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Ex vivo fluorescence molecular tomography of the spine

机译:脊柱的离体荧光分子层析成像

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We investigated the potential of fluorescence molecular tomography to image ex vivo samples collected from a large animal model, in this case, a dog spine. Wide-field time-gated fluorescence tomography was employed to assess the impact of multiview acquisition, data type, and intrinsic optical properties on the localization and quantification accuracy in imaging a fluorescent inclusion in the intervertebral disk. As expected, the TG data sets, when combining early and late gates, provide significantly better performances than the CW data sets in terms of localization and quantification. Moreover, the use of multiview imaging protocols led to more accurate localization. Additionally, the incorporation of the heterogeneous nature of the tissue in the model to compute the Jacobians led to improved imaging performances. This preliminary imaging study provides a proof of concept of the feasibility of quantitatively imaging complex ex vivo samples nondestructively and with short acquisition times. This work is the first step towards employing optical molecular imaging of the spine to detect and characterize disc degeneration based on targeted fluorescent probes.
机译:我们研究了荧光分子层析成像技术对从大型动物模型(在本例中为狗脊柱)收集的离体样品成像的潜力。广域时间门控荧光层析成像技术用于评估多视图采集,数据类型和固有光学特性对椎间盘中荧光内含物成像的定位和定量精度的影响。不出所料,当组合早期和晚期门时,TG数据集在定位和量化方面提供了比CW数据集更好的性能。此外,多视图成像协议的使用导致更准确的定位。另外,将组织的异质性并入模型以计算雅可比矩阵导致了改进的成像性能。这项初步的成像研究为无损且采集时间短的复杂离体样品定量成像的可行性提供了概念证明。这项工作是采用脊柱光学分子成像技术来检测和表征基于靶向荧光探针的椎间盘退变的第一步。

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