一个基于分子建模和药物-聚合物相互作用研究的局部配方虚拟工厂。

IF 5.5 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Harshvardhan Modh, Ayça Altay Benetti, Abu Zayed Badruddoza, Jia Yan, Tomasz Panczyk, Jaymin Shah, Giorgia Pastorin, Matthias Gerhard Wacker
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引用次数: 0

摘要

局部给药为全身给药提供了一种具有成本效益和非侵入性的替代方案,但由于皮肤的屏障特性和半固体制剂的复杂流变学,面临着挑战。这需要更深入地了解制剂成分之间的相互作用及其对药物释放和治疗效果的影响。乳化双组分聚合物体系,作为油和表面活性剂的现成液体分散体,越来越多地用于简化制造过程。然而,它们与活性药物成分(api)的相互作用会不可预测地改变制剂的性质。本研究探讨了模型原料药(布比卡因、利多卡因和阿替洛尔)如何影响关键的制剂性质,如流变学、药物释放和制造效率。随着API浓度的增加,观察到粘度的系统性剂量依赖性降低,这是由于静电相互作用导致聚合物网络的破坏。这种效应在不同的胺类中保持一致,并成功地使用指数函数进行拟合。虽然配方pH值对粘度没有显著影响,但较低的pH值加速了药物释放,突出了凝胶微观结构、药物-聚合物相互作用和聚合物系统内释放动力学之间的相互作用。分子模拟表明,原料药在聚合物-油界面上优先定位,而未电离原料药则吸附在油表面。分离力模拟进一步量化了这些相互作用。离体皮肤渗透研究证实了黏度对药物渗透的影响,黏度越低的凝胶渗透速度越快。最后,在一种新颖的从分子到制造的方法中,这些多尺度的见解被集成到一个“虚拟工厂”模型中。该模型成功预测了API浓度对制造参数的影响,为优化设备选择、工艺参数和能耗提供了有价值的工具。这项工作为局部系统的合理设计提供了一个全面的框架,将分子相互作用与最终制造结果联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A virtual factory for topical formulations based on molecular modeling and drug-polymer interaction studies.

Topical drug delivery offers a cost-effective and non-invasive alternative to systemic drug administration but faces challenges due to the skin's barrier properties and the complex rheology of semisolid formulations. This necessitates a deeper understanding of the interplay between formulation components and their impact on drug release and therapeutic efficacy. Emulsifying two-component polymer system, supplied as ready-to-use liquid dispersions of oil and surfactant, is increasingly used to simplify manufacturing processes. However, their interaction with active pharmaceutical ingredients (APIs) can unpredictably alter formulation properties. This study investigates how the model APIs (bupivacaine, lidocaine, and atenolol) influence key formulation properties, such as rheology, drug release, and manufacturing efficiency. A systematic, dose-dependent reduction in viscosity was observed with increasing API concentration, an effect attributed to the disruption of the polymer network via electrostatic interactions. This effect remained consistent across different amine classes and was successfully fitted using an exponential function. While formulation pH did not significantly affect viscosity, lower pH values accelerated drug release, highlighting the interplay between gel microstructure, drug-polymer interactions, and release kinetics within this polymer system. Molecular modeling revealed preferential localization of ionized APIs at the polymer-oil interface, while unionized APIs adsorbed onto the oil surface. Detachment force simulations further quantified these interactions. Ex-vivo skin permeation studies confirmed the influence of viscosity on drug permeation, with lower viscosity gels exhibiting faster permeation rates. Finally, in a novel molecule-to-manufacturing approach, these multi-scale insights were integrated into a "Virtual Factory" model. This model successfully predicted the impact of API concentration on manufacturing parameters, offering a valuable tool to optimize equipment selection, process parameters, and energy consumption. This work provides a comprehensive framework for the rational design of topical systems, connecting molecular interactions to final manufacturing outcomes.

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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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