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
2013年
4期
1015-1019
,共5页
丁岚%马强%李文涛%马会娟%李晶瑞%孟宪双%陈云霞%白桦
丁嵐%馬彊%李文濤%馬會娟%李晶瑞%孟憲雙%陳雲霞%白樺
정람%마강%리문도%마회연%리정서%맹헌쌍%진운하%백화
纸质食品接触材料%亚甲基双硫氰酸酯%迁移量%高压液相色谱法
紙質食品接觸材料%亞甲基雙硫氰痠酯%遷移量%高壓液相色譜法
지질식품접촉재료%아갑기쌍류청산지%천이량%고압액상색보법
food contact paper materials%methylene dithiocyanate%migration%high pressure liquid chro-matography
目的建立纸质食品接触材料中亚甲基双硫氰酸酯迁移量的高压液相色谱测定方法。方法食品模拟物(水、3%乙酸水溶液、10%乙醇水溶液和橄榄油)中的亚甲基双硫氰酸酯通过高压液相色谱进行分离,采用二极管阵列检测器进行测定。水基食品模拟物直接进样,油基食品模拟物经乙腈萃取后进样,外标法定量。结果3种水基食品模拟物中,亚甲基双硫氰酸酯在0.5~50 mg/L范围内线性关系良好,定量下限为0.5 mg/L,平均回收率为88.2%~97.4%,相对标准偏差为0.44%~6.54%;油基食品模拟物中,亚甲基双硫氰酸酯在1.0~20 mg/kg范围内线性关系良好,定量下限为1.0 mg/kg,平均回收率为99.3%~104.7%,相对标准偏差为0.75%~3.15%。结论该方法准确、简便、快速,可用于纸质食品接触材料中亚甲基双硫氰酸酯迁移量的实际检验工作。
目的建立紙質食品接觸材料中亞甲基雙硫氰痠酯遷移量的高壓液相色譜測定方法。方法食品模擬物(水、3%乙痠水溶液、10%乙醇水溶液和橄欖油)中的亞甲基雙硫氰痠酯通過高壓液相色譜進行分離,採用二極管陣列檢測器進行測定。水基食品模擬物直接進樣,油基食品模擬物經乙腈萃取後進樣,外標法定量。結果3種水基食品模擬物中,亞甲基雙硫氰痠酯在0.5~50 mg/L範圍內線性關繫良好,定量下限為0.5 mg/L,平均迴收率為88.2%~97.4%,相對標準偏差為0.44%~6.54%;油基食品模擬物中,亞甲基雙硫氰痠酯在1.0~20 mg/kg範圍內線性關繫良好,定量下限為1.0 mg/kg,平均迴收率為99.3%~104.7%,相對標準偏差為0.75%~3.15%。結論該方法準確、簡便、快速,可用于紙質食品接觸材料中亞甲基雙硫氰痠酯遷移量的實際檢驗工作。
목적건립지질식품접촉재료중아갑기쌍류청산지천이량적고압액상색보측정방법。방법식품모의물(수、3%을산수용액、10%을순수용액화감람유)중적아갑기쌍류청산지통과고압액상색보진행분리,채용이겁관진렬검측기진행측정。수기식품모의물직접진양,유기식품모의물경을정췌취후진양,외표법정량。결과3충수기식품모의물중,아갑기쌍류청산지재0.5~50 mg/L범위내선성관계량호,정량하한위0.5 mg/L,평균회수솔위88.2%~97.4%,상대표준편차위0.44%~6.54%;유기식품모의물중,아갑기쌍류청산지재1.0~20 mg/kg범위내선성관계량호,정량하한위1.0 mg/kg,평균회수솔위99.3%~104.7%,상대표준편차위0.75%~3.15%。결론해방법준학、간편、쾌속,가용우지질식품접촉재료중아갑기쌍류청산지천이량적실제검험공작。
Objective An analytical method for the detection of methylene dithiocyanate migration from food contact paper materials by high pressure liquid chromatography was established. Methods Methylene dithiocyanate migrated into the food simulants (water, 3%aqueous acetic acid solution, 10%aqueous ethanol solution and refined olive oil) was separated and detected by high pressure liquid chromatography coupled with diode array detector. The water-based food simulants were subjected to instrumental analysis directly and the oil-based food simulant was extracted by acetonitrile and then analyzed and quantitated with external standard method. Results This method showed a good linearity for methylene dithiocyanate in the range of 0.5~50 mg/L in the 3 water-based food simulants with the limit of quantification of 0.5 mg/L. The mean recoveries at three spiked levels were in the range of 88.2%~97.4%with relative standard deviations of 0.44%~6.54%. Me-thylene dithiocyanate exhibited a good linearity in the range of 1.0~20 mg/kg with the limit of quantification of 1.0 mg/kg. The mean recoveries at 3 spiked levels were between 99.3% and 104.7% with relative standard deviations of 0.75%~3.15%. Conclusion The method is accurate, simple, and rapid, and it can be used for the determination of methylene dithiocyanate in food contact paper materials.