Comparison of different stationary phases for bioanalytical studies of biologically active compounds
Language English Country Germany Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Analgesics analysis chemistry metabolism MeSH
- Anti-Inflammatory Agents, Non-Steroidal analysis chemistry metabolism MeSH
- Antineoplastic Agents analysis chemistry metabolism MeSH
- Butanones analysis chemistry metabolism MeSH
- Fluorenes analysis chemistry metabolism MeSH
- Cocaine analysis chemistry metabolism MeSH
- Pharmaceutical Preparations analysis chemistry metabolism MeSH
- Humans MeSH
- Molecular Structure MeSH
- Nabumetone MeSH
- Reference Standards MeSH
- Tramadol analysis chemistry metabolism MeSH
- Chromatography, High Pressure Liquid methods standards MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Analgesics MeSH
- Anti-Inflammatory Agents, Non-Steroidal MeSH
- Antineoplastic Agents MeSH
- Butanones MeSH
- dimefluron MeSH Browser
- Fluorenes MeSH
- Cocaine MeSH
- Pharmaceutical Preparations MeSH
- Nabumetone MeSH
- Tramadol MeSH
In this study, the chromatographic behaviour of four mixtures of compounds was tested on columns possessing various surface properties. Cocaine, dimefluron, nabumetone, and tramadol were chosen as the test compounds. Cocaine is a tropane alkaloid, which is relatively often abused as a drug. This is why many papers have already been written about its determination in human biological samples. Dimefluron, a derivative of benzo[c]fluorene, is a new perspective drug being investigated for its potential antineoplastic effects. Nabumetone is a non-steroidal anti-inflammatory prodrug used for treatment of inflammatory and degenerative rheumatic diseases. Tramadol, derived from an opioid structure is used as an anodyne for treatment of severe pain. As a medicament it is usually determined either in biological samples or in pharmaceuticals. The above-mentioned model drugs were separated using chromatographic columns with C18, C8, palmitamidopropyl, and pentafluorophenylpropyl chains. The best conditions for separation of the individual compounds and their metabolites were chosen on the basis of resolution, retention times, and peak symmetry.
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