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机构地区:[1]河北省食品检验研究院,河北省食品安全重点实验室,河北石家庄050091 [2]河北衡水中学,河北衡水053000 [3]河北出入境检验检疫局,检验检疫技术中心,河北石家庄050051
出 处:《乳业科学与技术》2016年第2期17-20,共4页JOURNAL OF DAIRY SCIENCE AND TECHNOLOGY
基 金:河北省科技计划项目(15275505D)
摘 要:建立液态乳中2种紫外吸收剂(UV-326和UV-1577)和2种抗氧化剂(AO-1010、AO-2246)的高效液相色谱测定方法。前处理采用乙腈提取液态乳中目标化合物,样品用正己烷提取;检测经Agilent HC—C。反相色谱柱,以乙腈一水作为流动相,梯度洗脱程序进行分离,280nm波长下检测。结果表明:分析物在0.05-50μg/mL质量浓度范围内线性关系良好,线性相关系数〉0.9995,方法检出限为0.02~0.5mg/kg。方法在3个水平的加标回收率为69.08%~115.87%,相对标准偏差为0.43%-9.94%。该方法操作简单、灵敏度高、重现性好,适用于液态乳中紫外吸收剂和抗氧化剂的同时测定。A method was developed for the simultaneous determination of 2 ultraviolet absorbers UV-326, UV-1577 and 2 antioxidants AO-1010 and AO-2246 in milk by high performance liquid chromatography. Samples were extracted with acetonitrile. The effective separation of the target analytes was accomplished on Agilent HC-C8 (150 mm - 4.6 mm, 5.0 μm) column with gradient elution procedure using a mixture of water and acetonitrile as the mobile phase. External calibration was used for quantitative determination at detection wavelength of 280 nm. The linearity of 4 analytes were satisfactory with a correlation coefficient of 〉 0.9995 at concentrations ranging from 0.05 to 50 ktg/mL. The limits of detection of the method were 0.02-0.5 mg/kg, and the recoveries at different spiked levels and precision (RSD) were 69.08%-115.87% and 0.43%4.94%, respectively. The method is simple, sensitive, reproducible and suitable for the simultaneous determination of 2 ultraviolet absorbers and 2 antioxidants in milk.
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