Edholm L E, Kennedy B M, Bergquist S
Eur J Respir Dis Suppl. 1984;134:33-40.
Because of low drug concentrations and complex nature of the sample, analytical methods with sensitive and selective detection are necessary for pharmacokinetic studies of terbutaline. Up to now, for non-radiolabelled drugs, usually only methods based on gas chromatography plus mass spectrometry have met these requirements. As an alternative, we have developed an automated method based on liquid chromatography. The necessary sensitivity and selectivity were obtained by using electrochemical detection and a microprocessor-controlled column switching system. The accuracy of the method was compared with a method based on gas chromatography plus mass spectrometry. The overall precision expressed as per cent of the mean was +/- 3.5% and +/- 2.2% at 5 and 50 pmol/mL, respectively. The total absolute recovery for terbutaline and internal standard at these concentration levels were in the range 85-106%.
由于样本中药物浓度较低且性质复杂,对于特布他林的药代动力学研究,需要采用具有灵敏且选择性检测功能的分析方法。到目前为止,对于非放射性标记药物,通常只有基于气相色谱-质谱联用的方法能满足这些要求。作为一种替代方法,我们开发了一种基于液相色谱的自动化方法。通过使用电化学检测和微处理器控制的柱切换系统获得了所需的灵敏度和选择性。将该方法的准确度与基于气相色谱-质谱联用的方法进行了比较。以平均值的百分比表示的总体精密度在5 pmol/mL和50 pmol/mL时分别为±3.5%和±2.2%。在这些浓度水平下,特布他林和内标的总绝对回收率在85%-106%范围内。