Multiple-dose evaluation of intravenous hydromorphone pharmacokinetics in normal human subjects.

Abstract:

:We measured the pharmacokinetics of hydromorphone in normal volunteers given three doses of the drug (10, 20, and 40 micrograms/kg) as intravenous 45-s injections on different days. Concentrations of hydromorphone in plasma from serial blood samples were measured by a high-performance liquid chromatography method specific for hydromorphone with a detection limit of 0.1 ng/mL. In all cases, plasma hydromorphone concentration versus time data for individual subjects were best described by a triexponential (instead of mono- or biexponential) function. Furthermore, we found that the pharmacokinetics of hydromorphone was independent of dose across the range studied. Averaged across doses, the distribution and terminal elimination half-lives were 1.27 min (t1/2 pi), 14.7 min (t1/2 alpha), and 184 min (t1/2 beta), respectively. Average values for systemic clearance, initial dilution volume, and steady-state volume of distribution were 1.66 L/min (Cl), 24.4 L (Vc), and 295 L (Vdss). Our results indicate that hydromorphone pharmacokinetic parameters are linear across a fourfold range of doses that are usually employed clinically and that previously reported pharmacokinetic values for hydromorphone (based on radioimmunoassay measurements) deserve reconsideration.

journal_name

Anesth Analg

journal_title

Anesthesia and analgesia

authors

Hill HF,Coda BA,Tanaka A,Schaffer R

doi

10.1213/00000539-199103000-00009

subject

Has Abstract

pub_date

1991-03-01 00:00:00

pages

330-6

issue

3

eissn

0003-2999

issn

1526-7598

journal_volume

72

pub_type

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