Effects of prototypical microsomal enzyme inducers on cytochrome P450 expression in cultured human hepatocytes.
- A. Madan, R. Graham, A. Parkinson
- Biology, MedicineDrug Metabolism And Disposition
- 1 April 2003
It is generalized that beta-naphthoflavone induces CYP1A2 and isoniazid induces CyP2E1, whereas rifampin and, to a lesser extent phenobarbital, tend to significantly and consistently induce enzymes of the CYP2A, CYB2B, CYP 2C, CYp2E, and CYP3A subfamilies but not the 2D subfamily.
Determination of selected pyrimidines, purines and their metabolites in serum and urine by reversed-phase ion-pair chromatography.
- W. Voelter, K. Zech, P. Arnold, G. Ludwig
- Chemistry, BiologyJournal of Chromatography A
- 31 October 1980
Pharmacokinetics of pantoprazole in man.
- R. Huber, M. Hartmann, H. Bliesath, R. Lühmann, V. Steinijans, K. Zech
- Medicine, BiologyInternational journal of clinical pharmacology…
- 1 May 1996
Pantoprazole showed lack of cytochrome P450 interaction with concomitantly administered drugs in any of the studies conducted to date, and Lack of interaction was also demonstrated with a coadministered antacid.
The role of esterases in the metabolism of ciclesonide to desisobutyryl-ciclesonide in human tissue.
- E. Mutch, R. Nave, N. McCracken, K. Zech, F. Williams
- Biology, MedicineBiochemical Pharmacology
- 15 May 2007
Pharmacokinetics of [14C]Ciclesonide After Oral and Intravenous Administration to Healthy Subjects
Because of an almost complete first-pass metabolism, ciclesonide is undetectable in serum after oral administration, and any cicleonide swallowed after oral inhalation does not contribute to systemically available cicles onide or to its active metabolite.
Steady-State Pharmacokinetics of Roflumilast and Roflumilast N-Oxide in Patients with Mild and Moderate Liver Cirrhosis
- R. Hermann, N. Nassr, C. Mey
- MedicineClinical Pharmacokinetics
- 2007
It is suggested that roflumilast can be safely used in patients with mild and moderate liver cirrhosis without special precautions or dose adjustment and indicates modest average exposure increases to the sum of both compounds.
Population Pharmacokinetics and Pharmacodynamics of Ciclesonide
- S. Rohatagi, V. Arya, J. Barrett
- Biology, MedicineJournal of clinical pharmacology
- 1 April 2003
The estimated EC50 is similar to mean Cmax from an 800–μg dose, further suggesting CIC‐AP has little effect on cortisol suppression, and the influence of select covariates on PK and/or pharmacodynamic parameters is assessed.
Risk‐Benefit Value of Inhaled Glucocorticoids: A Pharmacokinetic/ Pharmacodynamic Perspective
- S. Rohatagi, S. Appajosyula, D. Banerji
- Biology, MedicineJournal of clinical pharmacology
- 1 January 2004
Current available inhaled glucocorticoids do not provide the complete pharmacokinetic/pharmacodynamic parameters to optimize RBV, leaving room for improvement in the development of future agents.
Plasma pharmacokinetics, tissue distribution and excretion of MnDPDP in the rat and dog after intravenous administration
- S. Hustvedt, D. Grant, T. Southon, K. Zech
- Biology, MedicineActa Radiologica
- 1 September 1997
The ligand does not appear to facilitate the transport of Mn into any organ except the kidney for subsequent excretion, and it reduces distribution to the heart.
A novel screening strategy to identify ABCB1 substrates and inhibitors
- O. Richter, H. Glavinas, P. Krajcsi, Stephanie Liehner, B. Siewert, K. Zech
- BiologyNaunyn-Schmiedeberg's Archives of Pharmacology
- 2008
The use of HDM-PAMPA in combination with ABCB1-ATPase offers a simple, inexpensive experimental approach capable of identifyingABCB1 inhibitors as well as transported substrates.
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