pkquest capillary permeability limitation and plasma protein binding – application to human inulin, dicloxacillin and ceftriaxone pharmacokineticspkquest局限性毛细血管通透性和血浆蛋白结合,应用人类菊粉,双氯青霉素和头孢曲松钠药物动力学.pdfVIP
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pkquest capillary permeability limitation and plasma protein binding – application to human inulin, dicloxacillin and ceftriaxone pharmacokineticspkquest局限性毛细血管通透性和血浆蛋白结合,应用人类菊粉,双氯青霉素和头孢曲松钠药物动力学
BMC Clinical Pharmacology BioMed Central
BMC Clinical Pharmacology x
2002, Open Access
2
Research article
PKQuest: capillary permeability limitation and plasma protein
binding – application to human inulin, dicloxacillin and ceftriaxone
pharmacokinetics
David G Levitt
Address: Department of Physiology, University of Minnesota, 6-125 Jackson Hall, 321 Church St. S. E., Minneapolis, MN 55455, USA
E-mail: levitt@
Published: 26 September 2002 Received: 4 April 2002
Accepted: 26 September 2002
BMC Clinical Pharmacology 2002, 2:7
This article is available from: /1472-6904/2/7
© 2002 Levitt; licensee BioMed Central Ltd. This article is published in Open Access: 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: It is generally assumed that the tissue exchange of antibiotics is flow limited
(complete equilibration between the capillary and the tissue water). This assumption may not be
valid if there is a large amount of plasma protein binding because the effective capillary permeability
depends on the product of the intrinsic capillary permeability (PS) and the fraction of solute that is
free in the blood (fwB). PKQuest, a new generic physiologically based pharmacokinetic software
routine (PBPK), provides a novel approach to modeling capillary permeability in which the only
adj
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