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Matrix and food processing induced changes in the accuracy of different commercial milk ELISA kits.

机译:基质和食品加工引起了不同商业牛奶ELISA试剂盒准确性的变化。

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摘要

Milk proteins are common functional food ingredients but major milk proteins are also allergens. Commercial milk ELISAs are widely used to detect milk residues in foods. However, these milk kits have not been well validated for their performance with processed food matrices. Thus, the recovery of spiked amounts of non-fat dry milk (NFDM) before and after processing from two different matrices was compared using 9 different milk ELISA kits.;The first matrix was wheat pastry squares spiked with NFDM which then underwent thermal (boiling, baking, frying, retorting, microwaving, radiofrequency) and non-thermal (high-pressure, acidification) processing. Initially from the unprocessed pastry squares, excellent recoveries were obtained with the beta-lactoglobulin kits, while recoveries were not nearly as good (average of 40% of the spiked amounts) for the total milk and casein kits. The results suggest that interactions are occurring between matrix components and milk proteins after addition of water. With the pastry matrix, thermal treatments resulted in even further reduced recovery, with baking completely eliminating the detection of milk proteins for many kits. Among non-thermal treatments, acidification resulted in an extremely reduced recovery of milk proteins. The effects of processing treatments on milk protein extraction and recovery were also concentration dependent. The findings suggest that attempts to use commercial milk ELISA kits to detect low levels of milk residue from complex food matrices may not be reliable in many circumstances.;Recoveries were much better (80% or more with most ELISAs) from a model liquid matrix following various thermal and non-thermal treatments. Differences encountered were dependent upon kit and milk protein concentration. Therefore, selection of the most appropriate kit should be approached carefully to ascertain the ELISA that works best with a particular processing method and matrix.;Attempts to improve milk protein recovery with new extraction buffers or enzyme treatment were not advantageous. Thus, especially for solid food matrices, the development of improved ELISAs is needed for more reliable detection of low-level milk residues.
机译:牛奶蛋白是常见的功能性食品成分,但主要的牛奶蛋白也是过敏原。商业牛奶ELISA被广泛用于检测食品中的牛奶残留。但是,这些牛奶套件在加工食品基质中的性能尚未得到充分验证。因此,使用9种不同的牛奶ELISA试剂盒比较了两种不同基质加工前后加标的脱脂奶粉(NFDM)的回收率。;第一个基质是加有NFDM的小麦糕饼块,然后对其进行加热(煮沸) ,烘烤,油炸,蒸煮,微波,射频)和非热(高压,酸化)处理。最初从未经加工的糕点方盒中,使用β-乳球蛋白试剂盒可获得极佳的回收率,而总牛奶和酪蛋白试剂盒的回收率却不及后者(平均加标量的40%)。结果表明,加水后基质成分与牛奶蛋白之间发生相互作用。对于糕点基质,热处理导致回收率进一步降低,而烘烤完全消除了许多试剂盒中牛奶蛋白的检测。在非热处理中,酸化导致牛奶蛋白的回收率大大降低。加工处理对乳蛋白提取和回收的影响也与浓度有关。研究结果表明,尝试使用商业牛奶ELISA试剂盒来检测复杂食品基质中低水平的牛奶残留可能在许多情况下都不可靠。;从以下模型液体基质中回收率要好得多(大多数ELISA的回收率为80%或更高)各种热处理和非热处理。遇到的差异取决于试剂盒和牛奶蛋白浓度。因此,应仔细选择最合适的试剂盒,以确保在特定的加工方法和基质下最适合使用ELISA。;尝试使用新的提取缓冲液或酶处理来提高牛奶蛋白的回收率是不利的。因此,特别是对于固体食品基质,需要开发改进的ELISA以更可靠地检测低水平的牛奶残留物。

著录项

  • 作者

    Bly, Brigitta.;

  • 作者单位

    The University of Nebraska - Lincoln.;

  • 授予单位 The University of Nebraska - Lincoln.;
  • 学科 Agriculture Food Science and Technology.;Health Sciences Toxicology.;Health Sciences Nutrition.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 291 p.
  • 总页数 291
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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