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Determination of triamterene in human plasma and urine after its cloud point extraction

机译:浊点萃取后的人血浆和尿液中锑的测定

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摘要

A new analytical approach was developed involving cloud point extraction (CPE) and spectrofluorimetric determination of triamterene (TM) in biological fluids. A urine or plasma sample was prepared and adjusted to pH 7, then TM was quickly extracted using CPE, using 0.05% (w/v) of Triton X-114 as the extractant. The main factors that affected the extraction efficiency (the pH of the sample, the Triton X-114 concentration, the addition of salt, the extraction time and temperature, and the centrifugation time and speed) were studied and optimized. The method gave calibration curves for TM with good linearities and correlation coefficients (r) higher than 0.99. The method showed good precision and accuracy, with intra- and inter-assay precisions of less than 8.50% at all concentrations. Standard addition recovery tests were carried out, and the recoveries ranged from 94.7% to 114%. The limits of detection and quantification were 3.90 and 11.7 µg L-1, respectively, for urine and 5.80 and 18.0 µg L-1, respectively, for plasma. The newly developed, environmentally friendly method was successfully used to extract and determine TM in human urine samples.
机译:开发了一种新的分析方法,涉及浊点提取(CPE)和光谱氟化物测定生物流体中的Triamterene(TM)。制备尿或等离子体样品并调节至pH7,然后使用CPE快速提取Tm,使用0.05%(w / v)作为萃取剂的Triton X-114。研究了影响提取效率的主要因素(样品的pH,Triton X-114浓度,加入盐,提取时间和温度,以及离心时间和速度)。该方法为TM提供了校准曲线,具有高于0.99的良好线性和相关系数(R)。该方法表现出良好的精度和精度,在所有浓度下具有少于8.50%的分析型和分析晶体积。进行标准添加回收试验,回收率范围为94.7%至114%。检测和定量的极限分别为3.90和11.7μg,分别用于尿液和5.80和18.0μgL-1,用于等离子体。新开发的环保方法已成功地用于提取和确定人类尿液样本中的TM。

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