Pan Ryh-Nan, Lin Chang-Ching, Huang Pei-Wei, Hsiong Cheng-Huei, Pao Li-Heng
Department of Disaster Management, Taiwan Police College, Taipei, Taiwan, ROC.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Sep 1;872(1-2):58-62. doi: 10.1016/j.jchromb.2008.07.014. Epub 2008 Jul 23.
A sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the determination of triazolam and its metabolites, alpha-hydroxytriazolam (alpha-OHTRZ) and 4-hydroxytriazolam (4-OHTRZ), was developed and validated. Triazolam-D4 was used as the internal standard (IS). This analysis was carried out on a Thermo C(18) column and the mobile phase was composed of acetonitrile:H(2)O:formic acid (35:65:0.2, v/v/v). Detection was performed on a triple-quadrupole tandem mass spectrometer using positive ion mode electrospray ionization (ESI) and quantification was performed by multiple reaction monitoring (MRM) mode. The MS/MS ion transitions monitored were m/z 343.1-->308.3, 359.0-->308.3, 359.0-->111.2 and 347.0-->312.0 for triazolam, alpha-OHTRZ, 4-OHTRZ and triazolam-D4, respectively. LLOQ of the analytical method was 0.05 ng/mL for triazolam and 0.1 ng/mL for alpha-OHTRZ and 4-OHTRZ. The within- and between-run precisions were less than 15.26% and accuracy was -8.08% to 13.33%. The method proved to be accurate and specific, and was applied to the pharmacokinetic study of triazolam in healthy Chinese volunteers.
建立并验证了一种灵敏且具选择性的液相色谱 - 串联质谱法(LC - MS/MS),用于测定三唑仑及其代谢物α - 羟基三唑仑(α - OHTRZ)和4 - 羟基三唑仑(4 - OHTRZ)。使用三唑仑 - D4作为内标(IS)。该分析在Thermo C(18)柱上进行,流动相由乙腈:水:甲酸(35:65:0.2,v/v/v)组成。在三重四极杆串联质谱仪上采用正离子模式电喷雾电离(ESI)进行检测,并通过多反应监测(MRM)模式进行定量。所监测的MS/MS离子跃迁分别为:三唑仑的m/z 343.1→308.3,α - OHTRZ的m/z 359.0→308.3,4 - OHTRZ的m/z 359.0→111.2以及三唑仑 - D4的m/z 347.0→312.0。该分析方法的三唑仑定量下限(LLOQ)为0.05 ng/mL,α - OHTRZ和4 - OHTRZ的LLOQ为0.1 ng/mL。批内和批间精密度均小于15.26%,准确度为 - 8.08%至13.33%。该方法被证明准确且具特异性,并应用于三唑仑在健康中国志愿者中的药代动力学研究。