首页> 外文期刊>Analytical methods >Simultaneous extraction and determination of trace amounts of olanzapine and fluoxetine from biological fluids: comparison of conventional hollow fiber supported liquid phase microextraction and pulsed electrically assisted liquid-phase microextraction techniques
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Simultaneous extraction and determination of trace amounts of olanzapine and fluoxetine from biological fluids: comparison of conventional hollow fiber supported liquid phase microextraction and pulsed electrically assisted liquid-phase microextraction techniques

机译:从生物液体中同时提取和测定痕量的奥氮平和氟西汀:常规中空纤维支持的液相微萃取和脉冲电辅助液相微萃取技术的比较

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In the current work, hollow fiber liquid phase microextraction (HF-LPME) and pulsed electromembrane extraction (PEME) coupled with high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection were compared for the extraction of olanzapine (OLZ) and fluoxetine (FLX) from human plasma and urine samples. The influences of extraction parameters affecting the extraction efficiency of OLZ and FLX were studied and optimized for both methods. Under passive extraction conditions, FLX and OLZ were extracted from alkaline samples (pH = 12) into 1-octanol immobilized in the pores of a porous hollow fiber of polypropylene (SLM), and then transported into 25 ??L of 25 mM HCl as the acceptor solution. Under electrokinetic migration conditions, FLX and OLZ were transported under applied voltage from acidic sample solutions (pH = 6) through 2-nitrophenyl pentyl ether (NPPE) immobilized in the pores of the hollow fiber into 25 ??L of 10 mM HCl as the acceptor solution. Under the optimized conditions, preconcentration factors in the range of 59 to 78 and 43 to 65 for PEME and HF-LPME, respectively, and satisfactory repeatabilities (3.4 relative standard deviation [RSD] 7.8) were obtained in different matrices. The obtained recoveries of the drugs in the range of 82.6a€“103.1% indicated the excellent capability of the developed methods for simultaneous extraction of FLX and OLZ from complex matrices. The results showed that in comparison with HF-LPME based on pH gradient, PEME is a more effective transport process, providing high extraction efficiencies in a short time.
机译:在当前的工作中,比较了中空纤维液相微萃取(HF-LPME)和脉冲电膜萃取(PEME)结合高效液相色谱(HPLC)和紫外(UV)检测的奥氮平(OLZ)和氟西汀的萃取(FLX)来自人类血浆和尿液样本。研究并优化了提取参数对OLZ和FLX提取效率的影响。在被动萃取条件下,将FLX和OLZ从碱性样品(pH = 12)中萃取到固定在聚丙烯多孔中空纤维(SLM)孔中的1-辛醇中,然后以25 mL HCl的形式输送至25升。受体解决方案。在电动迁移条件下,FLX和OLZ在施加电压的条件下从酸性样品溶液(pH = 6)通过固定在中空纤维孔中的2-硝基苯基戊基醚(NPPE)转运到25 µL 10 mM HCl中。受体溶液。在优化的条件下,PEME和HF-LPME的预浓缩系数分别在59至78和43至65的范围内,并且在不同的基质中均获得了令人满意的重复性(3.4 <相对标准偏差[RSD] <7.8)。药物的回收率在82.6a±103.1%的范围内,表明该开发的方法能够从复杂基质中同时提取FLX和OLZ。结果表明,与基于pH梯度的HF-LPME相比,PEME是一种更有效的转运过程,可在短时间内提供较高的提取效率。

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