首页> 外文期刊>International journal of petroleum science and technology >Simultaneous Spectrophotometric Determination Of Coumaric Acid, Rutin And Quercetin In Biological Fluids By Means Of Some Multivariate Calibration Methods
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Simultaneous Spectrophotometric Determination Of Coumaric Acid, Rutin And Quercetin In Biological Fluids By Means Of Some Multivariate Calibration Methods

机译:多元校正法同时分光光度法测定生物液中香豆酸,芦丁和槲皮素

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Due to biological activities of Coumaric acid (COR), and Rutin (RUT) and Quercetin (QUR) could be a decent lead compound for a new medication development. Thus, the simultaneous determination of three analytes with similarstructure is required. Additionally, investigates on the simultaneous analysis of COR, RUT, and QUR in biological specimens are rare by spectrometry [l-5].The use of multivariate calibration for the simultaneous determination of COR, RUT and QUR is depicted. Along these lines, a simple, quick and inexpensive method for the simultaneous determination of these anti-oxidants was explored and created with the support of chemometrics methods comparing the principal component regression (PCR) and partial least squares (PLS) models[6-9]. Despite the fact that the components demonstrate an important degree of spectral overlap, they have been simultaneously determined with high accuracy and precision, rapidly and with no need of nonaqueous solvents for dissolving the specimens. It is conceivable to acquire a model adjusted in accordance with the concentration values of the mixtures used in the calibration range[8]. UV-spectra were gathered in the 220-350 nm range.The standard curves were found to be linear over the concentration ranges of 0.1-5.00 μg/mL for COR, RUT and QUR. The PRESS for COR, RUT and QUR with PLS were 2.9915, 0.7292 and, 2.5817 that, those NPC were 4, 5, and 3 but in PCR model the PRESS were 2.7902, 2.4827, 4.057 and NPC were 6, 8, 5, respectively. This technique permits the simultaneous determination of anti-oxidant in synthetic and genuine samples.
机译:由于香豆酸(COR)的生物活性,而芦丁(RUT)和槲皮素(QUR)可能是新药开发中不错的先导化合物。因此,需要同时测定具有相似结构的三种分析物。另外,通过光谱分析法对生物样品中的COR,RUT和QUR进行同时分析的研究很少[1-5]。描述了使用多元校准同时测定COR,RUT和QUR的方法。沿着这些思路,在化学计量学方法的支持下,探索并创建了一种同时测定这些抗氧化剂的简单,快速,廉价的方法,该方法比较了主成分回归(PCR)模型和偏最小二乘(PLS)模型[6-9 ]。尽管组分显示出重要的光谱重叠程度,但已以高精度,高精度,快速且无需非水溶剂溶解样品的方式同时测定了它们。可以想象得到一个根据在校准范围内使用的混合物的浓度值而调整的模型[8]。紫外光谱在220-350 nm范围内收集.COR,RUT和QUR的标准曲线在0.1-5.00μg/ mL的浓度范围内呈线性关系。使用PLS的COR,RUT和QUR的PRESS分别为2.9915、0.7292和2.5817,其中NPC为4、5和3,但在PCR模型中,PRESS分别为2.7902、2.4827、4.057和NPC为6、8、5 。这项技术可以同时测定合成和真实样品中的抗氧化剂。

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