Department of Nuclear Medicine, Affiliated Hospital of Luzhou Medical College, Luzhou, Sichuan 646000, PR China.
Eur J Radiol. 2011 Sep;79(3):369-74. doi: 10.1016/j.ejrad.2010.10.021. Epub 2010 Nov 23.
The purpose of this study is to describe the synthesis of Gadolinium-diethylenetriamine pentaacetic acid-deoxyglucosamine (Gd-DTPA-DG) which is a d-glucosamine metabolic MR imaging contrast agent. We will also discuss its use in a pilot MRI study using a xenograft mouse model of human adenocarcinoma.
This novel contrast agent was specifically studied because of its ability to "target" metabolically active tumor tissues. In this study Gd-DTPA-DG is used to investigate how tumor tissues would react to a dose of 0.2 mmol Gd/kg over a 120 min exposure in a xenograft mouse model. These experiments used athymic mice implanted with human pulmonary adenocarcinoma (A549) as demonstrated by dynamic MRI. Alternately, another contrast agent that is not specific for targeting, Gd-DTPA, was used as the control at a similar dose of gadolinium. Efficacy of the targeted contrast agent was assessed by measuring relaxation rate in vitro and signal intensity (SI) in vivo. Statistical differences were calculated using one-way analysis of variance.
The synthesized Gd-DTPA-DG was shown to improve the contrast of tumor tissue in this model. Gd-DTPA-DG was also shown to have a similar pharmacokinetic rate but generated a higher relaxation rate in tumor tissues relative to the control contrast Gd-DTPA. In comparison to the pre-contrast imaging, the SI of tumor tissue in the experimental group was shown to be significantly increased at 15 min after injection of Gd-DTPA-DG (p<0.001). The enhanced signal intensity spread from the edge of the tumor to the center and seemed to strengthen the idea that MRI performance would be useful in different tumor tissues.
This preliminary study shows that this new chelated contrast agent, Gd-DTPA-DG, can be specifically targeted to accumulation in tumor tissue as compared to normal tissues. This targeted paramagnetic contrast agent has potential for specific cancer molecular imaging with MRI.
本研究旨在描述钆-二乙三胺五乙酸-葡糖胺(Gd-DTPA-DG)的合成,这是一种葡糖胺代谢性磁共振成像对比剂。我们还将讨论其在人类腺癌异种移植小鼠模型的初步 MRI 研究中的应用。
本研究特别研究了这种新型对比剂,因为它具有“靶向”代谢活跃的肿瘤组织的能力。在这项研究中,Gd-DTPA-DG 用于研究在异种移植小鼠模型中,在 120 分钟的暴露时间内,以 0.2mmol Gd/kg 的剂量,肿瘤组织将如何反应。这些实验使用植入人肺腺癌(A549)的裸鼠,如动态 MRI 所示。另外,使用一种非特异性靶向的对比剂 Gd-DTPA 作为类似剂量的钆的对照。通过体外测量弛豫率和体内信号强度(SI)来评估靶向对比剂的疗效。使用单向方差分析计算统计差异。
合成的 Gd-DTPA-DG 被证明可改善该模型中肿瘤组织的对比度。Gd-DTPA-DG 还显示出相似的药代动力学速率,但与对照对比剂 Gd-DTPA 相比,在肿瘤组织中产生更高的弛豫率。与预对比成像相比,实验组肿瘤组织的 SI 在注射 Gd-DTPA-DG 后 15 分钟显著增加(p<0.001)。信号强度的增强从肿瘤边缘扩散到中心,似乎强化了 MRI 性能在不同肿瘤组织中有用的观点。
这项初步研究表明,与正常组织相比,这种新的螯合对比剂 Gd-DTPA-DG 可以特异性靶向肿瘤组织的积累。这种靶向顺磁性对比剂具有通过 MRI 进行特定癌症分子成像的潜力。