Comparing computational times for simulations when using PBPK model template and stand-alone implementations of PBPK models.

IF 4.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2025-02-19 eCollection Date: 2025-01-01 DOI:10.3389/ftox.2025.1518769
Amanda S Bernstein, Paul M Schlosser, Dustin F Kapraun
{"title":"Comparing computational times for simulations when using PBPK model template and stand-alone implementations of PBPK models.","authors":"Amanda S Bernstein, Paul M Schlosser, Dustin F Kapraun","doi":"10.3389/ftox.2025.1518769","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>We previously developed a PBPK model template that consists of a single model \"superstructure\" with equations and logic found in many physiologically based pharmacokinetic (PBPK) models. Using the template, one can implement PBPK models with different combinations of structures and features.</p><p><strong>Methods: </strong>To identify factors that influence computational time required for PBPK model simulations, we conducted timing experiments using various implementations of PBPK models for dichloromethane and chloroform, including template and stand-alone implementations, and simulating four different exposure scenarios. For each experiment, we measured the required computational time and evaluated the impacts of including various model features (e.g., number of output variables calculated) and incorporating various design choices (e.g., different methods for estimating blood concentrations).</p><p><strong>Results: </strong>We observed that model implementations that treat body weight and dependent quantities as constant (fixed) parameters can result in a 30% time savings compared with options that treat body weight and dependent quantities as time-varying. We also observed that decreasing the number of state variables by 36% in our PBPK model template led to a decrease of 20-35% in computational time. Other factors, such as the number of output variables, the method for implementing conditional statements, and the method for estimating blood concentrations, did not have large impacts on simulation time. In general, simulations with PBPK model template implementations of models required more time than simulations with stand-alone implementations, but the flexibility and (human) time savings in preparing and reviewing a model implemented using the PBPK model template may justify the increases in computational time requirements.</p><p><strong>Conclusion: </strong>Our findings concerning how PBPK model design and implementation decisions impact computational speed can benefit anyone seeking to develop, improve, or apply a PBPK model, with or without the PBPK model template.</p>","PeriodicalId":73111,"journal":{"name":"Frontiers in toxicology","volume":"7 ","pages":"1518769"},"PeriodicalIF":4.6000,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11880222/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/ftox.2025.1518769","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: We previously developed a PBPK model template that consists of a single model "superstructure" with equations and logic found in many physiologically based pharmacokinetic (PBPK) models. Using the template, one can implement PBPK models with different combinations of structures and features.

Methods: To identify factors that influence computational time required for PBPK model simulations, we conducted timing experiments using various implementations of PBPK models for dichloromethane and chloroform, including template and stand-alone implementations, and simulating four different exposure scenarios. For each experiment, we measured the required computational time and evaluated the impacts of including various model features (e.g., number of output variables calculated) and incorporating various design choices (e.g., different methods for estimating blood concentrations).

Results: We observed that model implementations that treat body weight and dependent quantities as constant (fixed) parameters can result in a 30% time savings compared with options that treat body weight and dependent quantities as time-varying. We also observed that decreasing the number of state variables by 36% in our PBPK model template led to a decrease of 20-35% in computational time. Other factors, such as the number of output variables, the method for implementing conditional statements, and the method for estimating blood concentrations, did not have large impacts on simulation time. In general, simulations with PBPK model template implementations of models required more time than simulations with stand-alone implementations, but the flexibility and (human) time savings in preparing and reviewing a model implemented using the PBPK model template may justify the increases in computational time requirements.

Conclusion: Our findings concerning how PBPK model design and implementation decisions impact computational speed can benefit anyone seeking to develop, improve, or apply a PBPK model, with or without the PBPK model template.

比较使用PBPK模型模板和独立实现PBPK模型时的模拟计算时间。
我们之前开发了一个PBPK模型模板,该模板由一个单一的模型“上层结构”组成,其中包含许多基于生理的药代动力学(PBPK)模型中的方程和逻辑。使用模板,可以实现具有不同结构和特征组合的PBPK模型。方法:为了确定影响PBPK模型模拟所需计算时间的因素,我们使用不同的二氯甲烷和氯仿PBPK模型实现(包括模板和独立实现)进行了时序实验,并模拟了四种不同的暴露情景。对于每个实验,我们测量了所需的计算时间,并评估了包括各种模型特征(例如,计算输出变量的数量)和结合各种设计选择(例如,估计血液浓度的不同方法)的影响。结果:我们观察到,与将体重和依赖量视为时变的选项相比,将体重和依赖量视为恒定(固定)参数的模型实现可以节省30%的时间。我们还观察到,在我们的PBPK模型模板中减少36%的状态变量数量导致计算时间减少20-35%。其他因素,如输出变量的数量、实现条件语句的方法和估计血液浓度的方法,对模拟时间没有太大的影响。一般来说,使用PBPK模型模板实现模型的模拟比使用独立实现的模拟需要更多的时间,但是在准备和审查使用PBPK模型模板实现的模型时节省的灵活性和(人力)时间可能证明了计算时间需求的增加是合理的。结论:我们关于PBPK模型设计和实施决策如何影响计算速度的研究结果可以使任何寻求开发、改进或应用PBPK模型的人受益,无论是否使用PBPK模型模板。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
13 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信