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Determination of Free Catecholamines in Urine By Tandem Affinity/Ion-Pair Chromatography and Flow Injection Analysis

机译:HpLC法测定尿液中游离儿茶酚胺的含量 串联亲和/离子对色谱和流动 注射分析

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摘要

Background—A system was developed for the simultaneous measurement in urine of free catecholamines (i.e., dopamine, norepinephrine, epinephrine) and creatinine (i.e., an indicator of urine output and volume). This method was based on the use of tandem affinity/ion-pair HPLC and flow injection analysis.Methods—The free catecholamines were extracted directly from urine by using an on-line phenylboronic acid affinity column. The extracted solutes were then separated and measured by ionpair chromatography followed by amperometric detection. Creatinine was measured by an on-line flow injection analysis system based on the Jaffe reaction, which analyzed creatinine as it eluted nonretained from the phenylboronic acid column.Results—Various factors were considered in the design and optimization of the phenylboronic acid column, the tandem affinity/ion-pair HPLC columns and the flow injection analysis system. The total analysis time for the final combined system was approximately 16 min per injection at 1 ml/min. This method was found to have good agreement with the expected results for control urine samples. The limits of detection for 20 μl samples (S/N = 3.0) were 1.8, 1.0 and 4.3 μg/l for norepinephrine, epinephrine and dopamine, respectively, while the limit of detection of creatinine was 5.0 mg/l. The linear response of this method extended over a 450 to 930-fold range in concentration for the catecholamines and covered the range of clinical interest. The within-day precision of this method was ±2.0−2.7%.Conclusions—The ability of this method to simultaneously monitor both creatinine and other analytes makes this HPLC/FIA system an attractive method for use in monitoring urinary compounds. With this approach it was possible to provide fast results for small volumes of random urine samples that were collected as part of a psychological study. The same method could also be utilized with 12 or 24 h urine specimens.
机译:背景技术—开发了一种同时测量尿中游离儿茶酚胺(即多巴胺,去甲肾上腺素,肾上腺素)和肌酐(即尿量和尿量的指标)的系统。该方法基于串联亲和/离子对HPLC和流动注射分析的方法。方法-使用在线苯基硼酸亲和柱直接从尿液中提取游离儿茶酚胺。然后分离提取的溶质,并通过离子对色谱法进行测量,然后进行安培检测。通过基于Jaffe反应的在线流动注射分析系统对肌酐进行测量,该系统分析了肌酐在苯硼酸柱中未洗脱时的肌酐。结果-在设计和优化苯硼酸柱的串联和优化过程中考虑了多种因素亲和/离子对HPLC色谱柱和流动注射分析系统。最终组合系统的总分析时间约为每次注射1 ml / min时16分钟。发现该方法与对照尿液样品的预期结果具有很好的一致性。去甲肾上腺素,肾上腺素和多巴胺的20μl样品(S / N = 3.0)的检出限分别为1.8、1.0和4.3μg/ l,而肌酐的检出限为5.0 mg / l。该方法的线性响应使儿茶酚胺的浓度范围扩大了450到930倍,并涵盖了临床关注的范围。该方法的日内精度为±2.0-2.7%。结论—该方法能够同时监测肌酐和其他分析物的能力,使该HPLC / FIA系统成为用于监测尿中化合物的诱人方法。通过这种方法,可以为作为心理研究一部分而收集的少量随机尿液样本提供快速的结果。同样的方法也可用于12或24小时尿液样本。

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