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首页> 外文期刊>Central European Journal of Chemistry >The thermodynamic dissociation constants of methotrexate by the nonlinear regression and factor analysis of multiwavelength spectrophotometric pH-titration data
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The thermodynamic dissociation constants of methotrexate by the nonlinear regression and factor analysis of multiwavelength spectrophotometric pH-titration data

机译:通过多波长分光光度法pH滴定数据的非线性回归和因子分析对氨甲蝶呤的热力学解离常数

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摘要

The mixed dissociation constants of methotrexate - chemically (2S)-2-[(4-{[(2,4-diamino-7,8-dihydropteridin-6-yl)methyl] (methyl)amino}phenyl)formamido]pentanedioic acid (the cas number 59-05-2) at various ionic strengths I of range 0.01 - 0.4, and at temperatures of 25℃ and 37℃, were determined with the use of two different multiwavelength and multivariate treatments of spectral data, SPECFIT32 and SQUAD(84) nonlinear regression analyses and INDICES factor analysis according to a general rule of first,determining the number of components, and then calculating the spectral responses and concentrations of the components. Concurrently, the experimental determination of the thermodynamic dissociation constants was in agreement with its computational prediction of the PALLAS programme based on knowledge of the chemical structures of the drug. The factor analysis in the INDICES programme predicts the correct number of light-absorbing components when the data quality is high and the instrumental error is known. Three thermodynamic dissociation constants were estimated by nonlinear regression of {pKa, I} data: for methotrexate pK_(a1)T= 2.895(13), pK_(a2)T= 4.410(14), pK_(a3)T= 5.726(15) at 25℃ and pK_(a1)T= 3.089(15), pK_(a2)T= 4.392(12), pK_(a3)T= 5.585(11) at 37℃, where the figure in brackets is the standard deviation in last significant digits. The reliability of the dissociation constants of the drug were proven by conducting goodness-of-fit tests of the multiwavelength spectrophotometric pH-titration data.
机译:甲氨蝶呤的化学-(2S)-2-[(4-{[(2,4-二氨基-7,8-二氢蝶呤-6-基)甲基](甲基)氨基}苯基)甲酰胺基]戊二酸的混合解离常数使用两个不同的多波长和多元光谱数据处理方法(SPECFIT32和SQUAD),测定了离子强度I(范围为0.01-0.4)以及25℃和37℃的离子强度(CAS号59-05-2) (84)根据一般规则首先进行非线性回归分析和INDICES因子分析,确定组分的数量,然后计算组分的光谱响应和浓度。同时,热力学解离常数的实验确定与基于药物化学结构知识对PALLAS程序的计算预测一致。当数据质量高且已知仪器误差时,INDICES程序中的因子分析可预测光吸收组件的正确数量。通过{pKa,I}数据的非线性回归估计了三个热力学解离常数:对于甲氨蝶呤pK_(a1)T = 2.895(13),pK_(a2)T = 4.410(14),pK_(a3)T = 5.726(15) )在25℃且pK_(a1)T = 3.089(15),pK_(a2)T = 4.392(12),pK_(a3)T = 5.585(11),其中括号中的数字为标准偏差最后一位有效数字。通过对多波长分光光度法pH滴定数据进行拟合优度测试,证明了药物解离常数的可靠性。

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