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
12期
4102-4106
,共5页
魏晶晶%陈章捷%张艳燕%郝延涛%陈晓芳
魏晶晶%陳章捷%張豔燕%郝延濤%陳曉芳
위정정%진장첩%장염연%학연도%진효방
三聚氰胺%水产品%鳗鱼%高效液相色谱法
三聚氰胺%水產品%鰻魚%高效液相色譜法
삼취청알%수산품%만어%고효액상색보법
melamine%aquatic products%eel%high performance liquid chromatography
目的:建立高效液相色谱法检测鳗鱼中三聚氰胺残留量的方法。方法鳗鱼试样用1%三氯乙酸超声提取,以1%三氯乙酸饱和的二氯甲烷液液分配除脂,用混合型阳离子交换固相萃取小柱富集和净化,用SHISEIDO CAPCELL PAK CR(1:4)混合液相色谱柱分离, DAD检测器检测。结果三聚氰胺在0~25μg/mL浓度范围的线性相关系数为0.9999,加标水平在2.0、4.0、10.0 mg/kg的平均回收率分别为94.0%、95.3%、99.5%,相对标准偏差RSD(n=6)分别为2.73%、3.71%、5.79%,该方法检出限(S/N=10)为1.55 mg/kg。结论各项指标均符合GB/T 27404-2008《实验室质量控制规范食品理化检测》中检测方法确认的技术要求。
目的:建立高效液相色譜法檢測鰻魚中三聚氰胺殘留量的方法。方法鰻魚試樣用1%三氯乙痠超聲提取,以1%三氯乙痠飽和的二氯甲烷液液分配除脂,用混閤型暘離子交換固相萃取小柱富集和淨化,用SHISEIDO CAPCELL PAK CR(1:4)混閤液相色譜柱分離, DAD檢測器檢測。結果三聚氰胺在0~25μg/mL濃度範圍的線性相關繫數為0.9999,加標水平在2.0、4.0、10.0 mg/kg的平均迴收率分彆為94.0%、95.3%、99.5%,相對標準偏差RSD(n=6)分彆為2.73%、3.71%、5.79%,該方法檢齣限(S/N=10)為1.55 mg/kg。結論各項指標均符閤GB/T 27404-2008《實驗室質量控製規範食品理化檢測》中檢測方法確認的技術要求。
목적:건립고효액상색보법검측만어중삼취청알잔류량적방법。방법만어시양용1%삼록을산초성제취,이1%삼록을산포화적이록갑완액액분배제지,용혼합형양리자교환고상췌취소주부집화정화,용SHISEIDO CAPCELL PAK CR(1:4)혼합액상색보주분리, DAD검측기검측。결과삼취청알재0~25μg/mL농도범위적선성상관계수위0.9999,가표수평재2.0、4.0、10.0 mg/kg적평균회수솔분별위94.0%、95.3%、99.5%,상대표준편차RSD(n=6)분별위2.73%、3.71%、5.79%,해방법검출한(S/N=10)위1.55 mg/kg。결론각항지표균부합GB/T 27404-2008《실험실질량공제규범식품이화검측》중검측방법학인적기술요구。
Objective To develop a method for the detection of melamine residues in eel by high performance liquid chromatography.MethodsThe sample was extracted with 1% trichloroacetic acid by ultrasonic extraction, degreased through liquid-liquid distribution with methylene chloride saturated by 1% trichloroacetic acid, enriched and purified by mixed cation exchange column. SHISEIDO CAPCELL PAK CR (1:4) mixed liquid chromatographic column was used for separation, and DAD detector was used for determination.Results The correlation coefficient in the range of 0~25μg/mL was 0.9999. The recoveries of three different concentration (2.0, 4.0, and 10.0 mg/kg) were 94.0%, 95.3%, and 99.5%, respectively. The relative standard deviations (RSD,n=6) were 2.73%, 3.71% and 5.79%. The limit of detection was 1.55 mg/kg. ConclusionAll the parameters conform to technical specificationsof GB/T 27404-2008 “Criterion on quality control of laboratories-chemical testing of food”.