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探索依达拉奉在纯溶剂和二元混合物中的溶解度极限:实验与机器学习研究

Exploring the Solubility Limits of Edaravone in Neat Solvents and Binary Mixtures: Experimental and Machine Learning Study.

作者信息

Przybyłek Maciej, Jeliński Tomasz, Mianowana Magdalena, Misiak Kinga, Cysewski Piotr

机构信息

Department of Physical Chemistry, Pharmacy Faculty, Collegium Medicum of Bydgoszcz, Nicolaus Copernicus University in Toruń, Kurpińskiego 5, 85-096 Bydgoszcz, Poland.

出版信息

Molecules. 2023 Sep 29;28(19):6877. doi: 10.3390/molecules28196877.

Abstract

This study explores the edaravone solubility space encompassing both neat and binary dissolution media. Efforts were made to reveal the inherent concentration limits of common pure and mixed solvents. For this purpose, the published solubility data of the title drug were scrupulously inspected and cured, which made the dataset consistent and coherent. However, the lack of some important types of solvents in the collection called for an extension of the available pool of edaravone solubility data. Hence, new measurements were performed to collect edaravone solubility values in polar non-protic and diprotic media. Such an extended set of data was used in the machine learning process for tuning the parameters of regressor models and formulating the ensemble for predicting new data. In both phases, namely the model training and ensemble formulation, close attention was paid not only to minimizing the deviation of computed values from the experimental ones but also to ensuring high predictive power and accurate solubility computations for new systems. Furthermore, the environmental friendliness characteristics determined based on the common green solvent selection criteria, were included in the analysis. Our applied protocol led to the conclusion that the solubility space defined by ordinary solvents is limited, and it is unlikely to find solvents that are better suited for edaravone dissolution than those described in this manuscript. The theoretical framework presented in this study provides a precise guideline for conducting experiments, as well as saving time and resources in the pursuit of new findings.

摘要

本研究探索了涵盖纯溶剂和二元溶解介质的依达拉奉溶解度空间。努力揭示常见纯溶剂和混合溶剂的固有浓度极限。为此,对已发表的标题药物溶解度数据进行了严格审查和修正,使数据集一致且连贯。然而,收集的溶剂中缺少一些重要类型,这就需要扩展依达拉奉溶解度数据的可用库。因此,进行了新的测量,以收集依达拉奉在极性非质子和双质子介质中的溶解度值。这样一组扩展数据被用于机器学习过程,以调整回归模型的参数并构建用于预测新数据的集成模型。在模型训练和集成模型构建这两个阶段,不仅密切关注使计算值与实验值之间的偏差最小化,还确保新系统具有高预测能力和准确的溶解度计算。此外,基于常见绿色溶剂选择标准确定的环境友好特性也纳入了分析。我们应用的方案得出结论,普通溶剂定义的溶解度空间是有限的,不太可能找到比本手稿中描述的更适合依达拉奉溶解的溶剂。本研究提出的理论框架为进行实验提供了精确指导,同时在寻求新发现时节省了时间和资源。

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