三维打印 PVA 胶囊装置在配制药剂中的应用:设计参数对制药性能的影响

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2024-08-15 DOI:10.3390/pharmaceutics16081069
Juan Francisco Peña, Ivana Cotabarren, Loreana Gallo
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引用次数: 0

摘要

在制药领域,利用三维(3D)打印等创新技术创造具有个性化或创新功能的产品尤其值得关注,特别是在复方药剂领域。在这项工作中,设计并成功制造了不同壁厚(0.2、0.3、0.4、0.6 和 0.9 毫米)和尺寸的三维打印胶囊装置(CD),并改变了挤出温度、打印速度、材料流动百分比和喷嘴直径等打印参数。对这些 CD 的理化、制药和生物制药性能进行了评估,目的是获得与硬明胶胶囊(HGC)相媲美的即时药物释放特性,以便在磁性复合物中使用。研究发现,光盘的崩解时间随壁厚的增加而增加,这与药物释放速度减慢有关。壁厚为 0.4 毫米、大小与 0 号、1 号和 2 号 HGC 相当的 CD 显示出令人满意的重量均匀性、较短的崩解时间和即时的药物释放,这表明它们有望成为未来复方制剂应用中的有效设备。此外,还提出了一种改进的 Weibull 型模型,该模型将壁厚作为预测溶出曲线的一个新变量。该模型改进了选择特定壁厚的过程,从而在指定时间内达到理想的溶出率。
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Three-Dimensional Printing of PVA Capsular Devices for Applications in Compounding Pharmacy: Effect of Design Parameters on Pharmaceutical Performance.

The creation of products with personalized or innovative features in the pharmaceutical sector by using innovative technologies such as three-dimensional (3D) printing is particularly noteworthy, especially in the realm of compounding pharmacies. In this work, 3D printed capsule devices (CDs) with different wall thicknesses (0.2, 0.3, 0.4, 0.6, and 0.9 mm) and sizes were designed and successfully fabricated varying printing parameters such as extrusion temperature, printing speed, material flow percent, and nozzle diameter. The physicochemical, pharmaceutical, and biopharmaceutical performance of these CDs was evaluated with the aim of achieving an immediate drug release profile comparable to hard gelatin capsules (HGC) for use in magistral compounding. It was observed that the disintegration time of the CDs increased with wall thickness, which correlated with a slower drug release rate. CDs with configurations presenting 0.4 mm wall thickness and sizes comparable to HGC n° 0, 1, and 2 demonstrated satisfactory weight uniformity, short disintegration times, and immediate drug release, indicating their potential as effective devices in future compounding pharmacy applications. In addition, a modified Weibull-type model was proposed that incorporates wall thickness as a new variable in predicting dissolution profiles. This model improves the process of selecting a specific wall thickness to achieve the desired dissolution rate within a specified time frame.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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