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钆基造影剂在磁共振成像引导放疗中的安全性——利用弛豫测量法对螯合物稳定性的研究

Safety of gadolinium based contrast agents in magnetic resonance imaging-guided radiotherapy - An investigation of chelate stability using relaxometry.

作者信息

Mahmood Faisal, Nielsen Ulla Gro, Jørgensen Christian Brandt, Brink Carsten, Thomsen Henrik S, Hansen Rasmus Hvass

机构信息

Laboratory of Radiation Physics, Department of Oncology, Odense University Hospital, Kloevervaenget 19, Indgang 85, Pavillonen, Stuen, 5000 Odense C, Denmark.

Department of Clinical Research, University of Southern Denmark, Winsløwparken 19, 3. Sal, Odense C 5000, Denmark.

出版信息

Phys Imaging Radiat Oncol. 2022 Feb 26;21:96-100. doi: 10.1016/j.phro.2022.02.015. eCollection 2022 Jan.

Abstract

BACKGROUND AND PURPOSE

With the introduction of hybrid magnetic resonance linacs (MR-linac), improved imaging has enabled daily treatment adaptation. However, the use of gadolinium based contrast agents (GBCAs) is desired to further improve MR image contrast. GBCAs are in the form of a non-toxic metalorganic gadolinium complex, but toxic un-chelated aqueous gadolinium(III), Gd(aq), can be released in patients if the organic ligand is degraded by the radiation. In this study, T relaxation measurements were performed to study the effect of radiation on three GBCAs.

MATERIALS AND METHODS

GBCAs, gadoteric acid, gadobutrol and gadoxectic acid were investigated in a concentration range of 10-100 mM. Measurements were performed on a 500 MHz nuclear MR (NMR) spectrometer with a high-resolution inversion recovery sequence to determine T. Samples were irradiated with 7 MV photons on an MR-linac to a total dose of 100 Gy. The lower detection limit of Gd(aq) was established by estimating the overall measurement uncertainty and comparing to corresponding changes in R when replacing chelated Gd with gadolinium nitrate at predefined percentages.

RESULTS

The overall measurement uncertainty was estimated to ±0.0053 ms, corresponding to Gd(aq) detection levels 1%-1.5% or 1-4.5 micro molar at clinical GBCA dosage. No detectable differences in R were observed between irradiated and non-irradiated samples for any GBCA.

CONCLUSIONS

This study did not find any measurable degradation of GBCAs due to irradiation with high-energy X-rays, however, in-vivo investigations are needed to provide the clinical basis for safe use of contrast agents in a radiotherapy workflow.

摘要

背景与目的

随着混合型磁共振直线加速器(MR直线加速器)的引入,成像技术的改进使得每日治疗方案的调整成为可能。然而,人们期望使用基于钆的造影剂(GBCA)来进一步提高磁共振图像的对比度。GBCA为无毒金属有机钆络合物形式,但如果有机配体因辐射而降解,有毒的未螯合水合钆(III),即Gd(aq),可能会在患者体内释放。在本研究中,进行了T弛豫测量以研究辐射对三种GBCA的影响。

材料与方法

研究了钆特酸、钆布醇和钆塞酸三种GBCA,浓度范围为10 - 100 mM。在一台500 MHz核磁共振(NMR)光谱仪上,使用高分辨率反转恢复序列进行测量以确定T。样品在MR直线加速器上用7 MV光子照射,总剂量为100 Gy。通过估计总体测量不确定度并与在预定义百分比下用硝酸钆替代螯合钆时R的相应变化进行比较,确定了Gd(aq)的下限检测限。

结果

总体测量不确定度估计为±0.0053 ms,在临床GBCA剂量下对应Gd(aq)检测水平为1% - 1.5%或1 - 4.5微摩尔。对于任何GBCA,照射样品和未照射样品之间未观察到R有可检测到的差异。

结论

本研究未发现高能X射线照射导致GBCA有任何可测量的降解,然而,需要进行体内研究以为在放射治疗工作流程中安全使用造影剂提供临床依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8ea/8885577/addec7c2a459/gr1.jpg

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