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超声增强表面活性剂辅助分散液液微萃取-高效液相色谱法测定人血中酮康唑和硝酸益康唑。

Ultrasound-enhanced surfactant-assisted dispersive liquid-liquid microextraction and high-performance liquid chromatography for determination of ketoconazole and econazole nitrate in human blood.

机构信息

Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, China.

出版信息

Anal Bioanal Chem. 2012 Jan;402(3):1241-7. doi: 10.1007/s00216-011-5508-z. Epub 2011 Nov 6.

Abstract

A simple and efficient method, based on ultrasound-enhanced surfactant-assisted dispersive liquid-liquid microextraction (UESA-DLLME) followed by high-performance liquid chromatography (HPLC) has been developed for extraction and determination of ketoconazole and econazole nitrate in human blood samples. In this method, a common cationic surfactant, cetyltrimethylammonium bromide (CTAB), was used as dispersant. Chloroform (40 μL) as extraction solvent was added rapidly to 5 mL blood containing 0.068 mg mL(-1) CTAB. The mixture was then sonicated for 2 min to disperse the organic chloroform phase. After the extraction procedure, the mixture was centrifuged to sediment the organic chloroform phase, which was collected for HPLC analysis. Several conditions, including type and volume of extraction solvent, type and concentration of the surfactant, ultrasound time, extraction temperature, pH, and ionic strength were studied and optimized. Under the optimum conditions, linear calibration curves were obtained in the ranges 4-5000 μg L(-1) for ketoconazole and 8-5000 μg L(-1) for econazole nitrate, with linear correlation coefficients for both >0.99. The limits of detection (LODs, S/N = 3) and enrichment factors (EFs) were 1.1 and 2.3 μg L(-1), and 129 and 140 for ketoconazole and econazole nitrate, respectively. Reproducibility and recovery were good. The method was successfully applied to the determination of ketoconazole and econazole nitrate in human blood samples.

摘要

一种基于超声增强表面活性剂辅助分散液液微萃取(UESA-DLLME)结合高效液相色谱(HPLC)的简单高效方法已被开发用于人血样中酮康唑和硝酸益康唑的提取和测定。在该方法中,使用了一种常见的阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)作为分散剂。将 40 μL 氯仿(萃取溶剂)快速加入含有 0.068 mg mL(-1) CTAB 的 5 mL 血样中。然后将混合物超声处理 2 分钟以分散有机氯仿相。萃取后,将混合物离心以沉降有机氯仿相,收集用于 HPLC 分析。研究并优化了几种条件,包括萃取溶剂的类型和体积、表面活性剂的类型和浓度、超声时间、萃取温度、pH 值和离子强度。在最佳条件下,酮康唑的线性校准范围为 4-5000 μg L(-1),硝酸益康唑的线性校准范围为 8-5000 μg L(-1),两者的线性相关系数均大于 0.99。酮康唑和硝酸益康唑的检出限(LOD,S/N = 3)分别为 1.1 和 2.3 μg L(-1),富集因子(EF)分别为 129 和 140。重现性和回收率良好。该方法成功应用于人血样中酮康唑和硝酸益康唑的测定。

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