Lintelmann Jutta, Fischer Karin, Matuschek Georg
Institut für Okologische Chemie, GSF-Forschungszentrum für Umwelt und Gesundheit, GmbH, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.
J Chromatogr A. 2006 Nov 10;1133(1-2):241-7. doi: 10.1016/j.chroma.2006.08.038. Epub 2006 Sep 26.
A high-performance liquid chromatography-tandem mass spectrometric (LC-MS/MS) method with a rapid and simple sample preparation was optimized and validated for the determination of phenanthrene-9,10-dione, chrysene-5,6-dione, benzo[a]pyrene-1,6-dione, benzo[a]pyrene-3,6-dione, benzo[a]pyrene-4,5-dione, benzo[a]pyrene-6,12-dione, benzo[a]pyrene-7,8-dione, benzo[a]pyrene-11,12-dione and 6-oxo-7-oxa-benzo[a]pyrene in particulate matter. The mass spectrometer was operated in the multiple reaction monitoring (MRM) mode leading to high sensitivity and selectivity. The limits of quantification (S/N=10) ranged from ca. 0.1 pg/microl to ca. 5.8 pg/microl and matrix dependent recoveries varied between 49 and 92%. The applicability of the LC-MS/MS method was shown by the analysis of particulate matter (PM(2.5)) collected during the course of 2005 in the Munich area, Germany. All oxy-PAHs determined exhibited higher mean and peak concentrations in the winter months compared to the concentration levels in the warmer season.
优化并验证了一种高效液相色谱-串联质谱(LC-MS/MS)方法,该方法具有快速简单的样品制备过程,用于测定颗粒物中的菲-9,10-二酮、屈-5,6-二酮、苯并[a]芘-1,6-二酮、苯并[a]芘-3,6-二酮、苯并[a]芘-4,5-二酮、苯并[a]芘-6,12-二酮、苯并[a]芘-7,8-二酮、苯并[a]芘-11,12-二酮和6-氧代-7-氧杂苯并[a]芘。质谱仪在多反应监测(MRM)模式下运行,具有高灵敏度和选择性。定量限(S/N = 10)范围约为0.1 pg/微升至约5.8 pg/微升,且基质依赖性回收率在49%至92%之间变化。通过对2005年期间在德国慕尼黑地区采集的颗粒物(PM(2.5))进行分析,展示了LC-MS/MS方法的适用性。与温暖季节的浓度水平相比,所有测定的含氧多环芳烃在冬季月份的平均浓度和峰值浓度均更高。