首页> 外文期刊>Analytical methods >Development of pipette tip-based on molecularly imprinted polymer micro-solid phase extraction for selective enantioselective determination of (?)-(2S,4R) and (+)-(2R,4S) ketoconazole in human urine samples prior to HPLC-DAD
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Development of pipette tip-based on molecularly imprinted polymer micro-solid phase extraction for selective enantioselective determination of (?)-(2S,4R) and (+)-(2R,4S) ketoconazole in human urine samples prior to HPLC-DAD

机译:基于分子印迹聚合物微固相萃取的移液器吸头的开发,用于在HPLC-DAD之前选择性对映选择性测定人尿液样品中的(?)-(2S,4R)和(+)-(2R,4S)酮康唑

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In this work a simple and selective sample preparation technique employing pipette tip-based on molecularly imprinted polymer micro-solid phase extraction (PT-MIP-??-SPE) coupled to HPLC/DAD was developed for the determination of the cis-enantiomers of ketoconazole (KTZ) in human urine samples. Several parameters affecting the proposed PT-MIP-??-SPE technique were investigated, namely the washing solvent, type and volume of the eluent, amount of material (molecularly imprinted polymer, MIP), sample volume, pH and salt addition. The recoveries were around 100% using 5 ??g mLa?’1 for the (a?’)-(2S,4R) and (+)-(2R,4S) KTZ enantiomers. Optimum chromatographic conditions for determination of the (a?’)-(2S,4R) and (+)-(2R,4S)-KTZ enantiomers were found using the chiral stationary phase polysaccharide derived of amylose tris(3,5-dimethylphenylcarbamate). The mobile phase consisted of ethanol:water (95:5, v/v) at a flow rate of 1 mL mina?’1 and the detection was performed at 250 nm. The performance criteria for linearity, sensitivity, precision, accuracy, recovery, robustness and stability were assessed and they were within the recommended guidelines. The method showed to be linear over the concentration range from 6.25 to 650.00 ng mLa?’1 for each enantiomer, with the correlation coefficients of 0.9962 and 0.9952 for (+)-(2R,4S)-KTZ and (a?’)-(2S,4R)-KTZ, respectively. Within-day and between-day precision and accuracy assays for these analytes were studied at three concentration levels and were lower than 15%. The results for the application of the method in preliminary urinary excretion showed that there are not significant differences in the analyzed concentrations of KTZ cis-enantiomers in urine samples.
机译:在这项工作中,开发了一种简单,选择性的样品制备技术,该技术采用移液管吸头为基础,结合了HPLC / DAD的分子印迹聚合物微固相萃取(PT-MIP-β-SPE),用于测定HPLC的顺式对映异构体。人体尿液样本中的酮康唑(KTZ)。研究了影响拟议的PT-MIP-β-SPE技术的几个参数,即洗涤溶剂,洗脱液的类型和体积,材料量(分子印迹聚合物,MIP),样品量,pH和盐添加量。使用(a?’)-(2S,4R)和(+)-(2R,4S)KTZ对映体使用5 ?? g mLa?1进行回收率约为100%。使用直链淀粉三(3,5-二甲基苯基氨基甲酸酯)衍生的手性固定相多糖,可以找到确定(a?')-(2S,4R)和(+)-(2R,4S)-KTZ对映异构体的最佳色谱条件。流动相由乙醇:水(95:5,v / v)组成,流速为1 mL min-1?1,检测在250 nm处进行。评估了线性,灵敏度,精密度,准确性,回收率,鲁棒性和稳定性的性能标准,这些标准均在建议的准则之内。该方法在每种对映体的浓度范围为6.25至650.00 ng mLa?'1处显示出线性关系,(+)-(2R,4S)-KTZ和(a?')-的相关系数为0.9962和0.9952。 (2S,4R)-KTZ。这些分析物的日间和日间精密度和准确度分析是在三种浓度水平下进行的,并且低于15%。该方法在初步尿液排泄中的应用结果表明,尿液样品中分析的KTZ顺式对映体浓度没有显着差异。

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