首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Hand-held high-resolution fluorescence imaging system for fluorescence-guided surgery of patient and cell-line pancreatic tumors growing orthotopically in nude mice
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Hand-held high-resolution fluorescence imaging system for fluorescence-guided surgery of patient and cell-line pancreatic tumors growing orthotopically in nude mice

机译:手持式高分辨率荧光成像系统,用于在裸鼠体内原位生长的患者和细胞系胰腺肿瘤进行荧光引导手术

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Background In this study, we investigated the advantages of fluorescence-guided surgery (FGS) in mice of a portable hand-sized imaging system compared with a large fluorescence imaging system or a long-working-distance fluorescence microscope. Methods Mouse models of human pancreatic cancer for FGS included the following: (1) MiaPaCa-2-expressing green fluorescent protein, (2) BxPC3 labeled with Alexa Fluor 488-conjucated anti-carcinoembryonic antigen (CEA) antibody, and (3) patient-derived orthotopic xenograft (PDOX) labeled with Alexa Fluor 488-conjugated anti-carbohydrate antigen 19-9 antibody. Results Each device could clearly detect the primary MiaPaCa-2-green fluorescent protein tumor and any residual tumor after FGS. In the BxPC3 model labeled with Alexa Fluor 488-conjugated anti-CEA, each device could detect the primary tumor, but the MVX10 could not clearly detect the residual tumor remaining after FGS whereas the other devices could. In the PDOX model labeled with Alexa Fluor 488-conjugated anti-carbohydrate antigen 19-9, only the portable hand-held device could distinguish the residual tumor from the background, and complete resection of the residual tumor was achieved under fluorescence navigation. Conclusions The results described in the present report suggest that the hand-held mobile imaging system can be applied to the clinic for FGS because of its convenient size and high sensitivity which should help make FGS widely used.
机译:背景技术在这项研究中,我们调查了与大型荧光成像系统或长距离荧光显微镜相比,便携式手大小成像系统的小鼠中的荧光引导手术(FGS)的优势。方法用于FGS的人类胰腺癌小鼠模型包括:(1)表达MiaPaCa-2的绿色荧光蛋白,(2)用Alexa Fluor 488结合的抗癌胚抗原(CEA)抗体标记的BxPC3,以及(3)患者标记的Alexa Fluor 488结合抗碳水化合物抗原19-9抗体标记的原位异种移植物(PDOX)。结果每台设备均可清楚地检测出原发性MiaPaCa-2-green荧光蛋白肿瘤和FGS后残留的肿瘤。在用Alexa Fluor 488偶联的抗CEA标记的BxPC3模型中,每个设备都可以检测到原发性肿瘤,但是MVX10不能清晰地检测FGS后残留的残留肿瘤,而其他设备则可以。在用Alexa Fluor 488结合的抗碳水化合物抗原19-9标记的PDOX模型中,只有便携式手持设备才能将残留肿瘤与背景区分开,并且在荧光导航下可以完全切除残留肿瘤。结论本报告中描述的结果表明,该手持式移动成像系统具有方便的尺寸和较高的灵敏度,因此可以在FGS的临床应用,这将有助于FGS的广泛应用。

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