Search Results - "Lutz, Werner K"
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CYP2C9 genotype vs. metabolic phenotype for individual drug dosing--a correlation analysis using flurbiprofen as probe drug
Published in PloS one (16-03-2015)“…Currently, genotyping of patients for polymorphic enzymes responsible for metabolic elimination is considered a possibility to adjust drug dose levels. For a…”
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Statistical model to estimate a threshold dose and its confidence limits for the analysis of sublinear dose–response relationships, exemplified for mutagenicity data
Published in Mutation research (01-08-2009)“…Strongly sublinear dose–response relationships (slope increasing with dose) raise the question about a putative threshold dose below which no biologically…”
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Metabolic Profiling of Glucuronides in Human Urine by LC−MS/MS and Partial Least-Squares Discriminant Analysis for Classification and Prediction of Gender
Published in Analytical chemistry (Washington) (01-07-2006)“…Mass spectrometry (MS) is increasingly being used for metabolic profiling, but detection modes such as constant neutral loss or multiple reaction monitoring…”
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Nonmonotonic Dose-Response Relationships: Mechanistic Basis, Kinetic Modeling, and Implications for Risk Assessment
Published in Toxicological sciences (01-01-2004)“…Dose-response curves for the first interaction of a chemical with a biochemical target molecule are usually monotonic; i.e., they increase or decrease over the…”
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Quantification of cortisol and 6 beta-hydroxycortisol in human urine by LC-MS/MS, and gender-specific evaluation of the metabolic ratio as biomarker of CYP3A activity
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (01-01-2010)“…Drug–drug and food–drug interactions are often due to an inhibition or induction of drug-metabolizing cytochrome P450 (CYP) enzymes and may result in…”
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Correction: CYP2C9 genotype vs. metabolic phenotype for individual drug dosing--a correlation analysis using flurbiprofen as probe drug
Published in PloS one (13-04-2015)“…According to the study design, which also designated phenotyping for CYP2D6, 10 mg dextromethorphan in water (DEX, as dextromethorphan hydrobromide…”
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Ochratoxin A: 13-Week Oral Toxicity and Cell Proliferation in Male F344/N Rats
Published in Toxicological sciences (01-06-2007)“…Ochratoxin A (OTA) is nephrotoxic and a potent renal carcinogen. Male rats are most susceptible to OTA toxicity, and chronic administration of OTA (70 and 210…”
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Metabolite profiling in human urine by LC–MS/MS: Method optimization and application for glucuronides from dextromethorphan metabolism
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (15-08-2008)“…Analysis of human urine for specific compounds or metabolites is an established method for biomonitoring occupational or environmental exposures. Modern liquid…”
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9
Increased brain levels of 4-hydroxy-2-nonenal glutathione conjugates in severe Alzheimer's disease
Published in Neurochemistry international (01-06-2006)“…In the last decade an important role for the progression of neuronal cell death in Alzheimer's disease (AD) has been ascribed to oxidative stress…”
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Drug interactions with mitotane by induction of CYP3A4 metabolism in the clinical management of adrenocortical carcinoma
Published in Clinical endocrinology (Oxford) (01-11-2011)“…Summary Mitotane [1‐(2‐chlorophenyl)‐1‐(4‐chlorophenyl)‐2,2‐dichloroethane, (o,p’‐DDD)] is the only drug approved for the treatment for adrenocortical…”
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Strategies in case of positive in vivo results in genotoxicity testing
Published in Mutation research (16-08-2011)“…At the 2009 International Workshop on Genotoxicity Testing in Basel, an expert group gathered to provide guidance on suitable follow-up tests to describe risk…”
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LC–MS/MS analysis of dextromethorphan metabolism in human saliva and urine to determine CYP2D6 phenotype and individual variability in N-demethylation and glucuronidation
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (25-12-2004)“…In order to establish a fast screening method for the determination of the CYP2D6 metabolic phenotype a sensitive LC–MS/MS assay to quantify dextromethorphan…”
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Comparative Assessment of the Inhibition of Recombinant Human CYP19 (Aromatase) by Azoles Used in Agriculture and as Drugs for Humans
Published in Endocrine research (01-01-2004)“…Azoles (imidazoles and triazoles) are used as antifungal agents in agriculture and in medicine, and also for antiestrogen therapy, e.g., for breast cancer…”
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Different Types of Combination Effects for the Induction of Micronuclei in Mouse Lymphoma Cells by Binary Mixtures of the Genotoxic Agents MMS, MNU, and Genistein
Published in Toxicological sciences (01-08-2005)“…Distinction between dose addition and response addition for the analysis of the toxicity of mixtures may allow differentiation of the components regarding…”
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The Viracept (nelfinavir)—Ethyl methanesulfonate case: A threshold risk assessment for human exposure to a genotoxic drug contamination?
Published in Toxicology letters (12-11-2009)“…In May 2007, the F. Hoffmann-La Roche Company became aware of a contamination of Viracept (nelfinavir) tablets by the mutagenic DNA-ethylating agent ethyl…”
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Effect of Omeprazole and Dextromethorphan on the Urinary Metabolic Ratio of Flurbiprofen
Published in Basic & clinical pharmacology & toxicology (01-06-2016)Get full text
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Biomarkers of Furan Exposure by Metabolic Profiling of Rat Urine with Liquid Chromatography-Tandem Mass Spectrometry and Principal Component Analysis
Published in Chemical research in toxicology (01-03-2008)“…Furan has been found in a number of heated food items and is carcinogenic in the liver of rats and mice. Estimates of human exposure on the basis of…”
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Tests for genotoxicity and mutagenicity of furan and its metabolite cis-2-butene-1,4-dial in L5178Y tk +/− mouse lymphoma cells
Published in Mutation research (08-12-2008)“…Furan is found in various food items and is cytotoxic and carcinogenic in the liver of rats and mice. Metabolism of furan includes the formation of an…”
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Comparison of lanosterol-14α-demethylase (CYP51) of human and Candida albicans for inhibition by different antifungal azoles
Published in Toxicology (Amsterdam) (10-11-2006)“…Inhibition of fungal lanosterol-14α-demethylase (CYP51) is the working principle of the antifungal activity of azoles used in agriculture and medicine…”
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Inhibition of human CYP19 by azoles used as antifungal agents and aromatase inhibitors, using a new LC–MS/MS method for the analysis of estradiol product formation
Published in Toxicology (Amsterdam) (15-02-2006)“…Azoles are used as fungicides in agriculture or antifungal drugs in medicine. Their therapeutic activity is based on the inhibition of fungal…”
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