Criteria for opiate identification using liquid chromatography linked to tandem mass spectrometry: problems in routine practice
| Autor: | Keith R Allen, Shirley Twigger, Elizabeth J Fox |
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| Rok vydání: | 2009 |
| Předmět: |
Morphine Derivatives
Chromatography Codeine Chemistry Clinical Biochemistry Reproducibility of Results General Medicine Hydrogen-Ion Concentration Routine practice Tandem mass spectrometry Tandem Mass Spectrometry Humans Identification (biology) Drug identification Chromatography High Pressure Liquid Oxycodone Drug confirmation |
| Zdroj: | Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 46:50-57 |
| ISSN: | 1758-1001 0004-5632 |
| DOI: | 10.1258/acb.2008.008104 |
| Popis: | Background Liquid chromatography linked to tandem mass spectrometry (LC/MS/MS) is being increasingly used for drug confirmation. At present, no official criteria exist for drug identification using this technique although the European Union (EU) criteria for compound identification have been adopted. These criteria are evaluated with respect to opiate confirmation by LC/MS/MS and problems highlighted. Methods Urine samples screened positive for opiates by immunoassay were subjected to confirmation by LC/MS/MS using multiple reaction monitoring (MRM) and two separate buffer systems of pH 6.8 and 8.0, respectively. The EU criteria for compound identification were applied for confirmation of morphine, 6-monoacetylmorphine (6MAM), codeine and dihydrocodeine (DHC). Results Using the pH 6.8 buffer, confirmation could be achieved for 84%, 94%, 96% and 95%, respectively, for samples demonstrating MRM chromatographic peaks at retention times for morphine, 6MAM, codeine and DHC. Failure to meet the EU criteria was mainly attributed to low signal-to-noise (S:N) ratios or excessively high drug concentrations. Isobaric interferences and poor chromatography were also contributing factors. The identification of morphine was considerably improved with chromatography at pH 8.0 owing to resolution of interferences. Oxycodone metabolites were a potential problem for the identification of DHC. Conclusion Isobaric interferences can pose a problem with drug identification using LC/MS/MS. Optimizing chromatographic conditions is important to overcome these interferences. Consideration needs to be given to investigating drug metabolites as well as parent drugs in method development. |
| Databáze: | OpenAIRE |
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