食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
Journal of Food Safety & Quality
2015年
10期
3804-3809
,共6页
路杨%吕志强%刘印平%王丽英%常凤启%董彬%杨立新
路楊%呂誌彊%劉印平%王麗英%常鳳啟%董彬%楊立新
로양%려지강%류인평%왕려영%상봉계%동빈%양립신
工业染料%QuEChERS%超高效液相色谱法%豆制品%快速检测
工業染料%QuEChERS%超高效液相色譜法%豆製品%快速檢測
공업염료%QuEChERS%초고효액상색보법%두제품%쾌속검측
dye%QuECHERS%ultra performance liquid chromatography%bean products%rapid detection
目的:建立了豆皮、豆腐、腐竹及豆干4种豆制品中的9种工业染料的检测方法。方法以QuEChERS方法作为前处理技术,以超高效液相色谱技术作为检测技术,对方法的有效性进行了验证,并对实际样品进行检测。结果以空白的4种豆制品为基质,分别在3个水平进行加标实验,回收率分别在71.5%~126.4%、74.0%~106.5%、86%~124.5%和76.7%~107.5%之间。RSD (n=5)分别在1.9%~8.5%、1.8%~8.1%、1.8%~7.0%之间和1.7%~8.0%之间。各工业染料的检出限(S/N=3)在0.05~0.2 mg/kg之间,定量限(S/N=10)在0.15~0.6 mg/kg之间。结论该方法操作简单,稳定性好,适于在实际检测工作中推广应用。
目的:建立瞭豆皮、豆腐、腐竹及豆榦4種豆製品中的9種工業染料的檢測方法。方法以QuEChERS方法作為前處理技術,以超高效液相色譜技術作為檢測技術,對方法的有效性進行瞭驗證,併對實際樣品進行檢測。結果以空白的4種豆製品為基質,分彆在3箇水平進行加標實驗,迴收率分彆在71.5%~126.4%、74.0%~106.5%、86%~124.5%和76.7%~107.5%之間。RSD (n=5)分彆在1.9%~8.5%、1.8%~8.1%、1.8%~7.0%之間和1.7%~8.0%之間。各工業染料的檢齣限(S/N=3)在0.05~0.2 mg/kg之間,定量限(S/N=10)在0.15~0.6 mg/kg之間。結論該方法操作簡單,穩定性好,適于在實際檢測工作中推廣應用。
목적:건립료두피、두부、부죽급두간4충두제품중적9충공업염료적검측방법。방법이QuEChERS방법작위전처리기술,이초고효액상색보기술작위검측기술,대방법적유효성진행료험증,병대실제양품진행검측。결과이공백적4충두제품위기질,분별재3개수평진행가표실험,회수솔분별재71.5%~126.4%、74.0%~106.5%、86%~124.5%화76.7%~107.5%지간。RSD (n=5)분별재1.9%~8.5%、1.8%~8.1%、1.8%~7.0%지간화1.7%~8.0%지간。각공업염료적검출한(S/N=3)재0.05~0.2 mg/kg지간,정량한(S/N=10)재0.15~0.6 mg/kg지간。결론해방법조작간단,은정성호,괄우재실제검측공작중추엄응용。
ABSTRACT:Objective To establish a method for the detection of 9 kinds of industrial dyes in Yuba, tofu, beancurd sticks,and dried tofu .MethodsThe validity of the method was validated, which used to the actual sample, with QuEChERS as a pretreatment technology and ultra-high performance liquid chromatography as detection method.Results Blank bean products material were used as matrixes, and spiking experiments were carried out in high, medium and low level, respectively. Recoveries were between 71.5% to 126.4%, 74.0% to 106.5%, 86% to 124.5% and 76.7%~107.5%. RSD (n=5) were between 1.9% to 8.5%, 1.8% to 8.1%, 1.8% to 7.0% and 1.7% to 8.0%, the limits of detection (S/N=3) were between 0.05~0.2 mg/kg and the limit of quantification (S/N=10) was between 0.15~0.6 mg/kg. ConclusionThe method is simple to operate with a good stability and is suitable for the application in daily testing work.