Equilibrium solubilities, model analysis, solvent effect, molecular dynamic simulation, and thermodynamic properties of itopride hydrochloride in eleven organic pure solvents at different temperatures

IF 2.2 3区 工程技术 Q3 CHEMISTRY, PHYSICAL Journal of Chemical Thermodynamics Pub Date : 2023-12-12 DOI:10.1016/j.jct.2023.107224
Yuan Gao, Yuanhuai Luan, Mingjie Ren, Zidan Cao, Yu Li, Tao Li, Baozeng Ren
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Abstract

Itopride hydrochloride is a novel prokinetic drug used to relieve gastrointestinal diseases. In this paper, the equilibrium solubility of itopride hydrochloride in selected eleven pure solvents (methanol, ethanol, 1-propanol, 2-methoxyethanol, 2-ethoxyethanol, 2-propoxyethanol, acetonitrile, N-methyl-2-pyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide) was determined by the laser monitoring technique at temperatures ranging from 278.15 K to 323.15 K and pressures of 101.3 kPa. The experimental results showed that the equilibrium solubility of itopride hydrochloride in the selected pure solvents were all positively correlated with temperature and the order of equilibrium solubility at 298.15 K was: dimethyl sulfoxide (28.06)>methanol (16.63)>2-methoxyethanol (12.04)>N-methyl-2-pyrrolidone (8.020)>N,N-dimethylformamide (5.117)>N,N-dimethylacetamide(3.576)>2-ethoxyethanol (1.463)>ethanol (0.9341)>2-propoxyethanol (0.4850)>1-propanol (0.2504)>acetonitrile (0.1887). In addition, we used the λh model, modified Apelblat model, NRTL model and van't Hoff model to correlate the experimental data of the equilibrium solubility of itopride hydrochloride. Comparing the ARD and RMSD fitted by the four models, it was found that the NRTL model fitted the best, with the 100ARD value less than 5, and the mean values of 100ARD and 104RMSD were 2.15 and 1.61, respectively. Therefore, the NRTL model is more suitable for the correlation of equilibrium solubility data in this experiment. Furthermore, we analyzed the impact of different solvent properties on the equilibrium solubility of itopride hydrochloride, the molecular dynamics simulation was carried out and the interaction between solute and solvent molecules was analyzed by means of radial distribution functions (RDF). Finally, the apparent thermodynamic properties (ΔdisG°, ΔdisH°, ΔdisS°) of the phase equilibrium process of itopride hydrochloride in eleven organic pure solvents were analyzed by using the van't Hoff equation. The results of the analysis showed that it is entropically increasing and heat absorbing during the dissolution process of itopride hydrochloride.

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盐酸伊托必利在十一种有机纯溶剂中不同温度下的平衡溶解度、模型分析、溶剂效应、分子动力学模拟和热力学性质
盐酸伊托必利是一种新型促胃肠动力药,用于缓解胃肠道疾病。本文采用激光监测技术测定了盐酸伊托必利在选定的 11 种纯溶剂(甲醇、乙醇、1-丙醇、2-甲氧基乙醇、2-乙氧基乙醇、2-丙氧基乙醇、乙腈、N-甲基-2-吡咯烷酮、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、二甲亚砜)中的平衡溶解度,温度范围为 278.15 K 至 323.15 K,压力为 101.3 kPa。实验结果表明,盐酸伊托必利在所选纯溶剂中的平衡溶解度均与温度呈正相关,在 298.15 K 时的平衡溶解度顺序为:二甲亚砜(28.06)>甲醇(16.63)>2-甲氧基乙醇(12.04)>N-甲基-2-吡咯烷酮(8.020)>N,N-二甲基甲酰胺(5.117)>N,N-二甲基乙酰胺(3.576)>2-乙氧基乙醇(1.463)>乙醇(0.9341)>2-丙氧基乙醇(0.4850)>1-丙醇(0.2504)>乙腈(0.1887)。此外,我们还利用λh模型、改进的Apelblat模型、NRTL模型和van't Hoff模型对盐酸伊托必利的平衡溶解度实验数据进行了相关分析。比较四种模型拟合的 ARD 和 RMSD 发现,NRTL 模型拟合效果最好,100ARD 值小于 5,100ARD 和 104RMSD 的平均值分别为 2.15 和 1.61。因此,NRTL 模型更适合本实验中平衡溶解度数据的相关性分析。此外,我们还分析了不同溶剂性质对盐酸伊托必利平衡溶解度的影响,进行了分子动力学模拟,并通过径向分布函数(RDF)分析了溶质和溶剂分子之间的相互作用。最后,利用范特霍夫方程分析了盐酸伊托必利在 11 种有机纯溶剂中相平衡过程的表观热力学性质(ΔdisG°、ΔdisH°、ΔdisS°)。分析结果表明,盐酸伊托必利在溶解过程中呈熵增加和吸热状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemical Thermodynamics
Journal of Chemical Thermodynamics 工程技术-热力学
CiteScore
5.60
自引率
15.40%
发文量
199
审稿时长
79 days
期刊介绍: The Journal of Chemical Thermodynamics exists primarily for dissemination of significant new knowledge in experimental equilibrium thermodynamics and transport properties of chemical systems. The defining attributes of The Journal are the quality and relevance of the papers published. The Journal publishes work relating to gases, liquids, solids, polymers, mixtures, solutions and interfaces. Studies on systems with variability, such as biological or bio-based materials, gas hydrates, among others, will also be considered provided these are well characterized and reproducible where possible. Experimental methods should be described in sufficient detail to allow critical assessment of the accuracy claimed. Authors are encouraged to provide physical or chemical interpretations of the results. Articles can contain modelling sections providing representations of data or molecular insights into the properties or transformations studied. Theoretical papers on chemical thermodynamics using molecular theory or modelling are also considered. The Journal welcomes review articles in the field of chemical thermodynamics but prospective authors should first consult one of the Editors concerning the suitability of the proposed review. Contributions of a routine nature or reporting on uncharacterised materials are not accepted.
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