首页> 外文会议>Photonic Therapeutics and Diagnostics III; Progress in Biomedical Optics and Imaging; vol.8 no.1; Proceedings of SPIE-The International Society for Optical Engineering; vol.6424 >Analysis of 18F-fluorodeoxy-glucose PET Imaging Data Captured Before and After Pc 4-mediated Photodynamic Therapy of U87 Tumors in the Athymic Nude Rat
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Analysis of 18F-fluorodeoxy-glucose PET Imaging Data Captured Before and After Pc 4-mediated Photodynamic Therapy of U87 Tumors in the Athymic Nude Rat

机译:Pc 4介导的无胸腺裸鼠U87肿瘤光动力治疗前后捕获的18F-氟脱氧葡萄糖PET成像数据分析

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Introduction: Several workers have proposed the use of PET (Positron Emission Tomography) imaging for the outcome assessment of photodynamic therapy (PDT), especially for deep-seated tumors. We report on our study of 18F-fluorodeoxy-glucose (~(18)F-FDG) PET imaging following brain tumor Pc4-PDT. Our working hypothesis was that the tumor's metabolic activity would decline dramatically following Pc 4-PDT owing to tumor necrosis. Methods: Seven days after intraparenchymal implantation of U87 cells, the brains of 12 athymic nude rats were imaged by micro-CT and/or micro-MR. These animals were also ~(18)F-FDG micro-PET (μPET) scanned before and after Pc 4-PDT. ~(18)F-FDG was used to trace metabolic activity that was monitored via μPET. Occurrence of PDT was confirmed on histology. The analysis of ~(18)F-FDG dose and animal weight normalized μPET activity was studied over the 90 minute μPET scan. Results: Currently, μPET data have been studied for: (1) three of the animals that did not indicate tumor necrosis on histology and were assigned to a "Non-PDT" group, and (2) six animals that exhibited tumor necrosis on histology and were assigned to a "PDT" group. The μPET-detected ~(18)F-FDG uptake activity in the tumor region before and after photoirradiation increased in the Non-PDT group an average of 2.28 times, and in the PDT group it increased an average of 1.15 times. Discussion: We are investigating the cause of the increase in ~(18)F-FDG μPET activity that we observed in the PDT group. The methodology used in this study should be useful in determining whether this or other PET, SPECT, or MR functional imaging protocols will detect both the specificity and sensitivity of brain tumor necrosis following Pc 4-PDT.
机译:简介:几位工作人员已提议将PET(正电子发射断层扫描)成像用于光动力疗法(PDT)的结果评估,尤其是对于深部肿瘤。我们报告了我们对脑肿瘤Pc4-PDT之后的18F-氟脱氧葡萄糖(〜(18)F-FDG)PET成像的研究。我们的工作假设是,由于肿瘤坏死,Pc 4-PDT后肿瘤的代谢活性将急剧下降。方法:实质内植入U87细胞7天后,通过micro-CT和/或micro-MR对12只无胸腺裸鼠的大脑进行成像。在Pc 4-PDT前后对这些动物进行〜(18)F-FDG micro-PET(μPET)扫描。 〜(18)F-FDG用于追踪通过μPET监测的代谢活性。在组织学上证实PDT的发生。在90分钟的μPET扫描中研究了〜(18)F-FDG剂量和动物体重标准化μPET活性的分析。结果:目前,已对μPET数据进行了研究:(1)将三只在组织学上未显示肿瘤坏死的动物归为“非PDT”组,(2)在六只在组织学上显示肿瘤坏死的动物中并分配给“ PDT”组。在非PDT组中,μPET检测到的光照射前后肿瘤区域的〜(18)F-FDG摄取活性平均增加了2.28倍,而在PDT组中平均增加了1.15倍。讨论:我们正在研究在PDT组中观察到的〜(18)F-FDGμPET活性增加的原因。这项研究中使用的方法学应该用于确定此或其他PET,SPECT或MR功能成像方案是否将检测Pc 4-PDT后脑肿瘤坏死的特异性和敏感性。

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