## Abstract The metabolism of 1‐(2‐methyl‐4‐methoxyphenyl)‐4‐[(3‐hydroxypropyl)amino]‐6‐methyl‐2,3‐dihydropyrrolo[3,2c]quinoline (DBM‐819), a new H^+^/K^+^ ATPase inhibitor, has been studied by HPLC with spectrometric detection and on‐line LC‐electrospray mass spectrometry. __In vitro__ incubation
Study of Phenformin Metabolism in Rat Liver Microsomes by HPLC, CE and On-Line HPLC-Electrospray Ionization Mass Spectrometry
✍ Scribed by Elena B. C. Llambias; Jinli Luo
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 342 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0269-3879
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✦ Synopsis
Methods for the analysis of phenformin and its metabolite by high-performance liquid chromatography (HPLC), capillary electrophoresis (CE) and high-performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-ESIMS) are developed. The effects of pH, buffer concentration and proportion of organic modifier on the retention of the compounds in HPLC have been studied. The optimum condition was used for the separation and identification of phenformin and its metabolite in microsomal metabolism by HPLC-ESIMS. A simple CE method is also described for the separation of these compounds. Optimum incubation conditions and cofactor requirements for the formation of 4-hydroxyphenformin by microsomal preparations of rat liver were determined. A linear response in the formation of product was found with increasing concentrations of protein and up to 15 min incubation. High concentrations of phenformin inhibited its metabolite formation, and K , was 4 PM.
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