Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento, 6, 61029 Urbino (PU), Italy.
Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento, 6, 61029 Urbino (PU), Italy.
Int J Pharm. 2022 Jul 25;623:121960. doi: 10.1016/j.ijpharm.2022.121960. Epub 2022 Jun 24.
During the past decades, 3D printing has revolutionised different areas of research. Despite the considerable progress achieved in 3D printing of pharmaceuticals, the limited choice of suitable materials remains a challenge to overcome. The growing search for sustainable excipients has led to an increasing interest in biopolymers. Poly(3-hydroxybutyrate) (PHB) is a biocompatible and biodegradable biopolymer obtained from bacteria that could be efficiently employed in the pharmaceutical field. Here we aimed to demonstrate its potential application as a thermoplastic material for personalised medicine through 3D printing. More specifically, we processed PHB by using direct powder extrusion, a one-step additive manufacturing technique. To assess and denote the feasibility and versatility of the process, a 3D square model was manufactured in different dimensions (sidexheight: 12x2 mm; 18x2 mm; 24x2 mm) and loaded with increasing percentages of a model drug (up to 30% w/w). The manufacturing process was influenced by the drug content, and indeed, an increase in the amount of the drug determined a reduction in the printing temperature, without affecting the other parameters (such as the layer height). The composition of the model squares was investigated using Fourier-transform infrared spectroscopy, the resulting spectra confirmed that the starting materials were successfully incorporated into the final formulations. The thermal behaviour of the printed systems was characterized by differential scanning calorimetry, and thermal gravimetric analysis. Moreover, the sustained drug release profile of the formulations was performed over 21 days and showed to be dependent on the dimensions of the printed object and on the amount of loaded drug. Indeed, the formulation with 30% w/w in the dimension 24x2 mm released the highest amount of drug. Hence, the results suggested that PHB and direct powder extrusion technique could be promising tools for the manufacturing of prolonged release and personalised drug delivery forms.
在过去的几十年中,3D 打印技术已经彻底改变了各个领域的研究。尽管在药物 3D 打印方面已经取得了相当大的进展,但合适材料的有限选择仍然是一个需要克服的挑战。对可持续赋形剂的不断探索,导致人们对生物聚合物的兴趣日益增加。聚(3-羟基丁酸酯)(PHB)是一种由细菌获得的生物相容性和可生物降解的生物聚合物,可在制药领域得到有效应用。在这里,我们旨在通过 3D 打印证明其作为热塑性材料在个性化医疗中的潜在应用。更具体地说,我们使用直接粉末挤压法(一种一步式增材制造技术)来处理 PHB。为了评估和表示该过程的可行性和多功能性,我们制造了不同尺寸的 3D 方形模型(边长×高度:12x2mm;18x2mm;24x2mm),并以不同的百分比(最高可达 30%w/w)加载模型药物。药物含量会影响制造过程,事实上,药物含量的增加会降低打印温度,而不会影响其他参数(如层厚)。使用傅里叶变换红外光谱法研究了模型方块的组成,所得光谱证实起始材料已成功地掺入最终配方中。使用差示扫描量热法和热重分析法对打印系统的热行为进行了表征。此外,还进行了制剂的持续药物释放曲线的研究,结果表明,药物释放曲线依赖于打印物体的尺寸和加载药物的量。事实上,在尺寸为 24x2mm 的制剂中,30%w/w 的药物释放了最高量的药物。因此,结果表明 PHB 和直接粉末挤压技术可能是制造延长释放和个性化药物输送形式的有前途的工具。