Molecular Imaging Program at Stanford (MIPS), Department of Radiology and Bio-X Program, Canary Center at Stanford for Cancer Early Detection, Stanford University, Stanford, California 94305, USA.
J Nucl Med. 2012 Oct;53(10):1579-84. doi: 10.2967/jnumed.111.098541. Epub 2012 Aug 17.
Cerenkov luminescence imaging (CLI) is an emerging new molecular imaging modality that is relatively inexpensive, easy to use, and has high throughput. CLI can image clinically available PET and SPECT probes using optical instrumentation. Cerenkov luminescence endoscopy (CLE) is one of the most intriguing applications that promise potential clinical translation. We developed a prototype customized fiberscopic Cerenkov imaging system to investigate the potential in guiding minimally invasive surgical resection.
All experiments were performed in a dark chamber. Cerenkov luminescence from (18)F-FDG samples containing decaying radioactivity was transmitted through an optical fiber bundle and imaged by an intensified charge-coupled device camera. Phantoms filled with (18)F-FDG were used to assess the imaging spatial resolution. Finally, mice bearing subcutaneous C6 glioma cells were injected intravenously with (18)F-FDG to determine the feasibility of in vivo imaging. The tumor tissues were exposed, and CLI was performed on the mouse before and after surgical removal of the tumor using the fiber-based imaging system and compared with a commercial optical imaging system.
The sensitivity of this particular setup was approximately 45 kBq (1.21 μCi)/300 μL. The 3 smallest sets of cylindric holes in a commercial SPECT phantom were identifiable via this system, demonstrating that the system has a resolution better than 1.2 mm. Finally, the in vivo tumor imaging study demonstrated the feasibility of using CLI to guide the resection of tumor tissues.
This proof-of-concept study explored the feasibility of using fiber-based CLE for the detection of tumor tissue in vivo for guided surgery. With further improvements of the imaging sensitivity and spatial resolution of the current system, CLE may have a significant application in the clinical setting in the near future.
切伦科夫发光成像是一种新兴的分子成像模式,相对便宜、易于使用且具有高通量。CLI 可以使用光学仪器对临床可用的 PET 和 SPECT 探针进行成像。切伦科夫发光内窥镜(CLE)是最具吸引力的应用之一,有望实现潜在的临床转化。我们开发了一种定制的纤维内窥镜切伦科夫成像系统原型,以研究在指导微创手术切除方面的潜力。
所有实验均在暗室内进行。含有放射性衰变的 18F-FDG 样品的切伦科夫发光通过光纤束传输,并通过增强型电荷耦合器件相机进行成像。使用充满 18F-FDG 的体模评估成像空间分辨率。最后,通过静脉内注射 18F-FDG 使皮下 C6 神经胶质瘤细胞荷瘤小鼠,以确定体内成像的可行性。在使用纤维成像系统和商业光学成像系统对肿瘤进行手术切除前后,暴露肿瘤组织并进行 CLI。
该特定设置的灵敏度约为 45 kBq(1.21 μCi)/300 μL。通过该系统可以识别商业 SPECT 体模中的 3 个最小的圆柱孔组,表明系统的分辨率优于 1.2mm。最后,体内肿瘤成像研究表明,使用 CLI 引导肿瘤组织切除是可行的。
这项概念验证研究探索了使用纤维内窥镜 CLE 检测体内肿瘤组织以进行引导手术的可行性。随着当前系统的成像灵敏度和空间分辨率的进一步提高,CLE 可能在不久的将来在临床环境中具有重要的应用。