药代动力学
丙谷胺
药理学
苯甲酰胺
半衰期
医学
化学
内科学
敌手
立体化学
受体
胆囊收缩素受体
作者
Angelo Bignamini,Paolo Casula,Andrea Rovati
出处
期刊:PubMed
日期:1979-01-01
卷期号:29 (4): 639-42
被引量:6
摘要
In order to explain the long-term therapeutic activity of (+/-)-4-benzamide-N,-di-n-propylglutaramic acid (proglumide, Milid) a pharmacokinetic study was carried out in rats by three administration routes. As a result, experimental data could have been fitted to a tri- or tetra-exponential equation, with terminal half-life of about 24 h. Since human pharmacokinetics was found to be rather similar to that in rats, it can be extrapolated that steady state plasma level of drug during therapeutic dosage regimen should range around 60% of peak level of single administration.
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