中国调味品
中國調味品
중국조미품
CHINESE CONDIMENT
2014年
4期
124-127
,共4页
陈勇%花锦%潘亚利%王静慧%刘海峰
陳勇%花錦%潘亞利%王靜慧%劉海峰
진용%화금%반아리%왕정혜%류해봉
超高效液相色谱-电喷雾串联质谱%工业染料%调味品%熟肉制品
超高效液相色譜-電噴霧串聯質譜%工業染料%調味品%熟肉製品
초고효액상색보-전분무천련질보%공업염료%조미품%숙육제품
Ultra Performance Liquid Chromatography and Electrospray Tandem Mass Spectrometry%industrial dyes%condiments%cooked meat products
建立了超高效液相色谱-电喷雾串联质谱法(UPLC-MS/MS)测定调味品与熟肉制品中碱性橙Ⅱ、碱性橙21、碱性橙22、酸性橙Ⅱ、酸性红1号和碱性玫瑰精6种工业染料分析方法。样品用V(乙腈)∶V(水)7∶3的溶液提取,取上清液过滤,以 BEH C18柱(1.7μm,2.1×50 mm)为分离柱,甲醇和10 mmol/L乙酸铵(含0.1%甲酸)梯度洗脱,在优化的实验条件下,碱性橙Ⅱ、碱性橙21、碱性橙22、酸性橙Ⅱ和碱性玫瑰精的检出限均为0.5μg/kg ,定量限为1μg/kg;酸性红1号检出限为50μg/kg ,定量限为100μg/kg;碱性橙Ⅱ、碱性橙21、碱性橙22、酸性橙Ⅱ和碱性玫瑰精的线性范围为1~50μg/kg,相关系数均大于0.99。酸性红1号的线性范围为50~1000μg/kg,相关系数大于0.99。样品在三个添加水平下平均回收率在75.6%~99.7%之间,相对标准偏差在0.9%~10.7%。可用于调味品与熟肉制品中6种工业染料的检测。
建立瞭超高效液相色譜-電噴霧串聯質譜法(UPLC-MS/MS)測定調味品與熟肉製品中堿性橙Ⅱ、堿性橙21、堿性橙22、痠性橙Ⅱ、痠性紅1號和堿性玫瑰精6種工業染料分析方法。樣品用V(乙腈)∶V(水)7∶3的溶液提取,取上清液過濾,以 BEH C18柱(1.7μm,2.1×50 mm)為分離柱,甲醇和10 mmol/L乙痠銨(含0.1%甲痠)梯度洗脫,在優化的實驗條件下,堿性橙Ⅱ、堿性橙21、堿性橙22、痠性橙Ⅱ和堿性玫瑰精的檢齣限均為0.5μg/kg ,定量限為1μg/kg;痠性紅1號檢齣限為50μg/kg ,定量限為100μg/kg;堿性橙Ⅱ、堿性橙21、堿性橙22、痠性橙Ⅱ和堿性玫瑰精的線性範圍為1~50μg/kg,相關繫數均大于0.99。痠性紅1號的線性範圍為50~1000μg/kg,相關繫數大于0.99。樣品在三箇添加水平下平均迴收率在75.6%~99.7%之間,相對標準偏差在0.9%~10.7%。可用于調味品與熟肉製品中6種工業染料的檢測。
건립료초고효액상색보-전분무천련질보법(UPLC-MS/MS)측정조미품여숙육제품중감성등Ⅱ、감성등21、감성등22、산성등Ⅱ、산성홍1호화감성매괴정6충공업염료분석방법。양품용V(을정)∶V(수)7∶3적용액제취,취상청액과려,이 BEH C18주(1.7μm,2.1×50 mm)위분리주,갑순화10 mmol/L을산안(함0.1%갑산)제도세탈,재우화적실험조건하,감성등Ⅱ、감성등21、감성등22、산성등Ⅱ화감성매괴정적검출한균위0.5μg/kg ,정량한위1μg/kg;산성홍1호검출한위50μg/kg ,정량한위100μg/kg;감성등Ⅱ、감성등21、감성등22、산성등Ⅱ화감성매괴정적선성범위위1~50μg/kg,상관계수균대우0.99。산성홍1호적선성범위위50~1000μg/kg,상관계수대우0.99。양품재삼개첨가수평하평균회수솔재75.6%~99.7%지간,상대표준편차재0.9%~10.7%。가용우조미품여숙육제품중6충공업염료적검측。
A method has been established for the determination of 6 industrial dyes,Basic OrangeⅡ, Basic Orange 21,Basic Orange 22,Acid Orange Ⅱ,Azophloxine I and Rhodamine Bextra in condi-ments and cooked meat products by ultra performance liquid chromatography combined with electros-pray tandem mass spectrometry (UPLC-MS/MS).Samples are extracted with solution of acetonitrile and water (7∶3).The supernatant is separated on BEH C18 column (1.7μm,2.1 ×50 mm)by gra-dient elution with methanol and 10 mmol/L ammonium acetate with 0.1% (volume ratio)formic acid. Under the optimal experimental conditions,LODs of Basic OrangeⅡ,Basic Orange 21 ,Basic Orange 22,Acid Orange Ⅱ and Rhodamine Bextra are all 0.5μg/kg,LOQs are all 1μg/kg;LOD of Azo-phloxineI is 50μg/kg,and LOQ is 100μg/kg .The method shows a good linearity of Basic OrangeⅡ, Basic Orange 21,Basic Orange 22,Acid Orange Ⅱand Rhodamine Bextra in the range of 1~50μg/kg with correlation coefficients more than 0 .9 9;The range of linearity and correlation coefficient of Azo-phloxine I are respectively 50~100μg/kg and more than 0.99.Recoveries for samples spiked at three levels range from 7 5 .6%to 9 9 .7%with RSDs from 0 .9%to 1 0 .7%.This method is suitable for the determination of industrial dyes in condiments and cooked meat products.