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
9期
2697-2704
,共8页
谢继安%刘柏林%冯慧%赵紫微%韦莹
謝繼安%劉柏林%馮慧%趙紫微%韋瑩
사계안%류백림%풍혜%조자미%위형
超高效液相色谱-串联质谱(UPLC-MS/MS)%环己基氨基磺酸钠%甜蜜素%食品
超高效液相色譜-串聯質譜(UPLC-MS/MS)%環己基氨基磺痠鈉%甜蜜素%食品
초고효액상색보-천련질보(UPLC-MS/MS)%배기기안기광산납%첨밀소%식품
ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)%sodium cyclamate%(beet) molasses%food
目的:建立食品中环己基氨基磺酸钠(甜蜜素)的超高效液相色谱-串联质谱(UPLC-MS/MS)检测方法。方法样品经水溶液溶解,超声提取,高速离心后取上清液供UPLC-MS/MS检测,采用电喷雾电离,负离子扫描,多反应检测模式(MRM),外标法定量。结果环己基氨基磺酸钠的线性范围为1.0~200μg/L,相关系数r≥0.999,最低检出限为0.01 mg/kg。3个不同水平(0.05 mg/kg、0.2 mg/kg和1.0 mg/kg)的加标平均回收率为82.8%~103.5%,相对标准偏差小于10%。结论所建立的方法具有较好的回收率和精密度,准确度和灵敏度高,符合食品中环己基氨基磺酸钠的检测要求,为大通量样品的食品安全检测提供了更灵敏、高效的技术支持。
目的:建立食品中環己基氨基磺痠鈉(甜蜜素)的超高效液相色譜-串聯質譜(UPLC-MS/MS)檢測方法。方法樣品經水溶液溶解,超聲提取,高速離心後取上清液供UPLC-MS/MS檢測,採用電噴霧電離,負離子掃描,多反應檢測模式(MRM),外標法定量。結果環己基氨基磺痠鈉的線性範圍為1.0~200μg/L,相關繫數r≥0.999,最低檢齣限為0.01 mg/kg。3箇不同水平(0.05 mg/kg、0.2 mg/kg和1.0 mg/kg)的加標平均迴收率為82.8%~103.5%,相對標準偏差小于10%。結論所建立的方法具有較好的迴收率和精密度,準確度和靈敏度高,符閤食品中環己基氨基磺痠鈉的檢測要求,為大通量樣品的食品安全檢測提供瞭更靈敏、高效的技術支持。
목적:건립식품중배기기안기광산납(첨밀소)적초고효액상색보-천련질보(UPLC-MS/MS)검측방법。방법양품경수용액용해,초성제취,고속리심후취상청액공UPLC-MS/MS검측,채용전분무전리,부리자소묘,다반응검측모식(MRM),외표법정량。결과배기기안기광산납적선성범위위1.0~200μg/L,상관계수r≥0.999,최저검출한위0.01 mg/kg。3개불동수평(0.05 mg/kg、0.2 mg/kg화1.0 mg/kg)적가표평균회수솔위82.8%~103.5%,상대표준편차소우10%。결론소건립적방법구유교호적회수솔화정밀도,준학도화령민도고,부합식품중배기기안기광산납적검측요구,위대통량양품적식품안전검측제공료경령민、고효적기술지지。
Objective To establish an ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of sodium cyclamate in food. Methods The samples were extracted with water and ultrasonic-assisted, after high speed centrifuged and determined by UPLC-MS/MS. Identification was achieved by electrospray ionization in negative mode (ESI-) using multiple reaction monitoring (MRM). The quantification was performed by external standard method. Results The sodium cyclamate from 1.0μg/L to 200μg/L showed an excellent linear relationship (r≥0.999). The limit of detection of the sodium cyclamate was 0.01mg/kg. The average recoveries were 82.8%~103.5% at the spiked three concentration levels (add 0.05 mg/kg, 0.2 mg/kg and 1.0 mg/kg). The relative standard deviations (RSD) was less than 10%. Conclusion The established method has a good recovery and precision, high accuracy and sensitivity, and comply with the regulations for the determination of sodium cyclamate in food, provided more sensitive and efficient technical support of the large throughput sample for food safety determination.