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他非诺喹的药代动力学模型:对优化疟疾治疗策略的见解

Pharmacokinetic Models of Tafenoquine: Insights for Optimal Malaria Treatment Strategies.

作者信息

Santos Luisa Oliveira, Alves Izabel Almeida, Azeredo Francine Johansson

机构信息

Laboratory of Pharmacokinetics and Pharmacometrics, Faculty of Pharmacy, Federal University of Bahia, Salvador 40170-110, Brazil.

Center for Pharmacometrics & System Pharmacology, Department of Pharmaceutics, College of Pharmacy, University of Florida, Orlando, FL 32827, USA.

出版信息

Pharmaceutics. 2024 Aug 26;16(9):1124. doi: 10.3390/pharmaceutics16091124.

Abstract

Tafenoquine (TQ) is a new 8-aminoquinoline antimalarial drug developed by the US Army for malaria treatment. Modeling and simulation are essential tools for drug development and improving rationality in pharmacotherapy, and different modeling approaches are used. This study aims to summarize and explore the pharmacokinetic (PK) models available for tafenoquine in the literature. An integrative methodology was used to collect and review published data. Fifteen articles were identified using three modeling approaches: non-compartmental analysis (NCA), population pharmacokinetic analysis (popPK), and pharmacokinetic/pharmacodynamic analysis (PK/PD). An NCA was mainly used to describe the PK profile of TQ and to compare its PK profile alone to those obtained in association with other drugs. PopPK was used to assess TQ population PK parameters, covariates' impact, and dose selection. PK/PD helped understand the relationship between TQ concentrations, some adverse events common for 8-aminoquilones, and the efficacy assessment for . In summary, pharmacokinetic models were widely used during TQ development. However, there is still a need for different modeling approaches to support further therapeutic questions, such as treatment for special populations and potential drug-drug interactions.

摘要

他非诺喹(TQ)是美国陆军研发的一种用于疟疾治疗的新型8-氨基喹啉类抗疟药物。建模与模拟是药物研发及提高药物治疗合理性的重要工具,且使用了不同的建模方法。本研究旨在总结并探索文献中可用于他非诺喹的药代动力学(PK)模型。采用综合方法收集并回顾已发表的数据。使用三种建模方法确定了15篇文章:非房室分析(NCA)、群体药代动力学分析(popPK)和药代动力学/药效学分析(PK/PD)。NCA主要用于描述TQ的PK特征,并将其单独的PK特征与其他药物联合使用时获得的特征进行比较。PopPK用于评估TQ群体PK参数、协变量的影响及剂量选择。PK/PD有助于理解TQ浓度、8-氨基喹啉类常见的一些不良事件以及疗效评估之间的关系。总之,药代动力学模型在TQ研发过程中被广泛应用。然而,仍需要不同的建模方法来支持进一步的治疗问题,如特殊人群的治疗及潜在的药物相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/989b/11434791/60ed3e04c516/pharmaceutics-16-01124-g001.jpg

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