Polymeric Drug Nanocarrier Production by Nanoprecipitation-Solvent Neutralization: A Chemically Driven Route to Rapid Solvent Removal

IF 5.8 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Nano Materials Pub Date : 2026-10-16 Epub Date: 2026-08-12 DOI:10.1021/acsanm.6c01923
Gabriela Spingolon, Matheus Stecker Andrade, Daniela Lana Tommasi Schmitt, Felipe Schlichta de Gouveia, Gabriel Fraga Ribas, Natália Elisa Turra de Castro, Marcelo Jung Eberhardt, Fabiano Severo Rodembusch, Karina Paese, Tanira Alessandra Silveira Aguirre, Fernanda Poletto
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引用次数: 0

Abstract

We report a bottom-up strategy, termed nanoprecipitation-solvent neutralization, for the preparation of drug-loaded polymeric nanospheres and nanocapsules for pharmaceutical applications. The method is compatible with hydrolysis-sensitive drug molecules and accommodates pharmaceutically approved polymers and excipients that are water-insoluble across the entire pH range. In this approach, an organic phase containing polymer and, when appropriate, additional hydrophobic components dissolved in glacial acetic acid is combined with an aqueous phase containing a stabilizer, inducing nanoparticle nucleation and growth via the Ouzo effect. Glacial acetic acid serves both as the nanoprecipitation solvent and as a chemically removable species that can be converted into a water-soluble salt through a simple acid−base reaction. Following particle formation, solvent neutralization substantially reduces solvent-removal times relative to conventional evaporation-based nanoprecipitation without the need for specialized equipment. No significant degradation of polymers-drugs, or stabilizers was observed by GPC and HPLC analyses despite the presence of hydrolysis-sensitive bonds. The use of a weak base following the transient acidic step was fundamental for maintaining formulation stability by generating a buffering system in the near-neutral pH range. Mechanistic insights obtained using an environment-sensitive photophysical probe revealed a transition in the medium polarity and pH consistent with efficient solvent-to-salt conversion following nanoparticle formation. The method was effective across systems containing hydrophobic components and enabled the preparation of nanoparticles stabilized with nonionic, anionic, or cationic surfactants, allowing modulation of surface charge. The resulting nanoparticles exhibited diameters ranging from 146 to 272 nm and spherical morphology with smooth surfaces, as confirmed by TEM. The salt formed during solvent neutralization could be readily removed without affecting nanoparticle properties. Overall, this approach establishes a chemically driven route to nanoprecipitation in which solvent removal is not governed by mass transport, providing a simple and versatile platform for the production of polymeric nanoparticles for pharmaceutical applications.

纳米沉淀-溶剂中和法制备高分子药物纳米载体:一种化学驱动的快速溶剂去除途径
我们报告了一种自下而上的策略,称为纳米沉淀-溶剂中和,用于制备药物负载的聚合物纳米球和纳米胶囊。该方法与水解敏感的药物分子兼容,并适应在整个pH范围内不溶于水的药学上批准的聚合物和赋形剂。在这种方法中,将含有聚合物的有机相和(适当时)溶解在冰醋酸中的其他疏水组分与含有稳定剂的水相结合,通过Ouzo效应诱导纳米颗粒成核和生长。冰醋酸既可以作为纳米沉淀溶剂,也可以作为一种化学可去除的物质,通过简单的酸碱反应可以转化为水溶性盐。在颗粒形成后,相对于传统的基于蒸发的纳米沉淀法,溶剂中和大大减少了溶剂去除时间,而不需要专门的设备。尽管存在水解敏感键,但GPC和HPLC分析并未观察到聚合物-药物或稳定剂的明显降解。在短暂的酸性步骤之后使用弱碱是通过在接近中性的pH范围内产生缓冲系统来保持配方稳定性的基础。利用环境敏感光物理探针获得的机理揭示了介质极性和pH值的转变,与纳米颗粒形成后有效的溶剂到盐转化一致。该方法在含有疏水组分的体系中都是有效的,并且可以制备由非离子、阴离子或阳离子表面活性剂稳定的纳米颗粒,从而可以调节表面电荷。透射电镜证实,所制得的纳米颗粒直径在146 ~ 272 nm之间,呈球形,表面光滑。在溶剂中和过程中形成的盐可以很容易地去除而不影响纳米颗粒的性质。总的来说,这种方法建立了一种化学驱动的纳米沉淀途径,其中溶剂去除不受质量传输的控制,为制药应用的聚合物纳米颗粒的生产提供了一个简单而通用的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.30
自引率
3.40%
发文量
1601
期刊介绍: ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.
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