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Determination of Trace Amounts of Aluminum in Environmental and Biological Fluids by Reversed-Phase Ion-Pair Liquid Chromatography with Fluorometric Detection Using 5-Sulfoquinoline-8-ol

机译:反相离子对液相色谱-5-磺基喹啉-8-ol荧光检测法测定环境和生物液体中的痕量铝

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Background: Aluminum is a toxic metal and is widespread in nature. Therefore, evaluation of aluminum level in environmental and biological fluids has received considerable attention. Among instrumental analytical techniques used for determination of aluminum, HPLC has advantages of selective separation and wide linear dynamic range. However, most of the HPLC methods reported for the analysis of aluminum involve pre-column derivatization with chromogenic chelating reagents and separation of aluminum with the mobile phases free from the reagents, which need to maintain the experimental conditions such as temperature and flow rate of the mobile phase strictly constant in order to obtain reliable results. Methods: In this study a reversed-phase ion-pair HPLC method for determination of trace amounts of aluminum was developed using 5-sulfoquinoline-8-ol (HQS) as the derivatization reagent for fluorometric detection. In order to suppress the appearance of system peaks on the chromatograms, the solutions injected into the HPLC column were prepared so that the compositions of the solutions were the same as that of the mobile phase except only for aluminum originating from the samples. Results: The calibration curve of aluminum standard solutions was linear over the range 0.05-10 μg L-1 with a correlation coefficient, r~2, of 0.9997. The limit of detection defined as three times the standard deviation of the blank signal was found to be 18 ng L-1 (0.67 nM). The aluminum concentrations in certified reference materials of river water determined by this method were in excellent agreement with the certified values. This method was also successfully applied for the determination of aluminum in urine and glucose parenteral solution as well as river water and tap water samples. Conclusion: HPLC determination of trace amounts of aluminum in environmental and biological fluids was performed with high accuracy and precision by suppressing the fluctuation of the baseline and detecting the Al-HQS complex at equilibrium of the complexation reaction.
机译:背景:铝是一种有毒金属,在自然界中广泛存在。因此,对环境和生物液体中铝含量的评估已引起广泛关注。在用于测定铝的仪器分析技术中,HPLC具有选择性分离和宽线性动态范围的优点。但是,报告的大多数用于分析铝的HPLC方法都涉及用生色螯合剂进行柱前衍生化以及将铝与流动相分离而不含试剂的方法,这需要保持实验条件,例如温度和流速。流动相严格恒定以便获得可靠的结果。方法:在本研究中,使用5-磺基喹啉-8-ol(HQS)作为衍生化试剂进行荧光检测,开发了一种反相离子对HPLC法测定痕量铝的方法。为了抑制色谱图中系统峰的出现,制备了注入HPLC柱的溶液,使溶液的成分与流动相相同,只是铝源于样品。结果:铝标准溶液的校准曲线在0.05-10μgL-1范围内呈线性,相关系数r〜2为0.9997。发现的检测限定义为空白信号标准偏差的三倍,为18 ng L-1(0.67 nM)。用这种方法测定的经过认证的河水参考材料中的铝浓度与经认证的值高度吻合。该方法还成功地用于尿液和葡萄糖肠胃外溶液以及河水和自来水样品中铝的测定。结论:通过抑制基线波动并在络合反应平衡时检测Al-HQS络合物,HPLC可以高精度,高精度地测定环境和生物液体中的痕量铝。

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