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采用基于光纤二极管阵列检测器的在线耦合等速电泳-毛细管区带电泳法直接测定人尿液中的塞利洛尔。

Direct determination of celiprolol in human urine using on-line coupled ITP-CZE method with fiber-based DAD.

作者信息

Mikus Peter, Maráková Katarína, Marák Jozef, Planková Alexandra, Valásková Iva, Havránek Emil

机构信息

Department of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University, Slovak Republic.

出版信息

Electrophoresis. 2008 Nov;29(22):4561-7. doi: 10.1002/elps.200800079.

Abstract

The present work illustrated possibilities of column-coupling electrophoresis combined with DAD for the direct quantitative determination of trace drug (celiprolol, CEL) in clinical human urine samples. ITP, on-line coupled with CZE, served as an ideal injection technique (high sample load capacity, narrow and sharp drug zone). Moreover, the ITP provided an effective on-line sample pretreatment (preseparation, purification and preconcentration of the drug) producing analyte zone suitable for its direct detection and quantitation in CZE stage. Spectral DAD in comparison with single wavelength ultraviolet detection enhanced value of analytical information (i) verifying purity (i.e., spectral homogeneity) of drug zone (according to differences in spectrum profiles when compared tested and reference drug spectra) and (ii) indicating zones/peaks with spectra similar to the drug spectrum (potential structurally related metabolites). The characterization of trace analyte signals superposed on the baseline noise was more definite thanks to the application of background correction and smoothing procedure to the raw DAD spectra (producing relevant spectral response). The proposed ITP-CZE-DAD method was characterized by favorable performance parameters for CEL in urine matrices {e.g., the lower limit of quantification was 9.7 ng/mL, RSD and relative error of the determinations were lower than 3% (precision) and 1% (accuracy), respectively, analyte peak exhibited spectral homogeneity (reflecting separation selectivity), separation efficiency was 84,500 theoretical plates} and successfully applied in a trial pharmacokinetic study of CEL.

摘要

本研究阐述了柱耦合电泳结合二极管阵列检测器(DAD)直接定量测定临床人尿样中痕量药物(塞利洛尔,CEL)的可能性。等速电泳(ITP)与毛细管区带电泳(CZE)在线联用,作为一种理想的进样技术(高样品负载能力、窄且尖锐的药物区带)。此外,ITP提供了有效的在线样品预处理(药物的预分离、纯化和预富集),产生适合在CZE阶段直接检测和定量的分析物区带。与单波长紫外检测相比,光谱DAD增强了分析信息的价值:(i)验证药物区带的纯度(即光谱均匀性)(根据测试药物光谱与对照药物光谱比较时的光谱轮廓差异);(ii)指示光谱与药物光谱相似的区带/峰(潜在的结构相关代谢物)。由于对原始DAD光谱应用了背景校正和平滑程序(产生相关的光谱响应),叠加在基线噪声上的痕量分析物信号的表征更加明确。所提出的ITP-CZE-DAD方法在尿样基质中对CEL具有良好的性能参数{例如,定量下限为9.7 ng/mL,测定的相对标准偏差(RSD)和相对误差分别低于3%(精密度)和1%(准确度),分析物峰表现出光谱均匀性(反映分离选择性),分离效率为84,500理论塔板数},并成功应用于CEL的试验性药代动力学研究。

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