Aresta Antonella, Cioffi Nicola, Palmisano Francesco, Zambonin Carlo G
Dipartimento di Chimica, Università degli Studi di Bari, Via E. Orabona 4, I-70126 Bari, Italy.
J Agric Food Chem. 2003 Aug 27;51(18):5232-7. doi: 10.1021/jf034385r.
A solid-phase microextraction (SPME) method, coupled to liquid chromatography with diode array UV detection (LC-UV/DAD), for the simultaneous determination of cyclopiazonic acid, mycophenolic acid, tenuazonic acid, and ochratoxin A is described. Chromatographic separation was achieved on a propylamino-bonded silica gel stationary phase using acetonitrile/methanol/ammonium acetate buffer mixture (78:2:20, v/v/v) as mobile phase. SPME adsorption and desorption conditions were optimized using a silica fiber coated with a 60 microm thick polydimethylsiloxane/divinylbenzene film. Estimated limits of detection and limits of quantitation ranged from 3 to 12 ng/mL and from 7 to 29 ng/mL, respectively. The method has been applied to cornflake samples. Samples were subjected to a preliminary short sonication in MeOH/2% KHCO(3) (70:30, v/v); the mixture was evaporated to near dryness and reconstituted in 1.5 mL of 5 mM phosphate buffer (pH 3) for SPME followed by LC-UV/DAD. The overall procedure had recoveries (evaluated on samples spiked at 200 ng/g level) ranging from 74 +/- 4 to 103 +/- 9%. Samples naturally contaminated with cyclopiazonic and tenuazonic acids were found; estimated concentrations were 72 +/- 9 and 25 +/- 6 ng/g, respectively.
描述了一种固相微萃取(SPME)方法,该方法与配有二极管阵列紫外检测的液相色谱(LC-UV/DAD)联用,用于同时测定环匹阿尼酸、霉酚酸、细交链孢菌酮酸和赭曲霉毒素A。在丙基氨基键合硅胶固定相上进行色谱分离,使用乙腈/甲醇/醋酸铵缓冲液混合物(78:2:20,v/v/v)作为流动相。使用涂有60微米厚聚二甲基硅氧烷/二乙烯基苯膜的硅胶纤维对SPME的吸附和解吸条件进行了优化。估计的检测限和定量限分别为3至12 ng/mL和7至29 ng/mL。该方法已应用于玉米片样品。样品先在甲醇/2%碳酸氢钾(70:30,v/v)中进行短时间超声处理;混合物蒸发至近干,然后用1.5 mL 5 mM磷酸盐缓冲液(pH 3)复溶,用于SPME,随后进行LC-UV/DAD分析。整个过程的回收率(在添加水平为200 ng/g的样品上评估)为74±4%至103±9%。发现了天然受环匹阿尼酸和细交链孢菌酮酸污染的样品;估计浓度分别为72±9 ng/g和25±6 ng/g。