Analysis of free amino acids with unified chromatography-mass spectrometry—application to food supplements

• Published in: Journal of Chromatography A 2020-04, Vol.1616, p.460772, Article 460772
• Main Authors: Raimbault, Adrien, Noireau, Angéline, West, Caroline
• Format: Article
• Language: English
• Subjects: Chemical Sciences; Dietary supplements; Native amino acids; Supercritical fluid chromatography; Unified chromatography; Zwitterionic stationary phases
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2019.460772

•Free amino acids analyzed in unified chromatography from SFC to HPLC.•Adapted operating conditions to optimize run time and efficiency.•Separation of isobaric isomers of leucine and isoleucine.•Quantification with ESI(+)-MS detection in dietary supplements. Amino acids are most often analyzed in reversed-phase liquid chromatography after a derivatization procedure to render them sufficiently hydrophobic and detectable with UV or fluorimetric detection. Simpler methods should be possible to avoid additional chemical reactions. We present an improved method to analyze free amino acids with unified chromatography, that is to say with a wide elution gradient starting with supercritical fluid chromatography (SFC) conditions (high percentage of carbon dioxide) and ending with high-performance liquid chromatography (HPLC) conditions (100% co-solvent). The mobile phase composition was carefully adjusted to permit the elution of 21 natural amino acids (among which 19 proteinogenic) with very good peak shapes from a zwitterionic cinchona-based stationary phase (Chiralpak ZWIX(+)). Chiral separation was not desired. The mobile phase finally selected comprised carbon dioxide and a co-solvent (methanol containing 2% water and 20 mM methanesulfonic acid), ranging from 10 to 100% in 7 min followed by 3 min re-equilibration at 25 °C. A reversed pressure gradient (15 to 11 MPa) and a reversed flow rate gradient (3 to 1 mL/min) were applied to avoid reaching the upper pressure limit of the pumping system (40 MPa) and to favor high chromatographic efficiency at every stage of the elution gradient. Detection was achieved with electrospray ionization-mass spectrometry (ESI(+)-MS). The method is then fast and straightforward as no derivatization step is necessary, and all isobaric species were chromatographically resolved. To demonstrate the applicability of the method, it was applied to the quantitation of amino acids in food supplements commonly consumed by sportsmen, containing taurine (a common natural amino acid) or branched-chain amino acids (BCAA), namely valine, and the isobaric leucine and isoleucine. A standard addition method was examined for sensitivity, linearity, repeatability and intermediate precision.