Abstract
Background: Co-trimoxazole is frequently used in the prophylaxis and treatment of Pneumocystis carinii pneumonia. High plasma concentrations of sulfamethoxazole or trimethoprim are correlated with toxicity. There is, however, a large variation in PK observed which can lead to underexposure or toxicity. Results: We developed a novel LC-MS/MS method to analyze the components of co-trimoxazole, trimethoprim and sulfamethoxazole and its metabolite sulfamethoxazole-N-acetyl. This new method is expeditious due to its limited sample preprocessing and a relatively short run-time of only 3 min. Conclusion: This new method met the US FDA requirements on linearity, selectivity, precision, accuracy, matrix effects, recovery and stability and is suitable for routine analysis and future prospective studies.
Original language | English |
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Pages (from-to) | 2741-2749 |
Number of pages | 9 |
Journal | Bioanalysis |
Volume | 7 |
Issue number | 21 |
DOIs | |
Publication status | Published - Nov-2015 |
Keywords
- PNEUMOCYSTIS-CARINII-PNEUMONIA
- HIV-INFECTED PATIENTS
- TRIMETHOPRIM-SULFAMETHOXAZOLE
- THERAPY
- TUBERCULOSIS
- PROPHYLAXIS
- METAANALYSIS
- HPLC