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Zoekresultaten - 35 results
Evaluation of a screening system for obesogenic compounds: screening of endocrine disrupting compounds and evaluation of the PPAR dependency of the effect.
adipogenesis model, and direct fluorescent measurement using Nile red lipid staining technique. In a first phase, we characterised the assay using the acknowledged obesogens rosiglitazone and tributyltin. Based ...
A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations
Analysis 2010, Issue Belgian Society of Pharmaceutical Sciences (2012) Keywords: acid ALL an Analyses analysis Area AS at bias Comparison differences DRUG effect Folic Acid function LEVEL levels measurement ...
A targeted proteomics method to detect urinary biomarkers of kidney disease
blood Carbon care Categories chronic Clinical conference Creatinine detection Diagnosis disease Diseases effect effects Evolution factors general general population General-population intervention IS ...
A validated Ultra High Pressure Liquid Chromatographic method for the characterisation of confiscated illegal slimming products containing anorexics.
ammonium acetate buffer pH 5.0 as aqueous phase and acetonitrile as organic modifier. The obtained method was fully validated based on its measurement uncertainty (accuracy profile). Calibration lines for ...
Influenza A/H1N1 vaccine in patients treated by kidney transplant or dialysis: a cohort study36521
Bernard Brochier; Isabelle Thomas; Abramowicz,D. Source: Clin.J.Am.Soc.Nephrol., Volume 6, Issue 11, Number 2578, p.2573- 2578 (2011) Keywords: 0 2009 a administration & dosage Adult adverse effects ...
A fast ultra high pressure liquid chromatographic method for qualification and quantification of pharmaceutical combination preparations containing paracetamol, acetyl salicylic acid and/or antihistaminics.
mm, 1.7 μm) with a gradient using an ammonium acetate buffer pH 4.0 as aqueous phase and methanol as organic modifier. The obtained method was fully validated based on its measurement uncertainty ...
A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations.
measurement uncertainty (accuracy profile) and robustness tests. A UHPLC method was obtained for the identification and quantification of folic acid in pharmaceutical preparations, which will cut analysis times ...
Validation of two real-time RT-PCR methods for foot-and-mouth disease diagnosis: RNA-extraction, matrix effect, uncertainty of measurement and precision.
determine analytical and diagnostic sensitivity and specificity, a thorough validation in terms of establishing optimal RNA-extraction conditions, matrix effect, uncertainty of measurement and precision is ...
Validation of a liquid chromatography-mass spectrometric assay for tacrolimus in peripheral blood mononuclear cells.
respectively. Intra-assay and interassay imprecisions ranged from 9.3% to 12% and 10.7% to 12.2%, respectively, across the analytical range. Mean TAC extraction efficiency was 80.9% +/- 8.3%. Matrix effects were ...
Novel highly potent mu-opioid receptor antagonist based on endomorphin-2 structure4392
synthesis chemistry Cho Cells Chromatography,High Pressure Liquid Cricetinae Cricetulus Drug Design drug effects electronic EVALUATION im improve in vivo Institute IS IT journal Laboratories Less medical ...