Exploration of solubilisation effects facilitated by the combination of Soluplus® with ionic surfactants.

IF 4.3 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2024-11-15 DOI:10.1016/j.ejps.2024.106957
Justus Johann Lange, Lukas Enzner, Martin Kuentz, Patrick J O'Dwyer, Wiebke Saal, Brendan T Griffin, Nicole Wyttenbach
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Abstract

Preclinical testing of new drug candidates frequently necessitates high-dose solution formulations to support robust testing in rodent models. This study aimed to expand the range of high solubilisation capacity formulations by exploring the solubilisation effects of the polymeric surfactant Soluplus® in combination with ionic surfactants. The interactions between Soluplus® and three ionic surfactants, sodium dodecyl sulfate, dioctyl sodium succinate, and sodium oleate, with a primary focus on solubility enhancement were investigated over a range of ionic surfactant concentrations. The solubilisation profiles for seven model drugs were obtained, and the vehicles were characterized by their visual characteristics, dynamic light scattering, and viscosity measurements. The solubilisation profiles were non-linear, indicating the formation of different colloidal species with individual solubilisation strengths depending on surfactant type and concentration, demonstrating substantial solubility enhancement. For certain drugs more than additive solubilisation, facilitated by synergistic interactions between Soluplus® and the ionic surfactants, was obtained. Overall, the solubility increase provided by the excipient combinations resulted in non-linear and drug specific solubilisation profiles. The non-linearities observed were reflected in visual observations of the vehicles appearance, DLS and viscosity measurements, which collectively indicated a change in polymer aggregation with increasing concentration of anionic surfactant. This investigation highlights that already low quantities of ionic surfactants introduced to Soluplus® may substantially enhance solubility, which offers a promising approach for further exploration in preclinical drug development where more conventional solubilising formulation strategies may fall short.

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探索 Soluplus® 与离子表面活性剂结合后的增溶效果。
新药候选物的临床前测试通常需要高剂量溶液配方,以支持啮齿动物模型的稳健测试。本研究旨在通过探索聚合物表面活性剂 Soluplus® 与离子表面活性剂结合的增溶效果,扩大高增溶能力制剂的范围。研究了 Soluplus® 与三种离子表面活性剂(十二烷基硫酸钠、琥珀酸二辛酯钠和油酸钠)之间的相互作用,主要重点是在一定浓度的离子表面活性剂中提高溶解度。获得了七种模型药物的增溶曲线,并通过视觉特征、动态光散射和粘度测量对载体进行了表征。增溶曲线是非线性的,表明根据表面活性剂的类型和浓度形成了不同的胶体物种,其各自的增溶强度也不同,这表明药物的溶解度得到了大幅提高。Soluplus® 与离子表面活性剂之间的协同作用促进了某些药物的增溶。总之,辅料组合带来的溶解度增加导致了非线性和药物特定的溶解曲线。观察到的非线性现象反映在对载体外观的目测、DLS 和粘度测量中,这些结果共同表明,随着阴离子表面活性剂浓度的增加,聚合物的聚集情况也会发生变化。这项研究表明,在 Soluplus® 中加入少量离子表面活性剂就能大大提高溶解度,这为临床前药物开发提供了一种很有前景的方法,因为在临床前药物开发中,传统的增溶配方策略可能会出现不足。
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来源期刊
CiteScore
9.60
自引率
2.20%
发文量
248
审稿时长
50 days
期刊介绍: The journal publishes research articles, review articles and scientific commentaries on all aspects of the pharmaceutical sciences with emphasis on conceptual novelty and scientific quality. The Editors welcome articles in this multidisciplinary field, with a focus on topics relevant for drug discovery and development. More specifically, the Journal publishes reports on medicinal chemistry, pharmacology, drug absorption and metabolism, pharmacokinetics and pharmacodynamics, pharmaceutical and biomedical analysis, drug delivery (including gene delivery), drug targeting, pharmaceutical technology, pharmaceutical biotechnology and clinical drug evaluation. The journal will typically not give priority to manuscripts focusing primarily on organic synthesis, natural products, adaptation of analytical approaches, or discussions pertaining to drug policy making. Scientific commentaries and review articles are generally by invitation only or by consent of the Editors. Proceedings of scientific meetings may be published as special issues or supplements to the Journal.
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