Lindberg C, Jönsson S, Paulson J, Tunek A
Bioanalytical Chemistry, AB Draco, Lund, Sweden.
Biomed Environ Mass Spectrom. 1990 Apr;19(4):218-24. doi: 10.1002/bms.1200190403.
(R,S)-Bambuterol was isolated from plasma and urine by solid-phase extraction and analysed as its trimethylsilyl derivative by gas chromatography/chemical ionization mass spectrometry with ammonia as the reagent gas. Deuterium-labelled bambuterol was used as internal standard. An esterase inhibitor was added to plasma to prevent hydrolysis of bambuterol in the plasma sample. Bambuterol could be measured in plasma down to 1 nmol l-1 with a within-day variation of less than 5% (coefficient of variation). The lower limit of measurement in urine was judged to be 8 nmol l-1, a concentration at which the within-day variation was 5.4% (coefficient of variation).
通过固相萃取从血浆和尿液中分离出(R,S)-班布特罗,并以氨作为反应气,通过气相色谱/化学电离质谱法将其作为三甲基硅烷基衍生物进行分析。氘标记的班布特罗用作内标。向血浆中添加酯酶抑制剂以防止血浆样品中班布特罗的水解。血浆中班布特罗的检测下限可达1 nmol/L,日内变异小于5%(变异系数)。尿液中的检测下限判定为8 nmol/L,该浓度下日内变异为5.4%(变异系数)。