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Nanosecond scanned x-ray sheet imaging for time-resolved luminescence tomography

机译:纳秒扫描X射线板成像,用于时间分辨发光断层扫描

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Biomedical imaging techniques are often limited by the loss of resolution with depth due to light scattering inbiological tissue. Beyond a few millimeters in depth, diffuse transport dominates and makes high resolution imagingimpossible using conventional techniques. In this work, light sheet imaging using x-ray photons was developed witha keV x-ray source. This partially overcomes this scattering by generating light within tissue at depth. The lightexcites fluorescent probes that can be used for tumor tracking based upon molecular targeting. Most of the fluorescentprobes have a lifetime in the nanosecond range. In this study, the use of a portable linear accelerator delivering 30-nsx-ray pulses was explored. Using x-ray excitable fluorophores, light was generated within a tissue phantom. Imagestacks were acquired using an intensified camera (PiMAX4 – Princeton Instrument – USA) placed perpendicularly tothe slicing direction of the sample. A solid-state silicon photomultiplier was used to gate acquisition. Although thisdelayed acquisition slightly, it improved the fluorescence signal-to-noise ratio (SNR). A deconvolution algorithmcounteracted the blurring effects of tissue, and image stacks were converted to 3D reconstructions. In summary,nanosecond x-ray pulses can be used to excite fluorophores through radioluminescence phenomenon. Combined withslice imaging, this approach shows promise for time-resolved x-ray luminescence.
机译:生物医学成像技术通常受到由于光散射而具有深度的分辨率的限制生物组织。超过几毫米深度,漫反射占主导地位并使高分辨率成像不可能使用传统技术。在这项工作中,使用X射线光子的光板成像一个kev X射线源。这部分地克服了在深度内的组织内产生光。光明激发荧光探针,其可用于基于分子靶向的肿瘤跟踪。大多数荧光灯探针在纳秒范围内有一生。在本研究中,使用便携式线性加速器提供30-NS探索了X射线脉冲。使用X射线激发荧光团,在组织幻像内产生光。图片使用强化相机(Pimax4 - Princeton仪器 - USA)垂直于样品的切片方向。使用固态硅光电倍增管浇筑。虽然这一点稍微延迟采集,改善了荧光信噪比(SNR)。一种解卷积算法抵消组织的模糊效果,并且图像堆叠被转换为3D重建。总之,纳秒X射线脉冲可用于通过放射发光现象来激发荧光团。结合切片成像,这种方法显示了时间解决的X射线发光的承诺。

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