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总蛋白检测方法及其在降低食品蛋白质掺假风险方面的潜在用途。

Total Protein Methods and Their Potential Utility to Reduce the Risk of Food Protein Adulteration.

作者信息

Moore Jeffrey C, DeVries Jonathan W, Lipp Markus, Griffiths James C, Abernethy Darrell R

机构信息

Authors Moore, Lipp, Griffiths, and Abernethy are with the US Pharmacopeial Convention, 12601 Twinbrook Parkway, Rockville, MD 20852-1790, U.S.A. Author DeVries is a member of the US Pharmacopeial Convention's Food Ingredients Expert Committee. Author Abernethy is now with the Office of Clinical Pharmacology, Food and Drug Administration, Silver Spring, MD 20993, U.S.A. Direct inquiries to author Moore (E-mail:

出版信息

Compr Rev Food Sci Food Saf. 2010 Jul;9(4):330-357. doi: 10.1111/j.1541-4337.2010.00114.x.

Abstract

Kjeldahl and combustion (Dumas) methods are widely accepted for total protein determination but lack analytical selectivity for protein because they measure protein on the basis of sample nitrogen content. Adulteration incidents exploiting this analytical vulnerability (for example, melamine) demonstrate that these methods are no longer sufficient to protect the public health. This article explores the challenges and opportunities to move beyond total nitrogen based methods for total protein measurement. First, it explores the early history of protein measurement science, complexities of current global protein measurement activities, and ideal analytical performance characteristics for new methods. Second, it comprehensively reviews the pros and cons of current and emerging approaches for protein measurement, including their selectivity for protein, ability to detect adulteration, and practicality for routine use throughout the supply chain. It concludes that some existing highly selective methods for food protein measurement have potential for routine quality control. It also concludes that their successful implementation will require matrix-specific validation and the use of supporting reference materials. These methods may be suitable only for food ingredients that have a low degree of compositional variability and are not complex finished food products.

摘要

凯氏定氮法和燃烧(杜马斯)法在总蛋白质测定中被广泛接受,但由于它们是基于样品氮含量来测定蛋白质,因此缺乏对蛋白质的分析选择性。利用这种分析弱点的掺假事件(例如三聚氰胺)表明,这些方法已不足以保护公众健康。本文探讨了超越基于总氮的方法进行总蛋白质测量所面临的挑战和机遇。首先,探讨了蛋白质测量科学的早期历史、当前全球蛋白质测量活动的复杂性以及新方法的理想分析性能特征。其次,全面回顾了当前和新兴蛋白质测量方法的优缺点,包括它们对蛋白质的选择性、检测掺假的能力以及在整个供应链中常规使用的实用性。得出的结论是,一些现有的高选择性食品蛋白质测量方法具有用于常规质量控制的潜力。还得出结论,这些方法的成功实施将需要进行特定基质的验证并使用配套的参考材料。这些方法可能仅适用于成分变异性较低且不是复杂成品食品的食品成分。

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