Khater, Syame, et al. Journal of pharmaceutical and biomedical analysis, 2015, 102, 321-325.
The therapeutic effects of provitamin B5 are solely attributed to its D-form (dexpanthenol), making precise determination of its enantiomeric purity in cosmetic products essential. This study presents a swift and effective chiral supercritical fluid chromatography (SFC) method for the quantitative analysis of panthenol enantiomers in various cosmetic formulations, including creams, lotions, wipes, and exfoliants.
Determination Method
· The samples were prepared using liquid-liquid extraction followed by solid-phase extraction with amino cartridges. Various enantioselective columns were tested to reverse the elution order so that the minor enantiomer would elute first. The optimal separation of the enantiomers and the internal standard, N-acetyl-l-alanine, was accomplished on a 3 μm-amylose-type immobilized polysaccharide chiral stationary phase in under 6 minutes, using a simple mobile phase of carbon dioxide and 11% methanol, at a flow rate of 2.3 mL/min, 25 °C, and a backpressure of 150 bar.
· The technique employed supercritical fluid chromatography, paired with an optical diode-array detector and a user-friendly single-quadrupole mass spectrometer featuring an electrospray ionization source. This online coupling enhances the method's informative capacity and detection sensitivity, particularly beneficial since underivatized panthenol exhibits weak UV absorption. The limit of quantification (LOQ) was determined to be 0.5 μg/mL using single-ion recording.