Somogyi A, Gugler R
Fortschr Med. 1980 Nov 20;98(43):1707-10.
The pharmacokinetics and bioavailability of theophylline have been investigated in eight healthy subjects following application of the drug in form of a tablet, a retard tablet (enteric-coated), and a suppository (Euphyllin) in comparison with an intravenous preparation. Peak plasma concentrations were measured 1.5 hours (tablet), 6 hours (retard tablet) and 4 hours (suppository) after drug administration, respectively. The absolute bioavailability was of th tablet 105 +/- 25%, of the retard table 81 +/- 23%, of the suppository 74 +/- 25%. The variations observed were primarily due to variations in the other pharmacokinetic parameters, only to a lesser extent to variable absorption of theophylline.
在八名健康受试者中,对茶碱以片剂、缓释片(肠溶包衣)和栓剂(优菲林)形式给药后的药代动力学和生物利用度进行了研究,并与静脉制剂进行了比较。给药后分别在1.5小时(片剂)、6小时(缓释片)和4小时(栓剂)测量血浆峰浓度。片剂的绝对生物利用度为105±25%,缓释片为81±23%,栓剂为74±25%。观察到的差异主要是由于其他药代动力学参数的变化,仅在较小程度上是由于茶碱吸收的变化。