Steinijans V W, Schulz H U, Böhm A, Beier W
Byk Gulden Research Centre, Konstanz, Federal Republic of Germany.
Eur J Clin Pharmacol. 1987;33(5):523-6. doi: 10.1007/BF00544248.
The effect of different intravenous infusions on the absolute bioavailability of theophylline from a sustained-release formulation has been investigated. Oral administration of 750 mg theophylline (2 capsules Euphylong 375) was referenced to intravenous aminophylline infusions corresponding to 506 mg theophylline over 8 h (63 mg.h-1) in Study 1, and to 749 mg theophylline over 14 h in Study 2. A reduction in the infusion rate from 69 to 33 mg.h-1 was made in Study 2 after 8 h in order to mimic the concentration/time profile of the oral formulation as closely as possible. The absolute bioavailability was 100 (89, 115)% in Study 1 and 88 (73, 105)% in Study 2. The lower clearance values and, as a consequence, the lower bioavailability ratios observed with the higher intravenous dose, although not significant, indicate that the absolute bioavailability of theophylline might appear to depend on the choice of the intravenous reference standard.
已研究了不同静脉输注方式对茶碱缓释制剂绝对生物利用度的影响。在研究1中,口服750 mg茶碱(2粒优菲龙375胶囊),与8小时内静脉输注相当于506 mg茶碱(63 mg·h⁻¹)的氨茶碱进行对照;在研究2中,与14小时内静脉输注749 mg茶碱进行对照。在研究2中,8小时后将输注速率从69 mg·h⁻¹降至33 mg·h⁻¹,以便尽可能模拟口服制剂的浓度/时间曲线。研究1中的绝对生物利用度为100(89,115)%,研究2中的绝对生物利用度为88(73,105)%。尽管差异不显著,但较高静脉剂量下观察到的清除率值较低,因此生物利用度比值也较低,这表明茶碱的绝对生物利用度可能似乎取决于静脉参考标准的选择。