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首页> 外文期刊>Journal of food protection >Evaluation of Alkaline Phosphatase Detection in Dairy Products Using a Modified Rapid Chemiluminescent Method and Official Methods
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Evaluation of Alkaline Phosphatase Detection in Dairy Products Using a Modified Rapid Chemiluminescent Method and Official Methods

机译:使用改良的快速化学发光法和官方方法评估乳制品中碱性磷酸酶的检测

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摘要

Alkaline phosphatase is a ubiquitous milk enzyme that historically has been used to verify adequate pasteurization of milk for public health purposes. Current approved methods for detection of alkaline phosphatase in milk include the use of enzyme photoactivated substrates to give readings in milliunits per liter. The U.S. and European public health limit for alkaline phosphatase in pasteurized drinks is 350 mU/liter. A modified chemiluminescent method, fast alkaline phosphatase, was compared with the approved fluorometric and chemiluminescent alkaline phosphatase methods to determine whether the modified method was equivalent to the approved methods and suitable for detecting alkaline phosphatase in milk. Alkaline phosphatase concentrations in cow's, goat's, and sheep's milk and in flavored drinks and cream were determined by three methods. Evaluations in each matrix were conducted with pasteurized samples spiked with raw milk to produce alkaline phosphatase concentrations of 2 to 5,000 mU/liter. The tests were performed by the method developer and then reproduced at a laboratory at the National Center for Food Safety and Technology following the criteria for a single laboratory validation. The results indicated that the fast alkaline phosphatase method was not significantly different from the approved chemiluminescent method, with a limit of detection of 20 to 50 mU/liter in all the studied matrices. This modified chemiluminescent method detects alkaline phosphatase in the 350 mU/liter range with absolute differences from triplicate data that are lower and within the range of the allowed intralaboratory repeatability values published for the approved chemiluminescent method.
机译:碱性磷酸酶是一种普遍存在的牛奶酶,历史上一直被用于验证牛奶用于公共卫生目的是否经过足够的巴氏杀菌。当前批准的检测牛奶中碱性磷酸酶的方法包括使用酶光活化的底物,以毫升/升为单位显示读数。美国和欧洲公共卫生对巴氏消毒饮料中碱性磷酸酶的限制为350 mU /升。将改良的化学发光方法快速碱性磷酸酶与批准的荧光法和化学发光碱性磷酸酶方法进行比较,以确定改良的方法是否等同于批准的方法并且适合检测牛奶中的碱性磷酸酶。用三种方法测定了牛,山羊和绵羊奶,调味饮料和奶油中的碱性磷酸酶浓度。在每个矩阵中进行的评估是使用加有生奶的巴氏灭菌样品进行的,以产生2至5,000 mU /升的碱性磷酸酶浓度。测试由方法开发人员执行,然后按照单个实验室验证的标准在国家食品安全与技术中心的实验室进行复制。结果表明,快速碱性磷酸酶方法与批准的化学发光方法没有显着差异,在所有研究的基质中检测限为20至50 mU /升。这种改良的化学发光方法可检测到350 mU /升范围内的碱性磷酸酶,且与三次重复数据的绝对差值较低,并且在批准的化学发光方法公布的允许实验室内重复性值范围内。

著录项

  • 来源
    《Journal of food protection》 |2011年第7期|1144-1154|共11页
  • 作者单位

    National Center for Food Safety and Technology, Summit-Argo, Illinois 60455;

    U.S. Food and Drug Administration, 6502 South Archer Road, Summit-Argo, Illinois 60455;

    Charm Sciences Inc., 659 Andover Street, Lawrence, Massachusetts 01843, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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