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理想 PET 灌注示踪剂的特性:新的 PET 示踪剂案例和数据。

Properties of an ideal PET perfusion tracer: new PET tracer cases and data.

机构信息

Department of Molecular and Medical Pharmacology (Nuclear Medicine), David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA 90095-7064, USA.

出版信息

J Nucl Cardiol. 2012 Feb;19 Suppl 1:S30-7. doi: 10.1007/s12350-011-9491-8.

Abstract

An ideal positron emission tomography (PET) tracer should be highly extractable by the myocardium and able to provide high-resolution images, should enable quantification of absolute myocardial blood flow (MBF), should be compatible with both pharmacologically induced and exercise-induced stress imaging, and should not require an on-site cyclotron. The PET radionuclides nitrogen-13 ammonia and oxygen-15 water require an on-site cyclotron. Rubidium-82 may be available locally due to the generator source, but greater utilization is limited because of its relatively low myocardial extraction fraction, long positron range, and generator cost. Flurpiridaz F 18, a novel PET tracer in development, has a high-extraction fraction, short positron range, and relatively long half-life (as compared to currently available tracers), and may be produced at regional cyclotrons. Results of early clinical trials suggest that both pharmacologically and exercise-induced stress PET imaging protocols can be completed more rapidly and with lower patient radiation exposure than with single-photon emission computerized tomography (SPECT) tracers. As compared to SPECT images in the same patients, flurpiridaz F 18 PET images showed better defect contrast. Flurpiridaz F 18 is a potentially promising tracer for assessment of myocardial perfusion, measurement of absolute MBF, calculation of coronary flow reserves, and assessment of cardiac function at the peak of the stress response.

摘要

理想的正电子发射断层扫描(PET)示踪剂应该高度可被心肌提取,并能够提供高分辨率的图像,应该能够量化绝对心肌血流(MBF),应该与药物诱导和运动诱导的应激成像兼容,并且不需要现场回旋加速器。PET 放射性核素氮-13 氨和氧-15 水需要现场回旋加速器。由于发生器源,铷-82 可能在当地可用,但由于其相对较低的心肌提取分数、较长的正电子射程和发生器成本,其利用率受到限制。氟吡拉嗪 F18 是一种正在开发的新型 PET 示踪剂,具有高提取分数、短正电子射程和相对较长的半衰期(与目前可用的示踪剂相比),并且可以在区域回旋加速器中生产。早期临床试验结果表明,与单光子发射计算机断层扫描(SPECT)示踪剂相比,药物和运动诱导的应激 PET 成像方案可以更快地完成,并且患者的辐射暴露更低。与同一患者的 SPECT 图像相比,氟吡拉嗪 F18 PET 图像显示出更好的缺陷对比度。氟吡拉嗪 F18 是一种有潜力的示踪剂,可用于评估心肌灌注、测量绝对 MBF、计算冠状动脉血流储备以及评估应激反应峰值时的心脏功能。

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