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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Limited sampling strategy of mycophenolic acid in adult kidney transplant recipients: Influence of the post-transplant period and the pharmacokinetic profile
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Limited sampling strategy of mycophenolic acid in adult kidney transplant recipients: Influence of the post-transplant period and the pharmacokinetic profile

机译:成年肾移植受者中麦考酚酸的有限采样策略:移植后时期和药代动力学特征的影响

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摘要

We aimed to develop an accurate and convenient LSS for predicting MPA-AUC0-12hours in Tunisian adult kidney transplant recipients whose immunosuppressive regimen consisted of MMF and tacrolimus combination with regards to the post-transplant period and the pharmacokinetic profile. Each pharmacokinetic profile consisted of eight blood samples collected during the 12-hour dosing interval. The AUC0-12hourswas calculated according to the linear trapezoidal rule. The MPA concentrations at each sampling time were correlated by a linear regression analysis with the measuredAUC0-12. We analyzed all the developed models for their ability to estimate the MPA-AUC0-12hours. The best multilinear regression model for predicting the full MPA-AUC0-12hourswas found to be the combination of C1, C4, and C6. All the best correlated models and the most convenient ones were verified to be also applicable before 5 months after transplantation and thereafter. These models were also verified to be applicable for patients having or not the second peak in their pharmacokinetic profiles. For practical reasons we recommend a LSS using C 0, C1, and C4 that provides a reasonable MPA-AUC0- 12hoursestimation.
机译:我们旨在开发一种准确便捷的LSS,用于预测突尼斯成年肾移植受者的MPA-AUC0-12小时,其免疫抑制方案由MMF和他克莫司组成,涉及移植后的时期和药代动力学特征。每个药代动力学图由在12小时给药间隔内收集的八份血液样本组成。根据线性梯形法则计算AUC0-12小时。通过线性回归分析将每个采样时间的MPA浓度与测得的AUC0-12相关联。我们分析了所有已开发的模型的估算MPA-AUC0-12小时的能力。发现用于预测整个MPA-AUC0-12小时的最佳多线性回归模型是C1,C4和C6的组合。验证了所有最佳相关模型和最方便的模型在移植后5个月之前和之后也适用。这些模型也被证实适用于具有或没有第二代药物动力学特征的患者。出于实际原因,我们建议使用C 0,C1和C4的LSS提供合理的MPA-AUC0-12小时刺激。

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