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在吸入疗法背景下对帕拉米韦药代动力学特征的体外和体内评估。

In Vitro and In Vivo Assessment of Pharmacokinetic Profile of Peramivir in the Context of Inhalation Therapy.

作者信息

Dong Liuhan, Hu Juanwen, Zhang Qiannan, Yang Mengmeng, Zhang Wenpeng, Zhuang Xiaomei

机构信息

State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.

出版信息

Pharmaceuticals (Basel). 2025 Jan 29;18(2):181. doi: 10.3390/ph18020181.

Abstract

OBJECTIVE

The aim was to evaluate the pharmacokinetics and underlying mechanisms of peramivir, a clinically approved antiviral agent for severe influenza, subsequent to airway inhalation in rats, thereby surmounting the constraints associated with the sole currently available intravenous formulation.

METHODS

Pharmacokinetic and tissue distribution investigations of peramivir were carried out in rats following both intravenous and inhaled administration. In vitro cell models were verified to investigate peramivir's transmembrane transport and cellular uptake across diverse cell systems.

RESULTS

In vivo, peramivir exhibited restricted permeability, predominantly localizing within the alveolar epithelial lining fluid and lung tissue after inhalation, accompanied by minimal systemic dissemination. In vitro, it manifested low permeability across cell models, with no participation of efflux transporters. Despite the low rate of A549 uptake, the underlying uptake transport mechanism was still revealed. Peramivir was verified as an OCTN2 substrate. A robust correlation was observed between the in vitro and in vivo findings.

CONCLUSIONS

A preclinical pharmacokinetic platform applicable to inhaled medications was established. Inhalation of peramivir augments exposure at the target site while diminishing systemic exposure, presenting potential therapeutic benefits in terms of efficacy and safety and suggesting it as a favorable alternative administration pathway.

摘要

目的

旨在评估帕拉米韦(一种临床上已获批用于治疗重症流感的抗病毒药物)经大鼠气道吸入后的药代动力学及潜在机制,从而克服目前仅有的静脉制剂所带来的限制。

方法

对帕拉米韦进行静脉注射和吸入给药后,在大鼠体内开展药代动力学和组织分布研究。验证体外细胞模型,以研究帕拉米韦在不同细胞系统中的跨膜转运和细胞摄取情况。

结果

在体内,帕拉米韦表现出有限的通透性,吸入后主要定位于肺泡上皮衬液和肺组织内,全身扩散极少。在体外,它在细胞模型中表现出低通透性,且无外排转运体参与。尽管A549细胞摄取率较低,但仍揭示了其潜在的摄取转运机制。帕拉米韦被证实为有机阳离子转运体2(OCTN2)的底物。体外和体内研究结果之间存在显著相关性。

结论

建立了适用于吸入药物的临床前药代动力学平台。吸入帕拉米韦可增加靶部位的暴露量,同时减少全身暴露,在疗效和安全性方面具有潜在的治疗优势,并表明其为一种有利的替代给药途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44f/11858854/de3a1a4ece96/pharmaceuticals-18-00181-g001.jpg

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