Pan Xiaoping, Zhang Baohong, Tian Kang, Jones Lindsey E, Liu Jun, Anderson Todd A, Wang Jia-Sheng, Cobb George P
The Institute of Environmental and Human Health (TIEHH), and Department of Environmental Toxicology, Texas Tech University, Lubbock, TX 79409-1163, USA.
Rapid Commun Mass Spectrom. 2006;20(14):2222-6. doi: 10.1002/rcm.2576.
A quantitative liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) method was developed for the analysis of the explosive, octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX). In negative ionization mode, HMX forms an acetate adduct ion M + CH(3)COO, m/z 355, in the presence of a small amount of acetic acid in the mobile phase. The ESI collision-induced dissociation (CID) spectrum of m/z 355 was acquired and the transitions m/z 355 --> 147 and m/z 355 --> 174 were chosen for the determination of HMX in samples. Using this quantification technique, the method detection limit was 1.57 microg/L and good linearity was achieved in the range 5-500 microg/L. This method will help to unambiguously analyze environmentally relevant concentrations of HMX.
开发了一种定量液相色谱/电喷雾电离串联质谱(LC/ESI-MS/MS)方法用于分析炸药八氢-1,3,5,7-四硝基-1,3,5,7-四氮杂环辛烷(HMX)。在负离子化模式下,在流动相中存在少量乙酸的情况下,HMX形成乙酸加合物离子M + CH(3)COO,质荷比为355。获取了质荷比为355的ESI碰撞诱导解离(CID)谱,并选择质荷比355 --> 147和质荷比355 --> 174的跃迁用于样品中HMX的测定。采用这种定量技术,方法检测限为1.57微克/升,在5 - 500微克/升范围内实现了良好的线性。该方法将有助于明确分析与环境相关浓度的HMX。