Solubility Enhancement of Active Pharmaceutical Ingredients through Liquid Hydrotrope Addition: A Thermodynamic Analysis

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Pharmaceutics Pub Date : 2025-02-13 DOI:10.1021/acs.molpharmaceut.4c0111710.1021/acs.molpharmaceut.4c01117
Sahar Nasrallah,  and , Mirjana Minceva*, 
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Abstract

The poor water solubility of active pharmaceutical ingredients (APIs) poses a significant challenge in pharmaceutical development, affecting their bioavailability and therapeutic efficacy. Consequently, there is an urgent demand for strategies to improve API solubility, with hydrotropy emerging as one of the most effective approaches. Hydrotropes, which can act as excipients in pharmaceutical formulations, enhance solubility by solubilizing hydrophobic compounds in aqueous solutions through mechanisms other than micellar solubilization. However, identifying the right hydrotropic agent requires a screening from a large pool of candidates. This work aims to analyze hydrotropy from a thermodynamic perspective by investigating the influence of the molecular interactions among the API, hydrotrope, and water on the API solubility in water at different temperatures. For this systematic study, hypothetical ternary systems were used and only liquid hydrotropes were considered. Utilizing the Two-Suffix Margules equation to model the liquid phase nonideality, the study revealed that strong API–hydrotrope interactions notably enhance the API solubility in water. Additionally, the interaction between the hydrotrope and water significantly influences API solubility; weaker hydrotrope–water interactions allow for increased API solubility in water. However, when hydrotrope–water interactions are stronger than API–hydrotrope interactions, this effect is diminished. The theoretical findings were validated using solubility experimental data of syringic acid with alkanediols in water from the literature. The results of this work will aid in selecting suitable liquid hydrotropes for enhancing the API solubility in aqueous solutions.

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活性药物成分(API)的水溶性较差,影响了其生物利用度和治疗效果,给药物开发带来了巨大挑战。因此,人们急需改善原料药溶解度的策略,而水溶解是最有效的方法之一。水合作用剂可作为药物制剂中的辅料,通过胶束增溶以外的机制使水溶液中的疏水性化合物增溶,从而提高溶解度。然而,要确定合适的亲水剂,需要从大量候选物质中进行筛选。本研究旨在从热力学角度分析亲水作用,研究不同温度下原料药、亲水剂和水之间的分子相互作用对原料药在水中溶解度的影响。在这项系统性研究中,使用了假设的三元体系,并且只考虑了液态水托品。该研究利用马格力斯(Two-Suffix Margules)方程对液相非理想性进行建模,结果表明,强烈的原料药-水媒相互作用会显著提高原料药在水中的溶解度。此外,水胶与水之间的相互作用也会对原料药的溶解度产生重大影响;水胶与水之间较弱的相互作用会增加原料药在水中的溶解度。然而,当水胶与水的相互作用强于原料药与水胶的相互作用时,这种影响就会减弱。利用文献中丁香酸与烷二醇在水中的溶解度实验数据,对理论研究结果进行了验证。这项工作的结果将有助于选择合适的液体水托品来提高原料药在水溶液中的溶解度。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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