School of Pharmacy, Heilongjiang University of Chinese Medicine, 24 Heping Road, Xiangfang District, Harbin 150040, Heilongjiang, China.
Molecules. 2018 Jun 28;23(7):1573. doi: 10.3390/molecules23071573.
A simple and high sensitive ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the simultaneous determination of peimine and peiminine in beagle dog plasma after the oral administration of Maxim and Miq powder. Chromatographic separation was achieved on an ACQUIT UPLC BEH C column (1.7 μm, 2.1 × 100 mm) in a gradient elution way with a mobile phase consisting of acetonitrile and water containing 0.1% formic acid at a flow rate of 0.4 mL/min. The plasma samples were prepared by a liquid⁻liquid extraction (LLE) method with ethyl acetate. The analytes were detected with a triple quadrupole tandem mass spectrometry (MS) in multiple reaction monitoring (MRM) mode and a positive ion electrospray ionization (ESI) of the transitions at / 432.4→414.4 for peimine and / 430.3→412.3 for peiminine. The method was linear for two analytes over the investigated range with all determined correlation coefficients exceeding 0.9900. The lower limit of quantification (LLOQ) was 0.988 ng/mL for peimine and 0.980 ng/mL for peiminine. The mean extraction recoveries of peimine and peiminine at three quality control samples (QC) levels were ranged from 82.56 to 88.71%, and matrix effects ranged from 92.06 to 101.2%. The intra-day and inter-day precision and accuracy were within the acceptable limits at LLOQ and QC levels. The method was effectively and successfully applied to the pharmacokinetics of peimine and peiminine after oral administration of powder to beagle dogs. The obtained results may be help to guide the clinical application of Maxim and Miq.
建立并验证了一种简单、灵敏的超高效液相色谱-串联质谱法(UPLC-MS/MS),用于同时测定犬口服 Maxim 和 Miq 粉后血浆中的贝母辛和贝母辛宁。采用 ACQUIT UPLC BEH C 柱(1.7μm,2.1×100mm)进行色谱分离,以含 0.1%甲酸的乙腈-水为流动相进行梯度洗脱,流速为 0.4mL/min。血浆样品采用乙酸乙酯液-液萃取(LLE)法提取。采用三重四极杆串联质谱(MS),以正离子电喷雾电离(ESI),在多反应监测(MRM)模式下检测分析物,贝母辛和贝母辛宁的离子对分别为/432.4→414.4 和/430.3→412.3。两种分析物在考察范围内均呈良好的线性关系,所有测定的相关系数均大于 0.9900。贝母辛和贝母辛宁的定量下限(LLOQ)分别为 0.988ng/mL 和 0.980ng/mL。3 个质控样品(QC)水平的贝母辛和贝母辛宁的平均提取回收率在 82.56%88.71%之间,基质效应在 92.06%101.2%之间。LLOQ 和 QC 水平的日内和日间精密度和准确度均在可接受范围内。该方法成功地应用于犬口服粉后贝母辛和贝母辛宁的药代动力学研究。所得结果可能有助于指导 Maxim 和 Miq 的临床应用。