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Extraction and determination of trace amounts of chlorpromazine in biological fluids using magnetic solid phase extraction followed by HPLC

机译:磁性固相萃取-HPLC提取和测定生物体液中痕量氯丙嗪

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A simple, rapid and sensitive method termed as magnetic solid phase extraction (MSPE) combined with high-performance liquid chromatography-ultraviolet detector (HPLC-UV) has been proposed for the determination of trace amounts of chlorpromazine (CPZ) in water, urine and plasma samples. The separation and determination was performed on a C18 column under the optimal chromatographic conditions. Several factors influencing the extraction efficiency of CPZ, such as pH, surfactant and adsorbent amounts, ionic strength, extraction time, sample volume and desorption conditions, were studied and optimized. Under the optimal MSPE conditions, the extraction percentage of CPZ was 74%, 27% and 16% in water, urine and plasma samples, respectively. The limits of detection (LODs) of the proposed approach were 0.1, 5.0 and 10ng/mL in water, urine and plasma samples, respectively. The relative standard deviations (RSDs) based on five replicate determinations at 10ng/mL level of CPZ was 1.2%. Good linear behaviors over the investigated concentration ranges (0.25–300ng/mL) with good coefficient of determination, R 2 >0.9998, were obtained. Good spike recoveries with relative errors less than 9.0% were obtained when applying the proposed method to water, urine and plasma samples.
机译:提出了一种称为磁性固相萃取(MSPE)结合高效液相色谱-紫外检测器(HPLC-UV)的简单,快速,灵敏的方法,用于测定水,尿液和尿液中的痕量氯丙嗪(CPZ)。血浆样品。在最佳色谱条件下,在C18色谱柱上进行分离和测定。研究和优化了影响CPZ萃取效率的几个因素,例如pH,表面活性剂和吸附剂的量,离子强度,萃取时间,样品量和脱附条件。在最佳MSPE条件下,水,尿液和血浆样品中CPZ的提取率分别为74%,27%和16%。该方法在水,尿液和血浆样品中的检出限(LOD)分别为0.1、5.0和10ng / mL。基于CPZ浓度为10ng / mL的五次重复测定,相对标准偏差(RSD)为1.2%。在所研究的浓度范围(0.25-300ng / mL)内具有良好的线性行为,并具有良好的测定系数,R 2> 0.9998。将本方法应用于水,尿液和血浆样品时,可获得良好的加标回收率,相对误差小于9.0%。

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