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首页> 外文期刊>Pharmaceutics >In Vitro–In Vivo Correlations Based on In Vitro Dissolution of Parent Drug Diltiazem and Pharmacokinetics of Its Metabolite
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In Vitro–In Vivo Correlations Based on In Vitro Dissolution of Parent Drug Diltiazem and Pharmacokinetics of Its Metabolite

机译:基于体外溶解的母体药物Diltiazem的体外相关性,其代谢物的药代动力学

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In this study a novel type of in vitro–in vivo correlation (IVIVC) is proposed: The correlation of the in vitro parent drug dissolution data with the in vivo pharmacokinetic data of drug’s metabolite after the oral administration of the parent drug. The pharmacokinetic data for the parent drug diltiazem (DTZ) and its desacetyl diltiazem metabolite (DTZM) were obtained from an in vivo study performed in 19 healthy volunteers. The pharmacokinetics of the parent drug and its metabolite followed a pseudomono-compartmental model and deconvolution of the DTZ or DTZM plasma concentration profiles was performed with a Wagner–Nelson-type equation. The calculated in vivo absorption fractions were correlated with the in vitro DTZ dissolution data obtained with USP 2 apparatus. A linear IVIVC was obtained for both DTZ and DTZM, with a better correlation observed for the case of the metabolite. This type of correlation of the in vitro data of the parent compound with the in vivo data of the metabolite could be useful for the development of drugs with active metabolites and prodrugs.
机译:在这项研究中,提出了一种新型的体外体内相关性(IVIVC):在口服药物口服药物后,体外母体药物溶解数据与药物代谢物的体内药代动力学数据的相关性。母体药物Diltiazem(DTZ)的药代动力学数据及其去乙酰达替纳佐姆代谢物(DTZM)是在19个健康志愿者中进行的体内研究中获得。母体药物及其代谢物的药代动力学伴随着瓦格纳 - 纳尔逊型方程进行了伪分区的伪分区模型和DTZ或DTZM血浆浓度谱的去卷积。在体内吸收级分中的计算与用USP 2装置获得的体外DTZ溶解数据相关。为DTZ和DTZM获得线性IVIVC,对于代谢物的情况,观察到的相关性更好。本母体化合物的体外数据与代谢物的体内数据的这种类型的相关性可用于发育具有活性代谢物和前药的药物。

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