet precisely determined. To develop ideal contrast agents for image-guided surgery, we need to consider the following criteria: (1) excitation and emission wavelengths in the near-infrared (NIR) window, (2) optimized optical characteristics for high in vivo performance, (3) overcoming or harnessing biodistribution and clearance, and (4) reducing nonspecific uptake. The design considerations should be focused on optimizing the optical and physicochemical property criteria. Biodistribution and clearance should first be considered because they mediate the fate of a contrast agent in the body such as how long after intravenous injection a contrast agent reaches the peak signal-to-background ratio (SBR) and how long the signal lasts (retention).

摘要

生物成像和纳米医学的最新进展使得分子光学成像在图像引导手术中得以应用;然而,介导造影剂最佳性能的参数尚未精确确定。为了开发用于图像引导手术的理想造影剂,我们需要考虑以下标准:(1)近红外(NIR)窗口中的激发和发射波长,(2)针对高体内性能优化的光学特性,(3)克服或利用生物分布和清除,以及(4)减少非特异性摄取。设计考量应聚焦于优化光学和物理化学性质标准。首先应考虑生物分布和清除,因为它们决定了造影剂在体内的命运,例如静脉注射后造影剂达到峰值信号与背景比(SBR)所需的时间以及信号持续的时长(滞留时间)。

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