使用人体大小的脉冲电子顺磁共振成像仪对兔子肿瘤进行氧成像。

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Molecular Imaging and Biology Pub Date : 2024-06-01 Epub Date: 2023-09-15 DOI:10.1007/s11307-023-01852-3
Boris Epel, Navin Viswakarma, Subramanian V Sundramoorthy, Nitin J Pawar, Mrignayani Kotecha
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引用次数: 0

摘要

目的:肿瘤缺氧的空间异质性是调节肿瘤生长、发展、侵袭性、转移和影响治疗效果的最重要因素之一。已知大多数实体瘤都存在缺氧或低氧(pO2 ≤10 托)。电子顺磁共振氧成像(EPROI)是一种新兴的氧绘图技术。EPROI 利用可注射的 OX071 三苯甲基自旋探针的弛豫速率与氧分压(pO2)之间的线性关系。然而,由于仪器尺寸的限制,大多数 EPROI 研究仅限于实体瘤小鼠模型。这项工作的目的是开发一种人体大小的 9 mT(共振频率 250 MHz,孔径 60 cm)脉冲 EPROI 仪器,并评估其在兔 VX-2 肿瘤氧成像中的性能:使用人体大小的 EPROI 仪器和 2.25 英寸 ID 容积线圈对小腿肌肉中长有 3.2 厘米 VX-2 肿瘤的新西兰白兔进行成像。该动物接受了约 8 分钟的 OX071 静脉注射(总容量为 5.2 mL,浓度为 72 mM),75 分钟后接受了瘤内注射(总容量为 120 μL,浓度为 5 mM OX071),并接受了 EPROI。实验结束后,使用临床前 9.4-T 核磁共振成像系统进行核磁共振成像,以勾勒出肿瘤边界:结果:首次建立了60厘米孔径/250兆赫频率的人体尺寸脉冲EPROI仪器,并利用兔子肿瘤氧成像进行了评估。这是首次在如此大的动物身上全身静脉注射对氧敏感的三苯甲基 OX071 自旋探针。静脉注射产生的 EPROI 图像显示肿瘤完全覆盖。瘤内注射后获得的图像显示肿瘤上叶局部覆盖,这表明需要改进瘤内注射方案:这项研究证明了世界上第一台人体大小的脉冲 EPROI 仪器的性能。结论:这项研究证明了世界上第一台人体大小的脉冲 EPROI 仪器的性能,同时也证明了可以通过全身注射一定量的自旋探针来对大型动物进行 EPROI。这使 EPROI 离癌症疗法的临床应用更近了一步。氧成像是一种平台技术,这里开发的仪器和技术也将用于其他临床应用。
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Oxygen Imaging of a Rabbit Tumor Using a Human-Sized Pulse Electron Paramagnetic Resonance Imager.

Purpose: Spatial heterogeneity in tumor hypoxia is one of the most important factors regulating tumor growth, development, aggressiveness, metastasis, and affecting treatment outcome. Most solid tumors are known to have hypoxia or low oxygen levels (pO2 ≤10 torr). Electron paramagnetic resonance oxygen imaging (EPROI) is an emerging oxygen mapping technology. EPROI utilizes the linear relationship between the relaxation rates of the injectable OX071 trityl spin probe and the partial oxygen pressure (pO2). However, most of the EPROI studies have been limited to mouse models of solid tumors because of the instrument-size limitations. The purpose of this work was to develop a human-sized 9-mT (250 MHz resonance frequency, 60 cm bore size) pulse EPROI instrument and evaluate its performance with rabbit VX-2 tumor oxygen imaging.

Methods: A New Zealand white rabbit with a 3.2-cm VX-2 tumor in the calf muscle was imaged using the human-sized EPROI instrument and a 2.25-in. ID volume coil. The animal received a ~8-min intravenous injection of OX071 (5.2 mL total volume at 72 mM concentration) and, after 75 min, an intratumoral injection (120 μL total at 5 mM OX071 concentration) and underwent EPROI. At the end of the experiments, MRI was performed using a preclinical 9.4-T MRI system to outline the tumor boundaries.

Results: For the first time, a human-sized pulse EPROI instrument with a 60-cm bore size/250-MHz frequency was built and evaluated using rabbit tumor oxygen imaging. For the first time, the systemic IV injection of the oxygen-sensitive trityl OX071 spin probe was used for an animal of this size. The resulting EPROI image from the IV injection showed complete tumor coverage. The image obtained after intratumoral injection showed localized coverage in the upper lobe of the tumor, demonstrating the need for improved intratumoral injection protocol.

Conclusions: This study demonstrates the performance of the world's first human-sized pulse EPROI instrument. It also demonstrates that the EPROI of larger animals can be performed using the systemic injection of a manageable amount of the spin probe. This brings EPROI one step closer to clinical applications in cancer therapies. Oxygen imaging is a platform technology, and the instrument and techniques developed here will also be useful for other clinical applications.

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来源期刊
CiteScore
6.90
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3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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