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A highly sensitive sandwich ELISA for the determination of glycomacropeptide to detect liquid whey in raw milk

机译:高灵敏的夹心ELISA法测定糖巨肽以检测原料奶中的乳清

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摘要

Milk processing industries and distributors have problems with adulteration of liquid milk by the addition of bovine cheese whey. Recently, the detection of fraudulent manipulation of milk with whey has focused on the identification of glycomacropeptide (GMP). Current non-immunological methods to detect GMP in dairy products are expensive and time-consuming or have low sensitivity. In this study, a novel sandwich enzyme-linked immunosorbent assay (ELISA) for the detection and quantification of whey in raw milk was developed, using a polyclonal rabbit anti-GMP antibody. Calibration curves were constructed by analyzing raw milk standards containing different known concentrations of liquid cheese whey (0.02–20%). The method had a detection limit of 0.047% (v/v) and a quantification limit of 0.14% (v/v). The antibody showed high specificity and no cross-reaction with milk components (other than κ-casein) and was successful in detecting GMP in dairy commercial products. The recovery ratio was between 95.62% and 113.88% for all matrices tested. The intra-assay and interassay coefficients of variation were <6% and <7%, respectively. Finally, it can be stored for 3 months in the form of a ready-to-use kit, while maintaining its accuracy and reproducibility.
机译:牛奶加工行业和分销商因添加牛奶酪乳清而使液态牛奶掺假存在问题。近来,利用乳清对牛奶进行欺诈性操作的检测已集中在糖巨肽(GMP)的鉴定上。当前检测乳制品中GMP的非免疫方法昂贵,费时或灵敏度低。在这项研究中,使用多克隆兔抗GMP抗体,开发了一种用于检测和定量生乳中乳清的新型夹心酶联免疫吸附测定(ELISA)。通过分析包含不同已知浓度的液态干酪乳清(0.02–20%)的原奶标准品来构建校准曲线。该方法的检出限为0.047%(v / v),定量限为0.14%(v / v)。该抗体显示出高特异性,并且与牛奶成分(κ-酪蛋白除外)没有交叉反应,并成功检测了乳制品中的GMP。所有测试基质的回收率在95.62%至113.88%之间。批内和批间变异系数分别<6%和<7%。最后,它可以即用型试剂盒的形式保存3个月,同时保持其准确性和可重复性。

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