PHARMACOKINETICS OF DIGOXIN - RELATIONSHIP BETWEEN RESPONSE INTENSITY AND PREDICTED COMPARTMENTAL DRUG LEVELS IN MAN

被引:65
作者
KRAMER, WG
KOLIBASH, AJ
LEWIS, RP
BATHALA, MS
VISCONTI, JA
REUNING, RH
机构
[1] OHIO STATE UNIV,COLL PHARM,DIV PHARMACEUT & PHARMACEUT CHEM,COLUMBUS,OH 43210
[2] OHIO STATE UNIV,SCH MED,DIV CARDIOL,COLUMBUS,OH 43210
[3] OHIO STATE UNIV HOSP,CTR DRUG INFORMAT,COLUMBUS,OH 43210
来源
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS | 1979年 / 7卷 / 01期
关键词
digoxin; pharmacokinetics; radioimmunoassay; response kinetics; serum digoxin kinetics; systolic time intervals; three-compartment model;
D O I
10.1007/BF01059440
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A study designed to investigate the relationship between the pharmacokinetics of digoxin and a measure of its pharmacological effect has been conducted. Serum digoxin concentrations and systolic time intervals were measured concurrently in 12 normal male volunteers following a 1.0 mg i.v. bolus injection. The averaged serum digoxin concentration- time and response-time data were analyzed pharmacokinetically using a three-compartment open model and nonlinear least- squares fitting. When only the serum level-time data were analyzed, a close relationship was found between calculated digoxin levels in the slowly distributing (deep) peripheral compartment and response of the heart to digoxin, as measured by changes in the QS2 index δQS2I. Although it was not possible to distinguish clearly a linear from a nonlinear relationship between digoxin levels in the deep compartment and δQS2I, the nonlinear relationship gave the best overall fit when both serum digoxin and δQS2I data were fitted simultaneously. The simultaneous fityielded a total body clearance of digoxin of 3.6 ml/min/kg and a terminal t1/2 of 42 hr. © 1979 Plenum Publishing Corporation.
引用
收藏
页码:47 / 61
页数:15
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