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In vivo fluorescence enhanced optical tomography reconstruction of lungs cancer of non immersed small animals

机译:体内荧光增强光学体层摄影术重建非浸没小动物肺癌

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摘要

Fluorescence enhanced diffuse optical tomography (fDOT) is envisioned to be useful to collect functional information from small animal models. For oncology applications, cancer-targeted fluorescent markers can be used as a surrogate of the cancer activity. We are developing a continuous wave fDOT bench intended to be integrated in systems dedicated to whole body small animal fluorescence analyses. The focus is currently put on the reconstruction of non immersed small animals imaged by a CCD camera. The reconstruction stage already corrects the tissue heterogeneity artifacts through the computation of an optical heterogeneity map. We will show how this formalism coupled with the determination of the animal boundaries performed by a laser scanner, can be used to manage non contact acquisitions. The time of reconstruction for a 10 × 9 laser source positions, 45 × 40 detector elements and 14 × 11 × 14 mesh voxels is typically 10 minutes on a 3GHz PCs corresponding to the acquisition time allowing the two tasks to be performed in parallel. The system is validated on an in vivo experiment performed on three healthy nude mice and a mouse bearing a lung tumor at 10, 12 and 14 days after implantation allowing the follow up of the disease. The 3D fluorescence reconstructions of this mouse are presented and the total fluorescence amounts are compared.
机译:设想荧光增强漫射光学层析成像(fDOT)可用于从小型动物模型收集功能信息。对于肿瘤学应用,可以将靶向癌症的荧光标记物用作癌症活性的替代物。我们正在开发连续波fDOT实验台,该实验台将集成到专门用于全身小动物荧光分析的系统中。目前的重点是重建由CCD相机成像的未浸入水中的小动物。重建阶段已经通过光学异质图的计算纠正了组织异质伪影。我们将展示这种形式主义与激光扫描仪对动物边界的确定相结合,如何用于管理非接触式获取。在3 GHz PC上,对10×9激光源位置,45×40检测器元件和14×11×14网格体素的重建时间通常为10分钟,这与采集时间相对应,从而可以并行执行两项任务。该系统在植入后10、12和14天对三只健康的裸鼠和患有肺肿瘤的小鼠进行的体内实验中得到验证,从而可以对该疾病进行随访。介绍了该小鼠的3D荧光重建,并比较了总荧光量。

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