Beveridge T, Nüesch E, Ohnhaus E E
Arzneimittelforschung. 1978;28(4):701-3.
Ten healthy male volunteers each received 0.5 mg digoxin orally and i.v. in a randomised, cross-over sequence with at least two weeks between doses. Plasma concentration and cumulative urinary excretion of digoxin were measured up to 6 and 144 h, respectively, after administration using a radioimmunoassay method. Absolute bioavailability (i.e. the percentage absorption from tablets compared to i.v. injection) was calculated by four methods: by comparing areas under plasma concentration/time curves (AUC) up to 6 h and to infinity, also by comparing cumulative urinary excretion up to 144 h (t max.) and to infinity. The mean of the two extrapolated values for the absolute bioavailability of digoxin (Sandoz) tablets is 78%.
十名健康男性志愿者每人以随机交叉顺序口服和静脉注射0.5毫克地高辛,两次给药之间至少间隔两周。给药后分别在6小时和144小时内,使用放射免疫分析法测量地高辛的血浆浓度和累积尿排泄量。通过四种方法计算绝对生物利用度(即片剂吸收百分比与静脉注射相比):比较6小时和无限时间的血浆浓度/时间曲线下面积(AUC),也比较144小时(t max.)和无限时间的累积尿排泄量。地高辛(山德士)片剂绝对生物利用度的两个外推值的平均值为78%。