Synthesis and evaluation of [18F]cinacalcet for the imaging of parathyroid hyperplasia

被引:7
作者
Pees, Anna [1 ]
Beaino, Wissam [1 ]
Kooijman, Esther J. M. [1 ]
Schreurs, Maxime [1 ]
Verlaan, Mariska [1 ]
Schuit, Robert C. [1 ]
Vosjan, Maria J. W. D. [2 ]
Engelsman, Anton F. [3 ]
Windhorst, Albert D. [1 ]
Vugts, Danielle J. [1 ]
机构
[1] Vrije Univ Amsterdam, Radionuclide Ctr, Radiol & Nucl Med, Amsterdam UMC, Boelelaan 1085c, Amsterdam, Netherlands
[2] BV Cyclotron VU, Boelelaan 1081, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Surg, Amsterdam UMC, Amsterdam, Netherlands
基金
荷兰研究理事会;
关键词
Parathyroid hyperplasia; Cinacalcet; Calcimimetic; Calcium-sensing receptor; F-18]trifluoromethylation; Pre-operative localization; CALCIUM-SENSING RECEPTOR; ARYL BORONIC ACIDS; CALCIMIMETIC AGENT; SECONDARY HYPERPARATHYROIDISM; CINACALCET; TRIFLUOROMETHYLATION; METABOLISM; EXPRESSION;
D O I
10.1016/j.nucmedbio.2021.10.003
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
Introduction: Parathyroid hyperplasia is a disease characterized by overactive parathyroid glands secreting increased levels of parathyroid hormone. Surgical removal of the parathyroid glands is the standard treatment but requires precise pre-operative localization of the glands. However, currently available imaging modalities show limited sensitivity. Since positron emission tomography (PET) is a molecular imaging technique with high accuracy and sensitivity, our aim was to develop a new PET tracer for overactive parathyroid glands imaging by radiolabelling cinacalcet, a drug binding to the calcium-sensing receptor of the parathyroid glands. Methods: [F-18]Cinacalcet was synthesized by copper-catalysed [F-18]trifluoromethylation of a boronic acid precursor using high molar activity [F-18]fluoroform. Ex vivo biodistribution and metabolism were evaluated in 12 healthy male Wistar rats at 5, 15, 45 and 90 min. PET scans were performed at baseline and after blocking with NPS R-568. Results: [F-18]Cinacalcet was obtained in an overall radiosynthesis time of 1 h with a radiochemical purity of 98 +/- 1%, a radiochemical yield of 8 +/- 4% (overall, n=7, corrected for decay) and a molar activity of 40 +/- 11 GBq/mu mol (n = 7, at EOS). The ex vivo biodistribution showed uptake in the thyroid and parathyroid glands as well as in other glands such as adrenals, salivary glands and pancreas. The tracer was rapidly cleared from the blood via liver and kidneys and showed fast metabolism. PET images confirmed uptake in the target organ. However, in a blocking study with NPS R-568 specific binding of [F-18]cinacalcet to the CaSR could not be confirmed. Conclusions: [F-18]Cinacalcet was successfully synthesized. First in vivo experiments in healthy rats showed uptake of the tracer in the target organ and fast metabolism, encouraging further in vivo evaluation of this tracer. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:97 / 105
页数:9
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