In vivo evaluation of IGF1R/IR PET ligand [18F]BMS-754807 in rodents

被引:8
作者
Prabhakaran, Jaya [1 ,2 ]
Dewey, Stephen L. [3 ]
McClure, Richard [4 ,5 ]
Simpson, Norman R. [2 ]
Tantawy, Mohammed N. [4 ]
Mann, J. John [1 ,2 ]
Pham, Wellington [4 ,5 ]
Kumar, J. S. Dileep [2 ]
机构
[1] Columbia Univ, Dept Psychiat, Med Ctr, New York, NY USA
[2] New York State Psychiat Inst & Hosp, Mol Imaging & Neuropathol Div, New York, NY 10032 USA
[3] Hofstra North Shore LIJ Sch Med, Feinstein Inst Med Res, Manhasset, NY USA
[4] Vanderbilt Univ, Dept Radiol, Inst Imaging Sci, 221 Kirkland Hall, Nashville, TN 37235 USA
[5] Vanderbilt Univ, Dept Biomed Engn, 221 Kirkland Hall, Nashville, TN 37235 USA
关键词
IGF1R; IR; Insulin; Radiotracer; MicroPET; GROWTH-FACTOR-I; FACTOR RECEPTOR INHIBITORS; BREAST-CANCER XENOGRAFTS; BEARING NUDE-MICE; CELL LUNG-CANCER; BINDING-PROTEINS; INSULIN; IGF-1R; VITRO; BIODISTRIBUTION;
D O I
10.1016/j.bmcl.2016.12.086
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In vivo evaluation of [F-18]BMS-754807 binding in mice and rats using microPET and biodistribution methods is described herein. The radioligand shows consistent binding characteristics, in vivo, in both species. Early time frames of the microPET images and time activity curves of brain indicate poor penetration of the tracer across the blood brain barrier (BBB) in both species. However, microPET experiments in mice and rats show high binding of the radioligand outside the brain to heart, pancreas and muscle, the organs known for higher expression of IGF1R/1R. Biodistribution analysis 2 h after injection of [F-18]BMS-754807 in rats show negligible [F-18]defluorination as reflected by the low bone uptake and clearance from blood. Overall, the data indicate that [F-18]BMS-754807 can potentially be a radiotracer for the quantification of IGF1R/IR outside the brain using PET. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:941 / 943
页数:3
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