Novel Chemistries For Activatable Molecular Imaging Probes Applicable To Magnetic Resonance Imaging And Positron Emission Tomography
适用于磁共振成像和正电子发射断层扫描的可激活分子成像探针的新型化学物质
基本信息
- 批准号:RGPIN-2015-05796
- 负责人:
- 金额:$ 1.46万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2019
- 资助国家:加拿大
- 起止时间:2019-01-01 至 2020-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Enzymes and highly reactive, naturally occurring small molecules are the workhorses of the cell, and exert their effects on physiology through well-defined chemical mechanisms. The activity of these biochemical species is well regulated during health, but often changes substantially during disease processes. By measuring the activity of these biochemical workhorses, the subcellular processes that may ultimately result in the onset of disease, or its reversal through treatment efforts, can be detected very early on before any outward signs or symptoms occur. Molecular imaging is an emerging field that is specifically concerned with imaging these sorts of subcellular activities, and is heavily reliant on novel chemistries through which imaging tracers can be developed. These small molecule tracers are injected prior to imaging, and are acted upon by the workhorse target of interest to change their behavior in the area of disease, for example in a tumor. This results in a chemical change to the tracer that can be detected non-invasively through magnetic resonance imaging (MRI) or positron emission tomography (PET) scans. MRI and PET are important tools for fundamental research regarding disease and treatment, as well as clinical medicine, offering non-invasive, three-dimensional images with resolution and sensitivity unmatched by other imaging modalities. While MRI and PET molecular imaging holds promise to enhance the way health and disease can be studied and tracked, it has not yet reached its potential due to a lack of tracer chemistry available to interrogate workhorse activities using these modalities. My work has proved the principle of a new molecular imaging strategy: designing small molecule tracers that self-assemble into large structures in cells and tissues when a particular workhorse is present and active. The proposed research program will move this molecular imaging strategy of self-assembly into practice. New chemical approaches will be developed to design a large self-assembly toolbox containing tracer chemistry platforms applicable to a broad range of workhorse targets for both MR and PET imaging. The research program will also reevaluate the safety of materials currently used as MRI tracers, since there have been concerns regarding their necessary incorporation of heavy metal atoms. Materials will be made that lack these toxic heavy metals but that can still produce imaging contrast for MRI. With these new chemical tools for tracer design, the capacity to interrogate the activity of important biochemical workhorses would have substantial short term impact on studying fundamental processes in disease and innovative treatments, and a potential for long term impact on clinical molecular imaging in Canada and the management of disease.
酶和高度活跃的、自然产生的小分子是细胞的主力,它们通过明确定义的化学机制对生理学产生影响。这些生化物种的活性在健康期间受到很好的调节,但在疾病过程中往往会发生重大变化。通过测量这些生化主力的活动,可能最终导致疾病发病或通过治疗努力逆转的亚细胞过程可以在任何外部迹象或症状出现之前很早就被检测到。分子成像是一个新兴的领域,它特别涉及到对这些类型的亚细胞活动进行成像,并且严重依赖于可以开发成像示踪剂的新型化学物质。这些小分子示踪剂在成像前注射,并由感兴趣的主要靶点作用,以改变它们在疾病领域的行为,例如在肿瘤中。这会导致示踪剂发生化学变化,可通过磁共振成像(MRI)或正电子发射断层扫描(PET)进行非侵入性检测。磁共振成像和正电子发射计算机断层扫描是疾病和治疗以及临床医学基础研究的重要工具,它们提供了非侵入性的三维图像,其分辨率和灵敏度是其他成像方式所无法比拟的。虽然MRI和PET分子成像有望增强研究和跟踪健康和疾病的方式,但由于缺乏可用的示踪剂化学来使用这些模式询问主力活动,它尚未发挥其潜力。我的工作证明了一种新的分子成像策略的原理:设计小分子示踪剂,当特定的主力存在并活跃时,它会在细胞和组织中自组装成大结构。拟议的研究计划将把这种自组装的分子成像策略付诸实践。将开发新的化学方法来设计一个大型自组装工具箱,其中包含示踪化学平台,适用于广泛的主要目标,用于磁共振和正电子发射计算机断层扫描。该研究计划还将重新评估目前用作核磁共振示踪剂的材料的安全性,因为人们一直担心它们必须包含重金属原子。将制造出不含这些有毒重金属的材料,但仍能为核磁共振产生成像对比度。有了这些用于示踪剂设计的新化学工具,询问重要生化主力的活动的能力将对研究疾病的基本过程和创新治疗产生重大的短期影响,并可能对加拿大的临床分子成像和疾病管理产生长期影响。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Shuhendler, Adam其他文献
Fingerprinting Biogenic Aldehydes through Pattern Recognition Analyses of Excitation-Emission Matrices
- DOI:
10.1002/cbic.201800427 - 发表时间:
2019-02-15 - 期刊:
- 影响因子:3.2
- 作者:
Lazurko, Caitlin;Radonjic, Ivana;Shuhendler, Adam - 通讯作者:
Shuhendler, Adam
Doxorubicin and mitomycin C co-loaded polymer-lipid hybrid nanoparticles inhibit growth of sensitive and multidrug resistant human mammary tumor xenografts
- DOI:
10.1016/j.canlet.2012.08.008 - 发表时间:
2013-07-01 - 期刊:
- 影响因子:9.7
- 作者:
Prasad, Preethy;Shuhendler, Adam;Wu, Xiao Yu - 通讯作者:
Wu, Xiao Yu
Positron emission tomography imaging of drug-induced tumor apoptosis with a caspase-triggered nanoaggregation probe.
- DOI:
10.1002/anie.201303422 - 发表时间:
2013-09-27 - 期刊:
- 影响因子:16.6
- 作者:
Shen, Bin;Jeon, Jongho;Palner, Mikael;Ye, Deju;Shuhendler, Adam;Chin, Frederick T.;Rao, Jianghong - 通讯作者:
Rao, Jianghong
Cytotoxicity and mechanism of action of a new ROS-generating microsphere formulation for circumventing multidrug resistance in breast cancer cells
- DOI:
10.1007/s10549-009-0473-3 - 发表时间:
2010-06-01 - 期刊:
- 影响因子:3.8
- 作者:
Liu, Qun;Shuhendler, Adam;Wu, Xiao Yu - 通讯作者:
Wu, Xiao Yu
Shuhendler, Adam的其他文献
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{{ truncateString('Shuhendler, Adam', 18)}}的其他基金
Contrast Agents & Radiotracers As Activity-Based Sensors of Faulty Metabolism
造影剂
- 批准号:
RGPIN-2021-03387 - 财政年份:2022
- 资助金额:
$ 1.46万 - 项目类别:
Discovery Grants Program - Individual
Contrast Agents & Radiotracers As Activity-Based Sensors of Faulty Metabolism
造影剂
- 批准号:
RGPIN-2021-03387 - 财政年份:2021
- 资助金额:
$ 1.46万 - 项目类别:
Discovery Grants Program - Individual
Novel Chemistries For Activatable Molecular Imaging Probes Applicable To Magnetic Resonance Imaging And Positron Emission Tomography
适用于磁共振成像和正电子发射断层扫描的可激活分子成像探针的新型化学物质
- 批准号:
RGPIN-2015-05796 - 财政年份:2020
- 资助金额:
$ 1.46万 - 项目类别:
Discovery Grants Program - Individual
Novel Chemistries For Activatable Molecular Imaging Probes Applicable To Magnetic Resonance Imaging And Positron Emission Tomography
适用于磁共振成像和正电子发射断层扫描的可激活分子成像探针的新型化学物质
- 批准号:
RGPIN-2015-05796 - 财政年份:2018
- 资助金额:
$ 1.46万 - 项目类别:
Discovery Grants Program - Individual
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