Ahmed Yasser, Alshami Ali S, Al-Goraee Ashraf, Obeng Collins P, Kennedy Rebecca, Abdelaziz Hesham, Striker Ryan
Biomedical Engineering Department, University of North Dakota, Grand Forks, ND, 58202, USA.
Department of Chemical Engineering, University of North Dakota, Grand Forks, ND, 58202, USA.
Ann Biomed Eng. 2025 Jun 5. doi: 10.1007/s10439-025-03752-9.
While fabrication of bone scaffolds is important for the development of tissue engineering, traditional techniques have typically been prone to either scaling or reproducibility issues. This paper highlights a strategy for automated 3D printing and bioprinting techniques that enhance precision and efficiency in the production of PLGA-HA scaffolds. We realized significant improvements in efficiency, reproducibility, and scalability through optimization of 3D printing parameters, improvement of material handling, and refinement of the fabrication process. Precise measurement consequently minimized material waste; the introduction of a mesh filter allowed for high-throughput experimentation without compromising the integrity of individual scaffolds, streamlining the workflow. Combining automated casting with state-of-the-art 3D bioprinting, our experimental methodology precisely applied the bioactive materials, reducing the processing time fivefold and enhancing precision. Besides, automated casting produced thicker, better-quality scaffolds averaging 0.02354 g, which is against 0.01169 g using the manual approach, effectively doubling the retention of the PLGA-HA coating on a PVA mold. Excellent cell viability and adhesion on automated scaffolds have been further underlined for application in tissue engineering during in vitro studies using multipotent mesenchymal stromal cells. Although conventional techniques, such as injection molding, are standard for large lots, 3D printing has advantages in scaffold fabrication regarding control over geometry and homogeneous material properties. Equally important, these characteristics are necessary to achieve repeatable and up-scaled experimental results.
虽然骨支架的制造对于组织工程的发展很重要,但传统技术通常容易出现放大或可重复性问题。本文重点介绍了一种用于自动3D打印和生物打印技术的策略,该策略可提高PLGA-HA支架生产的精度和效率。我们通过优化3D打印参数、改进材料处理和完善制造工艺,在效率、可重复性和可扩展性方面实现了显著提升。精确测量因此将材料浪费降至最低;引入滤网允许进行高通量实验,同时不影响单个支架的完整性,简化了工作流程。将自动浇铸与最先进的3D生物打印相结合,我们的实验方法精确地应用了生物活性材料,将处理时间缩短了五倍并提高了精度。此外,自动浇铸生产出的支架更厚、质量更好,平均重量为0.02354克,而手动方法生产的支架重量为0.01169克,有效地使PLGA-HA涂层在PVA模具上的保留率提高了一倍。在使用多能间充质基质细胞进行的体外研究中,自动支架上出色的细胞活力和粘附性进一步凸显了其在组织工程中的应用潜力。尽管传统技术,如注塑成型,是大批量生产的标准方法,但3D打印在支架制造方面具有控制几何形状和均匀材料特性的优势。同样重要地,这些特性对于获得可重复和放大的实验结果是必要的。