Prediction of metabolism and solubility of tablet-form drugs according to the biopharmaceutical drug disposition classification system.

IF 5.1 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2025-09-17 eCollection Date: 2025-01-01 DOI:10.5599/admet.2945
Yaroslava Pushkarova, Galina Zaitseva, Kaouthar Bouaalam
{"title":"Prediction of metabolism and solubility of tablet-form drugs according to the biopharmaceutical drug disposition classification system.","authors":"Yaroslava Pushkarova, Galina Zaitseva, Kaouthar Bouaalam","doi":"10.5599/admet.2945","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and purpose: </strong>Prediction of metabolism and solubility of tablet-form drugs is essential in pharmaceutical development, impacting drug efficacy, safety and formulation strategies. This study aimed to develop predictive models for classifying drugs according to metabolism and solubility within the Biopharmaceutical Drug Disposition Classification System.</p><p><strong>Experimental approach: </strong>A dataset of 220 tablet-form drugs characterized by eleven molecular descriptors was analysed. The Kruskal-Wallis test identified relevant descriptors for metabolism (extensive vs. poor) and solubility (high vs. low) classifications. Probabilistic Neural Networks were employed for predictive modelling, with model parameters optimized to enhance accuracy.</p><p><strong>Key results: </strong>Six molecular descriptors (hydrogen bond acidity, logarithm of the partition coefficient, distribution coefficient, hydrogen bond acceptor count, molecular weight and polar surface area) predicted metabolism class with 97 % accuracy. For solubility classification, five descriptors (dipolarity/polarizability, logarithm of the partition coefficient, distribution coefficient, hydrogen bond donor count and molecular weight) achieved 88 % accuracy. Removal of key descriptors significantly reduced model performance, confirming their importance.</p><p><strong>Conclusion: </strong>The developed models demonstrate robust predictive capability for drug metabolism and solubility classes as defined by the Biopharmaceutical Drug Disposition Classification System, supporting early-stage drug screening based solely on molecular structure. The lower accuracy observed for solubility prediction reflects its complex and multifactorial nature, highlighting the need for further refinement of molecular descriptors. These findings advance the field by providing effective computational tools to predict key biopharmaceutical properties, potentially accelerating the drug development process.</p>","PeriodicalId":7259,"journal":{"name":"ADMET and DMPK","volume":"13 5","pages":"2945"},"PeriodicalIF":5.1000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662240/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ADMET and DMPK","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5599/admet.2945","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background and purpose: Prediction of metabolism and solubility of tablet-form drugs is essential in pharmaceutical development, impacting drug efficacy, safety and formulation strategies. This study aimed to develop predictive models for classifying drugs according to metabolism and solubility within the Biopharmaceutical Drug Disposition Classification System.

Experimental approach: A dataset of 220 tablet-form drugs characterized by eleven molecular descriptors was analysed. The Kruskal-Wallis test identified relevant descriptors for metabolism (extensive vs. poor) and solubility (high vs. low) classifications. Probabilistic Neural Networks were employed for predictive modelling, with model parameters optimized to enhance accuracy.

Key results: Six molecular descriptors (hydrogen bond acidity, logarithm of the partition coefficient, distribution coefficient, hydrogen bond acceptor count, molecular weight and polar surface area) predicted metabolism class with 97 % accuracy. For solubility classification, five descriptors (dipolarity/polarizability, logarithm of the partition coefficient, distribution coefficient, hydrogen bond donor count and molecular weight) achieved 88 % accuracy. Removal of key descriptors significantly reduced model performance, confirming their importance.

Conclusion: The developed models demonstrate robust predictive capability for drug metabolism and solubility classes as defined by the Biopharmaceutical Drug Disposition Classification System, supporting early-stage drug screening based solely on molecular structure. The lower accuracy observed for solubility prediction reflects its complex and multifactorial nature, highlighting the need for further refinement of molecular descriptors. These findings advance the field by providing effective computational tools to predict key biopharmaceutical properties, potentially accelerating the drug development process.

根据生物制药药物处置分类系统预测片剂药物的代谢和溶解度。
背景与目的:预测片剂药物的代谢和溶解度在药物开发中至关重要,影响药物的疗效、安全性和处方策略。本研究旨在建立生物制药药物处置分类系统中根据代谢和溶解度对药物进行分类的预测模型。实验方法:分析了由11个分子描述符表征的220种片剂药物的数据集。Kruskal-Wallis测试确定了代谢(广泛vs.差)和溶解(高vs.低)分类的相关描述符。采用概率神经网络进行预测建模,并对模型参数进行优化,提高预测精度。关键结果:6个分子描述符(氢键酸度、分配系数、分布系数的对数、氢键受体数、分子量和极性表面积)预测代谢类别的准确率为97%。对于溶解度分类,五个描述符(双极性/极化性、分配系数的对数、分配系数、氢键供体计数和分子量)的准确率达到88%。删除关键描述符显著降低了模型性能,确认了它们的重要性。结论:所建立的模型对生物制药药物处置分类系统定义的药物代谢和溶解度类别具有强大的预测能力,支持仅基于分子结构的早期药物筛选。溶解度预测的较低准确性反映了其复杂性和多因素的性质,突出了进一步改进分子描述符的必要性。这些发现通过提供有效的计算工具来预测关键的生物制药特性,从而推动了该领域的发展,有可能加速药物开发过程。
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
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
×
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
小红书