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the pharmacokinetics of the interstitial space in humans人类的药物动力学的间隙空间
BMC Clinical Pharmacology BioMed Central
Research article Open Access
The pharmacokinetics of the interstitial space in humans
David G Levitt*
Address: Department of Physiology University of Minnesota
Email: David G Levitt* - levit001@
* Corresponding author
Published: 30 July 2003 Received: 17 April 2003
Accepted: 30 July 2003
BMC Clinical Pharmacology 2003, 3:3
This article is available from: /1472-6904/3/3
© 2003 Levitt; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for
any purpose, provided this notice is preserved along with the articles original URL.
Abstract
Background: The pharmacokinetics of extracellular solutes is determined by the blood-tissue
exchange kinetics and the volume of distribution in the interstitial space in the different organs. This
information can be used to develop a general physiologically based pharmacokinetic (PBPK) model
applicable to most extracellular solutes.
Methods: The human pharmacokinetic literature was surveyed to tabulate the steady state and
equilibrium volume of distribution of the solutes mannitol, EDTA, morphine-6-glucuronide,
morphine-3-glucuronide, inulin and β-lactam antibiotics with a range of protein binding (amoxicillin,
piperacillin, cefatrizine, ceforanide, flucloxacillin, dicloxacillin). A PBPK data set was developed for
extracellular solutes based on the liter
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