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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Quantitative determination of nicotinic acid in micro liter volume of urine sample by drop-to-drop solvent microextraction coupled to matrix assisted laser desorption/ionization mass spectrometry
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Quantitative determination of nicotinic acid in micro liter volume of urine sample by drop-to-drop solvent microextraction coupled to matrix assisted laser desorption/ionization mass spectrometry

机译:滴滴溶剂微萃取-基质辅助激光解吸/电离质谱法定量测定尿样中微升体积中的烟酸

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摘要

Drop-to-drop solvent microextraction (DDSME) coupled with matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS) for quantitative determination of nicotinic acid in one drop of urine sample has been proposed. All parameters, such as type of organic solvent, extraction time, exposure volume solvent, pH of the sample solution that affecting the separation and preconcentration of nicotinic acid were investigated. Under the optimal conditions, the detection limit of the method was 20 ng mL~(-1) and the relative standard deviations (RSD) for determination of the nicotinic acid were in the range of 8.0-12.5%. The calculated calibration curves gave linearity in the range of 80-1000 ng mL~(-1). The main advantages of the proposed method are simple, fast, and small amount of sample solution is used for separation and preconcentration of nicotinic acid. This method could be also useful for the analysis of other interested analytes in small volume of biological samples, like plasma, saliva and urine, where the availability of samples are limited.
机译:提出了逐滴溶剂微萃取(DDSME)结合基质辅助激光解吸/电离质谱(MALDI-MS)定量测定一滴尿液样本中烟酸的方法。研究了影响烟酸分离和预富集的所有参数,例如有机溶剂的类型,萃取时间,溶剂的暴露量,样品溶液的pH。在最佳条件下,该方法的检出限为20 ng mL〜(-1),烟酸测定的相对标准偏差(RSD)为8.0-12.5%。计算出的校准曲线的线性范围为80-1000 ng mL〜(-1)。所提出方法的主要优点是简单,快速,并且少量的样品溶液用于烟酸的分离和预浓缩。该方法还可用于分析少量生物样品中其他感兴趣的分析物,例如血浆,唾液和尿液,其中样品的可用性受到限制。

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