P. Martins, A. Blanco, P. Crespo, M. Marques, R. Marques, P. M. Gordo, M. Kajetanowicz, G. Korcyl, L. Lopes, J. Michel, M. Palka, M. Traxler, A. Abrunhosa, M. Couceiro, P. Fonte
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Two features are mandatory in a preclinical PET system: a high Full Width at Half Maximum (FWHM) Spatial Resolution (SR), comprised between 0.40 and 0.27 mm for mice, so as to achieve the same level of detail of current state-of-the art PET scanners for humans [2], and a sensitivity as high as possible, to allow to differentiate and quantify a subtle signal in the presence of significant background counts [3]. Commercially available state-of-the-art preclinical PET systems make use of detectors based on segmented inorganic scintillation crystals coupled to photodetectors [2]. To reduce the complexity and cost, light multiplexing is used to decode the position of interaction of annihilation photons [3]. This scheme poses some limitations to the sensitivity and SR attained by preclinical PET systems, due to, among other problems, the difficulty of measuring efficiently the Depth-Of-Interaction [3]. The best reported values for the sensitivity and SR of current commercially available preclinical PET systems, are of, respectively, ~10% and ~1 mm FWHM [2]. Timing Resistive Plate Chambers (RPCs) are gaseous detectors with resistive parallel plate electrodes (made of glass) separated by small (~300 μm thick) and precise amplification gaps filled with an appropriate gas mixture. For the detection of photons, these are first converted into electrons in the resistive plates in an electronic cascade process. Some of the originated electrons will eventually escape to the amplification gap, where they will be accelerated by a uniform electric field, leading to a Townsend avalanche, which induces a current in a set of signal pickup strips. These low cost detectors have an excellent time resolution of 300 ps FWHM for 511 keV photon pairs, an excellent intrinsic SR, the readout being in almost full 3D mode. 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引用次数: 0
摘要
正电子发射断层扫描(PET)是一种强大的功能成像技术,用于体内生理和病理生理功能的定量和定位。在转基因和基因敲除小鼠中可能发生大量疾病,并有机会在个体基础上跟踪疾病的发病和治疗效果的演变,这使得PET成为新药疗法研发中第三大首选临床前成像技术(20%)[1]。临床前PET系统必须具备两个特征:高半最大全宽(FWHM)空间分辨率(SR),小鼠的分辨率在0.40至0.27 mm之间,以达到与当前最先进的人类PET扫描仪相同的细节水平[2],以及尽可能高的灵敏度,以便在存在显著背景计数的情况下区分和量化细微信号[3]。商用的最先进的临床前PET系统利用了基于分段无机闪烁晶体与光电探测器耦合的探测器[2]。为了降低复杂性和成本,采用光复用来解码湮灭光子相互作用的位置[3]。由于难以有效测量相互作用深度(Depth-Of-Interaction)等问题,该方案对临床前PET系统获得的灵敏度和SR存在一定限制[3]。目前市售的临床前PET系统的灵敏度和SR的最佳报告值分别为~10%和~1 mm FWHM[2]。定时电阻板室(rpc)是一种气体探测器,其电阻平行板电极(由玻璃制成)由小(~300 μm厚)和精确的放大间隙隔开,并填充适当的气体混合物。为了探测光子,这些光子首先在电子级联过程中在电阻板中转化为电子。一些产生的电子最终会逃到放大间隙,在那里它们会被一个均匀的电场加速,导致汤森雪崩,从而在一组信号接收带中产生电流。这些低成本探测器对511 keV光子对具有300 ps FWHM的出色时间分辨率,具有出色的本征SR,读数几乎为全3D模式。最近,我们开发了第一个功能齐全的小鼠临床前RPC-PET扫描仪原型,通过最大似然期望最大化类型算法重建图像后,显示出0.4 mm FWHM的SR。科英布拉大学核科学健康应用研究所(ICNAS - Instituto de Ciências Nucleares Applied às Saúde)在小鼠身上进行的初步测试表明,该系统能够清楚地识别小鼠非常小的大脑结构以及心脏壁。目前获得的结果非常有希望,揭示了前所未有的SR。
An ultra-high resolution preclinical positron emission tomography scanner
Positron Emission Tomography (PET) is a powerful functional imaging technique targeted for in vivo quantification and localization of physiological and pathophysiological functions. The possibility to develop a vast number of diseases in transgenic and knockout mice, and the chance to follow the onset of the diseases and the evolution of the treatment efficacy in an individual basis, made PET the third preferred preclinical imaging technique (20%) in research and development of new drug therapies [1]. Two features are mandatory in a preclinical PET system: a high Full Width at Half Maximum (FWHM) Spatial Resolution (SR), comprised between 0.40 and 0.27 mm for mice, so as to achieve the same level of detail of current state-of-the art PET scanners for humans [2], and a sensitivity as high as possible, to allow to differentiate and quantify a subtle signal in the presence of significant background counts [3]. Commercially available state-of-the-art preclinical PET systems make use of detectors based on segmented inorganic scintillation crystals coupled to photodetectors [2]. To reduce the complexity and cost, light multiplexing is used to decode the position of interaction of annihilation photons [3]. This scheme poses some limitations to the sensitivity and SR attained by preclinical PET systems, due to, among other problems, the difficulty of measuring efficiently the Depth-Of-Interaction [3]. The best reported values for the sensitivity and SR of current commercially available preclinical PET systems, are of, respectively, ~10% and ~1 mm FWHM [2]. Timing Resistive Plate Chambers (RPCs) are gaseous detectors with resistive parallel plate electrodes (made of glass) separated by small (~300 μm thick) and precise amplification gaps filled with an appropriate gas mixture. For the detection of photons, these are first converted into electrons in the resistive plates in an electronic cascade process. Some of the originated electrons will eventually escape to the amplification gap, where they will be accelerated by a uniform electric field, leading to a Townsend avalanche, which induces a current in a set of signal pickup strips. These low cost detectors have an excellent time resolution of 300 ps FWHM for 511 keV photon pairs, an excellent intrinsic SR, the readout being in almost full 3D mode. Recently, we developed a first fully functional prototype of a preclinical RPC-PET scanner for mice, which revealed a SR of 0.4 mm FWHM after image reconstruction by a Maximum Likelihood Expectation Maximization type algorithm. Preliminary tests with mice, preformed at the Institute of Nuclear Sciences Applied to Health (ICNAS - Instituto de Ciências Nucleares Aplicada às Saúde) of the University of Coimbra, shown the capability of the system to clearly identify the very small brain structures of mice, as well as the heart walls. The results obtained thus far are very promising, revealing unprecedented SR.