Literature DB >> 7096575

The physiological significance of total body clearance in pharmacokinetic studies.

W L Chiou.   

Abstract

The significance of the total body clearance (CL) is studied based on a physiological pharmacokinetic model. In the absence of evidence to the contrary, and for the sake of uniformity, it is proposed that the elimination rate of a drug at any time after various routes of dosing be assumed to be proportional to its systemic arterial plasma (blood) concentration with a proportionality constant equal to CL. The CL, calculated by the intravenous dose divided by the AUC, is defined as the hypothetical volume of the systemic arterial plasma (blood) completely cleared of drug per unit time even though the drug is eliminated by the lungs and venous plasma is assayed. A marked difference in the calculated elimination rate of lidocaine in patients based on arterial or venous plasma data is demonstrated. The calculated CLs which are sometimes greater than the cardiac output can be rationalized. The limitation of conventional multicompartmental mammillary modelling theory in the defining of CL is discussed.

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Year:  1982        PMID: 7096575     DOI: 10.1111/j.1365-2710.1982.tb00904.x

Source DB:  PubMed          Journal:  J Clin Hosp Pharm        ISSN: 0143-3180


  7 in total

1.  Relationship of apparent systemic clearance to individual organ clearances: effect of pulmonary clearance and site of drug administration and measurement.

Authors:  R Mehvar
Journal:  Pharm Res       Date:  1991-03       Impact factor: 4.200

Review 2.  The phenomenon and rationale of marked dependence of drug concentration on blood sampling site. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics (Part II).

Authors:  W L Chiou
Journal:  Clin Pharmacokinet       Date:  1989-10       Impact factor: 6.447

3.  Effect of a change in the luminal perfusion rate on intestinal drug absorption studied by a simple unified organ clearance approach.

Authors:  W L Chiou
Journal:  Pharm Res       Date:  1989-12       Impact factor: 4.200

4.  Effects of withdrawal of co-danthramer on use of laxatives in a district general hospital.

Authors:  D R Upton; J K Taylor; G K Holmes; J W Poston
Journal:  BMJ       Date:  1988-12-03

5.  Development of different analysis platforms with LC-MS for pharmacokinetic studies of protein drugs.

Authors:  Qiaozhen Lu; Xiaoyang Zheng; Thomas McIntosh; Hugh Davis; Jennifer F Nemeth; Chuck Pendley; Shiaw-Lin Wu; William S Hancock
Journal:  Anal Chem       Date:  2009-11-01       Impact factor: 6.986

6.  Correlation of unbound plasma clearances of fifteen extensively metabolized drugs between humans and rats.

Authors:  W L Chiou; F H Hsu
Journal:  Pharm Res       Date:  1988-10       Impact factor: 4.200

7.  Analysis of pethidine disposition in the pregnant rat by means of a physiological flow model.

Authors:  J L Gabrielsson; P Johansson; U Bondesson; M Karlsson; L K Paalzow
Journal:  J Pharmacokinet Biopharm       Date:  1986-08
  7 in total

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