P6A-1 Photoacoustic Imaging of Fibrosarcoma Using RGD-Cy 3 as a Targeted Contrast Agent

M. Mienkina, C. Friedrich, J. Waldeck, K. Hensel, N. Gerhardt, C. Bremer, M. Hofmann, G. Schmitz
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Abstract

Photoacoustics (PA) combines the high contrast of optical imaging modalities with the high resolution of clinical ultrasound. Fluorescence mediated tomography (FMT), on the other hand, offers a very high molecular contrast specificity. Therefore, a combination of PA imaging and FMT might be fruitful: e.g. PA imaging could provide valuable a priori information for optical-tomography reconstruction algorithms thereby improving the resolution of FMT. The fusion of PA and FMT will be facilitated by contrast agents that are detectable by both modalities. This study investigates the usage of RGD-Cy 3 as a multimodal contrast agent specific for M21 and HT-1080 tumor cells in vivo (fluorescence reflectance imaging, FRI) and ex vivo (PA). 1.6 muM of RGD-Cy 3 was injected into tumor bearing mice (n=4 M21, n=6 HT-1080). The mice were subjected to in vivo FRI. The FRI showed a typical tracer washout time response, however a statistically significant difference between tumor tissue and muscle tissue could not be shown due to auto-fluorescence and hemoglobin absorption. Similar results were obtained 24 h after the injection of the tracer in biodistribution experiments conducted using harvested organs. Subsequently, the organs were PA imaged using a commercial ultrasound system (Sonix RP) and a Nd:YAG laser (532 nm). The kidney exhibited a mean contrast to the noise-floor of 23.97 dB (plusmn 2.65 standard error of the mean (SEM)), the hearts 23.45 dB (plusmn 0.63 SEM), and the native tumor 26.09 dB. RGD-Cy 3 labeled tumors showed a gain of 0.26 dB (26.35 dB plusmn 0.22 SEM) compared to unlabeled tumors, which was not statistically significant. These results were consistent with in vitro measurements of Cy 3-gelatine mixture phantoms that only showed a 9.4 dB gain compared to the noise- floor for a concentration 81 times higher than in vivo. These findings suggest that RGD-Cy 3 might not be a suitable contrast agent for in vivo PA imaging, although similar fluorochromes like Indocyanine Green were already successfully used for PA imaging.
rgd - cy3靶向造影剂对纤维肉瘤P6A-1光声成像的影响
光声学(PA)结合了高对比度的光学成像模式和高分辨率的临床超声。另一方面,荧光介导的断层扫描(FMT)提供了非常高的分子对比特异性。因此,PA成像与FMT的结合可能是富有成效的:例如,PA成像可以为光学层析成像重建算法提供有价值的先验信息,从而提高FMT的分辨率。两种方式都可检测到的造影剂将促进PA和FMT的融合。本研究探讨了RGD-Cy 3作为M21和HT-1080肿瘤细胞体内(荧光反射成像,FRI)和体外(PA)特异性多模态造影剂的使用情况。1.6 muM rgd - cy3注入荷瘤小鼠(n=4 M21, n=6 HT-1080)。小鼠进行体内FRI, FRI表现出典型的示踪剂冲洗时间反应,但由于自身荧光和血红蛋白吸收,肿瘤组织和肌肉组织之间无法显示统计学上的显著差异。在用摘取的器官进行的生物分布实验中,在注射示踪剂24 h后也得到了类似的结果。随后,使用商用超声系统(Sonix RP)和Nd:YAG激光器(532 nm)对器官进行PA成像。肾脏显示出23.97 dB(平均标准误差为2.65),心脏23.45 dB(平均标准误差为0.63),原生肿瘤26.09 dB。与未标记的肿瘤相比,RGD-Cy 3标记的肿瘤的增益为0.26 dB (26.35 dB + 0.22 SEM),无统计学意义。这些结果与体外测量的Cy - 3-明胶混合模型一致,在比体内高81倍的浓度下,与噪声底相比仅显示9.4 dB增益。这些发现表明,RGD-Cy 3可能不是一种合适的体内PA成像造影剂,尽管类似的荧光染料如吲哚菁绿已经成功地用于PA成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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