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通过助溶作用阐明活性药物成分的溶解度增强:以局部麻醉剂为例。

Elucidating the Solubility Enhancement of Active Pharmaceutical Ingredients through Hydrotropy: A Case of Local Anesthetics.

作者信息

Nasrallah Sahar, Wendler Alexander, Hallweger Sebastian A, Kieslich Gregor, Minceva Mirjana

机构信息

Biothermodynamics, TUM School of Life Sciences, Technical University of Munich, Maximus-von Imhof-Forum 2, Freising 85354, Germany.

Department of Chemistry, TUM School of Natural Sciences, Technical University of Munich, Lichtenbergstraße 4, Garching 85748, Germany.

出版信息

Mol Pharm. 2025 Aug 4;22(8):4953-4968. doi: 10.1021/acs.molpharmaceut.5c00628. Epub 2025 Jul 4.

Abstract

Hydrotropy has emerged as a promising approach to enhance the solubility and the availability of hydrophobic active pharmaceutical ingredients (APIs). To understand the hydrotropic effect on API solubility, it is crucial to investigate the molecular interactions and phase behavior in the API-hydrotrope-water system. The solid-liquid equilibrium (SLE) phase diagram of the ternary system aids in quantifying the hydrotropic effect and can guide the selection of an effective hydrotrope and its concentration. However, experimental determination of the complete SLE phase diagram at different temperatures is challenging and labor-intensive. This study introduces a thermodynamic-based method for selecting hydrotropes to enhance the solubility of APIs in water, considering API-hydrotrope, API-water, and hydrotrope-water interactions. The approach was demonstrated using three APIs, lidocaine, procaine, and benzocaine, and three hydrotropes, nicotinamide, caffeine, and urea. The SLE phase diagram of the ternary API-hydrotrope-water systems was predicted using the melting properties of the system components and their activity coefficients in the liquid solution, calculated with the nonrandom two-liquid (NRTL) model. The NRTL model binary interaction parameters were obtained from experimental SLE data for API-hydrotrope, API-water, and hydrotrope-water binary systems. The predicted SLE diagrams of the ternary API-hydrotrope-water systems revealed that the studied systems are eutectic systems with maximum API solubility at the eutectic point. Moreover, the thermodynamic analysis has shown that an efficient hydrotrope strongly interacts with API and water, with nicotinamide yielding the highest API solubility enhancement for the studied systems. This study highlights the potential of thermodynamic modeling in guiding the selection of hydrotropes and their concentrations to achieve the targeted API solubility in water.

摘要

水促溶已成为一种有前景的方法,可提高疏水性活性药物成分(API)的溶解度和可利用性。为了解水促溶对API溶解度的影响,研究API-水促溶剂-水体系中的分子相互作用和相行为至关重要。三元体系的固液平衡(SLE)相图有助于量化水促溶效果,并可指导有效水促溶剂及其浓度的选择。然而,在不同温度下实验测定完整的SLE相图具有挑战性且劳动强度大。本研究引入了一种基于热力学的方法来选择水促溶剂,以提高API在水中的溶解度,该方法考虑了API-水促溶剂、API-水和水促溶剂-水之间的相互作用。使用三种API(利多卡因、普鲁卡因和苯佐卡因)以及三种水促溶剂(烟酰胺、咖啡因和尿素)对该方法进行了验证。利用体系组分的熔化性质及其在液相中的活度系数,通过非随机双液体(NRTL)模型计算,预测了三元API-水促溶剂-水体系的SLE相图。NRTL模型的二元相互作用参数从API-水促溶剂、API-水和水促溶剂-水二元体系的实验SLE数据中获得。三元API-水促溶剂-水体系的预测SLE相图表明,所研究的体系为共晶体系,在共晶点处API溶解度最大。此外,热力学分析表明,有效的水促溶剂与API和水强烈相互作用,在所研究的体系中烟酰胺使API溶解度提高得最多。本研究突出了热力学建模在指导水促溶剂及其浓度选择以实现水中目标API溶解度方面的潜力。

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