Galli Verónica, Barbas Coral
Facultad de CC. Experimentales y de la Salud, Universidad San Pablo-CEU, Urbanización Montepríncipe, Boadilla del Monte, 28668 Madrid, Spain.
J Chromatogr A. 2004 Apr 2;1032(1-2):299-304. doi: 10.1016/j.chroma.2003.09.028.
A simple and rapid capillary electrophoresis method for low-molecular mass carboxylic acids measurement in coffee has been optimised and validated. Regarding separation conditions, phosphate concentration in the background electrolyte, surfactant type [cetyltrimethylammonium bromide (CTAB), tetradecyltri methylammonium bromide (TTAB) and hexadimethrine bromide (HDB)], percentages of organic modifier and pH were assayed. The best conditions were: 500 mM phosphate buffer at pH 6.25 with CTAB 0.5 mM. The separation was carried out with an uncoated fused-silica capillary (57 cm x 50 microm i.d.) which was operated at -10 kV potential. Detection was performed at 200 nm. In such conditions 17 short-chain organic acids: oxalic, formic, fumaric, mesaconic, succinic, maleic, malic, isocitric, citric, acetic, citraconic, glycolic, propionic, lactic, furanoic, pyroglutamic, quinic acids plus nitrate were separated, identified and measured. Validation parameters of the method allow us to consider it lineal, accurate and precise and, therefore, reliable for its employment in food composition studies or for quality control. Results in coffees with different industrial treatment allow the detection of important differences in the organic acid profile.
一种用于测定咖啡中低分子量羧酸的简单快速毛细管电泳方法已得到优化和验证。关于分离条件,对背景电解质中的磷酸盐浓度、表面活性剂类型[十六烷基三甲基溴化铵(CTAB)、十四烷基三甲基溴化铵(TTAB)和溴化己二甲铵(HDB)]、有机改性剂的百分比和pH值进行了测定。最佳条件为:pH 6.25的500 mM磷酸盐缓冲液,含0.5 mM CTAB。使用未涂层熔融石英毛细管(57 cm×50μm内径)在-10 kV电压下进行分离。在200 nm处进行检测。在这些条件下,17种短链有机酸:草酸、甲酸、富马酸、甲基丙烯酸、琥珀酸、马来酸、苹果酸、异柠檬酸、柠檬酸、乙酸、柠康酸、乙醇酸、丙酸、乳酸、呋喃酸、焦谷氨酸、奎尼酸以及硝酸盐被分离、鉴定和测定。该方法的验证参数使我们能够认为它具有线性、准确性和精密度,因此可用于食品成分研究或质量控制。不同工业处理咖啡的结果能够检测出有机酸谱中的重要差异。