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Human physiologically based pharmacokinetic model for propofol
David G. Levitt, Thomas W. Schnider
Physiology
Research output
:
Contribution to journal
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Article
›
peer-review
66
Scopus citations
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Keyphrases
Propofol
100%
Physiologically-based Pharmacokinetic Model
100%
Pharmacokinetics
50%
Constant Rate Infusion
50%
Tissue Binding
33%
Bolus Dose
33%
Residual Error
33%
Weighted Residual Method
33%
Lung
16%
Obese Subjects
16%
Morbid Obesity
16%
Anesthesia
16%
NONMEM
16%
Bolus
16%
Model Fitting
16%
Pharmacokinetic Parameters
16%
Bolus Injection
16%
Adjustable Parameters
16%
High Lipid
16%
Multi-compartment Model
16%
Physiological Parameters
16%
Lipid Solubility
16%
Tissue Lipids
16%
Human Pharmacokinetics
16%
Lipid Fractions
16%
Long-term Sedation
16%
Anesthesiology
16%
Fat Fraction
16%
Compartmental Model
16%
Liver Clearance
16%
Oil-water Partition Coefficient
16%
Distributed Software
16%
Model Simulation
16%
Human Parameters
16%
Biochemistry, Genetics and Molecular Biology
Propofol
100%
Pharmacokinetics
100%
Lipid
20%
Pharmacokinetic Modeling Software
10%
Lipid Solubility
10%
Partition Coefficient
10%
Hepatic Clearance
10%