Abstract
A sample of 0.104 M nicardipine in methanol was photoirradiated with a Philips 400 W UV lamp for 3 h in a photochemical chamber. A total of four major photoproducts were found from the HPLC chromatogram. The same sample was used for taking LC-MS, while eight major photoproducts were observed and the structures elucidated by analyzing the CID patterns of their respective mass spectra. A reaction scheme of nicardipine is proposed that the photochemical reactions occur mainly via oxidation of 1,4-dihydropyridine moiety, following the stepwise photo-reduction of the m-nitro group and demethylation of the ester group at 5-position of the pyridine ring.
| Original language | English |
|---|---|
| Pages (from-to) | 1008-1012 |
| Number of pages | 5 |
| Journal | Biomedical Chromatography |
| Volume | 22 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2008 |
Keywords
- HPLC
- LC-MS
- Nicardipine
- Photoproducts
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Molecular Biology
- Pharmacology
- Drug Discovery
- Clinical Biochemistry