Anttila M, Tikkanen R, Nieminen L
Arzneimittelforschung. 1978;28(3):397-9.
A rapid, sensitive fluorometric method for the determination of ajmaline and N-propylajmaline (NPA) was used to follow serum concentrations after an i.v. administration of ajmaline, after an oral administration of ajmaline, and an oral dose of NPA bitartrate (NPAB) in beagle dogs. Ajmaline was eliminated from serum with an apparent half-life of approximately 1 h and NPA with one of approximately 4 h. 1 h after i.v. and oral administration of 50 mg of ajmaline the serum levels were of the same order of magnitude. The bioavailability of oral ajmaline, calculated from the area under the serum concentration/time curves, was about 90%. The peak serum concentrations of ajmaline and NPA after a single oral dose of 50 mg of ajmaline and NPAB were about 1.4 microgram/ml and 0.6 microgram/ml, respectively, the latter calculated as its bitartrate, with about the same peak time: 1 h.
采用一种快速、灵敏的荧光法测定阿马林和N-丙基阿马林(NPA),以跟踪比格犬静脉注射阿马林、口服阿马林及口服酒石酸N-丙基阿马林(NPAB)后的血清浓度。阿马林从血清中消除的表观半衰期约为1小时,NPA的约为4小时。静脉注射和口服50毫克阿马林1小时后,血清水平处于同一数量级。根据血清浓度/时间曲线下面积计算,口服阿马林的生物利用度约为90%。单次口服50毫克阿马林和NPAB后,阿马林和NPA的血清峰值浓度分别约为1.4微克/毫升和0.6微克/毫升(后者以其酒石酸盐计算),峰值时间大致相同:1小时。