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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >SEPARATION AND DETERMINATION OF AMINO ACIDS, CREATININE, BIOACTIVE AMINES AND NUCLEIC ACID BASES BY DUAL-MODE GRADIENT ION-PAIR CHROMATOGRAPHY
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SEPARATION AND DETERMINATION OF AMINO ACIDS, CREATININE, BIOACTIVE AMINES AND NUCLEIC ACID BASES BY DUAL-MODE GRADIENT ION-PAIR CHROMATOGRAPHY

机译:双模式梯度离子对色谱法分离测定氨基酸,肌酐,生物活性胺和核酸碱

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摘要

A simple and fast high-performance liquid chromatography method for the analysis of amino acids and biological bases such as creatinine was developed using a technique termed ''dual-mode gradient ion-pair chromatography''. A butyl-silica reversed-phase column and water-acetonitrile eluent containing sodium dodecyl sulfate (SDS) and perchloric acid were used for the separation. A concentration gradient of acetonitrile from 15 to 35% provided a good separation of such organic cations. Since change in concentration of acetonitrile causes change in distribution equilibrium of SDS between mobile and stationary phases, a complete regeneration of the column to the initial state is required for the reproducible separations. Completion of the reequilibrium was indicated by a system peak appearing in the UV chromatogram and by conductivity measurements. The formation mechanism of the system peak was revealed. A flow-rate gradient from 1 to 2 ml/min was introduced in addition to the concentration gradient to shorten the cycle time of the chromatography. More than twenty kinds of amino acids, creatine and creatinine were simultaneously separated within 50 min and the cycle time was 80 min including the reequilibration time. A post-column derivatization fluorescence detection system was usable as well as UV detection. This elution system was also useful for the separation of bioactive amines and nucleic acid bases. The developed method was applied to the simultaneous determination of urinary creatinine and diagnostic amino acids due to inherited metabolic disorders.
机译:使用一种称为``双模式梯度离子对色谱法''的技术开发了一种简单,快速的高效液相色谱法,用于分析氨基酸和生物碱(例如肌酐)。使用丁基硅胶反相柱和含有十二烷基硫酸钠(SDS)和高氯酸的水-乙腈洗脱液进行分离。乙腈的浓度梯度为15%至35%,可以很好地分离此类有机阳离子。由于乙腈浓度的变化会导致流动相和固定相之间SDS的分布平衡发生变化,因此对于可重现的分离,需要将色谱柱完全再生至初始状态。再平衡的完成由紫外色谱图中出现的系统峰和电导率测量指示。揭示了系统峰的形成机理。除了浓度梯度外,还引入了1-2 ml / min的流速梯度,以缩短色谱的循环时间。在50分钟内可同时分离出二十多种氨基酸,肌酸和肌酐,包括再平衡时间在内的循环时间为80分钟。柱后衍生荧光检测系统以及紫外线检测均可用。该洗脱系统还可用于分离生物活性胺和核酸碱基。该方法适用于同时测定遗传性代谢疾病引起的尿肌酐和诊断性氨基酸含量。

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