Leahey W J, Neill J D, Varma M P, Shanks R G
Eur J Clin Pharmacol. 1980 Jun;17(6):419-24. doi: 10.1007/BF00570158.
Observations were made in 5 healthy subjects who exercised before and 1, 3, 6, 8 and 24 h after the oral administration on separate occasions of 160 mg oxprenolol, 160 mg slow release oxprenolol, 160 mg long acting propranolol and 400 mg sotalol. Blood samples were obtained before and at 1, 2, 3, 6, 8, 10 and 24 h after drug administration and assayed for drug concentration. Although the plasma concentration of oxprenolol after S.R. oxprenolol was significantly less at 1 and 2 h and significantly greater at 24 h than after conventional oxprenolol, there was little difference between the effects of the two drugs on an exercise tachycardia. The plasma level of propranolol and the reduction in an exercise tachycardia after L.A. propranolol increased slowly to reach a peak at 6 h and then declined gradually to 24 h. The maximum plasma concentration and effect after sotalol occurred at 3 h and then declined with an elimination half-life of 12.1 h. At 24 h the percentage reduction in an exercise tachycardia was 8.3 +/- 2.5 after oxprenolol, 10.0 +/- 2.3 after S.R. oxprenolol, 18.0 +/- 3.2 after L.A. propranolol and 14.7 +/- 3.4% after sotalol.
对5名健康受试者进行了观察,他们在不同时间分别口服160毫克氧烯洛尔、160毫克缓释氧烯洛尔、160毫克长效普萘洛尔和400毫克索他洛尔之前以及服药后1、3、6、8和24小时进行运动。在给药前以及给药后1、2、3、6、8、10和24小时采集血样,并测定药物浓度。尽管缓释氧烯洛尔给药后1小时和2小时的氧烯洛尔血浆浓度显著低于普通氧烯洛尔,24小时时显著高于普通氧烯洛尔,但两种药物对运动性心动过速的影响几乎没有差异。长效普萘洛尔给药后普萘洛尔的血浆水平和运动性心动过速的降低幅度在6小时时缓慢上升至峰值,然后在24小时时逐渐下降。索他洛尔给药后的最大血浆浓度和效应出现在3小时,然后下降,消除半衰期为12.1小时。在24小时时,氧烯洛尔给药后运动性心动过速的降低百分比为8.3±2.5,缓释氧烯洛尔给药后为10.0±2.3,长效普萘洛尔给药后为18.0±3.2,索他洛尔给药后为14.7±3.4%。