Lucena M I, Moreno A, Fernandez M C, Garcia-Morillas M, Andrade R
Int J Clin Pharmacol Res. 1987;7(1):33-7.
The present study was carried out to evaluate the changes in digitoxin kinetics during ampicillin administration. Subjects were informed of the nature of the study and the treatment was applied to those who gave their written consent. Six healthy volunteers received a single oral dose of 1.0 mg of digitoxin. Three days later, they were given orally ampicillin trihydrate, 500 mg four times daily, for five consecutive days. Blood samples were taken at 24, 36, 48, 60, 72, 96, 120, 144, 168 and 192 hours after digitoxin. Compliance with ampicillin regimen was verified by fluorimetric measurement of serum ampicillin. Concentrations of serum digitoxin were determined by radioimmunoassay. The mean digitoxin elimination half-life changed from 162.8 +/- 12.9 h before to 181.3 +/- 10.1 h (mean +/- s.e. mean) after ampicillin. These differences were not significant. No consistent evidence of a kinetic interaction between digitoxin and the broad-spectrum antibiotic ampicillin was found.
本研究旨在评估氨苄西林给药期间洋地黄毒苷动力学的变化。向受试者告知了研究性质,并对给予书面同意的受试者进行治疗。六名健康志愿者口服单剂量1.0mg洋地黄毒苷。三天后,他们连续五天每天口服4次500mg三水合氨苄西林。在给予洋地黄毒苷后24、36、48、60、72、96、120、144、168和192小时采集血样。通过荧光法测定血清氨苄西林来验证对氨苄西林治疗方案的依从性。通过放射免疫测定法测定血清洋地黄毒苷浓度。洋地黄毒苷平均消除半衰期从氨苄西林给药前的162.8±12.9小时变为给药后的181.3±10.1小时(平均值±标准误平均值)。这些差异不显著。未发现洋地黄毒苷与广谱抗生素氨苄西林之间存在动力学相互作用的一致证据。