Yee Y G, Rubin P, Blaschke T F
J Chromatogr. 1979 Apr 1;171:357-62. doi: 10.1016/s0021-9673(01)95315-4.
A high-performance liquid chromatographic procedure using a fluorescence detector for the analysis of atenolol in plasma and whole blood is described. It employs a simple and rapid method of preparation. Atenolol and metoprolol as the internal standard are chromatographed as ion pairs with heptanesulfonic acid. The method is sensitive and reproducible with accurate detection at concentrations as low as 2 ng/ml in whole blood and plasma, and a coefficient of variation of 4.7% over the range 2 ng/ml to 1000 ng/ml.
描述了一种使用荧光检测器的高效液相色谱法,用于分析血浆和全血中的阿替洛尔。该方法采用简单快速的样品制备方法。阿替洛尔和作为内标的美托洛尔与庚烷磺酸形成离子对进行色谱分离。该方法灵敏且可重复,在全血和血浆中低至2 ng/ml的浓度下能准确检测,在2 ng/ml至1000 ng/ml范围内变异系数为4.7%。