Comparing fluorescent contrast agents for fluorescence guided surgery using 3-D cryo-imaging.

Augustino V Scorzo, Caleb Y Kwon, Rendall R Strawbridge, Ryan B Duke, William R Warner, Kristen L Chen, Chengpei Li, Xiaoyao Fan, David W Roberts, Keith D Paulsen, Scott C Davis
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Abstract

Fluorescence cryo-imaging is a high-resolution optical imaging technique that produces 3-D whole-body biodistributions of fluorescent molecules within an animal specimen. To accomplish this, animal specimens are administered a fluorescent molecule or reporter and are frozen to be autonomously sectioned and imaged at a temperature of -20°C or below. Thus, to apply this technique effectively, administered fluorescent molecules should be relatively invariant to low temperature conditions for cryo-imaging and ideally the fluorescence intensity should be stable and consistent in both physiological and cryo-imaging conditions. Herein, we assessed the mean fluorescence intensity of 11 fluorescent contrast agents as they are frozen in a tissue-simulating phantom experiment and show an example of a tested fluorescent contrast agent in a cryo-imaged whole pig brain. Most fluorescent contrast agents were stable within ~25% except for FITC and PEGylated FITC derivatives, which showed a dramatic decrease in fluorescence intensity when frozen.

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利用三维低温成像比较荧光引导手术的荧光造影剂。
荧光冷冻成像是一种高分辨率光学成像技术,可在动物标本内生成荧光分子的三维全身生物分布。为此,需要给动物标本注射荧光分子或荧光报告物,然后在零下 20 摄氏度或更低的温度下进行冷冻,以便自主切片和成像。因此,要有效地应用这项技术,给药的荧光分子应该对低温成像的低温条件具有相对不变性,而且在生理和低温成像条件下,荧光强度最好都能保持稳定和一致。在此,我们评估了 11 种荧光造影剂在组织模拟模型实验中冷冻时的平均荧光强度,并展示了在低温成像猪全脑中测试荧光造影剂的实例。除了 FITC 和 PEG 化 FITC 衍生物在冷冻后荧光强度急剧下降外,大多数荧光造影剂的荧光强度稳定在约 25% 的范围内。
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