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首页> 外文期刊>American Journal of PharmTech Research >Quantitative Structure-Pharmacokinetic Relationship (QSPkR) Analysis of the Serum Protein Binding Values for Antidiabetic Agents In Humans
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Quantitative Structure-Pharmacokinetic Relationship (QSPkR) Analysis of the Serum Protein Binding Values for Antidiabetic Agents In Humans

机译:人体抗糖尿病药血清蛋白结合值的定量结构-药代动力学关系(QSPkR)分析

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ABSTRACT An estimate of Serum protein binding (%SPB) is of paramount importance in assessing the efficacy of drugs used to treat diabetes in patients.  This study was conducted to develop Quantitative Structure Pharmacokinetic Relationship (QSPkR) for the prediction of %SPB in human for congeneric series of 23 antidiabetic drugs, using computer assisted Hansch approach.  The QSPkR correlations were duly analyzed using a battery of apt statistical  procedures and validated using leave-one-out (LOO) approach. Analysis of several hundreds of QSPkR correlations developed in this study revealed high degree of cross- validated coefficients (Q2) using LOO method (p
机译:摘要血清蛋白结合率(%SPB)的评估对于评估用于治疗糖尿病患者的药物的疗效至关重要。这项研究是为了开发定量结构药代动力学关系(QSPkR),使用计算机辅助的Hansch方法来预测23种抗糖尿病药物的同类人体内的%SPB。使用一系列适当的统计程序对QSPkR相关性进行了适当分析,并使用留一法(LOO)方法进行了验证。对本研究中开发的数百个QSPkR相关性进行的分析显示,使用LOO方法可以得到高度交叉验证的系数(Q2)(p

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