Molecular Imaging of Chemical Threats and Countermeasures

化学威胁的分子成像及对策

• 批准号: 9330941
• 负责人: JOHN M GERDES
• 金额: $ 79.95万
• 依托单位: UNIVERSITY OF MONTANA
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-08-01 至 2020-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9330941
• 关键词: Ache; Aging; Animal Model; Animals; Antidotes; Benchmarking; Biodistribution; Biological Assay; Cations; Cavia; Charge; Chemical Weapons; Chemicals; Clinical; Data; Development; Diagnostic; Drug Kinetics; Enzymes; Event; Exhibits; Fluorine; Functional Imaging; Goals; Government Agencies; Image; Imaging Device; Investigation; Kinetics; Label; Macaca mulatta; Measures; Methods; Military Personnel; Molecular; Nerve Tissue; Organophosphates; Oximes; Paraoxon; Performance; Peripheral; Pharmaceutical Preparations; Pharmacodynamics; Pharmacology; Pharmacology and Toxicology; Phase; Poisoning; Positron; Positron-Emission Tomography; Primates; Process; Property; Rattus; Recovery; Reporter; Reporting; Research; Research Personnel; Rodent; Sarin; Structure; Terrorism; Therapeutic; Therapeutic Agents; Time; Tissue imaging; Tissues; Tracer; Variant; Visual; adduct; analog; animal imaging; base; combat; comparative; design; imaging agent; imaging platform; in vivo; in vivo imaging; inhibitor/antagonist; insight; methylphosphonate; molecular imaging; nerve agent; neurotoxicity; nonhuman primate; novel; novel strategies; novel therapeutics; public health relevance; quantitative imaging; radioligand

 DESCRIPTION (provided by applicant): The possible deployment of organophosphate (OP) nerve agents by terrorists, rogue organizations, or by government agencies is of immediate concern and has prompted new investigations to better understand the properties of OP agents so that new therapeutics can be developed to combat and reverse the ill effects of OPs. These research endeavors are producing new approaches and molecular countermeasures to ameliorate the short- and long-term neurotoxicity associated with OPs. The objectives in this application are: (1) to provide quantitative and visual accounts of three OP structure types (VX, sarin and paraoxon) exposures in rats, guinea pigs and primates to advance our understanding of OP biodistribution; and (2) to provide quantitative and visual accounts of three oxime subtypes (cation, neutral and zwitterion) in rats, guinea pigs and primates to advance our understanding of oxime biodistribution; and (c) to develop new dynamic assays that evaluate, measure and validate new therapeutic agents in live subjects over time by employing positron emission tomography (PET) imaging. The approach will assess key pharmacokinetic (PK) and pharmacodynamic (PD) parameters and thus, this application will generate new 18F- and 11C-labeled organophosphate and oxime PET imaging tracers to demonstrate their functional imaging utility in live rodent/primate subjects, and validate their performance qualities in the presence of specific countermeasures. To accomplish these goals, rationally designed methylphosphonate PET radioligands will be prepared with the following progressive specific aims defined by two operational phases: Phase I (Specific Aims 1-2). Design and Synthesis of OP and Countermeasure PET Imaging Tracers and Phase II (Specific Aims 3-6). Establish and Confirm the Countermeasure Molecular Imaging Animal Platforms. Specific aims 1 and 2 will synthesize and validate the mechanism of action and pharmacology of the 18F- and 11C-labeled OP and oximes tracers. Specific Aims 3-4 will determine the PK/PD profiles of the 18F- and 11C-labeled OP and oxime tracers in rat and guinea pig. Specific aims 5-6 will advance the experimentation to combination approaches and evaluate the diagnostic capabilities of the 18F- and 11C-labeled tracers and use a candidate OP and oxime tracer in non-human primates. Specific aims 3-6 will collectively afford imaging platforms in each species.

 描述（由申请人提供）：恐怖分子、流氓组织或政府机构可能部署有机磷酸盐（OP）神经毒剂是一个紧迫的问题，并促使新的调查，以更好地了解OP剂的性质，以便开发新的治疗方法来对抗和逆转OP的不良影响。这些研究努力正在产生新的方法和分子对策，以改善与OP相关的短期和长期神经毒性。本研究的目的是：（1）提供三种OP结构类型的定量和可视化描述（VX、沙林和对氧磷）暴露于大鼠、豚鼠和灵长类动物中，以促进我们对OP生物分布的理解;和（2）提供三种肟亚型的定量和可视化描述（阳离子，中性和两性离子）在大鼠，豚鼠和灵长类动物，以促进我们对肟生物分布的理解;和（c）开发新的动态测定法，其通过采用正电子发射断层摄影术（PET）成像来评价、测量和验证新的治疗剂在活体受试者中随时间的变化。该方法将评估关键的药代动力学（PK）和药效学（PD）参数，因此，该应用将产生新的18 F和11 C标记的有机磷酸酯和肟PET成像示踪剂，以证明其在活啮齿动物/灵长类动物受试者中的功能成像效用，并在存在特定对策的情况下验证其性能质量。为了实现这些目标，将制备合理设计的甲基膦酸酯PET放射性配体，其具有由两个操作阶段定义的以下渐进式特定目标：第I阶段（特定目标1-2）。OP和对策PET成像示踪剂的设计和合成以及第II阶段（具体目标3-6）。建立并确认对抗性分子影像学动物平台。具体目标1和2将合成并验证18 F和11 C标记的OP和肟示踪剂的作用机制和药理学。特定目的3-4将确定大鼠和豚鼠中18 F和11 C标记的OP和肟示踪剂的PK/PD特征。具体目标5-6将把实验推进到组合方法，并评估18 F和11 C标记示踪剂的诊断能力，并在非人灵长类动物中使用候选OP和肟示踪剂。具体目标3-6将共同为每个物种提供成像平台。