Partial Acquisition of Spectral Projections Accelerates Four-dimensional Spectral-spatial EPR Imaging for Mouse Tumor Models: A Feasibility Study.

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Molecular Imaging and Biology Pub Date : 2024-06-01 Epub Date: 2024-05-29 DOI:10.1007/s11307-024-01924-y
Misa Oba, Mai Taguchi, Yohei Kudo, Koya Yamashita, Hironobu Yasui, Shingo Matsumoto, Igor A Kirilyuk, Osamu Inanami, Hiroshi Hirata
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Abstract

Purpose: Our study aimed to accelerate the acquisition of four-dimensional (4D) spectral-spatial electron paramagnetic resonance (EPR) imaging for mouse tumor models. This advancement in EPR imaging should reduce the acquisition time of spectroscopic mapping while reducing quality degradation for mouse tumor models.

Procedures: EPR spectra under magnetic field gradients, called spectral projections, were partially measured. Additional spectral projections were later computationally synthesized from the measured spectral projections. Four-dimensional spectral-spatial images were reconstructed from the post-processed spectral projections using the algebraic reconstruction technique (ART) and assessed in terms of their image qualities. We applied this approach to a sample solution and a mouse Hs766T xenograft model of human-derived pancreatic ductal adenocarcinoma cells to demonstrate the feasibility of our concept. The nitroxyl radical imaging agent 2H,15N-DCP was exogenously infused into the mouse xenograft model.

Results: The computation code of 4D spectral-spatial imaging was tested with numerically generated spectral projections. In the linewidth mapping of the sample solution, we achieved a relative standard uncertainty (standard deviation/| mean |) of 0.76 μT/45.38 μT = 0.017 on the peak-to-peak first-derivative EPR linewidth. The qualities of the linewidth maps and the effect of computational synthesis of spectral projections were examined. Finally, we obtained the three-dimensional linewidth map of 2H,15N-DCP in a Hs766T tumor-bearing leg in vivo.

Conclusion: We achieved a 46.7% reduction in the acquisition time of 4D spectral-spatial EPR imaging without significantly degrading the image quality. A combination of ART and partial acquisition in three-dimensional raster magnetic field gradient settings in orthogonal coordinates is a novel approach. Our approach to 4D spectral-spatial EPR imaging can be applied to any subject, especially for samples with less variation in one direction.

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部分获取光谱投影可加速小鼠肿瘤模型的四维光谱空间 EPR 成像:可行性研究
目的:我们的研究旨在加速小鼠肿瘤模型的四维(4D)光谱空间电子顺磁共振(EPR)成像的采集。EPR 成像的这一进步应能缩短光谱绘图的采集时间,同时减少小鼠肿瘤模型的质量下降:程序:部分测量磁场梯度下的 EPR 光谱,称为光谱投影。随后根据测量到的光谱投影计算合成额外的光谱投影。利用代数重建技术(ART)从后处理的光谱投影重建四维光谱空间图像,并评估其图像质量。我们将这种方法应用于样品溶液和小鼠 Hs766T 人源胰腺导管腺癌细胞异种移植模型,以证明我们概念的可行性。将硝基自由基成像剂 2H,15N-DCP 外源注入小鼠异种移植模型:结果:用数值生成的光谱投影测试了 4D 光谱空间成像的计算代码。在样本溶液的线宽映射中,我们实现了峰-峰第一衍生物 EPR 线宽的相对标准不确定性(标准偏差/平均值)为 0.76 μT/45.38 μT = 0.017。我们还研究了线宽图的质量以及光谱投影计算合成的影响。最后,我们获得了 Hs766T 肿瘤患者体内 2H、15N-DCP 的三维线宽图:结论:我们将 4D 光谱空间 EPR 成像的采集时间缩短了 46.7%,而图像质量却没有明显下降。在正交坐标的三维光栅磁场梯度设置中将 ART 和部分采集相结合是一种新方法。我们的 4D 光谱空间 EPR 成像方法可应用于任何对象,尤其是单向变化较少的样本。
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来源期刊
CiteScore
6.90
自引率
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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