Anadón A, Martínez-Larrañaga M R, Díaz M J, Vélez C, Bringas P
Department of Pharmacology, Faculty of Medicine, Complutense University, Madrid, Spain.
Am J Vet Res. 1990 Nov;51(11):1756-9.
The pharmacokinetics of pipemidic acid after 2 single doses were studied in broiler chickens. Chickens were given single IV and oral doses of 10 and 30 mg of pipemidic acid/kg of body weight. Blood samples were collected over 8 hours after each dose administration. High-pressure liquid chromatography with UV detection was used to determine concentrations in plasma of pipemidic acid. The plasma concentration-time curves after IV administration followed 2-compartment characteristics, rapid initial distribution phase, and a terminal elimination phase. The pharmacokinetic variables differed significantly between single doses of 10 and 30 mg of pipemidic acid/kg. Mean disposition variables were a half-life at alpha phase of 0.06 hours or 0.33 hours, a half-life at beta phase of 1.18 hours or 1.72 hours, a volume of distribution in the central compartment of 0.12 L/kg or 0.31 L/kg, a volume of distribution during the elimination beta phase of 1.64 L/kg or 1.05 L/kg, and a total plasma clearance of 0.97 L/h.kg or 0.41 L/h.kg, for the 10 or 30 mg/kg dose, respectively. After oral administration, the pipemidic acid plasma profile could be adequately described by a 1-compartment model. After the single oral doses of 10 and 30 mg of pipemidic acid/kg, pipemidic acid was absorbed rapidly (time to maximal concentration of 0.31 hours or 0.71 hours) and eliminated with a mean half-life of 0.86 hours or 0.61 hours, respectively. The bioavailability was 39% at 10 mg of pipemidic acid/kg and 61% at 30 mg of pipemidic acid/kg.
在肉鸡中研究了2次单剂量吡哌酸后的药代动力学。给鸡分别静脉注射和口服10mg/kg和30mg/kg体重的吡哌酸。每次给药后8小时内采集血样。采用带紫外检测的高压液相色谱法测定血浆中吡哌酸的浓度。静脉给药后的血浆浓度-时间曲线符合二室模型特征,有快速的初始分布相和终末消除相。10mg/kg和30mg/kg单剂量的吡哌酸药代动力学变量有显著差异。平均处置变量如下:α相半衰期分别为0.06小时或0.33小时,β相半衰期分别为1.18小时或1.72小时,中央室分布容积分别为0.12L/kg或0.31L/kg,消除β相分布容积分别为1.64L/kg或1.05L/kg,总血浆清除率分别为0.97L/h.kg或0.41L/h.kg,分别对应10mg/kg或30mg/kg剂量。口服给药后,吡哌酸的血浆曲线可用一室模型充分描述。口服10mg/kg和30mg/kg单剂量的吡哌酸后,吡哌酸吸收迅速(达峰时间分别为0.31小时或0.71小时),平均半衰期分别为0.86小时或0.61小时。吡哌酸在10mg/kg剂量时生物利用度为39%,在30mg/kg剂量时为61%。