Willmering Matthew M, Albert Brice J, Plummer Joseph W, Greer Josh, Walkup Laura L, Lindquist Diana M, Cleveland Zackary I
Center for Pulmonary Imaging Research (CPIR), Division of Pulmonary Medicine Cincinnati Children's Hospital Medical Center Cincinnati OH USA; Department of Pediatrics, University of Cincinnati OH USA.
Center for Pulmonary Imaging Research (CPIR), Division of Pulmonary Medicine Cincinnati Children's Hospital Medical Center Cincinnati OH USA.
J Magn Reson. 2025 Feb;371:107829. doi: 10.1016/j.jmr.2025.107829. Epub 2025 Jan 13.
Harmonizing and validating Xe gas exchange imaging across multiple sites is hampered by a lack of a quantitative standard that 1) displays the unique spectral properties of Xe observed from human subjects in vivo and 2) has short enough T times to enable practical imaging. This work describes and demonstrates the development of two dissolved-phase, thermally polarized phantoms that mimic the in-vivo, red blood cell and membrane resonances of Xe dissolved in human lungs. Following optimization, combinations of two common organic solvents, acetone and dimethyl sulfoxide, resulted in two in-vivo-like dissolved-phase Xe phantoms yielding chemical shifts of 212.4 ppm and 193.9 ppm. By doping the solutions with iron(iii) acetylacetonate, the longitudinal relaxation time was reduced T = 1.2 s for both phantoms at 3 T and 7 T. There was minimal change in chemical shift (+1.58 ppm) and T (+1.2 %) over 1 year. In a 2D Dixon-type acquisition with 3 mm in-plane resolution, Xe dissolved-phase images yielded signal-to-noise ratios 6 and 12 for the RBC and membrane phantoms, respectively. A simple scaling of these phantoms to clinically relevant volumes of several liters would result in an SNR of 7 for the RBC phantom acquired in less than one minute. These findings demonstrate the ability to fabricate robust, quantitative, thermally polarized dissolved-phase phantoms, which will be needed to validate and harmonize gas exchange imaging in multi-site clinical trials.
由于缺乏一种定量标准,使得在多个地点对氙气交换成像进行协调和验证受到阻碍。该定量标准需满足以下两点:一是能够显示在人体受试者体内观察到的氙气独特光谱特性;二是具有足够短的T时间以实现实际成像。这项工作描述并展示了两种溶解相热极化体模的开发,它们模拟了溶解在人肺中的氙气在体内的红细胞和膜共振情况。经过优化,两种常见有机溶剂丙酮和二甲基亚砜的组合产生了两种类似体内的溶解相氙气模体,其化学位移分别为212.4 ppm和193.9 ppm。通过用乙酰丙酮铁(III)掺杂溶液,在3 T和7 T场强下,两种模体的纵向弛豫时间均降低至T = 1.2 s。在1年的时间里,化学位移变化极小(+1.58 ppm),T变化也极小(+1.2%)。在平面分辨率为3 mm的二维狄克逊型采集中,溶解相氙气图像的红细胞模体和膜模体的信噪比分别为6和12。将这些模体简单放大到几升的临床相关体积,红细胞模体在不到一分钟的采集时间内信噪比将达到7。这些发现表明能够制造出稳健、定量的热极化溶解相模体,这对于在多中心临床试验中验证和协调气体交换成像将是必要的。