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首页> 外文期刊>Analytica chimica acta >Ultrasound-assisted hydrolysis and chemical derivatization combined to lab-on-valve solid-phase extraction for the determination of sialic acids in human biofluids by μ-liquid chromatography-laser induced fluorescence
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Ultrasound-assisted hydrolysis and chemical derivatization combined to lab-on-valve solid-phase extraction for the determination of sialic acids in human biofluids by μ-liquid chromatography-laser induced fluorescence

机译:超声辅助水解和化学衍生化-阀上固相萃取-μ-液相色谱-激光诱导荧光法测定人生物流体中的唾液酸

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摘要

The determination of sialic acids (SIAs) has recently gained interest because of their potential role as markers of inflammatory disorders or chronic diseases. Hydrolysis of conjugated derivatives, solid-phase extraction (SPE) and derivatization steps constitute sample preparation prior to insertion of the analytical sample into a μ-liquid chromatograph-laser induced fluorescence (μ-LC-LIF) detector in the present method for the determination of two representative SIAs of human metabolism. Ultrasound-accelerated hydrolysis released free SIAs, which were efficiently concentrated in a dynamic manner using a lab-on-valve (LOV) module that allows automation of SPE for preconcentration and cleanup. This step was on-line connected with DMB-labeling of SIAs (derivatization), which was shortened from 180 min required with the conventional heating method to 20 min with ultrasound assistance. Individual separation of the target analytes was achieved within 20 min by U--LC, while LIF detection endowed the overall method with high sensitivity. The LODs and LOQs provided by the method ranged 0.1-0.8 ng mL~(-1) and 0.4-1.0ngmL~(-1) (between 0.1 -0.8 pg and 0.4-1.0 pg expressed as on-column amount), respectively. High efficiency for interferents removal by SPE enabled the application of the method to four different biofluids—serum, urine, saliva and breast milk—for the determination of the target metabolites.
机译:唾液酸(SIA)的测定由于其作为炎症性疾病或慢性疾病的标志物的潜在作用,最近引起了人们的兴趣。共轭衍生物的水解,固相萃取(SPE)和衍生化步骤构成了样品制备,然后将分析样品插入本方法中的μ-液相色谱-激光诱导荧光(μ-LC-LIF)检测器中人类新陈代谢的两个代表性SIA。超声加速的水解释放出游离的SIA,然后使用阀门实验室(LOV)模块以动态的方式有效地对其进行浓缩,该模块允许SPE的自动化以进行预浓缩和净化。该步骤与SIA的DMB标记在线连接(衍生化),该步骤从传统加热方法所需的180分钟缩短为超声辅助下的20分钟。通过U--LC在20分钟内完成目标分析物的单独分离,而LIF检测使整个方法具有很高的灵敏度。该方法提供的LOD和LOQ分别在0.1-0.8 ng mL〜(-1)和0.4-1.0ngmL〜(-1)的范围内(以柱上量表示在0.1 -0.8 pg和0.4-1.0 pg之间)。通过SPE去除干扰物的高效率,使得该方法可应用于四种不同的生物流体(血清,尿液,唾液和母乳),以确定目标代谢物。

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