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作 者:王溪 韦娟 朱铭洪[1] 张昊[1] WANG Xi;WEI Juan;ZHU Ming-hong;ZHANG Hao(Jiangsu Provincial Center for Disease Control and Prevention,Jiangsu Nanjing 210009,China)
机构地区:[1]江苏省疾病预防控制中心,江苏南京210009
出 处:《江苏预防医学》2022年第3期277-279,283,共4页Jiangsu Journal of Preventive Medicine
基 金:江苏省医学重点学科(ZDXKA2016008);淮安市突发公共卫生事件应急检测重点实验室开放课题(ETPHI-K-04)。
摘 要:目的 建立1种冷冻饮品中赤藓红简单、准确的高效液相色谱检测法。方法 采用聚酰胺吸附样品中的赤藓红,乙醇-氨水-水溶液(7+2+1)解吸,解吸液蒸发至近干,甲醇-甲酸(6+4)复溶,微孔滤膜过滤后进行高效液相色谱仪检测。C18反相键合固定相色谱柱(250 mm×4.6 mm, 5μm)分离,20 mmol/L乙酸铵水溶液和甲醇为流动相,二极管阵列检测器530 nm作为检测波长,外标法定量。结果 赤藓红在质量浓度0.2~10.0 mg/L范围内线性良好(r>0.999);在冷冻饮品中加入低、中、高3个质量浓度水平标准溶液,加标回收率为89.9%~95.5%,相对标准偏差(RSD)均<5.0%。方法检出限为0.1 mg/kg,定量限为0.3 mg/kg,满足国标要求。结论 建立的方法能够用于冷冻饮品中赤藓红测定,方便快捷,准确可靠。Objective To establish a simple and accurate high performance liquid chromatography(HPLC) method for the determination of erythrosine in frozen drink samples. Methods The erythrosine in samples was absorbed by polyamide, desorbed by ethanol-ammonia-water(7+2+1) mixed solution, evaporated until nearly dry, and re-dissolved by methanol-formic acid(6+4),followed by filtration by microporous membrane, and sent to HPLC for analysis.The separation was performed on a C18 reverse-phase bonded stationary column(250 mm×4.6 mm, 5 μm) with 20 mmol/L ammonium acetate aqueous solution and methanol as mobile phase, and detected by a diode array detector at wavelength of 530 nm.The external standard method was used for quantitative analysis. Results The linearity of erythrosine was good in the mass concentration range of 0.2-10.0 mg/L(r>0.999).The average spiked recoveries of low medium and high levels were 89.9%-95.5% with relative standard deviations(RSD) <5.0%.The limit of detection was 0.1 mg/kg, and the limit of quantification was 0.3 mg/kg, which met the requirements of national standard. Conclusion The established method can be used for the determination of erythrosine in frozen drinks, and the results are accurate and reliable.
分 类 号:R113[医药卫生—公共卫生与预防医学]
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