Development and validation of a high-performance liquid chromatography–mass spectrometry assay for methylxanthines and taurine in dietary supplements
A procedure based on liquid chromatography–mass spectrometry (LC–MS) is described for determination of caffeine, theobromine, theophylline, taurine in different dietary supplements. After addition of tryptophan as internal standard, both solid and liquid specimens were extracted with 4 ml of hexane/...
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Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2005-03, Vol.37 (3), p.499-507 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A procedure based on liquid chromatography–mass spectrometry (LC–MS) is described for determination of caffeine, theobromine, theophylline, taurine in different dietary supplements. After addition of tryptophan as internal standard, both solid and liquid specimens were extracted with 4
ml of hexane/isopropanol (9:1).
Chromatography was performed on a C
18 reversed-phase column using water/methanol/acetic acid (75:20:5, v/v/v) as a mobile phase. Analytes were determined in LC–MS single ion monitoring mode with atmospheric pressure ionization-electrospray (ESI) interface. The method was validated in the range 0.1–500 and 0.06–500
μg/ml or μg/g for taurine and caffeine, respectively; 0.06–100
μg/ml or μg/g for theobromine and theophylline. Mean recoveries ranged between 70.1 and 94.4% for different analytes. The quantification limits were 0.1
μg/ml or μg/g for taurine and 0.06
μg/ml or μg/g for methylxanthines either in liquid samples or in solid samples. The method was applied to the analysis of various dietary supplements containing methylxanthines and taurine. Energetic drinks contained amounts of taurine in the range of hundreds to thousands μg/ml and ten times lower amounts of caffeine. Conversely, herbal powders, tablets and capsules mainly contained mg amounts of caffeine per gram of product with the other two methylxanthines in the range of ten to hundred μg/g. |
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ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/j.jpba.2004.11.013 |