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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of a fast and simple gas chromatographic protocol based on the combined use of alkyl chloroformate and solid phase microextraction for the assay of polyamines in human urine
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Development of a fast and simple gas chromatographic protocol based on the combined use of alkyl chloroformate and solid phase microextraction for the assay of polyamines in human urine

机译:基于组合使用烷基氯仿和固相微萃取的快速和简单的气相色谱协议的研制在人尿中多胺的测定

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摘要

Polyamines are aliphatic amines with low molecular weight that are widely recognized as one of the most important cancer biomarkers for early diagnosis and treatment. The goal of the work herein presented is the development of a rapid and simple method for the quantification of free polyamines (i.e., putrescine, cadaverine, spermidine, spermine) and N-monoacetylated polyamines (i.e., N-1-Acetylspermidine, N-8-Acetylspermidine, and N-1-Acetylspermine) in human urine. A preliminary derivatization with propyl chloroformate combined with the use of solid phase microextraction (SPME) allowed for an easy and automatable protocol involving minimal sample handling and no consumption of organic solvents. The affinity of the analytes toward five commercial SPME coatings was evaluated in univariate mode, and the best result in terms of analyte extraction was achieved using the divinyl-benzene/carboxen/polydimethylsiloxane fiber. The variables affecting the performance of SPME analysis were optimized by the multivariate approach of experimental design and, in particular, using a central composite design (CCD). The optimal working conditions in terms of response values are the following: extraction temperature 40 degrees C, extraction time of 15 min and no addition of NaCl. Analyses were carried out by gas chromatography-triple quadrupole mass spectrometry (GC-QqQ-MS) in selected reaction monitoring (SRM) acquisition mode. The developed method was validated according to the guidelines issued by the Food and Drug Administration (FDA). The satisfactory performances reached in terms of linearity, sensitivity (LOQs between 0.01 and 0.1 mu g/mL), matrix effect (68-121%), accuracy, and precision (inter-day values between -24% and +16% and in the range 3.3-28.4%, respectively) make the proposed protocol suitable to be adopted for quantification of these important biomarkers in urine samples. (C) 2018 Elsevier B.V. All rights reserved.
机译:多胺是具有低分子量的脂族胺,广泛认为是早期诊断和治疗中最重要的癌症生物标志物之一。本文的工作的目的是发展快速和简单的方法,用于定量自由多胺(即Putrescine,野生胺,亚精胺,精子)和N-单乙酰化多胺(即,N-1-乙酰哌啶,N-8 - 在人尿中的 - 乙酰哌啶和N-1-乙酰孢胺。用氯甲酸丙酯的初步衍生化与使用固相微萃取(SPME)的使用允许易于自动的协议,涉及最小的样品处理和无有机溶剂的消耗。分析物朝向五种商业SPME涂层的亲和力在单变量模式中评价,使用二乙烯基 - 苯/羧烯烯/聚二甲基硅氧烷纤维实现分析物提取的最佳结果。影响SPME分析性能的变量通过实验设计的多变量方法进行了优化,特别是使用中央复合设计(CCD)进行了优化。在响应值方面的最佳工作条件如下:提取温度40℃,提取时间为15分钟,没有添加NaCl。通过在选定的反应监测(SRM)采集模式中通过气相色谱 - 三倍四极杆质谱(GC-QQQ-MS)进行分析。根据食品和药物管理局(FDA)发出的指导方针验证了开发的方法。线性度方面达到了满意的性能,灵敏度(定量限亩0.01至0.1克/毫升),基体效应(68-121%),准确度和精确度(-24%之间和+ 16%,而在日间值分别为3.3-28.4%的范围,使拟议的方案适用于定量尿液样本中这些重要的生物标志物。 (c)2018年elestvier b.v.保留所有权利。

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