Josefsson K, Magni L, Nord C E
Scand J Infect Dis. 1982;14(2):131-3. doi: 10.3109/inf.1982.14.issue-2.11.
Single oral doses of phenoxymethylpenicillin were administered to 12 healthy volunteers, and their serum, saliva, and urine phenoxymethylpenicillin concentrations were determined. At all dose levels (0.4, 1, 2 and 3 g) phenoxymethylpenicillin was rapidly absorbed usually giving peak serum concentrations after 0.75 h. The relationship between mean peak serum concentration and dose was nonlinear (p less than 0.001); between area under serum concentration vs. time curve (AUC) and dose, it did not deviate from linearity (NS). Very low penicillin concentrations were obtained in saliva and the changes in the normal microflora were minor. The urinary excretion during the 10 h period after drug administration was 37-43 % of the given doses. After the 3 g doses, 3 volunteers had loose stools.
对12名健康志愿者单次口服苯氧甲基青霉素,并测定他们血清、唾液和尿液中的苯氧甲基青霉素浓度。在所有剂量水平(0.4、1、2和3克)下,苯氧甲基青霉素均迅速吸收,通常在0.75小时后达到血清峰值浓度。平均血清峰值浓度与剂量之间的关系呈非线性(p小于0.001);血清浓度-时间曲线下面积(AUC)与剂量之间未偏离线性关系(无显著性差异)。唾液中青霉素浓度非常低,正常微生物群的变化很小。给药后10小时内的尿排泄量为给药剂量的37%-43%。服用3克剂量后,3名志愿者出现腹泻。