肉类研究
肉類研究
육류연구
MEAT RESEARCH
2011年
10期
26-28
,共3页
郑海松%陈雪娇%杨小娇%余晓峰%孙娟娟%李云飞%李刚
鄭海鬆%陳雪嬌%楊小嬌%餘曉峰%孫娟娟%李雲飛%李剛
정해송%진설교%양소교%여효봉%손연연%리운비%리강
酶联免疫分析(ELISA)%莱克多巴胺%食品%快速检测
酶聯免疫分析(ELISA)%萊剋多巴胺%食品%快速檢測
매련면역분석(ELISA)%래극다파알%식품%쾌속검측
enzyme-linked immunosorbent assay (ELISA)%ractopamine%food%rapid detection
建立一种肉及其制品中莱克多巴胺的酶联免疫分析方法。对莱克多巴胺残留量进行选择性(交义反应)、特异性与检测限以及回收率和精密度测试。结果显示,选择酶联免疫法来检测样品中的莱克多巴胺准确性较好,其对莱克多巴胺结构类似物的交叉反应率都小于1%,出口猪肉罐头和牛肉中的检测限(LOD)分别为(0.28±0.30)μg/kg和(0.26±0.21)μg/kg,样品甲均回收率在82.9%-91.1%之间,相对标准偏差为4.3%~8.7%,经高效液相色谱(HPLC)确证假阳性率小于等于2.0%,表明酶联免疫分析定量泫可快速、准确实现对食品中莱克多巴胺残留量的快速筛选。
建立一種肉及其製品中萊剋多巴胺的酶聯免疫分析方法。對萊剋多巴胺殘留量進行選擇性(交義反應)、特異性與檢測限以及迴收率和精密度測試。結果顯示,選擇酶聯免疫法來檢測樣品中的萊剋多巴胺準確性較好,其對萊剋多巴胺結構類似物的交扠反應率都小于1%,齣口豬肉罐頭和牛肉中的檢測限(LOD)分彆為(0.28±0.30)μg/kg和(0.26±0.21)μg/kg,樣品甲均迴收率在82.9%-91.1%之間,相對標準偏差為4.3%~8.7%,經高效液相色譜(HPLC)確證假暘性率小于等于2.0%,錶明酶聯免疫分析定量泫可快速、準確實現對食品中萊剋多巴胺殘留量的快速篩選。
건립일충육급기제품중래극다파알적매련면역분석방법。대래극다파알잔류량진행선택성(교의반응)、특이성여검측한이급회수솔화정밀도측시。결과현시,선택매련면역법래검측양품중적래극다파알준학성교호,기대래극다파알결구유사물적교차반응솔도소우1%,출구저육관두화우육중적검측한(LOD)분별위(0.28±0.30)μg/kg화(0.26±0.21)μg/kg,양품갑균회수솔재82.9%-91.1%지간,상대표준편차위4.3%~8.7%,경고효액상색보(HPLC)학증가양성솔소우등우2.0%,표명매련면역분석정량현가쾌속、준학실현대식품중래극다파알잔류량적쾌속사선。
This paper describes an enzyme-linked immunosorbent assay (ELISA) to determine ractopamine in meat and meat products. The proposed method was highly accurate in determining ractopamine and showed a cross-reactivity of less than 1% with all ractopamine analogues investigated. The limits of detection (LODs) for exported canned pork and exported beef were (0.28±0.30) μg/kg and (0.26±0.21) μg/kg, respectively, with an average spike recovery of 82.9%-91.1% (n = 15) and a relative standard deviation of 4.3%-8.7%. Using high performance liquid chromatography (HPLC), the false posiitve rate of this method was confirmed as less than 2.0%, suggesting that it can enable accurate and rapid determination of ractopamine residues in foods.