Lin Li, Liu Jian-Xun, Zhang Ying, Lin Cheng-Ren, Duan Chang-Ling
Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
Yao Xue Xue Bao. 2008 Nov;43(11):1123-7.
A sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the quantification of tetrahydropalmatine (THP) and dehydrocorydaline (DHC) in rat plasma. The compounds were simply pretreated by protein precipitation using acetone. Chromatographic separation was achieved on a reversed-phase SB-C18 column with the mobile phase of acetonitrile-ammonium acetate (0. 1% acetic acid) and step gradient elution resulted at a flow rate of 0.80 mL x min(-1). A tandem mass spectrometer equipped with electrospray ionization source was used as detector and operated in the positive ion mode. Quantification was performed using multiple reaction monitoring (MRM) of the transitions m/z 356. 2 --> m/z 191.9 and m/z 366. 2 --> m/z 350.2 for THP and DHC respectively. The method showed excellent linearity over the concentration range 1-1 000 ng x mL(-1) of two components (r = 0.994 for THP and r = 0.992 for DHC). The low limits of quantification were both 1 ng x mL(-1). The extract recoveries of analytes were from 71.71% to 91.59% for THP and from 83.27% to 103.15% for DHC. The precisions, the accuracy and the stability of the analytes meet the requirements. The method was applied to a pharmacokinetic study of THP and DHC after oral administration of the total alkaloid extraction of Rhizoma Corydalis (Yanhusuo). The AUC were (1.90 +/- 0.04), (2.58 +/- 0.08) and (4.34 +/- 0.19) mg x L(-1) h for low, medium and high doses of THP, respectively. While the DHC concentrations in plasma of low dose and medium dose were too lower to be detected, the AUC of high dose was (0.0896 +/- 0.0002) mg x L(-1) h.
建立了一种灵敏的液相色谱 - 串联质谱(LC - MS/MS)法并进行了验证,用于定量大鼠血浆中的延胡索乙素(THP)和去氢紫堇碱(DHC)。化合物通过用丙酮进行蛋白沉淀进行简单预处理。在反相SB - C18柱上进行色谱分离,流动相为乙腈 - 醋酸铵(0.1%乙酸),采用梯度洗脱,流速为0.80 mL·min⁻¹。配备电喷雾电离源的串联质谱仪用作检测器,在正离子模式下运行。分别采用多反应监测(MRM)对m/z 356.2→m/z 191.9和m/z 366.2→m/z 350.2的跃迁进行THP和DHC的定量。该方法在两种成分1 - 1000 ng·mL⁻¹的浓度范围内显示出良好的线性(THP的r = 0.994,DHC的r = 0.992)。定量下限均为1 ng·mL⁻¹。THP的分析物提取回收率为71.71%至91.59%,DHC的提取回收率为83.27%至103.15%。分析物的精密度、准确度和稳定性均符合要求。该方法应用于延胡索(延胡索)总生物碱提取物口服给药后THP和DHC的药代动力学研究。低、中、高剂量THP的AUC分别为(1.90±0.04)、(2.58±0.08)和(4.34±0.19)mg·L⁻¹·h。低剂量和中剂量血浆中DHC浓度过低无法检测,高剂量的AUC为(0.0896±0.0002)mg·L⁻¹·h。