Key Laboratory of Forest Plant Ecology, Ministry of Education, Northeast Forestry University, Harbin 150040, PR China.
J Pharm Biomed Anal. 2011 Dec 5;56(4):841-5. doi: 10.1016/j.jpba.2011.07.038. Epub 2011 Jul 30.
A rapid and sensitive method for the determination of pinostrobin in rat plasma was developed using liquid chromatography tandem mass spectrometry (LC-MS/MS) for the first time. Isoliquiritigenin was used as an internal standard in rat plasma. Chromatographic separation was performed on an HiQ Sil C(18) column with isocratic elution at a flow rate of 1mL/min. The mobile phase consisted of water and methanol (9:91, v/v) containing 0.1% formic acid. The quantification limit was 10ng/mL within a linear range of 10-1000ng/mL (R=0.9984). The intra- and inter-day assay precision ranged from 3.8-5.3% to 3.2-5.2%, respectively, and the intra- and inter-day assay accuracy was between 93.2-95.1% and 95.5-104.3%, respectively. Our results indicated that the LC-MS/MS method is effective for pharmacokinetic study of pinostrobin in rat plasma.
首次建立了液相色谱-串联质谱法(LC-MS/MS)测定大鼠血浆中紫檀芪的方法。以异甘草素为内标,采用 HiQ Sil C18 柱,以水-甲醇(9:91,v/v)为流动相,含 0.1%甲酸,流速为 1mL/min,等度洗脱。紫檀芪在 10-1000ng/mL 范围内线性关系良好(R=0.9984),定量下限为 10ng/mL。日内和日间精密度分别为 3.8-5.3%至 3.2-5.2%,准确度分别为 93.2-95.1%至 95.5-104.3%。结果表明,该 LC-MS/MS 法可有效用于大鼠血浆中紫檀芪的药代动力学研究。