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Pharmacokinetics of a sustained-release theophylline formulation.

机译:缓释茶碱制剂的药代动力学。

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摘要

1 Plasma theophylline concentrations following administration of sustained-release (SR) theophylline tablets were determined in ten healthy volunteers using a dose of 190 mg or 380 mg 12 hourly. 2 The plasma theophylline levels during the first 12 h period confirmed the sustained-release formulation characteristics, with the plasma drug concentrations reaching a plateau for the last 6 hours. 3 During the fifth 12 h dosing period the mean maximum and minimum plasma theophylline concentrations were 7.25 and 4.30 microgram/ml after 190 mg SR theophylline 12 hourly (n = 6) and 12.96 and 7.36 microgram/ml after 380 mg 12 hourly (n = 5), although there was marked between-subject variation in plasma theophylline concentrations. 4 One subject withdrew from the study due to side effects, which were more common when the higher dose of SR theophylline was given.
机译:1在十名健康志愿者中,每12小时测定190 mg或380 mg的剂量,确定服用缓释(SR)茶碱片后的血浆茶碱浓度。 2在最初的12小时内血浆茶碱水平证实了缓释制剂的特征,在最后6小时内血浆药物浓度达到平稳。 3在第五个12小时的服药期间,平均190 mg SR茶碱12小时(n = 6)后平均最大和最小血浆茶碱浓度为7.25和4.30微克/ ml,而380 mg 12小时后12.96和7.36微克/ ml(n = 5),尽管血浆茶碱浓度存在明显的受试者间差异。 4一名受试者由于副作用而退出研究,当给予更高剂量的SR茶碱时,这种情况更为常见。

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