咖啡因在不同纯溶剂中的汉森溶解度参数研究

María Ángeles Peña, Angeliki. Kaproulia, D. R. Delgado, A. Jouyban, José María Machuca, F. Martínez
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摘要

本文的主要目的是通过汉森溶解度参数(HSP)和 KAT-LSER 模型来解释分子性质差异和分子间相互作用对溶解度的影响。研究设计:溶解度是一种分子性质,在从药物开发和设计到最终药物制剂和生产的整个过程中起着决定性作用,本文的主要目的是通过汉森溶解度参数(HSP)和 KAT-LSER 模型解释分子性质差异和分子间相互作用对溶解度的影响。研究地点和时间:药学院生物医学科学系。2023 年 4 月至 2024 年 4 月。研究方法:在药物制剂、纯化和晶体形成过程中使用的几类化学键的纯单溶剂中测量药物的溶解度。对 HSP 进行了测试,以确定咖啡因的部分溶解度参数。以实验溶解度分子分数的对数 ln X2 作为因变量。KAT-LSER 模型表明,溶质与溶剂之间的相互作用主要归因于二极性/极化性相互作用和氢键碱性。对原始粉末和用纯溶剂平衡后的固相进行了差示扫描量热法(DSC)和傅立叶变换红外光谱法(FT-IR)分析。结果:采用三参数和四参数溶解度模型得到了良好的结果。由于不同药物的分散参数变化不大,因此不同溶剂之间溶解度的变化主要是由双极参数和氢键参数造成的,这一点在其他小分子量药物中也得到了一致的证实。通过 DSC 和 FT-IR 可以检测固相热性质的可能变化,并验证起始材料的无水性质。结论结果表明,咖啡因的溶解度主要受极性和/或氢键的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation on Hansen Solubility Parameter of Caffeine Dissolved in Different Pure Solvents
Aims: Solubility is a molecular property decisive in the entire process from drug development and design to the final drug formulation and production, the main objective of this paper is to explain the effect of the variance in molecular properties and intermolecular interaction on dissolution by Hansen Solubility Parameter (HSP) and KAT-LSER model. Study Design: Solubility is a molecular property decisive in the entire process from the drug development and design to the final drug formulation and production, the main objective of this paper is to explain the effect of the variance in molecular properties and intermolecular interaction on dissolution by Hansen Solubility Parameter (HSP) and KAT-LSER model. Place and Duration of Study: Department of Biomedical Sciences, Faculty of Pharmacy. Between April 2023-April 2024. Methodology: The solubility of the drug was measured in pure mono solvents of several chemical classes keys in formulation, purification, and crystal formation of drugs. HSP was tested to determine the partial solubility parameters of caffeine. The logarithm of the mole fraction experimental solubility ln X2 as the dependent variable was used. KAT-LSER model was used to show that solute-solvent interactions are principally attributed to the dipolarity/polarizability interaction and the hydrogen bonding basicity. Differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FT‐IR) were performed for the original powder and the solid phase after equilibration with the pure solvents. Results: Good results were obtained with the model of three- and four-partial parameters of solubility. Since the dispersion parameter does not greatly vary from one drug to another, the variation of solubility among solvents is largely due to the dipolar and hydrogen bonding parameters, a fact that is consistently found for other drugs of small molecular weight. DSC and FT-IR allow the detection of possible changes in the thermal properties of the solid phase and verify the anhydrous nature of the starting material. Conclusion: The results showed that the solubility of caffeine is mostly affected by polarity and/or hydrogen bonding.
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