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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >The influence of sample collection, handling and low temperature storage upon NMR metabolic profiling analysis in human synovial fluid
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The influence of sample collection, handling and low temperature storage upon NMR metabolic profiling analysis in human synovial fluid

机译:样品收集,处理和低温储存对人滑液NMR代谢分析分析的影响

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摘要

The impact of metabolism upon the altered pathology of joint disease is rapidly becoming recognized as an important area of study. Synovial joint fluid is an attractive and representative biofluid of joint disease. A systemic review revealed little evidence of the metabolic stability of synovial joint fluid collection, handling or storage, despite recent reports characterizing the metabolic phenotype in joint disease. We aim to report the changes in small molecule detection within human synovial fluid (HSF) using nuclear magnetic resonance (NMR) spectroscopy at varying storage temperatures, durations and conditions. HSF was harvested by arthrocentesis from patients with isolated monoarthropathy or undergoing joint replacement (n = 30). Short-term storage (0-12h, 4 degrees C & 18 degrees C) and the effect of repeated freeze-thaw cycles (-80 degrees C to 18 degrees C) was assessed. Long-term storage was evaluated by early (-80 degrees C, <21days) and late analysis (-80 degrees C, 10-12 months). 1D NMR spectroscopy experiments, NOESYGPPRID and CPMG identified metabolites and semi-quantification was performed. Samples demonstrated broad stability to freeze-thaw cycling and refrigeration of <4 h. Short-term room temperature or refrigerated storage showed significant variation in 2-ketoisovalerate, valine, dimethylamine, succinate, 2-hydroxybutyrate, and acetaminophen glucuronide. Lipid and macromolecule detection was variable. Long-term storage demonstrated significant changes in: acetate, acetoacetate, creatine, N,N-dimethylglycine, dimethylsulfone, 3-hydroxybutyrate and succinate. Changeable metabolites during short-term storage appeared to be energy-synthesis intermediates. Most metabolites were stable for the first four hours at room temperature or refrigeration, with notable exceptions. We therefore recommend that HSF samples should be kept refrigerated for no more than 4 hours prior to freezing at -80 degrees C. Furthermore, storage of HSF samples for 10-12 months before analysis can affect the detection of selected metabolites. Crown Copyright (C) 2021 Published by Elsevier B.V. All rights reserved.
机译:代谢对关节疾病病理改变的影响正迅速成为一个重要的研究领域。滑膜关节液是关节疾病中一种极具吸引力和代表性的生物流体。一项系统性综述显示,尽管最近的报告描述了关节疾病的代谢表型,但几乎没有证据表明滑膜关节液收集、处理或储存的代谢稳定性。我们的目的是报告在不同的储存温度、持续时间和条件下,使用核磁共振(NMR)光谱技术检测人体滑液(HSF)中小分子的变化。单纯性单关节病患者或正在进行关节置换的患者(n=30)通过关节穿刺术获取HSF。评估短期储存(0-12小时,4摄氏度和18摄氏度)和重复冻融循环(-80摄氏度至18摄氏度)的效果。通过早期(-80摄氏度,<21天)和后期分析(-80摄氏度,10-12个月)评估长期储存。1D核磁共振波谱实验、NOESYGPPRID和CPMG鉴定代谢物并进行半定量。样品在冻融循环和<4小时的冷藏中表现出广泛的稳定性。短期室温或冷藏显示2-酮异戊酸盐、缬氨酸、二甲胺、琥珀酸盐、2-羟基丁酸盐和对乙酰氨基酚葡萄糖醛酸盐存在显著变化。脂质和大分子检测是可变的。长期储存表明:乙酸盐、乙酰乙酸盐、肌酸、N,N-二甲基甘氨酸、二甲基砜、3-羟基丁酸盐和琥珀酸盐发生显著变化。短期储存期间的可变代谢物似乎是能量合成中间体。大多数代谢物在室温或冷藏条件下的前四个小时内是稳定的,但有明显的例外。因此,我们建议HSF样品在-80°C下冷冻前应冷藏不超过4小时。此外,在分析前将HSF样品储存10-12个月可能会影响所选代谢物的检测。皇冠版权(C)2021由爱思唯尔B.V.出版保留所有权利。

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