NanoBioCel Research Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad 7, 01006, Vitoria Gasteiz, Spain.
NanoBioCel Research Group, Vitoria Gasteiz, Spain.
Drug Deliv Transl Res. 2024 Dec;14(12):3385-3403. doi: 10.1007/s13346-023-01506-5. Epub 2024 Jan 7.
Traditional approaches to solid rectal therapies have halted progress, leading to a continual decline in the use of conventional suppositories. Additive manufacturing techniques have been recently explored as a suitable innovative tool for suppository fabrication. However, little advancement has been made in composition materials for 3D-printed suppository (3DPS) manufacturing and still, conventional vehicles are often used for construct fabrication, hindering the growth in the field. As a novelty, this study unveils a ground-breaking Laponite-alginate hydrogel-based 3DPS. Interestingly, this study proposes a novel approach for loading drugs into the 3DPS employing for the first time the post-printing loading. Thus, a passive loading strategy of molecular models is developed, demonstrating the versatility and capacity to load molecules of different charges and molecular sizes within the matrix systems. This novel strategy allows adapting the load of a wide range of drugs into a single ink, which simplifies and speeds up the 3DPS technological development process for drugs with different physico-chemical properties. Additionally, in this research, a displacement strategy of the three-dimensional Laponite matrices is developed in order to enhance the drug release capacity through the 3DPS and their disintegration capacity, resulting in a significant improvement of the drug diffusion through the hydrogel matrix and a rapid disintegration of the 3DPS. Finally, our study demonstrates that the obtained 3DPS have a suitable in vivo behavior, being non-obstructive and allowing the normal motility of the rats intestine.
传统的直肠固体制剂方法已经停滞不前,导致传统栓剂的使用不断下降。增材制造技术最近被探索作为栓剂制造的合适创新工具。然而,在 3D 打印栓剂(3DPS)制造的组成材料方面几乎没有进展,并且仍然经常使用传统载体进行构建,阻碍了该领域的发展。作为一种新颖性,本研究揭示了一种基于 Laponite-海藻酸盐水凝胶的突破性 3DPS。有趣的是,本研究提出了一种将药物加载到 3DPS 中的新方法,首次采用了打印后加载。因此,开发了一种分子模型的被动加载策略,证明了在基质系统内加载不同电荷和分子大小的分子的多功能性和能力。这种新策略允许将多种药物的负载适应到单个墨水中,从而简化和加快具有不同物理化学性质的药物的 3DPS 技术发展过程。此外,在这项研究中,开发了一种三维 Laponite 基质的置换策略,以通过 3DPS 及其崩解能力增强药物释放能力,从而显著改善药物通过水凝胶基质的扩散和 3DPS 的快速崩解。最后,我们的研究表明,所获得的 3DPS 具有合适的体内行为,不会造成阻塞,并允许大鼠肠道的正常运动。