Gural R P, Chungi V S, Shrewsbury R P, Dittert L W
J Pharm Pharmacol. 1985 Jun;37(6):443-5. doi: 10.1111/j.2042-7158.1985.tb03035.x.
The gastrointestinal absorption of disodium etidronate (as [14C]disodium etidronate) was investigated in the rat proximal jejunum in-situ. Studies using various initial concentrations of the drug suggested that etidronate absorption occurred by passive diffusion at initial concentrations below 0.08 M. At initial concentrations above 0.08 M, the rate of absorption was significantly greater than would be expected if passive diffusion was the only mechanism responsible for absorption. Etidronate absorption is not mediated by the carrier mechanism responsible for phosphate ion absorption.
在大鼠近端空肠原位研究了依替膦酸二钠(以[14C]依替膦酸二钠形式)的胃肠道吸收。使用该药物的各种初始浓度进行的研究表明,在初始浓度低于0.08 M时,依替膦酸通过被动扩散吸收。在初始浓度高于0.08 M时,吸收速率明显高于如果被动扩散是唯一负责吸收的机制所预期的速率。依替膦酸的吸收不是由负责磷酸根离子吸收的载体机制介导的。