Department of Toxicology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
Environ Monit Assess. 2013 May;185(5):3637-44. doi: 10.1007/s10661-012-2815-6. Epub 2012 Aug 16.
This study reports the feasibility of applying directly suspended liquid-phase microextraction (DSLPME)-gas chromatography detection for the pre-concentration and determination of low levels of eight polychlorinated biphenyls (PCBs) in aqueous samples. The technique requires minimal sample preparation, analysis time and solvent consumption and represents significant advantages over conventional analytical methods. The experimental parameters such as salt content, sample temperature, stirring rate, extraction time, micro-drop volume and breakthrough volume were investigated and found to have significant influences on DSLPME. Under the optimal experimental conditions, the enrichment factor ranged from 578 to 729, and the recovery was above 93 %. Calibration curves possessed good linearity (R(2) > 0.99) over a wide concentration range of 0.1-10.0 μg L(-1) with limits of detection ranging from 0.01 to 0.07 μg L(-1). The relative standard deviations for 1.0 μg L(-1) of PCBs in water by using internal standard were in the range 2-14 % (n = 3). The proposed simple, accurate and sensitive analytical method was applied successfully to the determination of trace amounts of PCBs in water samples.
本研究报告了直接悬浮液相微萃取(DSLPME)-气相色谱检测在预浓缩和测定水样中低浓度的八种多氯联苯(PCBs)中的应用可行性。该技术需要最少的样品制备、分析时间和溶剂消耗,与传统分析方法相比具有显著优势。研究了盐含量、样品温度、搅拌速度、萃取时间、微滴体积和突破体积等实验参数,发现它们对 DSLPME 有显著影响。在最佳实验条件下,富集因子范围为 578 至 729,回收率高于 93%。校准曲线在 0.1-10.0 μg L(-1) 的宽浓度范围内具有良好的线性(R(2) > 0.99),检出限范围为 0.01 至 0.07 μg L(-1)。使用内标时,水中 1.0 μg L(-1) 的 PCBs 的相对标准偏差在 2-14%(n = 3)范围内。该简单、准确和灵敏的分析方法成功应用于水样中痕量 PCBs 的测定。