Validation of gallbladder absorbed radiation dose reduction simulation: human dosimetry of [18F]fluortriopride

被引:6
作者
Doot, Robert K. [1 ]
Dubroff, Jacob G. [1 ]
Scheuermann, Joshua S. [1 ]
Labban, Kyle J. [1 ]
Cai, Jenny [1 ]
Hsieh, Chia-Ju [1 ]
Li, Shihong [1 ]
Lee, Hsiaoju [1 ]
Schubert, Erin K. [1 ]
Hou, Catherine [1 ]
Sheffer, Regan [1 ]
Schmitz, Alexander [1 ]
Xu, Kuiying [1 ]
Mach, Robert H. [1 ]
机构
[1] Univ Penn, Dept Radiol, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
PET; F-18]fluortriopride; Dopamine; Dosimetry; Gallbladder absorbed dose; POSITRON-EMISSION-TOMOGRAPHY; DOPAMINE-RECEPTORS; CHOLECYSTOKININ-CHOLESCINTIGRAPHY; THERAPEUTIC AGENTS; D-3; SCHIZOPHRENIA; BINDING; PET;
D O I
10.1186/s40658-018-0219-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background[F-18]Fluortriopride (FTP) was developed as a dopamine D3-selective radiotracer, thought to be important to neurobiological reward pathways and implicated in drug addiction, Parkinson's disease, and schizophrenia. Preclinical radiation dosimetry studies found the gallbladder wall received the highest dose. A gallbladder dose reduction intervention was simulated using a novel reduction model for healthy adults following fatty-meal consumption. The goals of this study were to assess whole body FTP human dosimetry and determine the feasibility of reducing absorbed dose to the gallbladder wall.ResultsEffective dose without a fatty meal was 0.0220.002mSv/MBq (+/- standard deviation) with highest organ dose of 0.436 +/- 0.178mSv/MBq to the gallbladder wall (n=10). Predicted gallbladder dose reduction with fatty meal consumed was 67.4% (n=10). Meal consumption by four repeat volunteers decreased average gallbladder dose by 71.3% (n=4) compared to the original ten volunteers.Conclusions Observed effective doses were adequately low to continue studying FTP uptake in humans. Validated dosimetry simulations indicate up to a 71% reduction in gallbladder dose can be achieved by employing intrinsic physiology to contract the gallbladder via fatty meal ingestion. This methodology for predicting gallbladder absorbed dose reduction from fatty meal consumption can be applied to other radiopharmaceuticals and radiotherapies.
引用
收藏
页数:12
相关论文
共 28 条
[1]  
[Anonymous], 1995, Ann ICRP, V25, P1
[2]   Modification of cocaine self-administration by buspirone (buspar®): potential involvement of D3 and D4 dopamine receptors [J].
Bergman, Jack ;
Roof, Rebecca A. ;
Furman, Cheryse A. ;
Conroy, Jennie L. ;
Mello, Nancy K. ;
Sibley, David R. ;
Skolnick, Phil .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2013, 16 (02) :445-458
[3]   Cholecystokinin-Cholescintigraphy in Adults: Consensus Recommendations of an Interdisciplinary Panel [J].
DiBaise, John K. ;
Richmond, Bryan K. ;
Ziessman, Harvey A. ;
Everson, Gregory T. ;
Fanelli, Robert D. ;
Maurer, Alan H. ;
Ouyang, Ann ;
Shamamian, Peter ;
Simons, Richard J. ;
Wall, Laura A. ;
Weida, Thomas J. ;
Tulchinsky, Mark .
CLINICAL NUCLEAR MEDICINE, 2012, 37 (01) :63-70
[4]   Imaging Nicotine- and Amphetamine-Induced Dopamine Release in Rhesus Monkeys with [11C]PHNO vs [11C]raclopride PET [J].
Gallezot, Jean-Dominique ;
Kloczynski, Tracy ;
Weinzimmer, David ;
Labaree, David ;
Zheng, Ming-Qiang ;
Lim, Keunpoong ;
Rabiner, Eugenii A. ;
Ridler, Khanum ;
Pittman, Brian ;
Huang, Yiyun ;
Carson, Richard E. ;
Morris, Evan D. ;
Cosgrove, Kelly P. .
NEUROPSYCHOPHARMACOLOGY, 2014, 39 (04) :866-874
[5]   Effects of lorazepam administration on striatal dopamine D-2 receptor binding characteristics in man - a positron emission tomography study [J].
Hietala, J ;
Kuoppamaki, M ;
Nagren, K ;
Lehikoinen, P ;
Syvalahti, E .
PSYCHOPHARMACOLOGY, 1997, 132 (04) :361-365
[6]   Liver uptake of radiolabeled targeting proteins and peptides: considerations for targeting peptide conjugate design [J].
Hosseinimehr, Seyed Jalal ;
Tolmachev, Vladimir ;
Orlova, Anna .
DRUG DISCOVERY TODAY, 2012, 17 (21-22) :1224-1232
[7]  
ICRP, 2007, ANN ICRP, V103, P1
[8]   Performance evaluation of the Ingenuity TF PET/CT scanner with a focus on high count-rate conditions [J].
Kolthammer, Jeffrey A. ;
Su, Kuan-Hao ;
Grover, Anu ;
Narayanan, Manoj ;
Jordan, David W. ;
Muzic, Raymond F. .
PHYSICS IN MEDICINE AND BIOLOGY, 2014, 59 (14) :3843-3859
[9]  
Laforest R, 2016, AM J NUCL MED MOLEC, V6, P301
[10]   Progress in developing D3 dopamine receptor ligands as potential therapeutic agents for neurological and neuropsychiatric disorders [J].
Luedtke, RR ;
Mach, RH .
CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (08) :643-671