Population pharmacokinetic modeling of cefadroxil renal transport in wild-type andPept2knockout mice
Author:
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00498254.2015.1080881
Reference44 articles.
1. A PHARMACOKINETIC COMPARISON OF CEFADROXIL AND CEPHALEXIN AFTER ADMINISTRATION OF 250, 500 AND 1000 MG SOLUTION DOSES
2. Prediction-Corrected Visual Predictive Checks for Diagnosing Nonlinear Mixed-Effects Models
3. Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter.
4. Cefadroxil, a New Broad-Spectrum Cephalosporin
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2. Physiologically Based Pharmacokinetic Modeling of Cefadroxil in Mouse, Rat, and Human to Predict Concentration–Time Profile at Infected Tissue;Frontiers in Pharmacology;2021-12-23
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4. Semi-Mechanistic Population Pharmacokinetic Modeling of L-Histidine Disposition and Brain Uptake in Wildtype and Pht1 Null Mice;Pharmaceutical Research;2018-01
5. Species Differences in Human and Rodent PEPT2-Mediated Transport of Glycylsarcosine and Cefadroxil in Pichia Pastoris Transformants;Drug Metabolism and Disposition;2016-11-11
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