Guo P, Li Z, Li T, Wang X, Li F
Faculty of Pharmacy, West China University of Medical Sciences, People's Republic of China.
Biomed Chromatogr. 1999 Feb;13(1):61-4. doi: 10.1002/(SICI)1099-0801(199902)13:1<61::AID-BMC819>3.0.CO;2-D.
An HPLC method has been developed for the determination of pseudoephedrine in plasma using column switching. Preparation of the sample was simple in that only 1000 microL of water was added to 200 microL of plasma before injection. A 900 microL aliquot was injected onto the precolumn. Double distilled water was used to elute and remove proteins and polar components in the sample. The components retained on the precolumn were flushed forward onto the analytical column by the mobile phase (acetonitrile-0.2 mol/L ammonium sulphate, 10:90 v/v) with automated column switching. The limit of determination of pseudoephedrine in plasma was 12 ng/mL. The relative standard deviations of intra- and inter-assay for the determination of pseudoephedrine in plasma were 1.2-9.8% over the concentration range 1020-21.8 ng/mL. The mean recovery by on-line solid phase extraction was 94.76% (RSD = 1.1%).
已开发出一种采用柱切换技术测定血浆中伪麻黄碱的高效液相色谱法。样品制备简单,只需在进样前向200微升血浆中加入1000微升水。取900微升等分试样注入预柱。用双蒸水洗脱并去除样品中的蛋白质和极性成分。通过自动柱切换,流动相(乙腈-0.2摩尔/升硫酸铵,10:90 v/v)将保留在预柱上的成分冲洗至分析柱上。血浆中伪麻黄碱的测定限为12纳克/毫升。在1020-21.8纳克/毫升的浓度范围内,血浆中伪麻黄碱测定的批内和批间相对标准偏差为1.2-9.8%。在线固相萃取的平均回收率为94.76%(相对标准偏差=1.1%)。