Hendeles L, Weinberger M, Bighley L
Am J Hosp Pharm. 1977 May;34(5):525-7.
The absolute bioavailability of theophylline was investigated by comparing the areas under concentration-time curves for intravenous theophylline with a plain uncoated anhydrous theophylline tablet and a theophylline solution. Twenty asthmatic adults received approximately 7.5 mg/kg theophylline intravenously over 30 minutes; either seven days before or after the i.v. dose, 10 of these patients received tablets and the remainder solution in a similar dose. Blood samples were obtained at 0, 10, 20, 30, 45, 60, 90, 120, 180 and 240 minutes and then every two hours for at least 12 hours. Theophylline concentration was measured in serum by high-pressure cation exchange chromatography. The fraction of the dose absorbed averaged 0.96 +/- 0.03 for the tablet while the value for the solution was 0.99 +/- 0.02. The time of peak absorption averaged 2 +/- 0.3 hours for the tablets and 1.4 +/- 0.3 hours for the solution. The maximum serum concentration attained was 15.3 +/- 0.7 microng/ml after a dose of 7.6 +/- 0.4 mg/kg of the tablet, and 14.6 +/- 0.6 microng/ml after a dose of 7.3 +/- 0.2 mg/kg of the solution. Absorption of the tested theophylline tablets and solution approached 100% of the available drug.
通过比较静脉注射氨茶碱、普通无包衣无水氨茶碱片和氨茶碱溶液的浓度-时间曲线下面积,研究了氨茶碱的绝对生物利用度。20名成年哮喘患者在30分钟内静脉注射约7.5mg/kg氨茶碱;在静脉注射剂量前或后的七天,其中10名患者服用片剂,其余患者服用相同剂量的溶液。在0、10、20、30、45、60、90、120、180和240分钟采集血样,然后每两小时采集一次,至少采集12小时。通过高压阳离子交换色谱法测定血清中的氨茶碱浓度。片剂吸收的剂量分数平均为0.96±0.03,而溶液的该值为0.99±0.02。片剂的平均达峰吸收时间为2±0.3小时,溶液为1.4±0.3小时。服用7.6±0.4mg/kg片剂后达到的最大血清浓度为15.3±0.7μg/ml,服用7.3±0.2mg/kg溶液后为14.6±0.6μg/ml。受试氨茶碱片和溶液的吸收接近可用药物的100%。