Spahn H, Mutschler E
Arzneimittelforschung. 1985;35(1):167-9.
The influence of aluminium hydroxide (given as a suspension, Aludrox) on the oral bioavailability of feprazone was tested. The degree and speed of absorption of feprazone from capsules (400 mg feprazone as a single dose; 8 volunteers) was investigated by determining plasma levels of feprazone and one of its metabolites using an HPLC method. No statistically significant change in feprazone kinetics caused by the antacid was evident. Cmax (means +/- SEM) decreased from 40.6 +/- 2.9 to 36.25 +/- 1.4 micrograms/ml; the mean area under the plasma level time curve was somewhat higher after additional administration of aluminium hydroxide (n. s.).
测试了氢氧化铝(以混悬液Aludrox形式给药)对非普拉宗口服生物利用度的影响。通过使用高效液相色谱法测定非普拉宗及其一种代谢物的血浆水平,研究了非普拉宗从胶囊(400mg非普拉宗单剂量;8名志愿者)中的吸收程度和速度。抗酸剂引起的非普拉宗动力学无统计学显著变化。Cmax(平均值±标准误)从40.6±2.9降至36.25±1.4μg/ml;额外给予氢氧化铝后血浆水平-时间曲线下的平均面积略高(无统计学意义)。