Literature DB >> 3251034

The sojourn time and its prospective use in pharmacology.

G Segre1.   

Abstract

Sojourn time in a given compartment i when the material has been injected in compartment i (Sji) corresponds to the average time spent by the particles of the material in i before their definitive exit from that compartment. Sojourn time is different from the mean residence time (tji), which is the average age of the particles leaving the system. If K denotes the transfer matrix of the compartmental system, then -K-1 provides the sojourn times in each compartment given initial arrival in each of the other compartments. It can be shown that Sji = xi(s)/xj. 0/s = 0, corresponds to the value of AUC in compartment i. Since AUCi/xj,0 = Fji.AUC/xi,0 (Fji = fraction of the dose in j reaching i), one has Sji = FjiSii.AUCi corresponds to a rectangle of height equal to xj,0 and base equal to Sii. Therefore in a compartment i a drug acts on the average for a time equal to Sii and the number of molecules in it depends on the dose and on Fji. In compartments which are not sampled the value of AUC can be calculated by a simulated curve or by -K-1. From the height of the rectangle whose area is equal to AUC one should subtract the threshold theta for a given effect; the resulting rectangle should indicate the intrinsic efficacy of the drug. These considerations could be applied in pharmacology, toxicology, and chemotherapy.

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Year:  1988        PMID: 3251034     DOI: 10.1007/bf01062016

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  10 in total

1.  Pharmacokinetic analysis of the effect of theophylline on pulmonary function in asthmatic children.

Authors:  G Levy; R Koysooko
Journal:  J Pediatr       Date:  1975-05       Impact factor: 4.406

2.  Kinetics of interaction between drugs and biological systems.

Authors:  G Segre
Journal:  Farmaco Sci       Date:  1968-10

3.  Kill kinetics and regrowth pattern of bacteria exposed to antibiotic concentrations simulating those observed in vivo.

Authors:  J P Guggenbichler; E Semenitz; P König
Journal:  J Antimicrob Chemother       Date:  1985-01       Impact factor: 5.790

4.  On pharmacokinetics in target tissues.

Authors:  M Weiss
Journal:  Biopharm Drug Dispos       Date:  1985 Jan-Mar       Impact factor: 1.627

5.  Mean hepatic transit time in the determination of mean absorption time.

Authors:  W L Chiou
Journal:  J Pharm Sci       Date:  1983-11       Impact factor: 3.534

6.  On some stochastic formulations and related statistical moments of pharmacokinetic models.

Authors:  J H Matis; T E Wehrly; C M Metzler
Journal:  J Pharmacokinet Biopharm       Date:  1983-02

7.  Statistical moments in pharmacokinetics.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharmacokinet Biopharm       Date:  1978-12

8.  The application of statistical moment theory to the evaluation of in vivo dissolution time and absorption time.

Authors:  S Riegelman; P Collier
Journal:  J Pharmacokinet Biopharm       Date:  1980-10

9.  Moment analysis for the separation of mean in vivo disintegration, dissolution, absorption, and disposition time of ampicillin products.

Authors:  Y Tanigawara; K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharm Sci       Date:  1982-10       Impact factor: 3.534

10.  Moment analysis for disposition kinetics of several cephalosporin antibiotics in rats.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharm Pharmacol       Date:  1983-01       Impact factor: 3.765

  10 in total
  1 in total

1.  Mean time parameters for generalized physiological flow models (semihomogeneous linear systems).

Authors:  D Verotta; L B Sheiner; S L Beal
Journal:  J Pharmacokinet Biopharm       Date:  1991-06
  1 in total

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