首页> 外文期刊>Journal of separation science. >Three-phase hollow-fiber microextraction combined with ion-pair high-performance liquid chromatography for the simultaneous determination of five components of compound alpha-ketoacid tablets in human urine
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Three-phase hollow-fiber microextraction combined with ion-pair high-performance liquid chromatography for the simultaneous determination of five components of compound alpha-ketoacid tablets in human urine

机译:三相中空纤维微萃取-离子对高效液相色谱法同时测定人尿中复方α-酮酸片的五种成分

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The determination of alpha-ketoacid concentration is demanded to evaluate the absorption and metabolic behavior of compound alpha-ketoacid tablets taken by chronic kidney disease patients. To eliminate the interference of endogenous substance of urine and enrich the analytes, a three-phase hollow-fiber liquid-phase microextraction combined with ion-pair high-performance liquid chromatography method was established for the determination of D,L-alpha-hydroxymethionine calcium, D, L-alpha-ketoisoleucine calcium, alpha-ketovaline calcium, alpha-ketoleucine calcium, and alpha-ketophenylalanine calcium of compound alpha-ketoacid tablets in human urine samples. The extraction parameters, such as organic solvent, pH of donor phase and acceptor phase, stirring rate, and extraction time were optimized. Under the optimal conditions, the obtained enrichment factors were up to 11-, 110-, 198-, 202-, and 50-fold, respectively. The calibration curves for these analytes were linear over the range of 0.110 mg/L for alpha-ketovaline calcium, D, L-alpha-ketoisoleucine calcium, and alpha-ketoleucine calcium, 0.5-10 mg/L for D, L-alpha-hydroxymethionine calcium, and alpha-ketophenylalanine calcium with r > 0.99. The relative standard deviations (n = 5) were less than 6.27% and the LODs were 100.7, 10.0, 5.8, 7.8, and 8.6 mu g/L (based on S/N = 3), respectively. Good recoveries from spiked urine samples (92-118%) were obtained. The proposed method demonstrated excellent sample clean-up and analytes enrichment to determine the five components in human urine.
机译:需要确定α-酮酸浓度以评估慢性肾脏病患者服用的复合α-酮酸片剂的吸收和代谢行为。为了消除尿液中的内源性物质的干扰并富集分析物,建立了三相中空纤维液相微萃取-离子对高效液相色谱法测定D,L-α-羟基蛋氨酸钙的方法。人尿液样本中的D,L,L-α-酮基异亮氨酸钙,α-酮基缬氨酸钙,α-酮亮氨酸钙和α-酮基苯丙氨酸钙。优化了萃取参数,如有机溶剂,供体相和受体相的pH,搅拌速率和萃取时间。在最佳条件下,获得的富集因子分别高达11倍,110倍,198倍,202倍和50倍。这些分析物的校准曲线在0.110 mg / L的范围内呈线性关系,其中α-酮戊环酸钙,D,L-α-酮异亮氨酸钙和α-酮基亮氨酸钙为0.5-10 mg / L,D,L-α-α-酮羟基蛋氨酸钙和α-酮基苯丙氨酸钙,r> 0.99。相对标准偏差(n = 5)小于6.27%,LOD分别为100.7、10.0、5.8、7.8和8.6μg / L(基于S / N = 3)。从加标的尿液样品中回收率高(92-118%)。所提出的方法展示了出色的样品净化能力和分析物富集度,可确定人尿中的五种成分。

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