食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
16期
94-96
,共3页
丁娟芳%樊艳%吕玉珍%韦林洪
丁娟芳%樊豔%呂玉珍%韋林洪
정연방%번염%려옥진%위림홍
超高效液相色谱%双氰胺%原料乳
超高效液相色譜%雙氰胺%原料乳
초고효액상색보%쌍청알%원료유
ultra high performance liquid chromatography%dicyandiamide%saw milk
建立了超高效液相色谱检测原料乳中双氰胺的分析方法。采用甲醇提取样品中的双氰胺,HILICS色谱柱为分析柱,流动相为乙腈-10 mmol/L乙酸铵(90∶10,体积比),流速0.4 mL/min,检测波长230 nm。双氰胺在0.006 mg/L~10.0 mg/L范围内具有良好的线性关系,标准曲线方程为y=90.336x+0.9946,R2=0.9999。方法检出限为0.05 mg/kg,不同添加水平平均回收率在87.0%~91.6%之间,变异系数<3.84%(n=6)。此方法操作简便,可在15 min内完成快速检测,适用于原料乳中双氰胺残留的快速筛查。
建立瞭超高效液相色譜檢測原料乳中雙氰胺的分析方法。採用甲醇提取樣品中的雙氰胺,HILICS色譜柱為分析柱,流動相為乙腈-10 mmol/L乙痠銨(90∶10,體積比),流速0.4 mL/min,檢測波長230 nm。雙氰胺在0.006 mg/L~10.0 mg/L範圍內具有良好的線性關繫,標準麯線方程為y=90.336x+0.9946,R2=0.9999。方法檢齣限為0.05 mg/kg,不同添加水平平均迴收率在87.0%~91.6%之間,變異繫數<3.84%(n=6)。此方法操作簡便,可在15 min內完成快速檢測,適用于原料乳中雙氰胺殘留的快速篩查。
건립료초고효액상색보검측원료유중쌍청알적분석방법。채용갑순제취양품중적쌍청알,HILICS색보주위분석주,류동상위을정-10 mmol/L을산안(90∶10,체적비),류속0.4 mL/min,검측파장230 nm。쌍청알재0.006 mg/L~10.0 mg/L범위내구유량호적선성관계,표준곡선방정위y=90.336x+0.9946,R2=0.9999。방법검출한위0.05 mg/kg,불동첨가수평평균회수솔재87.0%~91.6%지간,변이계수<3.84%(n=6)。차방법조작간편,가재15 min내완성쾌속검측,괄용우원료유중쌍청알잔류적쾌속사사。
An ultra high performance liquid chromatography method was developed for determination of dicyandiamide in saw milk. Dicyandiamide was extracted by methanol, the sample was isolated on a HILIC column,using a mobile phase made up of acetonitrile and 10mmol/L ammonium acetate (90∶10, V/V) at a flow rate of 0.4 mL/min, and detected at 230 nm. Dicyandiamide was well separated with a good linear relationship in the range of 0.006 mg/L-10.0 mg/L,caffeine standard curve equation:y=90.336x+ 0.994 6,R2=0.999 9.The detection limit was 0.05 mg/kg, recovery rate was in the range of 87.0%-91.6%at several spiked levels, and the coefficient of variance of method was less than 3.84%(n=6).This method is simple, the whole determination process was completed within 15 min, making it applicable for analysis in dicyandiamide monitoring programmes in saw milk.