Microemulsion electrokinetic chromatography for the analysis of green tea catechins: Effect of the cosurfactant on the separation selectivity

被引:58
作者
Pomponio, R [1 ]
Gotti, R [1 ]
Luppi, B [1 ]
Cavrini, V [1 ]
机构
[1] Univ Bologna, Dipartimento Sci Farmaceut, I-40126 Bologna, Italy
关键词
capillary electrophoresis; catechins; cosurfactants; green tea; microemulsion electrokinetic chromatography;
D O I
10.1002/elps.200305391
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microemulsion electrokinetic chromatography (MEEKC) was applied to the separation of six catechins and caffeine, the major constituents of the green tea. The developed methods involved the use of sodium dodecyl sulfate (SDS) as surfactant, n-heptane as organic solvent and an alcohol as cosurfactant. The separations were performed under acidic conditions (pH 2.5 phosphate buffer, 50 mm) to ensure good stability of the catechins, with reversed polarity (anodic outlet). The effect of the alcohol nature on the MEEKC selectivity was evaluated; nine alcohols were used as cosurfactant: 1-butanol, tert-butanol, 1-pentanol, 2-pentanol, 3-pentanol, cyclopentanol, 1-hexanol, 2-hexanol, and cyclohexanol. The migration order of (+)-catechin (C), (-)-epicatechin (EC), (-)-epigallocatechin (EGC), (-)-gallocatechin (GC), (-)-epigallocatechin gallate (EGCG), (-)-epicatechin gallate (ECG), caffeine and theophylline was significantly affected by the alcohol used as cosurfactant. Using nine microemulsions, four different selectivities were achieved: A (cyclohexanot); B (2-pentanol, 3-pentanol, 1-hexanol, 2-hexanol); C (1-butanol, 1-pentanol, cyclopentanol); D (tert-butanol). MEEKC methods, based on 2-hexanol and cyclohexanol as cosurfactant were validated and successfully applied to the analysis of catechins and caffeine in commercial green tea products.
引用
收藏
页码:1658 / 1667
页数:10
相关论文
共 60 条
[31]   Why drinking green tea could prevent cancer [J].
Jankun, J ;
Selman, SH ;
Swiercz, R ;
SkrzypczakJankun, E .
NATURE, 1997, 387 (6633) :561-561
[32]   Separations of flavan-3-ols and dimeric proanthocyanidins by capillary electrophoresis [J].
Kreimeyer, J ;
Petereit, F ;
Nahrstedt, A .
PLANTA MEDICA, 1998, 64 (01) :63-67
[33]   Separation of tea polyphenols using micellar electrokinetic chromatography with diode array detection [J].
Larger, PJ ;
Jones, AD ;
Dacombe, C .
JOURNAL OF CHROMATOGRAPHY A, 1998, 799 (1-2) :309-320
[34]  
LIDE DR, 1998, HDB CHEM PHYS, P6
[35]  
Mahuzier PE, 2001, ELECTROPHORESIS, V22, P3819, DOI 10.1002/1522-2683(200109)22:17<3819::AID-ELPS3819>3.0.CO
[36]  
2-E
[37]   Selective and quantitative analysis of 4-hydroxybenzoate preservatives by microemulsion electrokinetic chromatography [J].
Mahuzier, PE ;
Altria, KD ;
Clark, BJ .
JOURNAL OF CHROMATOGRAPHY A, 2001, 924 (1-2) :465-470
[38]   Mass spectrometry of selected components of biological interest in green tea extracts [J].
Miketova, P ;
Schram, KH ;
Whitney, JL ;
Kerns, EH ;
Valcic, S ;
Timmermann, BN ;
Volk, KJ .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (04) :461-467
[39]   The use of microemulsion electrokinetic chromatography in pharmaceutical analysis [J].
Miola, MF ;
Snowden, MJ ;
Altria, KD .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 18 (4-5) :785-797
[40]   Protective activity of green tea against free radical- and glucose-mediated protein damage [J].
Nakagawa, T ;
Yokozawa, T ;
Terasawa, K ;
Shu, S ;
Juneja, LR .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (08) :2418-2422