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Dispersive liquid-liquid microextraction based on solidification of floating organic droplet followed by spectrofluorimetry for determination of carvedilol in human plasma

机译:基于悬浮有机液滴凝固后分光荧光法测定人血浆中卡维地洛的分散液-液微萃取

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摘要

Background: Simple, chip and rapid analytical methods are required in biomedical analysis laboratories to support therapeutic drug monitoring units in hospitals. The present work aimed to provide such a method for quantitative determination of carvedilol in plasma samples. Results: A new, simple, precise and efficient method was developed for the determination of carvedilol in human plasma using a dispersive liquid-liquid microextraction based on solidification of floating organic droplet, followed by spectrofluorimetry method. Some important parameters such as types and volumes of extraction and disperser solvents, pH, salt effect and sample volume were optimized. Under the optimized experimental conditions, the method provided a linear range of 40 to 300 ng ml-1, with a correlation coefficient of 0.996. The limit of detection, lower limit of quantification and upper limit of quantification were 18, 40 and 300 ng ml-1, respectively. The found recovery was from 98.2 to 102.2%, the mean intra-and inter-day precisions were 8.3 and 6.4%, respectively. The relative error for accuracy varied from 0.4 to 2.2%. The short-term temperature and freeze-thaw stability studies showed that carvedilol in human plasma was stable for sample preparation and analysis after storage. Conclusion: The proposed method provided reasonable acceptable results and could be used for therapeutic monitoring of carvedilol.
机译:背景:生物医学分析实验室需要简单,芯片和快速的分析方法来支持医院的治疗药物监测部门。本工作旨在提供一种定量测定血浆样品中卡维地洛的方法。结果:建立了一种新的,简单,准确和高效的方法,该方法使用基于悬浮有机液滴固化的分散液-液微萃取,然后采用荧光光谱法测定人血浆中的卡维地洛。优化了一些重要参数,例如萃取和分散剂溶剂的类型和体积,pH,盐效应和样品量。在优化的实验条件下,该方法提供了40至300 ng ml-1的线性范围,相关系数为0.996。检测限,定量下限和定量上限分别为18、40和300 ng ml-1。发现的恢复率为98.2%至102.2%,日内和日间平均精度分别为8.3%和6.4%。精度的相对误差在0.4到2.2%之间变化。短期温度和冻融稳定性研究表明,人血浆中卡维地洛对保存后的样品制备和分析是稳定的。结论:该方法提供了合理的可接受结果,可用于卡维地洛的治疗监测。

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