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首页> 外文期刊>Bioanalysis >Comparison of UHPLC and HPLC methods for the assay of prostanoids: 'are the methods equivalent in terms of accuracy and precision?'.
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Comparison of UHPLC and HPLC methods for the assay of prostanoids: 'are the methods equivalent in terms of accuracy and precision?'.

机译:比较UHPLC和HPLC分析前列腺素的方法:“就准确性和精密度而言,这些方法是否等效?”。

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BACKGROUND: As new methods are developed to increase efficiency and higher analytical performance, it is necessary to evaluate their quality in comparison to standard methods. To understand how the analytical performance changes between methods, it is common to compare the validation parameters; sensitivity, linearity, accuracy and precision. Here, we compare an UHPLC-UV method to the HPLC-UV method (reference method) for the simultaneous determination of seven prostanoids. Though the basic chromatography theory is the same for HPLC and UHPLC, the instrumentation has been modified to accommodate higher pressures, lower flow rates and smaller sample size. The differences in analytical instrumentation and procedures can give rise to method inequivalencies. Our approach evaluates the UHPLC and HPLC methods and poses the question: are the methods equivalent? To answer this question a statistical comparison of the analytical performance and method parameters is necessary. RESULTS: Statistical comparisons were performed using the t-test, F-test, regression analyses (ordinary linear regression and Deming regression) and Bland-Altman analyses. Statistical comparison of the results, suggested that the precision (amount of variability) is different (p < 0.05) for the HPLC and UHPLC methods. Whereas, the accuracy (method bias and the means) is similar (p > 0.05) for 8-isoprostane, 11-dehydro TXB, PGE PGF(2alpha), PGD and 15-deoxy Delta(1)(2),(1) PGJ. DISCUSSION: Ordinary linear regression shows that the methods are well correlated for all compounds. The Deming regression, which assumes error in both the methods, suggests the existence of a proportional and constant bias for 11-dehydro TXB and only proportional bias for 8-isoprostane, PGF(2alpha), PGD and 15-deoxy Delta(12,14) PGJ between the two methods. According to Deming regression, the two methods are statistically similar for 6-keto PGF(1alpha) and PGE. The Bland-Altman analyses indicate the two methods are commutable.
机译:背景:随着新方法的发展,以提高效率和更高的分析性能,与标准方法相比,有必要评估其质量。要了解分析方法之间的分析性能如何变化,通常需要对验证参数进行比较。灵敏度,线性,准确性和精确度。在这里,我们将UHPLC-UV方法与HPLC-UV方法(参考方法)进行比较,以同时测定7种前列腺素。尽管HPLC和UHPLC的基本色谱理论是相同的,但仪器已进行了修改,以适应更高的压力,更低的流速和更小的样品大小。分析仪器和程序的差异可能导致方法不对等。我们的方法评估了UHPLC和HPLC方法,并提出了一个问题:这些方法是否等效?为了回答这个问题,必须对分析性能和方法参数进行统计比较。结果:采用t检验,F检验,回归分析(常规线性回归和Deming回归)和Bland-Altman分析进行统计比较。结果的统计比较表明,HPLC和UHPLC方法的精度(可变性量)不同(p <0.05)。而对于8-异前列腺素,11-脱氢TXB,PGE PGF(2alpha),PGD和15-脱氧Delta(1)(2),(1),准确性(方法偏倚和均值)相似(p> 0.05)。 PGJ。讨论:普通线性回归表明,所有化合物的方法均具有良好的相关性。 Deming回归假设两种方法均存在误差,表明11-脱氢TXB存在比例偏差和恒定偏差,而8-异前列腺素,PGF(2alpha),PGD和15-脱氧Delta仅存在比例偏差(12,14 )两种方法之间的PGJ。根据Deming回归,这两种方法对于6-酮PGF(1alpha)和PGE在统计学上相似。 Bland-Altman分析表明这两种方法是可交换的。

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