Campillo Natalia, Peñalver Rosa, Hernández-Córdoba Manuel
Department of Analytical Chemistry, Faculty of Chemistry, University of Murcia, E-30071 Murcia, Spain.
J Chromatogr A. 2006 Aug 25;1125(1):31-7. doi: 10.1016/j.chroma.2006.05.051.
A rapid and solvent-free method for the determination of nine chlorophenol (CP) compounds in honey samples using headspace solid-phase microextraction (HS-SPME) and gas chromatography with atomic emission detection (GC-AED) is developed. The different factors affecting the efficiency of the extraction and derivatization steps were carefully optimized. The polydimethylsiloxane-divinylbenzene (PDMS/DVB) fiber was the most suitable for preconcentrating the analytes from the headspace of an aqueous solution containing the dissolved honey samples where the chlorophenols had been submitted to acetylation. When the matrix effect was evaluated for different samples, it was concluded that standard addition calibration was required for quantification purposes. Detection limits roughly ranged from 0.1 to 2.4 ng g(-1), depending on the compound and the honey sample analyzed, with a fiber time exposure of only 15 min at 75 degrees C. The optimized method was successfully applied to different samples, some of the studied chlorophenols being detected in some of the analyzed honeys at concentration levels 0.6-9.4 ng g(-1).
建立了一种快速、无溶剂的方法,用于测定蜂蜜样品中的九种氯酚(CP)化合物,该方法采用顶空固相微萃取(HS-SPME)和带原子发射检测的气相色谱法(GC-AED)。仔细优化了影响萃取和衍生化步骤效率的不同因素。聚二甲基硅氧烷-二乙烯基苯(PDMS/DVB)纤维最适合从含有溶解蜂蜜样品的水溶液顶空中预浓缩分析物,其中氯酚已进行乙酰化处理。在评估不同样品的基质效应时,得出结论,为了定量目的需要采用标准加入校准法。检测限大致在0.1至2.4 ng g⁻¹范围内,这取决于所分析的化合物和蜂蜜样品,在75℃下纤维暴露时间仅为15分钟。该优化方法成功应用于不同样品,在一些分析的蜂蜜中检测到了部分所研究的氯酚,浓度水平为0.6 - 9.4 ng g⁻¹。