食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2014年
3期
801-807
,共7页
蔡增轩%胡玲玲%王军淋%柳家鹏%任一平
蔡增軒%鬍玲玲%王軍淋%柳傢鵬%任一平
채증헌%호령령%왕군림%류가붕%임일평
奶制品%黄曲霉毒素M1%黄曲霉毒素M2%超高效液相色谱法%大体积流通池
奶製品%黃麯黴毒素M1%黃麯黴毒素M2%超高效液相色譜法%大體積流通池
내제품%황곡매독소M1%황곡매독소M2%초고효액상색보법%대체적류통지
milk products%aflatoxin M1%aflatoxin M2%ultra high performance liquid chromatography%large volume flow cell
目的:建立一种免疫亲和柱净化-超高效液相色谱法同时测定奶及奶制品中M族黄曲霉毒素的方法。方法以乙腈为提取剂和蛋白沉淀剂,采用涡旋混合及超声提取,免疫亲和柱净化。结果经 Welch Ultimate XB-C18色谱柱(100 mm×2.1 mm,1.8μm)分离,应用大体积流通池荧光检测,流动相为水和乙腈/甲醇(1:1)。线性范围在0.01~5.00 ng/mL之间,线性系数均大于0.999,黄曲霉毒素M1、M2的检出限为0.003μg/kg。免疫亲和柱对黄曲霉毒素M1、M2的回收率均在80%以上,液态奶中添加0.05、0.2、1.0μg/kg的回收率在85.6%~106.4%之间,奶粉中添加0.5、2.0、10.0μg/kg的回收率在81.5%~93.4%之间。结论该方法可以适用于奶粉、液态奶中M族黄曲霉毒素检测。
目的:建立一種免疫親和柱淨化-超高效液相色譜法同時測定奶及奶製品中M族黃麯黴毒素的方法。方法以乙腈為提取劑和蛋白沉澱劑,採用渦鏇混閤及超聲提取,免疫親和柱淨化。結果經 Welch Ultimate XB-C18色譜柱(100 mm×2.1 mm,1.8μm)分離,應用大體積流通池熒光檢測,流動相為水和乙腈/甲醇(1:1)。線性範圍在0.01~5.00 ng/mL之間,線性繫數均大于0.999,黃麯黴毒素M1、M2的檢齣限為0.003μg/kg。免疫親和柱對黃麯黴毒素M1、M2的迴收率均在80%以上,液態奶中添加0.05、0.2、1.0μg/kg的迴收率在85.6%~106.4%之間,奶粉中添加0.5、2.0、10.0μg/kg的迴收率在81.5%~93.4%之間。結論該方法可以適用于奶粉、液態奶中M族黃麯黴毒素檢測。
목적:건립일충면역친화주정화-초고효액상색보법동시측정내급내제품중M족황곡매독소적방법。방법이을정위제취제화단백침정제,채용와선혼합급초성제취,면역친화주정화。결과경 Welch Ultimate XB-C18색보주(100 mm×2.1 mm,1.8μm)분리,응용대체적류통지형광검측,류동상위수화을정/갑순(1:1)。선성범위재0.01~5.00 ng/mL지간,선성계수균대우0.999,황곡매독소M1、M2적검출한위0.003μg/kg。면역친화주대황곡매독소M1、M2적회수솔균재80%이상,액태내중첨가0.05、0.2、1.0μg/kg적회수솔재85.6%~106.4%지간,내분중첨가0.5、2.0、10.0μg/kg적회수솔재81.5%~93.4%지간。결론해방법가이괄용우내분、액태내중M족황곡매독소검측。
Objectives To develop the method of simultaneous determination of M aflatoxins in milk and milk products by ultra high performance liquid chromatography (UPLC) coupled with immunoaffinity column (IAC) clean-up. Methods Samples were extracted with acetonitrile after vortex mixing and ul-trasound, meanwhile, acetonitrile was used as an protein precipitant, then extraction solution was clean-up with IAC. Results The analytes were separated on Welch Ultimate XB-C18 (100 mm×2.1 mm, 1.8 μm), and eluted with a mobile phase consisting of (a) waters and (b) acetonitrile: methanol (50: 50, v/v). The separated compounds were detected with fluorescence detection (FLD) equipped with a large volume flow cell. Meanwhile, high correlation coefficient (R2>0.999) was obtained within linear range from 0.01 to 5.0 ng/mL, and the limits of determination (LOD) of M aflatoxins were 0.003 μg/kg. Reasonable recove-ries (above 80%) were demonstrated for aflatoxin M1 and M2 with aflatoxin M1 immunoaffinity column, and recoveries (85.6%~106.4%) were in 3 spiked levels (0.05, 0.2, 1.0 μg/kg) for milk, and recoveries (81.5%~93.4%) were in 3 spiked levels (0.5, 2. 0, 10.0 μg/kg) for milk powder. Conclusion This quan-titative method can be applied to the determination and quantification of M aflatoxins in milk and milk products.