Zhao Yonggang, Chen Xiaohong, Li Xiaoping, Yao Shanshan, Jin Micong
Ningbo Municipal Center for Disease Control and Prevention, Ningbo Key Laboratory of Poison Research and Control, Ningbo 315010, China.
Se Pu. 2011 Oct;29(10):988-94.
The influences of ion-suppressors on retention behaviors of nine food additives, i.e., acesulfame, saccharin, caffeine, aspartame, benzoic acid, sorbic acid, stevioside, dehydroacetic acid and neotame in reversed-phase high performance liquid chromatographic (RP-HPLC) separation were investigated. The organic modification effects of acids, i. e. , trifluoroacetic acid (TFA) and buffer salts, i. e. , TFA-ammonium acetate (AmAc) were studied emphatically. The relationships between retention factors of solutes and volume percentages of ion-suppressors in the mobile phase systems of acetonitrile-TFA aqueous solution and acetonitrile-TFA-AmAc aqueous solution were quantitatively established, separately. The separation of nine food additives was completed by a gradient elution with acetonitrile-TFA (0.01%, v/v)-AmAc (2. 5 mmol/L) aqueous solution as the mobile phases. An RP-HPLC method was established for the simultaneous determination of nine food additives in red wine. In the range of 10. 0 - 100. 0 mg/L, nine food additives showed good linearity with the correlation coefficients ( r2 ) larger than 0. 999 1. The limits of detection (LODs) were in the range of 0. 33 - 2. 36 mg/L and the limits of quantification (LOQs) were in the range of 1. 11 - 7. 80 mg/L. The spiked recoveries were between 87. 61% and 108. 4% with the relative standard deviations (RSDs) of 2. 2% -9. 4%. These results are of referential significance for the rapid establishment and accu- rate optimization of RP-HPLC separation for the simultaneous determination of food additives in other foods.
研究了离子抑制剂对9种食品添加剂(乙酰磺胺酸钾、糖精、咖啡因、阿斯巴甜、苯甲酸、山梨酸、甜菊糖苷、脱氢乙酸和纽甜)在反相高效液相色谱(RP-HPLC)分离中保留行为的影响。重点研究了酸(即三氟乙酸(TFA))和缓冲盐(即TFA-乙酸铵(AmAc))的有机改性效果。分别定量建立了溶质保留因子与乙腈-TFA水溶液和乙腈-TFA-AmAc水溶液流动相体系中离子抑制剂体积百分比之间的关系。以乙腈-TFA(0.01%,v/v)-AmAc(2.5 mmol/L)水溶液为流动相进行梯度洗脱,完成了9种食品添加剂的分离。建立了一种RP-HPLC方法用于同时测定红酒中的9种食品添加剂。在10.0 - 100.0 mg/L范围内,9种食品添加剂呈现良好的线性,相关系数(r2)大于0.999 1。检测限(LOD)在0.33 - 2.36 mg/L范围内,定量限(LOQ)在1.11 - 7.80 mg/L范围内。加标回收率在87.61%至108.4%之间,相对标准偏差(RSD)为2.2% - 9.4%。这些结果对于快速建立和准确优化RP-HPLC分离以同时测定其他食品中的食品添加剂具有参考意义。