Gyllenhaal O, Vessman J
J Chromatogr. 1983 Mar 11;273(1):129-39. doi: 10.1016/s0378-4347(00)80929-9.
A method for the determination of therapeutic levels of metoprolol in human plasma is presented. Metoprolol and the internal standard are extracted from the buffered plasma sample to an organic phase containing 4 X 10(-3) M phosgene. After 10 min the organic phase is taken to dryness. The residue is dissolved in ethyl acetate and the formed oxazolidine derivatives are analyzed by gas chromatography with nitrogen-selective detection. With packed columns, rectilinear standard curves through the origin were obtained down to 80 nmoles/l of plasma. The precision of the method at 200 nmoles/l was 1.5% (n = 8). The sensitivity of the method was improved by using capillary column gas chromatography. Linear standard curves were obtained down to 10 nmoles/l of metoprolol in plasma. The precision of the method at the 50 nmoles/l level was 2.2% (n = 7). With this simple and straightforward method using extractive derivatization 30 samples can be handled in a day.
本文介绍了一种测定人血浆中美托洛尔治疗浓度的方法。美托洛尔和内标从缓冲血浆样品中萃取至含有4×10⁻³M光气的有机相中。10分钟后,将有机相蒸干。残渣溶于乙酸乙酯,生成的恶唑烷衍生物用带氮选择性检测的气相色谱法分析。使用填充柱时,得到通过原点的直线标准曲线,血浆浓度低至80纳摩尔/升。该方法在200纳摩尔/升时的精密度为1.5%(n = 8)。使用毛细管柱气相色谱法提高了该方法的灵敏度。血浆中美托洛尔浓度低至10纳摩尔/升时得到直线标准曲线。该方法在50纳摩尔/升水平时的精密度为2.2%(n = 7)。采用这种简单直接的萃取衍生化方法,一天可处理30个样品。