Khater Syame, West Caroline
Université d'Orléans, ICOA, CNRS UMR 7311, Pôle de Chimie, rue de Chartres, 45067 Orléans cedex 2, France.
Université d'Orléans, ICOA, CNRS UMR 7311, Pôle de Chimie, rue de Chartres, 45067 Orléans cedex 2, France.
J Pharm Biomed Anal. 2015 Jan;102:321-5. doi: 10.1016/j.jpba.2014.09.036. Epub 2014 Oct 13.
A rapid and efficient chiral supercritical fluid chromatography (SFC) method has been developed for the quantitative determination of panthenol enantiomers in cosmetic formulations (cream, lotion, wipe, and exfoliant). Indeed, the pharmacological effect only depends on the D form (Dexpanthenol) thus accurate measurement of its enantiomeric purity in formulated cosmetic products is of interest. The samples were prepared with liquid-liquid extraction followed by solid-phase extraction on Adsorbex amino cartridges. After testing several enantioselective columns in an attempt at reversing the elution order to have the minor enantiomer eluted first, the best separation of enantiomers and internal standard (N-acetyl-L-alanine) was achieved on a 3 μm-amylose-type immobilized polysaccharide chiral stationary phase (Chiralpak IA) in less than 6 min with a simple mobile phase comprising carbon dioxide and 11% methanol pumped at 2.3 mL/min, 25°C and 150 bar backpressure. Supercritical fluid chromatography coupled to both an optical diode-array detector and a user-friendly single-quadrupole mass spectrometer (Waters QDa) equipped with electrospray ionization source has been used. The on-line coupling ensures the technique to be more informative and improves detection sensitivity, as underivatized panthenol has a poor UV absorption. The limit of quantification (LOQ) achieved with single-ion recording was 0.5 μg/mL. The method was validated in terms of linearity, precision and accuracy and satisfactory results were obtained.
已开发出一种快速高效的手性超临界流体色谱(SFC)方法,用于定量测定化妆品配方(面霜、乳液、擦拭巾和去角质剂)中的泛醇对映体。实际上,药理作用仅取决于D型(右旋泛醇),因此准确测量其在配方化妆品中的对映体纯度很有意义。样品通过液液萃取制备,然后在Adsorbex氨基柱上进行固相萃取。在测试了几种对映体选择性柱以试图颠倒洗脱顺序使次要对映体先洗脱后,在3μm直链淀粉型固定化多糖手性固定相(Chiralpak IA)上,使用由二氧化碳和11%甲醇组成的简单流动相,以2.3 mL/min的流速泵送,在25°C和150 bar背压下,不到6分钟就实现了对映体和内标(N-乙酰-L-丙氨酸)的最佳分离。已使用超临界流体色谱与配备电喷雾电离源的光学二极管阵列检测器和用户友好型单四极杆质谱仪(Waters QDa)联用。在线联用确保该技术更具信息性并提高检测灵敏度,因为未衍生化的泛醇紫外吸收较差。单离子记录实现的定量限(LOQ)为0.5μg/mL。该方法在线性、精密度和准确度方面进行了验证,并获得了满意的结果。