分析测试学报
分析測試學報
분석측시학보
JOURNAL OF INSTRUMENTAL ANALYSIS
2009年
7期
838-841
,共4页
蒋奕修%魏瑞霞%杨桂珍%罗晓东%李秀英%谢天尧
蔣奕脩%魏瑞霞%楊桂珍%囉曉東%李秀英%謝天堯
장혁수%위서하%양계진%라효동%리수영%사천요
磺胺类人工合成甜味剂%毛细管电泳%电导检测%糖精钠%安赛蜜%甜蜜素
磺胺類人工閤成甜味劑%毛細管電泳%電導檢測%糖精鈉%安賽蜜%甜蜜素
광알류인공합성첨미제%모세관전영%전도검측%당정납%안새밀%첨밀소
sulfanilamide artificial sweetener%capillary electrophoresis%conductivity detection%saccharin sodium%acesulfame potassium%sodium cyclamate
采用15 mmol/L Tris-10 mmol/L H3BO3-0.2 mmol/L EDTA为电泳运行液,0.2%四乙烯五胺为电渗流抑制剂,融硅石英毛细管(45 cm×50 μm),负高压分离(-15 kV),柱端接触式电导检测,建立了磺胺类人工合成甜味剂(糖精钠、安赛蜜、甜蜜素)的高效毛细管电泳/电导法分离检测方法.糖精钠、安赛蜜、甜蜜素的线性检测范围分别为0.8 ~120、1.1 ~120、1.5 ~120 μmol/L,检出限分别为0.3、0.4、0.6 μmol/L.详细讨论了电泳运行液的组成、浓度以及进样方式对灵敏度和分离度的影响.该法用于市售饮料中3种甜味剂的分离检测,结果满意.
採用15 mmol/L Tris-10 mmol/L H3BO3-0.2 mmol/L EDTA為電泳運行液,0.2%四乙烯五胺為電滲流抑製劑,融硅石英毛細管(45 cm×50 μm),負高壓分離(-15 kV),柱耑接觸式電導檢測,建立瞭磺胺類人工閤成甜味劑(糖精鈉、安賽蜜、甜蜜素)的高效毛細管電泳/電導法分離檢測方法.糖精鈉、安賽蜜、甜蜜素的線性檢測範圍分彆為0.8 ~120、1.1 ~120、1.5 ~120 μmol/L,檢齣限分彆為0.3、0.4、0.6 μmol/L.詳細討論瞭電泳運行液的組成、濃度以及進樣方式對靈敏度和分離度的影響.該法用于市售飲料中3種甜味劑的分離檢測,結果滿意.
채용15 mmol/L Tris-10 mmol/L H3BO3-0.2 mmol/L EDTA위전영운행액,0.2%사을희오알위전삼류억제제,융규석영모세관(45 cm×50 μm),부고압분리(-15 kV),주단접촉식전도검측,건립료광알류인공합성첨미제(당정납、안새밀、첨밀소)적고효모세관전영/전도법분리검측방법.당정납、안새밀、첨밀소적선성검측범위분별위0.8 ~120、1.1 ~120、1.5 ~120 μmol/L,검출한분별위0.3、0.4、0.6 μmol/L.상세토론료전영운행액적조성、농도이급진양방식대령민도화분리도적영향.해법용우시수음료중3충첨미제적분리검측,결과만의.
A new method for the rapid separation and sensitive determination of sulfanilamide artificial sweeteners,including saccharin sodium,acesulfame potassium and sodium cyclamate,by capillary electrophoresis with conductivity detection was developed.The optimum conditions were as follows:running buffer:15 mmol/L Tris-10 mmol/L H3BO3-0.2 mmol/L EDTA,electrocsmotic flow(EOF) inhibitor:0.2% tetraethylenepentamine,separation voltage:-15 kV,electrokinetic injection:-10 kV×10 s.Three analytes could be well separated within 11 min in a fused-silica capillary under the optimal conditions.The linear response ranges were 0.8-120,1.1-120,1.5-120 μmol/L with the LODs of 0.3,0.4,0.6 μmol/L for saccharin sodium,acesulfame potassium and sodium cyclamate,respectively.The relative standard deviations for the intra- and inter- day precisions were below 4.0%.Effects of the component of the running buffer and its concentration,and the injection mode on the sensitivity and separation for the method were discussed in detail.The established method was used to determine the analytes contents in different commercial beverages with satisfactory results.