广州化学
廣州化學
엄주화학
GUANGZHOU CHEMISTRY
2011年
3期
17-21
,共5页
缪璐%郭振华%莫佳琳%温韬%干宁军
繆璐%郭振華%莫佳琳%溫韜%榦寧軍
무로%곽진화%막가림%온도%간저군
超高效液相色谱%荧光检测器%罗丹明B
超高效液相色譜%熒光檢測器%囉丹明B
초고효액상색보%형광검측기%라단명B
ultra performance liquid chromatography%fluorescence detector%Rhodamine B
建立了固相萃取净化超高效液相荧光测定调味品中罗丹明B的方法。样品中的罗丹明B经水提取,Strata-X-CW SPE柱萃取净化,用超高效液相色谱(荧光检测器)进行测定。结果表明:罗丹明B在0.1~1 000.0 ng/mL范围内呈现良好的线性关系,相关系数为0.999 86;在1.0~100.0μg/kg添加水平时,平均回收率为72.0%~96.5%,相对标准偏差为1.9%~5.2%(n=6);定量检出限为0.1μg/kg。该方法灵敏度高,重复性好,快速,适用于调味品中罗丹明B的检测。
建立瞭固相萃取淨化超高效液相熒光測定調味品中囉丹明B的方法。樣品中的囉丹明B經水提取,Strata-X-CW SPE柱萃取淨化,用超高效液相色譜(熒光檢測器)進行測定。結果錶明:囉丹明B在0.1~1 000.0 ng/mL範圍內呈現良好的線性關繫,相關繫數為0.999 86;在1.0~100.0μg/kg添加水平時,平均迴收率為72.0%~96.5%,相對標準偏差為1.9%~5.2%(n=6);定量檢齣限為0.1μg/kg。該方法靈敏度高,重複性好,快速,適用于調味品中囉丹明B的檢測。
건립료고상췌취정화초고효액상형광측정조미품중라단명B적방법。양품중적라단명B경수제취,Strata-X-CW SPE주췌취정화,용초고효액상색보(형광검측기)진행측정。결과표명:라단명B재0.1~1 000.0 ng/mL범위내정현량호적선성관계,상관계수위0.999 86;재1.0~100.0μg/kg첨가수평시,평균회수솔위72.0%~96.5%,상대표준편차위1.9%~5.2%(n=6);정량검출한위0.1μg/kg。해방법령민도고,중복성호,쾌속,괄용우조미품중라단명B적검측。
Solid phase extraction followed by ultra performance liquid chromatography(UPLC) with fluorescence detector method was developed for the analysis of Rhodamine B in condiment.The separation of Rhodamine B from samples was extracted by water,and purified by Strata-X-CW SPE column,and determined by UPLC with fluorescence detector(FLD).The calibration curve of the method was linear over the range of 1.0 to 1 000.0 ng/mL with a correlation coefficient of 0.999 86.The recoveries for Rhodamine B standard spiked in the range of 1.0 to 100.0 μg/kg were between 72.0% and 96.5% with a relative standard deviation(RSD) being between 1.9% and 5.2%(n=6).The detection limit was 0.1 μg/kg.Owing to advantages of good linearity,low limit of detection,high precision and rapidity,this method is suitable for the determination of Rhodamine B in condiment.