Dose-dependent pharmacokinetics

Identifieur interne : 003637 ( Main/Exploration ); précédent : 003636; suivant : 003638

---

Dose-dependent pharmacokinetics

Auteurs : J. M. Van Rossum [Pays-Bas] ; G. Van Lingen [Pays-Bas] ; J. P. T. Burgers [Pays-Bas]

Source :

• Pharmacology and Therapeutics [ 0163-7258 ] ; 1983.

RBID : ISTEX:FB764D797E9FC1A353D5F76E5DA1EC671177FF53

English descriptors

• Teeft :
  • Acetylsalicylic acid, Aucv dose, Average number, Average plateau concentration, Bimolecular reaction, Binding protein, Bioavailability, Biopharm, Blood cells, Blood flow, Blood plasma, Blood volume, Body residence time, Burger, Cardiac output, Chlorthalidone, Clearance, Clearance decreases, Clin, Clinical pharmacokinetics, Compartmental analysis, Concentration range, Constant clearance, Contact time, Different doses, Distribution coefficient, Dos, Dose, Dose dependency, Drug concentration, Drug design, Drug disposition, Drug effects, Drug metab, Drug molecule, Drug molecules, Dynamic systems analysis, Entire system, Equilibrium conditions, Erythrocyte, Excretion, Excretion deficit, Experimental pharmacology, Extraction ratio, Fedn proc, Final value theorems, Free plasma concentration, Galactose, Galactose galactose, Gastrointestinal tract, Hepatic, Hepatic clearance, High affinity, High concentration, High dose, High doses, Higher doses, Injection site, Input function, Intestinal wall, Intravenous injection, Intravenous input function, Kinetic parameters, Kinetics, Laplace domain, Linear conditions, Linear kinetics, Linear systems, Lingen, Liver blood flow, Liver sinusoids, Maximum binding capacity, Mbrt, Metabolic enzymes, Nonlinear, Nonlinear fraction, Nonlinear kinetics, Nonlinear pharmacokinetics, Nonlinear processes, Nonlinearity, Oral administration, Oral dose, Overall bioavailability, Overall system equation, Partition coefficient, Pharmac, Pharmacokin, Pharmacokinetics, Plasma, Plasma concentration, Plasma concentrations, Plasma curve, Plasma curves, Plasma drug concentration, Plasma proteins, Plateau, Plateau concentration, Positive feedback system, Protein binding, Receptor, Receptor occupation, Recirculation, Recirculation model, Renal clearance, Renal excretion curves, Residence time, Residence times, Rossum, Rowland, Salicylic, Salicylic acid, Salicyluric acid, Sampling site, Saturable pathway, Springer verlag, Steady state, Steady state concentration, Strong binding, Such drugs, Theoretical plasma curves, Tissue binding, Total clearance, Total conc, Total drug concentration, Total plasma concentration, Total plasma drug concentration, Transfer functions, Transit time, Transit times, Transport function, Transport functions, Transport proteins, Unbound, Unbound drug, Urinary excretion, Various organs, Various processes, Venous, Venous blood pool, Venous pool, Venous return, Volterra operators.

Url:

• https://api.istex.fr/ark:/67375/6H6-Q39L0CKK-T/fulltext.pdf

DOI: 10.1016/0163-7258(83)90068-2

Affiliations:

• Pays-Bas

---

Links toward previous steps (curation, corpus...)

• to stream Istex, to step Corpus: 002336
• to stream Istex, to step Curation: 002336
• to stream Istex, to step Checkpoint: 002397
• to stream Main, to step Merge: 003714
• to stream Main, to step Curation: 003637

---

Le document en format XML

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003637 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003637 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:FB764D797E9FC1A353D5F76E5DA1EC671177FF53
   |texte=   Dose-dependent pharmacokinetics
}}

---

This area was generated with Dilib version V0.6.33. Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021