Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Felix Bredendiek"'
Autor:
Annika Lisa Jendretzki, Lukas Corbinian Harps, Yanan Sun, Felix Bredendiek, Matthias Bureik, Ulrich Girreser, Xavier de la Torre, Francesco M. Botrè, Maria Kristina Parr
Publikováno v:
Separations, Vol 10, Iss 8, p 427 (2023)
The aim of the study was a comprehensive and quantitative determination of salbutamol and its sulfoconjugated major metabolite in urine samples using achiral ultrahigh performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Therefor
Externí odkaz:
https://doaj.org/article/3e287129e2304d90bd8944c043026627
Autor:
Annika Lisa Jendretzki, Lukas Corbinian Harps, Yanan Sun, Felix Bredendiek, Matthias Bureik, Ulrich Girreser, Xavier De la Torre, Francesco Botrè, Maria Kristina Parr
It was the aim of this study to compare the ratio of salbutamol and its major metabolite salbutamol-4’-O-sulfate as well as the quantity excreted renally after oral and inhalative administration. Additionally, the excretion pattern after applicatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a169cd104e0164f04e9bc7db73c26b
https://doi.org/10.20944/preprints202302.0447.v1
https://doi.org/10.20944/preprints202302.0447.v1
Autor:
Lingyu Liu, Leonie Hobohm, Felix Bredendiek, Alexander Froschauer, Oliver Zierau, Maria Kristina Parr, Annekathrin M. Keiler
Publikováno v:
Archives of toxicology. 96(7)
In anti-doping science, the knowledge of drug metabolism is a prerequisite to identify analytical targets for the detection of misused prohibited substances. As the most obvious way to study xenobiotic metabolism, the administration to human voluntee
Autor:
Felix Bredendiek, Maria Kristina Parr, Lukas C. Harps, Bernhard Wuest, Sonja Schipperges, Andreas Borowiak
Publikováno v:
Journal of Chromatography A. 1617:460828
In this study a heart-cutting 2D-LC method was successfully developed and optimized in order to discriminate and quantitate (S)-propranolol, (R)-propranolol, and its hydroxy metabolites, namely the isomeric (S)-4′‑hydroxy propranolol, (R)-4′‑