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Development and Validation of HPLC-DAD Method for Simultaneous Determination of Seven Food Additives and Caffeine in Powdered Drinks

机译:HPLC-DAD方法的开发与验证同时测定七种食品添加剂和粉末饮料中的咖啡因

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摘要

The usage of food additives must respect the general legislation in force in the country and requires a reliable analytical method for surveillance. This research aimed to develop a high-performance liquid chromatography with diode array detection (HPLC-DAD) method for the simultaneous determination of seven food additives and caffeine in powdered drinks. Three factors likely to affect the chromatographic separation, namely, mobile phase composition at the beginning ( , 0–10% of the amount of methanol in the phosphate buffer) and the end ( , 60–100% of the amount of methanol in the phosphate buffer) of the gradient program and pH ( , 3–7), were evaluated with the aid of a Box–Behnken Design (BBD). Subsequently, multi-response optimizations for chromatographic resolutions ( ) and analysis time were performed using the response surface methodology (RSM) in conjunction with the desirability function (DF). Complete separation ( > 1.5) of seven food additives and caffeine was achieved in less than 16 min by applying 8.5% methanol in the phosphate buffer at the beginning and 90% at the end of the gradient program, in pH 6.7. The developed method was validated with low limits of detection (ranging from 1.16 mg kg (sodium saccharin) to 3.00 mg kg (acesulfame potassium)), low limits of quantification (ranging from 3.86 mg kg (sodium saccharin) to 10.02 mg kg (acesulfame potassium)), high precision (CV < 4%), and high accuracy (recoveries from 95 to 101% at 80, 100, and 120% of the target concentration). The method was successfully used to assess the seven food additives and caffeine in commercially available powdered drinks.
机译:食品添加剂的使用必须尊重该国的一般立法,并需要一种可靠的监督方法。该研究旨在开发具有二极管阵列检测(HPLC-DAD)方法的高性能液相色谱法,用于同时测定粉末饮料中的七种食品添加剂和咖啡因。可能影响色谱分离的三个因素,即在开始时的流动相组合物(磷酸盐缓冲液中甲醇的0-10%)和末端(磷酸盐中甲醇的60-100%借助于Box-Behnken设计(BBD)评估梯度程序和pH(3-7)的缓冲液。随后,使用响应表面方法(RSM)结合期望函数(DF)来执行用于色谱分辨率()和分析时间的多响应优化。通过在梯度计划结束时在梯度计划的磷酸盐缓冲液中施加8.5%甲醇,在pH6.7中在磷酸盐缓冲液中施加8.5%甲醇,在少于16分钟内完成七种食品添加剂和咖啡因的完全分离(> 1.5)。验证了开发的方法,低限制的检测限(1.16mg kg(糖精)至3.00mg kg(乙酰磺酸钾)),低定量限制(范围从3.86mg kg(糖精)至10.02mg kg(aceSulfame钾)),高精度(CV <4%),高精度(回收率为95至101%,在80,100和120%的目标浓度)。该方法已成功用于评估市售粉末饮料中的七种食品添加剂和咖啡因。

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