A Rapid Determination of Patulin Using Capillary Zone Electrophoresis and its Application to Analysis of Apple Juices

被引:12
作者
Guray, Tufan [1 ]
Tuncel, Muzaffer [2 ]
Uysal, Ulku Dilek [3 ]
机构
[1] Eskisehir Osmangazi Univ, Fac Arts & Sci, Dept Chem, TR-26480 Eskisehir, Turkey
[2] Anadolu Univ, Fac Pharm, Dept Analyt Chem, TR-26470 Eskisehir, Turkey
[3] Anadolu Univ, Fac Sci, Dept Chem, TR-26470 Eskisehir, Turkey
关键词
CHROMATOGRAPHY-MASS SPECTROMETRY; LIQUID-CHROMATOGRAPHY; ELECTROMIGRATION METHODS; MYCOTOXIN PATULIN; FOOD ANALYSIS; IDENTIFICATION; STABILITY; TOXIN; CELLS; FRUIT;
D O I
10.1093/chromsci/bms142
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This study describes a capillary zone electrophoretic method for the determination of patulin. An optimum run buffer was found to be 25 mM of sodium tetraborate and 10% acetonitrile (v/v) at pH 10. Optimum conditions were determined to be: an applied voltage of 25 kV (normal polarity), temperature of 25 degrees C and injection time of 10 s at 50 mbar; the signals of patulin and phenobarbital as internal standard were detected at 276 nm. The method was highly reproducible, with relative standard deviations of 0.02-0.85 for intra-day and 0.04-0.42 for inter-day for standard patulin. Acceptable linearity [y = 0.0020C (mu g/L) - 0.0680 (r = 0.9999)] was obtained over a concentration range of 0.25 to 4.99 mu g/mL of patulin. The limits of detection and quantification were calculated to be 5.9 x 10(-3) and 1.79 x 10(-2) mu g/mL, respectively. Recovery was 68.0%. The proposed method was applied to 21 apple juice samples purchased from different Turkish markets, and two were found to contain higher than the limits of the European Union Directive for patulin.
引用
收藏
页码:310 / 317
页数:8
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