高效液相色谱-柱后光化学衍生-荧光检测法测定强化食品中的叶酸  被引量:4

Determination of folic acidin fortified foods by high performance liquid chromatography with post-column photochemical derivatization

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作  者:赵海燕[1] 杨永红[1] 刘泰然[1] 李兵[1] 赵榕[1] 

机构地区:[1]北京市疾病预防控制中心,北京100013

出  处:《中国食品卫生杂志》2014年第4期347-350,共4页Chinese Journal of Food Hygiene

摘  要:目的建立柱后光化学衍生一高效液相色谱法(HPLC)测定强化食品中叶酸的分析方法。方法采用SunFireC18(4.6mm×250mm,5μm)色谱柱,以乙腈-50mmol/L磷酸二氢钾溶液(pH=5.0)为流动相梯度洗脱,叶酸在254nm紫外光照射下进行柱后衍生,荧光检测器检测,激发和发射波长分别为344和428nm。结果本方法的线性范围为0.01~2.0μg/ml,r=0.9999;方法的定性检出限和定量检出限分别为0.01和0.03μg/g;加标回收率为90.0%.98.0%,RSD均小于5%。结论本方法简便、快速、准确、重现性好,适用于强化食品中叶酸含量的测定。Objective To establish a method for the determination of folic acid in fortified foods by high performance liquid chromatography (HPLC) with postcolumn photochemical derivatization. Methods Chromatographic separation was carried out using a SunFire C18 column (4. 6 mm× 250 mm, 5 μm). The mobile phases was acetonitrile and 50 mmol/L potassium dihydrogen phosphate solution (pH = 5.0 ) with an optimized gradient elution. Post-column photochemical derivatization of folic acid was under UV-light irradiation at 254 nm. The fluorescence detection was performed with the excitation at 344 nm and the emission at 428 nm. Results The linear range was 0.01-2.0 μg/ml, r = 0. 999 9. The limit of detection (LOD) was 0.01 μg/g and the limit of quantification (LOQ) was 0.03 μg/g. The average recoveries were 90.0%-98.0% and the RSD of the method was less than 5%. Conclusion The method was simple, rapid, accurate, reproducible, and suitable for the determination of folic acid in fortified foods.

关 键 词:高效液相色谱 柱后光化学衍生 叶酸 强化食品 强化营养素 

分 类 号:O657[理学—分析化学] TS207.3[理学—化学]

 

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