药代动力学
加药
药理学
生物利用度
药效学
医学
分配量
人血浆
分布(数学)
化学
数学
色谱法
数学分析
作者
Ragini Vuppugalla,Ramola Sane,Michael Wichroski,Ashvini Kumar Gavai,Sarandeep S.S. Boyanapalli,Zheng Yang
出处
期刊:Xenobiotica
[Informa]
日期:2021-10-28
卷期号:51 (11): 1255-1263
标识
DOI:10.1080/00498254.2021.1934606
摘要
AbstractIntra-tumoral (I-TUMOUR) delivery is being widely explored for novel anti-cancer agents. This route is anticipated to result in high tumour concentrations leading to better efficacy and safety. Prediction of human systemic pharmacokinetics (PK) from non-clinical species facilitates understanding of pharmacokinetic-pharmacodynamic relationships, efficient dose selection, and risk assessment of novel drugs. However, there is limited knowledge on the predictability of human pharmacokinetics following I-TUMOUR delivery.In this publication, we present a case study wherein human systemic PK of a novel agent administered intra-tumourally was prospectively predicted and compared with observed human PK.Simple allometry was used to project the human clearance (10.5 mL/min/kg) and steady-state volume of distribution (1.4 L/kg) after intravenous (IV) dosing. Using these IV PK parameters and assuming rapid absorption and complete I-TUMOUR bioavailability, human plasma PK profile was simulated. The projected 30 min concentrations and AUC(0–6h) were within 1.9 to 2.5-fold and 1 to 1.4-fold of the observed PK indicating a reasonable concordance between predicted and observed PK.To our knowledge, this is the first article that prospectively projected human pharmacokinetics after I-TUMOUR dosing. The results from this study indicate that similar approaches can be used to project the human PK of other I-TUMOUR agents.Keywords: Human plasma pharmacokinetic predictionintra-tumoral pharmacokineticsnon-clinical to human translationintra-tumoral dosinghuman pharmacokinetic profile prediction AckowledgementsWe would like to thank R. M. Fancher and the technical services unit for their help in conducting the I-TUMOR study in MC38 mice. We would also like to thank Lorell Discenza for analyzing the samples from the above study by LC/MS/MS.Disclosure statementNo potential conflict of interest was reported by the author(s).
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