Feng Biting, Gan Zhiwei, Hu Hongwei, Sun Hongwen
Se Pu. 2014 Sep;32(9):930-5. doi: 10.3724/sp.j.1123.2014.05033.
The sample pretreatment method for the determination of four typical artificial sweeteners (ASs) including sucralose, saccharin, cyclamate, and acesulfame in soil by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was optimized. Different conditions of extraction, including four extractants (methanol, acetonitrile, acetone, deionized water), three kinds of ionic strength of sodium acetate solution (0.001, 0.01, 0.1 mol/L), four pH values (3, 4, 5 and 6) of 0.01 mol/L acetate-sodium acetate solution, four set durations of extraction (20, 40, 60, 120 min) and number of extraction times (1, 2, 3, 4 times) were compared. The optimal sample pretreatment method was finally set up. The sam- ples were extracted twice with 25 mL 0.01 mol/L sodium acetate solution (pH 4) for 20 min per cycle. The extracts were combined and then purified and concentrated by CNW Poly-Sery PWAX cartridges with methanol containing 1 mmol/L tris (hydroxymethyl) amino methane (Tris) and 5% (v/v) ammonia hydroxide as eluent. The analytes were determined by HPLC-MS/MS. The recoveries were obtained by spiked soil with the four artificial sweeteners at 1, 10, 100 μg/kg (dry weight), separately. The average recoveries of the analytes ranged from 86.5% to 105%. The intra-day and inter-day precisions expressed as relative standard deviations (RSDs) were in the range of 2.56%-5.94% and 3.99%-6.53%, respectively. Good linearities (r2 > 0.995) were observed between 1-100 μg/kg (dry weight) for all the compounds. The limits of detection were 0.01-0.21 kg/kg and the limits of quantification were 0.03-0.70 μg/kg for the analytes. The four artificial sweeteners were determined in soil samples from farmland contaminated by wastewater in Tianjin. This method is rapid, reliable, and suitable for the investigation of artificial sweeteners in soil.
优化了采用高效液相色谱 - 串联质谱法(HPLC - MS/MS)测定土壤中三氯蔗糖、糖精、甜蜜素和安赛蜜四种典型人工合成甜味剂(ASs)的样品前处理方法。比较了不同的萃取条件,包括四种萃取剂(甲醇、乙腈、丙酮、去离子水)、三种乙酸钠溶液离子强度(0.001、0.01、0.1 mol/L)、0.01 mol/L乙酸 - 乙酸钠溶液的四个pH值(3、4、5和6)、四个萃取设定时长(20、40、60、120分钟)以及萃取次数(1、2、3、4次)。最终确定了最佳样品前处理方法。样品用25 mL 0.01 mol/L乙酸钠溶液(pH 4)萃取两次,每次萃取20分钟。合并萃取液,然后用含1 mmol/L三(羟甲基)氨基甲烷(Tris)和5%(v/v)氢氧化铵的甲醇作为洗脱剂,通过CNW Poly - Sery PWAX小柱进行净化和浓缩。采用HPLC - MS/MS测定分析物。通过向土壤中分别添加1、10、100 μg/kg(干重)的四种人工合成甜味剂来获得回收率。分析物的平均回收率在86.5%至105%之间。日内和日间精密度以相对标准偏差(RSDs)表示,分别在2.56% - 5.94%和3.99% - 6.53%范围内。所有化合物在1 - 100 μg/kg(干重)之间均呈现良好的线性关系(r2 > 0.995)。分析物的检测限为0.01 - 0.21 μg/kg,定量限为0.03 - 0.70 μg/kg。测定了天津受废水污染农田土壤样品中的四种人工合成甜味剂。该方法快速、可靠,适用于土壤中人工合成甜味剂的调查。