Quantitative receptor occupancy PET
Quantitative receptor occupancy PET
批准号:
10024082
负责人:
Marc David Normandin
金额:
$19.89万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-25 至 2022-07-31
关键词:
3-DimensionalAdoptedAlgorithmsAnatomyAnimal ModelAntipsychotic AgentsBindingBiological AssayBrainBrain regionCentral Nervous System AgentsCentral Nervous System DiseasesClozapineDataData SetDevelopmentDopamine D2 ReceptorDoseEvaluationFailureImageJointsKineticsLigand BindingLigandsMapsMeasuresMethodologyMethodsModelingMonkeysMonte Carlo MethodNeuraxisNoisePatientsPenetrationPerformancePharmaceutical PreparationsPharmacologic SubstancePharmacologyPhasePlasmaPlayPositron-Emission TomographyRadiation exposureResearchRiskRoleSample SizeScanningSignal TransductionSiteTechniquesTechnologyTimeTracerTranslatingbaseclinical developmentcostdetectordrug candidatedrug developmentdrug discoverydrug testinghuman subjectimage reconstructionimprovedin vivokinetic modelnonhuman primatenovelnovel therapeuticsreceptorreceptor densityreconstructionstem
中文摘要
项目摘要
正电子发射断层扫描(PET)受体占用成像在肿瘤治疗中发挥着越来越重要的作用。
中枢神经系统(CNS)药物的发展,提供药物脑的关键信息
穿透、目标接合和剂量。测量CNS药物占有率的常规方法
在基线和给药后扫描受试者两次,
对每次扫描的数据进行重建和动力学建模,并通过测量分数
减少扫描之间的特异性配体结合。然而,这种方法的缺点是,
估计占用值的精度。我们提出了一种新的参数化重建
联合重建和分析基线中测量的动态预测的方法,
药物后扫描,导致直接,定量估计受体占有率图,
更高的信噪比。我们希望我们的方法能够显着提高精度和准确性,
占用定量,允许更稳健地表征剂量-占用关系,从而
大大提高了从PET占用研究中提取的信息的质量。拟议
将在动物模型中评价方法学。
英文摘要
PROJECT SUMMARY
Positron emission tomography (PET) receptor occupancy imaging plays an increasingly important role in
the development of central nervous system (CNS) drugs, providing critical information on drug brain
penetration, target engagement and dosing. The conventional approach to measure occupancy of a CNS drug
is to scan a subject twice, at baseline and after administration of the drug, independently apply image
reconstruction and kinetic modeling to the data of each scan, and compute occupancy by measuring fractional
reductions in specific ligand binding between the scans. The drawback of this approach, however, is the low
precision of the estimated occupancy values. We propose to develop a novel parametric reconstruction
approach that jointly reconstructs and analyzes the dynamic projections measured in the baseline and
post-drug scans, leading to direct, quantitative estimation of receptor occupancy maps with a drastically
higher signal-to-noise ratio. We expect our approach to significantly improve the precision and accuracy of
occupancy quantification, allowing more robust characterization of dose-occupancy relationships and thereby
greatly improving the quality of the information extracted from PET occupancy studies. The proposed
methodology will be evaluated in an animal model.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
TR&D3: Novel Imaging Agents & Physiological Modeling for Quantitative PET/MR
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批准号:10651783
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项目类别:
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资助金额:$59.64万
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财政年份:2017
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负责人:Marc David Normandin
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依托单位:
Pharmacokinetic Physiologic Modeling in Simultaneous PET/MR
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批准号:10263163
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资助金额:$37.09万
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财政年份:2017
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负责人:Marc David Normandin
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依托单位:
PEG-like Multimodal Nanoprobes for Imaging Enhanced Permeability Retention
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批准号:9263761
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资助金额:$38.91万
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财政年份:2014
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负责人:Marc David Normandin
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依托单位:
Combined PET and fMRI imaging of dopamine and serotonin responses in depression
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批准号:9265515
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项目类别:
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资助金额:$44.48万
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财政年份:2013
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负责人:Marc David Normandin
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依托单位:
Combined PET and fMRI imaging of dopamine and serotonin responses in depression
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批准号:8480550
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项目类别:
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资助金额:$62.12万
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财政年份:2013
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负责人:Marc David Normandin
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依托单位:
Combined PET and fMRI imaging of dopamine and serotonin responses in depression
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批准号:8650334
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项目类别:
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资助金额:$53.92万
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财政年份:2013
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负责人:Marc David Normandin
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依托单位:
Pharmacokinetic Physiologic Modeling in Simultaneous PET/MR
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批准号:9369483
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项目类别:
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资助金额:$33.01万
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财政年份:--
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负责人:Marc David Normandin
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依托单位:
海外基金