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使用优化的显色鲎试剂法检测磁共振成像造影剂中的内毒素

Endotoxin Detection in Magnetic Resonance Imaging Contrast Agent Using Optimising Chromogenic Limulus Amebocyte Lysate Assay.

作者信息

Ab Aziz Atiqah, Mappiare Sahrinanah, Nam Hui Yin, Devi Durga, Johan Mohd Rafie, Kamarul Tunku

机构信息

Tissue Engineering Group (TEG), National Orthopaedic Centre of Excellence for Research and Learning (NOCERAL), Department of Orthopaedic Surgery, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.

M. Kandiah Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, Selangor, Malaysia.

出版信息

Malays J Med Sci. 2024 Oct;31(5):284-291. doi: 10.21315/mjms2024.31.5.20. Epub 2024 Oct 8.

Abstract

Endotoxin contamination in magnetic resonance imaging (MRI) contrast agents can pose a risk to patient safety causing immune reactions. Strict endotoxin limits are enforced for implants and catheters inserted into the body, but there are not clear rules for MRI contrast agents. Here, we investigated the efficacy of chromogenic LAL assay test for screening endotoxin activity in MRI contrast media manufactured in Malaysia. The powdered agent was dissolved in water for injection and endotoxin levels were measured. The coefficient of efficiency value for the standard curve, exhibiting ≥ 0.98, along with the absence of interfering substances and endotoxin activity below the regulatory threshold of 0.5 EU/mL, support the conclusion that the agent is unlikely to be pyrogenic or induce pyrogenic effect.

摘要

磁共振成像(MRI)造影剂中的内毒素污染可能会对患者安全构成风险,引发免疫反应。对于植入体内的植入物和导管,执行严格的内毒素限制,但对于MRI造影剂却没有明确的规定。在此,我们研究了显色鲎试剂法检测在马来西亚生产的MRI造影剂中筛选内毒素活性的功效。将粉状试剂溶于注射用水中并测量内毒素水平。标准曲线的效率系数值≥0.98,且不存在干扰物质,内毒素活性低于0.5 EU/mL的监管阈值,这些都支持该试剂不太可能具有致热原性或诱导热原效应这一结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24d9/11477474/2182dc2d91e4/20mjms3105_bcf1.jpg

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