Gao C X, Krull I S, Trainor T
Department of Chemistry, Barnett Institute, Northeastern University, Boston, Massachusetts 02115.
J Chromatogr Sci. 1990 Mar;28(3):102-8. doi: 10.1093/chromsci/28.3.102.
An easy, rapid, and efficient method using on-line solid-phase derivatization in HPLC is developed for the trace determination of aliphatic amines in air. Some fundamental studies on stop-flow, on-line, solid-phase derivatizations in HPLC are also investigated, such as optimization of the reaction detection HPLC system and band broadening. Air is sampled with silica gel tubes from different sites, including sewage areas, fish cleaning and processing rooms, and an organoleptic lab of the U.S. Food & Drug Administration (FDA). The trapped amines are desorbed with an acidic aqueous-organic solution, followed by pH adjustment of the eluates to pH 10. The resulting solution is directly injected into an on-line, precolumn, solid-phase derivatization and reversed-phase HPLC-UV/FL system, not requiring any further sample workup steps. The percent derivatizations are as high as 88 +/- 5% (n = 3) for primary amines, and 75 +/- 4% (n = 3) for diethylamine under optimized conditions (60 degrees C for 10 min). The recoveries for all amines are above 90%. The method is validated by a single-blind, spiked experiment with 1.1-4.4% relative standard deviation (RSD) in the range of 15-47 ppm. These results are confirmed by a GC-FID method performed in another lab. Amines are quantitated via calibration plots, with final concentrations from 0.02 to 0.38 mg/m3 air. It is suggested that this newer approach for the determination of amines and polyamines, using polymeric solid-phase reagents on-line, precolumn in HPLC, should prove generally successful for other amines and other sample types in the future.
开发了一种在高效液相色谱(HPLC)中使用在线固相衍生化的简便、快速且高效的方法,用于痕量测定空气中的脂肪胺。还研究了HPLC中停流、在线固相衍生化的一些基础研究,如反应检测HPLC系统的优化和谱带展宽。使用硅胶管从不同地点采集空气样本,这些地点包括污水区域、鱼类清理和加工室以及美国食品药品监督管理局(FDA)的感官实验室。捕获的胺用酸性水-有机溶液解吸,然后将洗脱液的pH值调节至10。所得溶液直接注入在线柱前固相衍生化反相HPLC-UV/FL系统,无需任何进一步的样品后处理步骤。在优化条件下(60℃,10分钟),伯胺的衍生化率高达88±5%(n = 3),二乙胺的衍生化率为75±4%(n = 3)。所有胺的回收率均高于90%。该方法通过单盲加标实验进行验证,在15 - 47 ppm范围内相对标准偏差(RSD)为1.1 - 4.4%。这些结果在另一个实验室通过气相色谱-火焰离子化检测(GC-FID)方法得到证实。通过校准曲线对胺进行定量,空气中的最终浓度为0.02至0.38 mg/m³。建议这种使用HPLC柱前在线聚合物固相试剂测定胺和多胺的新方法,未来对于其他胺和其他样品类型通常应会取得成功。