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垂直热熔挤出:创新中的下一个挑战。

Vertical Hot-Melt Extrusion: The Next Challenge in Innovation.

作者信息

Gallas Maël, Medjahdi Ghouti, Boulet Pascal, de Margerie Victoire

机构信息

Rondol Industrie, 2 Allée André Guinier, 54000 Nancy Cedex, France.

Institut Jean Lamour (IJL), Université de Lorraine, CNRS, 2 Allée André Guinier, 54000 Nancy, France.

出版信息

Pharmaceutics. 2025 Jul 21;17(7):939. doi: 10.3390/pharmaceutics17070939.

Abstract

Hot-melt extrusion (HME) has become a key technology in pharmaceutical formulation, particularly for enhancing the solubility of poorly soluble Active Pharmaceutical Ingredients (APIs). While horizontal HME is widely adopted, vertical HME remains underexplored despite its potential benefits in footprint reduction, feeding efficiency, temperature control, and integration into continuous manufacturing. This study investigates vertical HME as an innovative approach in order to optimize drug polymer interactions and generate stable amorphous dispersions with controlled release behavior. Extrusion trials were conducted using a vertical hot-melt extruder developed by Rondol Industrie (Nancy, France). Acetylsalicylic acid (ASA) supplied by Seqens (Écully, France) was used as a model API and processed with Soluplus and Kollidon 12 PF (BASF, Ludwigshafen, Germany). Various process parameters (temperature, screw speed, screw profile) were explored. The extrudates were characterized by powder X-ray diffraction (PXRD) and small-angle X-ray scattering (SAXS) to evaluate crystallinity and microstructure. In vitro dissolution tests were performed under sink conditions using USP Apparatus II to assess drug release profiles. Vertical HME enabled the formation of homogeneous amorphous solid dispersions. PXRD confirmed the absence of residual crystallinity, and SAXS revealed nanostructural changes in the polymer matrix influenced by drug loading and thermal input. In vitro dissolution demonstrated enhanced drug release rates compared to crystalline ASA, with good reproducibility. Vertical HME provides a compact, cleanable, and modular platform that supports the development of stable amorphous dispersions with controlled release. It represents a robust and versatile solution for pharmaceutical innovation, with strong potential for cost-efficient continuous manufacturing and industrial-scale adoption.

摘要

热熔挤出(HME)已成为药物制剂中的一项关键技术,特别是在提高难溶性活性药物成分(API)的溶解度方面。虽然卧式HME已被广泛采用,但立式HME尽管在减少占地面积、进料效率、温度控制以及集成到连续制造方面具有潜在优势,却仍未得到充分探索。本研究将立式HME作为一种创新方法进行研究,以优化药物与聚合物的相互作用,并生成具有控释行为的稳定无定形分散体。使用由法国隆多尔工业公司(南锡)开发的立式热熔挤出机进行挤出试验。由法国塞肯公司(埃屈利)提供的乙酰水杨酸(ASA)用作模型API,并与Solup lus和科利通12 PF(德国巴斯夫公司,路德维希港)一起进行加工。探索了各种工艺参数(温度、螺杆速度、螺杆外形)。通过粉末X射线衍射(PXRD)和小角X射线散射(SAXS)对挤出物进行表征,以评估结晶度和微观结构。在漏槽条件下使用美国药典装置II进行体外溶出试验,以评估药物释放曲线。立式HME能够形成均匀的无定形固体分散体。PXRD证实没有残留结晶度,SAXS揭示了聚合物基质中受药物负载和热输入影响的纳米结构变化。体外溶出试验表明,与结晶型ASA相比,药物释放速率有所提高,且重现性良好。立式HME提供了一个紧凑、可清洁且模块化的平台,支持开发具有控释功能的稳定无定形分散体。它代表了一种强大且通用的药物创新解决方案,在具有成本效益的连续制造和工业规模应用方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0b2/12299094/d55a76eea80c/pharmaceutics-17-00939-g001.jpg

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