Instrumentation for microSPECT and microPET imaging
Instrumentation for microSPECT and microPET imaging
批准号:
7965517
负责人:
peter L choyke
金额:
$78.75万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Animal ExperimentationAnimalsAreaBasic ScienceBedsChargeChemicalsCollimatorComputer Systems DevelopmentComputer softwareCoupledCustomDAQData AnalysesDevelopmentDevicesDiagnosticElectronicsEvaluationEventFloodsFutureGamma CamerasGoalsGrowth and Development functionHumanImageImaging DeviceImaging technologyIndividualLabelLaboratory AnimalsLightMedicalMindMissionMusNational Cancer InstituteNuclearOpticsPathway interactionsPhotonsPositioning AttributePositron-Emission TomographyRadioisotopesRadionuclide ImagingResearchResearch PersonnelScientistSideSpeedStructureSupport GroupsSystemTechnologyTestingTimeTubeUltrasonographyValidationWorkbasecancer therapycomputerized data processingcostdesigndetectorflexibilityhuman subjectimprovedinstrumentationmolecular imagingnewsnovelphotomultiplierprogramssimulationsingle photon emission computed tomographythallium-doped sodium iodide
中文摘要
国家癌症研究所的分子成像计划(MIP)负责开发特定于与癌症的发展、生长和治疗相关的途径的化学探针。放射性核素标记的化合物是这类试剂的一个重要子集。成功开发的放射性核素标记化合物为用于医学诊断和管理目的的人体受试者提供了PET、SPECT和平面成像的最终前景,并在用于小型实验室动物的探针验证时在基础科学中具有同样强大的应用。MIP放射性核素仪器小组通过探索和实施新的放射性核素成像技术来支持这一基础科学任务,以改善或提高MIP小动物成像的状态。钻井平台及其(基本)合作者开展的开发工作基于定向探索的概念,其中技术机会在研究层面上进行审查(图1,小组A),但考虑到特定的系统级目标(小组B,图1)。图1(A):成像系统开发的研究领域:(B):当前聚焦系统级别的开发项目:用于单光子、高速动态全身生物分布研究的双伽马相机平面投影成像系统。为了说明这种并行性,在图1A所示的每个领域,钻井平台目前都在进行工作:LaBr3板材和NaI(TL)像素化探测器模块和支持电子开发(CIT-NIH/RIG);评估新的模块化DAQ系统(Thomas Jefferson National Accelerator Facility(JLAB),Newport News,VA/RIG);创建同时使用质心事件定位和高级最大似然(ML)定位的高速数据处理接口(RIG/CIT);以及评估用于图像显示和分析的商业系统(核Mac)(RIG/CIT)。这些子系统项目中的每一个都是根据目前的系统级目标进行评估的,即创造一种为老鼠成像的双平面伽马相机设备,同时提供每个技术领域的信息,供我们下一个系统级开发项目使用。例如,其中一个探测器模块(图1B中的M1或M2)将由一个矩形像素化NaI(TL)阵列组成,该阵列耦合到两个并排的滨松H8500位置灵敏光电倍增管(PSPMT,面板A,图2)。通过这种组合(图2中的B面板)获得的初始成像结果需要充分利用JLAB DAQ、CIT开发的电子设备和钻井平台开发的数据处理软件来采集和分析这些数据。图2.(A):NaI(TL)探测器模块和支持电子设备(CIT/RIG);(B):这个19 x 42(43 Mm X 94 Mm)像素模块的早期511 keV场泛洪图像。请注意,在两个并排的PSPMT之间的间隙中可以清楚地识别出2 mm x 2 mm像素。为该阵列设计了一个定制的准直器,每个像素都有自己的准直器孔。我们计划继续这项探索性工作,目标是将完成的双伽马相机系统移交给MIP科学家,随后审查累积的技术发现并指定下一个系统级项目。
英文摘要
The Molecular Imaging Program (MIP) of the National Cancer Institute is charged with the task of developing chemical probes specific to pathways associated with the development, growth and treatment of cancer. Radionuclide-labeled compounds are an important subset of such agents. Successfully developed radionuclide-labeled compounds offer the ultimate prospect of PET, SPECT and planar imaging in human subjects for medical diagnostic and management purposes, and equally powerful applications in basic science when used for probe validation in small laboratory animals. The MIP radionuclide instrumentation group supports this basic science mission by exploring and implementing new radionuclide imaging technologies that improve or advance the state of MIP small animal imaging. Development work carried out by the RIG and its (essential) collaborators is based on the notion of directed exploration where technological opportunities are examined at the research level (panel A, Figure 1) but with a particular systems level goal in mind (panel B, Figure 1). Figure 1. (A): Research areas in imaging system development: (B): current focused systems level development project: dual gamma camera planar projection imaging system for single photon, high-speed dynamic whole body bio-distribution studies in mice. To illustrate this parallelism, work is now underway in the RIG in each of the areas shown in Figure 1A: LaBr3 slab and NaI(Tl) pixelated detector modules and support electronics development (CIT-NIH/RIG); evaluation of a new, modular DAQ system (Thomas Jefferson National Accelerator Facility (JLAB), Newport News, VA/RIG); creation of a high speed data processing interface using both centroid event positioning and advanced Maximum Likelihood (ML) positioning (RIG/CIT); and evaluation of a commercial system (Nuclear Mac) for image display and analysis (RIG/CIT). Each of these sub-system projects are evaluated in light of the current systems level goal of creating a dual planar gamma camera device for imaging mice while at the same time providing information in each technical area for potential use in our next systems level development project. For example, one of the detector modules (M1 or M2 in Figure 1B) will be comprised of a rectangular pixelated NaI(Tl) array coupled to two side-by-side Hamamatsu H8500 position-sensitive photomultiplier tubes (PSPMTs, panel A, Figure2). Initial imaging results obtained with this combination (panel B, Figure 2) required full use of the JLAB DAQ, CIT developed electronics and RIG-developed data processing software for acquisition and analysis of these data. Figure 2. (A): NaI(Tl) detector module and supporting electronics (CIT/RIG); (B): early 511 keV field flood image from this 19 x 42 (43mm x 94 mm) pixel module. Note clear identification of the 2 mm x 2 mm pixels in the gap between the two side-by-side PSPMTs. A custom collimator has been designed for this array where each pixel has its own individual collimator hole. We plan to continue this exploratory work with the goal of turning over the completed dual gamma camera system to MIP scientists , followed by a review of accrued technical findings and designation of the next systems level project.
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海外基金