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Validation and Comparison of Analytical Methods Based on the Release of p-Nitrophenol to Determine Lipase Activity in Milk

机译:对硝基苯酚释放量测定牛奶中脂肪酶活性的分析方法的验证与比较

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Three methods of determining lipase activity were optimized, validated, and compared using skim and whole milk. A chromogenic ester (P-nitrophenyl capry- late) was used in all to quantify the enzyme activity through the release of p-nitrophenol. It was measured colorimetrically (method A) or spectrophotometrically (methods B and C) with a clarifying reagent to render the samples measurable. Methods B and C differed be- cause an inhibiting mixture was used in the latter method to better stop the enzymatic reaction. All the methods were reliable; they were linear in the range of 0 to 300 mU/ml of the enzyme, and the least detection and quantification limits were 9.31 and 31.03 mU/ml of lipase, respectively. Precision, measured as relative standard deviation, was between 1.52 and 4.94/100, and mean recoveries ranged between 81 and 90/100. Linearity, sensitivity, and accuracy were signifi- cantly different among the methods. Methods B and C had better linearity and sensitivity than method A, and the most accurate results were obtained with methods A and B in skim milk. Sensitivity was influenced by the fat content of the samples. On the other hand, the content of lipase did not influence the reliability of any method. Although, all of the methods were useful for routine analysis of quality control of milk, method B was most reliable. Moreover, it would be the method of choice because it was easier and less costly than the other methods.
机译:使用脱脂奶粉和全脂奶对三种确定脂肪酶活性的方法进行了优化,验证和比较。发色酯(对硝基苯基辛酸酯)用于定量通过对硝基苯酚释放的酶活性。用澄清剂比色法(方法A)或分光光度法(方法B和C)进行测量,以使样品可测量。方法B和C不同,因为在后一种方法中使用了抑制混合物来更好地终止酶促反应。所有方法均可靠。它们在酶的0到300 mU / ml范围内呈线性关系,最小检测限和定量限分别为9.31和31.03 mU / ml脂肪酶。以相对标准偏差衡量的精度在1.52和4.94 / 100之间,平均回收率在81和90/100之间。两种方法之间的线性,灵敏度和准确性显着不同。方法B和C具有比方法A更好的线性和灵敏度,并且使用方法A和B在脱脂牛奶中获得了最准确的结果。敏感性受样品中脂肪含量的影响。另一方面,脂肪酶的含量不影响任何方法的可靠性。尽管所有方法都可用于牛奶质量控制的常规分析,但方法B最可靠。而且,它将是选择的方法,因为它比其他方法更容易且成本更低。

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