Wang Jing, Zhang Yu, Guan Tingting, Lin Xia, Tang Xing, Xu Hui
Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Biomed Chromatogr. 2009 Sep;23(9):999-1006. doi: 10.1002/bmc.1214.
A novel, specific and rapid ultra performance liquid chromatography electrospray ionization tandem mass spectrometry method has been developed and validated for determination of teniposide in rat plasma. A one-step liquid-liquid extraction method was used and the separation was carried out on an Acquity UPLC(TM) BEH C(18) column with gradient elution using a mobile phase composed of acetonitrile and water (containing 0.1% formic acid) at a flow rate of 0.20 mL/min. A triple quadrupole tandem mass spectrometer in multiple-reaction monitoring mode via an electrospray ionization interface was used for the detection of teniposide. The detection was complete within 3.0 min. A linear calibration curve was obtained over the concentration range 10-10,000 ng/mL for teniposide, with a lower limit of quantification of 10 ng/mL. The intra-day precision and inter-day precision (relative standard deviation) were less than 10.23 and 13.09%, respectively. The developed method was applied for the first time to the pharmacokinetic study of teniposide in rats following a single intravenous administration of 4.5 mg/kg teniposide.
已开发并验证了一种新颖、特异且快速的超高效液相色谱-电喷雾电离串联质谱法,用于测定大鼠血浆中的替尼泊苷。采用一步液-液萃取法,在Acquity UPLC(TM) BEH C(18)柱上进行分离,流动相由乙腈和水(含0.1%甲酸)组成,梯度洗脱,流速为0.20 mL/min。通过电喷雾电离接口,采用三重四极杆串联质谱仪在多反应监测模式下检测替尼泊苷。检测在3.0分钟内完成。替尼泊苷在10 - 10,000 ng/mL浓度范围内获得线性校准曲线,定量下限为10 ng/mL。日内精密度和日间精密度(相对标准偏差)分别小于10.23%和13.09%。所开发的方法首次应用于大鼠单次静脉注射4.5 mg/kg替尼泊苷后的药代动力学研究。