摘要
建立了液-液-液微萃取与高效液相色谱联用同时测定血浆中西地那非和伐地那非的方法。考察了萃取溶剂、溶剂体积、接受相液滴大小、搅拌速度和萃取时间等因素对富集因子的影响,得到了萃取溶剂为300μL甲苯、接受相为2μL0·2mol/LHCl、搅拌速度为600r/min和萃取时间为40min的最佳实验条件。在该条件下,获得了较高的富集因子。两种组分的线性范围均为5μg/L^1·0mg/L,加标回收率高于87%,其相对标准偏差小于5%。以信噪比为3计,西地那非的检测限为1μg/L,伐地那非为0·5μg/L。该方法能有效地去除复杂基体的干扰,有机溶剂消耗少,萃取效率高,是一种有效的、灵敏的样品前处理方法,适用于血浆中微量西地那非和伐地那非的测定。
High performance liquid chromatography coupled with liquid-liquid-liquid microextraction was developed for the simultaneous determination of sildenafil and vardenafil in human plasma. The effects of extraction solvent, the volume of organic solvent, dropsize of acceptor phase, stirring rate and extraction time on the enrichment factors of analytes were investigated.The optimized experimental conditions, 300 μL toluene as the organic phase, 2 μL 0. 2 mol/LHCI as the acceptor phase, 600 r/min of the stirring rate, and 40 min of the extraction time,were gotten. Under these conditions, high enrichment factors were obtained. The linear range of studied analytes was from 5 μg/L to 1.0 mg/L. The relative standard deviation was lower than 5%. The limits of detection were 1 μg/L for sildenafil and 0.5 μg/L for vardenafil at signal-to-noise ratio of 3. The method with little solvent consumption may provide high analyte preconcentration and excellent sample clean-up, and it is a sensitive and suitable method for simultaneous determination of the above two substances in human plasma.
出处
《色谱》
CAS
CSCD
北大核心
2005年第4期358-361,共4页
Chinese Journal of Chromatography
基金
科技部"十五"国家重大科技专项(No.2003AA2Z3515)
湖南省自然科学基金资助项目(No.03JJY4009).
关键词
液-液-液微萃取
高效液相色谱
西地那非
伐地那非
血浆
liquid-liquid-liquid microextraction
high performance liquid chromatography
sildenafil
vardenafil
plasma
