Zhang Fan, Tang Ming-Hai, Chen Li-Juan, Li Rui, Wang Xian-Huo, Duan Jun-Guo, Zhao Xia, Wei Yu-Quan
State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Keyuan Road 4, Gaopeng Street, Chengdu 610041, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Oct 1;873(2):173-9. doi: 10.1016/j.jchromb.2008.08.008. Epub 2008 Aug 19.
A rapid, specific and sensitive liquid chromatography-tandem mass spectrometry (LC/MS/MS) method was developed for simultaneous quantitation of six Aconitum alkaloids, i.e. aconitine (AC), mesaconitine (MA), hypaconitine (HA), benzoylaconine (BAC), benzoylmesaconine (BMA) and benzoylhypaconine (BHA) in human plasma collected from 18 healthy volunteers after intravenous drop infusion of "SHEN-FU" injectable powder in three different dosages. Lappaconitine was selected as the internal standard (IS). LC/MS/MS system coupled with an electrospray ionization (ESI) source was performed in multiple-reaction monitoring (MRM) mode. The transitions of the Aconitum alkaloids executed as following: m/z 646.3-->586.0 for AC; m/z 632.4-->573.1 for MA; m/z 616.2-->556.1 for HA; m/z 604.2-->104.8 for BAC; m/z 590.1-->104.8 for BMA; m/z 574.1-->104.8 for BHA; m/z 585.2-->161.8 for IS. Sample preparation was performed with solid-phase extraction (SPE) on a 1 mL HLB cartridge prior to analysis. The separation was applied on a Waters C(18) column (1.7 microm, 2.1 mm x 100 mm) and a gradient elution of methanol and 0.1% formic acid-water was used as mobile phase. The retention time was less than 4.5 min. The concentrations ranged from 0.1 to 1000 ng/mL for all six Aconitum alkaloids and showed a good linearity with the correlation coefficient (r(2)) >0.995. The validated method was employed to simultaneous quantitation and successfully used for the first time for the pharmacokinetic evaluation of the six Aconitum alkaloids after intravenous drop administration of "SHEN-FU" injectable powder in phase I clinical trial.
建立了一种快速、特异且灵敏的液相色谱-串联质谱(LC/MS/MS)方法,用于同时定量测定18名健康志愿者静脉滴注三种不同剂量的“参附”注射用粉剂后采集的人血浆中6种乌头生物碱,即乌头碱(AC)、中乌头碱(MA)、次乌头碱(HA)、苯甲酰乌头碱(BAC)、苯甲酰中乌头碱(BMA)和苯甲酰次乌头碱(BHA)。选择拉巴乌头碱作为内标(IS)。LC/MS/MS系统与电喷雾电离(ESI)源联用,采用多反应监测(MRM)模式。乌头生物碱的跃迁如下:AC的m/z 646.3→586.0;MA的m/z 632.4→573.1;HA的m/z 616.2→556.1;BAC的m/z 604.2→104.8;BMA的m/z 590.1→104.8;BHA的m/z 574.1→104.8;IS的m/z 585.2→161.8。分析前采用1 mL HLB柱进行固相萃取(SPE)进行样品制备。在Waters C(18)柱(1.7μm,2.1 mm×100 mm)上进行分离,以甲醇和0.1%甲酸-水的梯度洗脱作为流动相。保留时间小于4.5分钟。所有6种乌头生物碱的浓度范围为0.1至1000 ng/mL,且具有良好的线性,相关系数(r(2))>0.995。验证后的方法用于同时定量,并首次成功用于I期临床试验中静脉滴注“参附”注射用粉剂后6种乌头生物碱的药代动力学评价。