de Leede L G, de Boer A G, van Velzen S L, Breimer D D
J Pharmacokinet Biopharm. 1982 Oct;10(5):525-37. doi: 10.1007/BF01059035.
In vivo and in vitro performances of a rectally applied osmotic delivery system containing a water-soluble derivative of theophylline were compared. The system was applied in six healthy volunteers during 72 h, and a comparison was made with two conventional dosage forms, a suppository and a solution administered orally, given once. In vitro, a perfect zero-order release rate with the osmotic system was obtained. In all subjects, application of the osmotic system resulted in a constant steady-state theophylline level just as in a long time zero-order i.v. infusion, which strongly suggests that the release rate in vivo is zero-order too. The release rate was not influenced by renewing the dosage form after 36 hr or by defecation. The in vivo and in vitro release rates were almost identical and subject-independent.
比较了含茶碱水溶性衍生物的直肠给药渗透给药系统的体内和体外性能。该系统在6名健康志愿者身上应用了72小时,并与两种传统剂型(一种栓剂和一种口服溶液,均单次给药)进行了比较。在体外,渗透系统获得了完美的零级释放速率。在所有受试者中,渗透系统的应用导致茶碱水平达到恒定的稳态,就如同长时间的零级静脉输注一样,这强烈表明体内释放速率也是零级。36小时后更换剂型或排便对释放速率没有影响。体内和体外释放速率几乎相同且与受试者无关。