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Evaluation of Enzyme Substrate Radiotracers as PET/MRS Hybrid Imaging Agents
被引:4
|作者:
Brooks, Allen F.
[1
]
Drake, Lindsey R.
[2
]
Shao, Xia
[1
]
Zhao, Austin
[1
]
Scott, Peter J. H.
[1
,2
]
Kilhourn, Michael R.
[1
]
机构:
[1] Univ Michigan, Sch Med, Dept Radiol, 1301 Catherine St, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Med Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
来源:
ACS MEDICINAL CHEMISTRY LETTERS
|
2018年
/
9卷
/
11期
关键词:
Hybrid imaging;
carbon-11;
positron emission tomography;
magnetic resonance spectroscopy;
neuroimaging;
MONOAMINE-OXIDASE-A;
RAT-BRAIN;
IN-VITRO;
ANALOGS;
DESIGN;
PROBE;
D O I:
10.1021/acsmedchemlett.8b00402
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
The development of a positron emission tomography (PET)/magnetic resonance spectroscopy (MRS) hybrid imaging agent allows for functional imaging by both methods with a single imaging agent. Enzyme substrates that are cleaved to form two metabolites present an interesting opportunity, as the unique metabolites generated might each be detected by a different modality. To be successful, such enzyme substrates would require administration of doses that (a) reach the in vivo target tissue at concentrations necessary for MRS imaging, (b) do not show substrate inhibition of tissue uptake or enzymatic activity, and (c) provide PET images that still reflect the action of the enzyme. We report in vitro and in vivo proof-of-concept studies of a carbon-11 small molecule substrate for brain monoamine oxidases that, upon enzyme-mediated cleavage, produces two metabolites, one detectable by PET and the other by MRS.
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页码:1140 / 1143
页数:7
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