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采用改良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。

Evaluation of alkaline phosphatase detection in dairy products using a modified rapid chemiluminescent method and official methods.

机构信息

National Center for Food Safety and Technology, 6502 South Archer Road, Summit-Argo, Illinois 60455, USA.

出版信息

J Food Prot. 2011 Jul;74(7):1144-54. doi: 10.4315/0362-028X.JFP-10-422.

Abstract

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.

摘要

碱性磷酸酶是一种普遍存在的牛奶酶,历史上一直用于验证牛奶巴氏消毒的充分性,以保障公共卫生。目前用于检测牛奶中碱性磷酸酶的方法包括使用酶光激活底物,以毫单位/升(mU/L)为单位进行读数。美国和欧洲公共卫生机构规定,巴氏消毒饮料中的碱性磷酸酶含量上限为 350mU/L。本文将一种改良的化学发光法(快速碱性磷酸酶法)与已批准的荧光法和化学发光法进行了比较,以确定该改良方法是否与已批准的方法等效,是否适合检测牛奶中的碱性磷酸酶。通过三种方法测定了牛奶(包括牛乳、山羊奶和绵羊奶)、调味饮料和奶油中的碱性磷酸酶浓度。在每种基质中进行评估时,使用巴氏消毒样品中添加生乳,以产生 2 至 5000mU/L 的碱性磷酸酶浓度。测试由方法开发者进行,然后由国家食品安全与技术中心的实验室按照单一实验室验证标准进行重复。结果表明,快速碱性磷酸酶法与已批准的化学发光法无显著差异,在所有研究的基质中,检测限为 20 至 50mU/L。该改良的化学发光法可在 350mU/L 范围内检测碱性磷酸酶,与已批准的化学发光法公布的允许实验室内部重复性值范围内的重复数据的绝对差异较低。

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