王川丕,孙文闪,董叶箐,钟寒辉,郑剑峰,俞 婕,刘 静,林 婷.复合固相萃取净化-液相色谱法同时测定奶粉中的5种核苷酸[J].食品安全质量检测学报,2021,12(15):5997-6002
复合固相萃取净化-液相色谱法同时测定奶粉中的5种核苷酸
Simultaneous determination of 5 kinds of nucleotides in milk powder by liquid chromatography with composite solid phase extraction
投稿时间:2021-03-31  修订日期:2021-07-29
DOI:
中文关键词:  液相色谱法  复合固相萃取  核苷酸  奶粉
英文关键词:liquid chromatography  composite solid phase extraction  nucleotides  milk powder
基金项目:国家重点研发计划资助项目(2018YFC1602800)
作者单位
王川丕 绿城农科检测技术有限公司 
孙文闪 绿城农科检测技术有限公司 
董叶箐 绿城农科检测技术有限公司 
钟寒辉 绿城农科检测技术有限公司 
郑剑峰 绿城农科检测技术有限公司 
俞 婕 绿城农科检测技术有限公司 
刘 静 绿城农科检测技术有限公司 
林 婷 绿城农科检测技术有限公司 
AuthorInstitution
WANG Chuan-Pi Greentown Agricultural Testing Technology Co., Ltd 
SUN Wen-Shan Greentown Agricultural Testing Technology Co., Ltd 
DONG Ye-Jing Greentown Agricultural Testing Technology Co., Lt d 
ZHONG Han-Hui Greentown Agricultural Testing Technology Co., Ltd 
ZHENG Jian-Feng Greentown Agricultural Testing Technology Co., Ltd 
YU-Jie Greentown Agricultural Testing Technology Co., Ltd 
LIU Jing Greentown Agricultural Testing Technology Co., Ltd 
LIN Ting Greentown Agricultural Testing Technology Co., Ltd 
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中文摘要:
      目的 建立复合固相萃取净化-液相色谱法同时测定婴幼儿配方奶粉中的5种核苷酸含量的分析方法。方法 样品用纯水涡旋提取, 10%乙酸水溶液调pH到4.1, 离心将上清液全部转移到25 mL容量瓶中, 用纯水定容, 混匀。提取液用复合固相萃取小柱(弱阴离子交换和强阳离子交换固相萃取小柱)净化, 以磷酸盐缓冲液和甲醇为流动相, 等度洗脱, Spursil C18柱(250 mm×4.6 mm, 5 μm)色谱分离, 液相色谱-紫外检测器进行测定, 外标法定量。结果 5种核苷酸在一定范围内(0.1~10 mg/L、0.2~20 mg/L)线性关系良好, 相关系数均大于0.999, 定量限为1.0、2.0 mg/kg, 检出限为0.3、0.6 mg/kg。3水平加标浓度(1.0、5.0、10.0 mg/kg, 2.0、10.0、20.0 mg/kg)的回收率在91.0%~103%之间, 精密度在8%以内。结论 该方法具有操作简单、灵敏度高、重现性好等特点, 为奶粉中核苷酸含量测定提供一个简单准确的方法。
英文摘要:
      Objective To establish a method for the simultaneous determination of 5 kinds of nucleotides in infant formula by liquid chromatography (LC) with composite solid phase extraction. Methods The sample was extracted with ultrapure water in vortex. The pH was adjusted to 4.1 with 10% acetic acid water. The supernatant was centrifugally transferred to 25 mL volumetric flask, constanted to scale mark with ultrapure water, and mixed well. The extract was purified by composite solid-phase extraction column (weak anion exchange and strong cation exchange solid-phase extraction column). Phosphate buffer and methanol were used as mobile phase on isocratic elution. spursil C18 column (250 mm×4.6 mm, 5 μm) was used for chromatographic separation and quantification by external standard method. Results Under the optimized conditions, good linearity (0.1-10 mg/L, 0.2-20 mg/L) was observed for nucleotides. The quantitative limits were 1.0 and 2.0 mg/kg, and the detection limits of the method were 0.3 and 0.6 mg/kg. The method recoveris at the three standard levels (1.0, 5.0 and 10.0 mg/kg; 2.0, 10.0 and 20.0 mg/kg) were between 91.0%-103% and the precision was within 8%. Conclusion The method has the characteristics of simple operation, high sensitivity and good reproducibility, which provides a simple and accurate method for the determination of nucleotide content in infant formula.
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