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多次口服和静脉给药后β-甲基地高辛的生物利用度和药代动力学

Bioavailability and pharmacokinetics of beta-methyldigoxin after multiple oral and intravenous doses.

作者信息

Rietbrock N, Guggenmos J, Kuhlmann J, Hess U

出版信息

Eur J Clin Pharmacol. 1976 Mar 22;09(5-6):373-9. doi: 10.1007/BF00606551.

Abstract

To obtain true half lives, glycoside elimination from six healthy subjects was studied for 14 days after multiple intravenous doses or oral administration of a daily maintenance dose of beta-methyldigoxin 0.3 mg. After oral or intravenous administration of beta-methyldigoxin ceased, the plasma concentrations declined from the 14th to the 16th days with a half life of 1.7 days. From the 16th to the 20th day a change from a shorter to a longer half life of 2.8 and 2.9 days was observed. Similar half lives were found in urine: after the last dose the initial slope from the 14th to the 16th day had a half life of 1.8 days, and the terminal slope had one of 3.2 days. The results indicate release of the glycoside from slowly equilibrating tissues.

摘要

为获得真正的半衰期,在6名健康受试者多次静脉注射或口服每日维持剂量0.3毫克β-甲基地高辛14天后,研究了糖苷的消除情况。停止口服或静脉注射β-甲基地高辛后,血浆浓度在第14天至第16天下降,半衰期为1.7天。在第16天至第20天,观察到半衰期从较短的1.7天变为较长的2.8天和2.9天。尿液中也发现了类似的半衰期:最后一剂后,第14天至第16天的初始斜率半衰期为1.8天,终末斜率半衰期为3.2天。结果表明糖苷从缓慢平衡的组织中释放出来。

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