56 research outputs found
ChemInform Abstract: Cyclocondensation of 3(2H)-Benzo[b]thiophenone and Oxidation Products Obtained During These Reactions.
Application of triple-probe microdialysis for fast pharmacokinetic/pharmacodynamic evaluation of dopamimetic activity of drug candidates in the rat brain
Simple Procedures for Enrichment of Chlorinated Aromatic Pollutants from Fat, Water and Milk for Subsequent Analysis by High-Resolution Methods
IDENTIFICATION AND DETERMINATION OF PHENYLACETYLGLUTAMINE, A MAJOR NITROGENOUS METABOLITE IN PLASMA OF UREMIC PATIENTS
Hepatic excretion and metabolism of polyethylene glycols and mannitol in the cat
The biliary clearances of fluid phase markers like erythritol and mannitol have been used to estimate canalicular bile flow. Larger fluid phase marker molecules like polyethylene glycol (PEG) 900 are excreted more extensively into bile, and it has been suggested that the biliary clearance of these give a more accurate measure of canalicular water flux than those of erythritol and mannitol. In this study, the biliary excretion of PEG 900 was compared with that of mannitol during choleresis induced by either sodium taurocholate or secretin. The biliary excretion of PEG 900 exceeded that of mannitol by a factor of 94. The biliary clearance of these markers was not influenced by secretin-induced choleresis. Using ion-exchange chromatography and fast atom bombardment mass spectrometry (FABMS) it was demonstrated that 26% of the PEG molecules are excreted into bile after oxidation to carboxylic acids, whereas sulphate conjugation is negligible. The majority of the PEG molecules (74%) were secreted unchanged, which supports the hypothesis of a mainly passive movement of PEG with the water flux into bile. FABMS showed an enrichment of larger PEG molecules in bile, which supports a previous finding that among differently sized PEGs the 1074-Da molecules have the highest biliary excretion
Lipophilic ion exchangers for group separation of conjugated metabolites of xenobiotics
THE PRIMARY STRUCTURE OF ALCOHOL-DEHYDROGENASE FROM DROSOPHILA-LEBANONENSIS - EXTENSIVE VARIATION WITHIN INSECT SHORT-CHAIN ALCOHOL-DEHYDROGENASE LACKING ZINC
Isolation of bile acid glucosides and N-acetylglucosaminides from human urine by ion-exchange chromatography and reversed-phase high-performance liquid chromatography
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