液滴沉积建模增材制造中的材料兼容性和加工挑战:聚乙烯吡咯烷酮/醋酸乙烯(PVP/VA)和聚己内酯(PCL)药用辅料研究。

IF 4.3 3区 医学 Q1 PHARMACOLOGY & PHARMACY European Journal of Pharmaceutical Sciences Pub Date : 2024-07-10 DOI:10.1016/j.ejps.2024.106850
Farnoosh Ebrahimi, Han Xu, Evert Fuenmayor, Ian Major
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引用次数: 0

摘要

快速成型制造(AM)可以生产复杂、轻质和定制化的优质部件。考虑到材料的热性能、可印刷性和层粘附性,选择合适的材料对基于熔融的 AM 技术至关重要。本研究调查了液滴沉积建模(DDM),这是一种利用热塑性颗粒的创新材料挤压工艺。DDM 的特点是制造时间更短,材料范围更广,有别于熔融长丝制造等传统材料挤出方法。我们使用两种常见的药用辅料对 DDM 的可印刷性和零件质量进行了研究:聚乙烯吡咯烷酮/醋酸乙烯酯 6:4 (PVP/VA)(脆性高)和聚己内酯 (PCL)(溶解度低,可控制药物释放)。通过热熔挤压(HME)将不同比例的 PVP/VA 和 PCL 混合物用于 DDM,研究成分含量对可印刷性和零件质量的影响,并采用几何模型评估材料的兼容性和可印刷性。研究结果表明,PVP/VA 含量的增加会导致粘度升高、流动性降低和沉积不均匀,PVP/VA 含量为 80% 和 100% 的配方加工性较差。相比之下,PVP/VA 含量分别为 60% 和 40% 的配方则可顺利加工并与 DDM 兼容。我们发现加工温度和液滴纵横比(DAR)是影响材料可印刷性和零件质量的关键因素。我们发现,加工温度升高和 DAR 降低会增加界面温度、减少扩散并可能导致 "象脚 "问题。此外,较小的液滴尺寸和材料特性(如 PCL 较高的界面张力)也可能导致凝聚。我们的研究结果凸显了优化 DDM 加工参数和混合材料的复杂性,强调了精心设计配方以实现高质量 3D 打印产品的必要性。
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Material Compatibility and Processing Challenges in Droplet Deposition Modelling Additive Manufacturing: A Study on Pharmaceutical Excipients Polyvinylpyrrolidone/vinyl acetate (PVP/VA) and Polycaprolactone (PCL)

Additive manufacturing (AM) enables the production of complex, lightweight, and customized components with superior quality. Selecting the right materials considering their thermal properties, printability, and layer adhesion is crucial in melting-based AM techniques. This study investigates Droplet Deposition Modelling (DDM), an innovative material extrusion process that utilizes thermoplastic granules. DDM is distinguished by its shorter manufacturing times and a wider range of materials, setting it apart from traditional material extrusion methods such as fused filament fabrication. We investigated the printability and part quality in DDM using two common pharmaceutical excipients: Polyvinylpyrrolidone/vinyl acetate 6:4 (PVP/VA), which is highly brittle, and Polycaprolactone (PCL), known for its low solubility and role in controlled drug release. Different ratios of PVP/VA and PCL were compounded via hot melt extrusion (HME) and used in DDM to study the impact of ingredient content on printability and part quality, employing geometrical models to assess material compatibility and printability. The study revealed that increasing PVP/VA content leads to higher viscosity, reduced flowability, and uneven deposition, with formulations of 80% and 100% PVP/VA showing poor processability. In contrast, formulations with 60% and 40% PVP/VA exhibited smooth processing and compatibility with DDM. We identified processing temperature and Drop Aspect Ratio (DAR) as key factors influencing material printability and part quality. Elevated processing temperatures and reduced DAR were found to increase interface temperatures, reduce diffusion, and potentially cause the 'elephant feet' issue. Additionally, smaller droplet sizes and material characteristics, such as higher interfacial tension in PCL, could lead to coalescence. Our findings highlight the complexities in optimizing DDM processing parameters and material blends, underscoring the need for careful formulation design to achieve high-quality 3D printed products.

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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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