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基于青蛙体外表征数据的经皮吸收模型能否预测体内吸收?

Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?

机构信息

Pharmacy, College of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.

One Health Research Group, Melbourne Veterinary School, University of Melbourne, Werribee, Victoria, Australia.

出版信息

PLoS One. 2020 Jul 29;15(7):e0235737. doi: 10.1371/journal.pone.0235737. eCollection 2020.

Abstract

The primary aim of in vitro testing of chemicals delivered via the percutaneous route is to predict the absorption that would ensue if exposure occurred in live animals. While there is mounting evidence that in vitro diffusion studies in mammalian skin can provide valid information regarding likely in vivo absorption, little is known whether such a correlation exists between in vitro diffusion testing and in vivo blood levels in amphibians. The current study used previously-reported in vitro absorption data for caffeine, benzoic acid, and ibuprofen across isolated skin from the cane toad (Rhinella marina) to produce a series of linear mixed-effect models of the absorption parameters flux and permeability coefficient (Kp). Models investigated the relative impacts of animal weight, physicochemical characteristics of the applied chemical (logP or molecular weight), and site of application. The top models were then used to predict the flux, Kp and serum concentrations of the same three model chemicals. Finally, the absorption of these chemicals was determined in live cane toads, and results compared to the model predictions. LogP and site of application were included in all top models. In vivo absorption rates were lower than predicted for all chemicals, however, the models provided reasonable predictions of serum concentration, with factors of difference (FOD) ranging from 2.5-10.5. Ibuprofen, the chemical with the highest relative lipophilicity, had the poorest predictive performance, consistently having the highest FOD for all predictions. This report presents the first models of percutaneous absorption in an amphibian. These models provide a basic method to establish the approximate in vivo absorption of hydrophilic and moderately-lipophilic chemicals through frog skin, and could therefore be used to predict absorption when formulating such chemicals for treatment of disease in frogs, or for risk-assessments regarding chemical pollutants in frog habitats.

摘要

经皮途径给予的化学品的体外测试的主要目的是预测如果在活体动物中发生暴露则会随之发生的吸收。虽然越来越多的证据表明,哺乳动物皮肤的体外扩散研究可以提供关于可能的体内吸收的有效信息,但对于在体外扩散测试与两栖动物体内血液水平之间是否存在这种相关性知之甚少。本研究使用先前报道的来自 cane toad(Rhinella marina)的分离皮肤的咖啡因、苯甲酸和布洛芬的体外吸收数据,生成一系列吸收参数通量和渗透系数(Kp)的线性混合效应模型。模型研究了动物体重、应用化学物质的物理化学特性(logP 或分子量)和应用部位对吸收的相对影响。然后,使用顶级模型预测相同的三种模型化学物质的通量、Kp 和血清浓度。最后,在活体 cane toads 中测定这些化学物质的吸收,并将结果与模型预测进行比较。logP 和应用部位均包含在所有顶级模型中。所有化学物质的体内吸收速率均低于预测值,但模型对血清浓度提供了合理的预测,差异因子(FOD)范围为 2.5-10.5。布洛芬是相对脂溶性最高的化学物质,其预测性能最差,所有预测的 FOD 均最高。本报告介绍了在两栖动物中经皮吸收的第一个模型。这些模型为通过青蛙皮肤建立亲水性和中等亲脂性化学物质的近似体内吸收提供了一种基本方法,因此可以用于预测此类化学物质用于治疗青蛙疾病或评估化学污染物在青蛙栖息地中的风险时的吸收。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71d1/7390353/7936d34710c7/pone.0235737.g001.jpg

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