College of Pharmacy and Health Sciences, St. John's University, NY 11432, United States.
College of Pharmacy and Health Sciences, St. John's University, NY 11432, United States.
Int J Pharm. 2024 Apr 25;655:123941. doi: 10.1016/j.ijpharm.2024.123941. Epub 2024 Feb 23.
Developing safe and effective formulations for the geriatric and pediatric population is a challenging task due to issues of swallowability and palatability. The lack of standardized procedures for pediatric formulations further complicates the process. Manipulating adult formulations for children can lead to suboptimal efficacy and safety concerns. To overcome these challenges, minitablets or spinklets are preferred for the geriatric and pediatric population due to their smaller size and flexible dose adjustment. The aim of this study is the development of a 3D printed spinklets formulation of celecoxib, a nonsteroidal anti-inflammatory drug, using hot melt extrusion to address the limitations of traditional manufacturing methods. Three different formulations of celecoxib were prepared using Poly-2-ethyl-tetra-oxazoline (Aquazol) with and without surfactant. Subsequently, the mechanical properties and solubility of the drug-loaded filaments were evaluated. Solid state characterization confirmed the drug conversion into an amorphous form during the extrusion process, Computer-aided design software facilitate sprinklets design for fused deposition modeling and scanning electron microscopy assess the surface morphology. Sophorolipids plasticize better than TPGS, resulting in lowering processing temperatures during melt extrusion. In vitro drug release showed successful enhancements in the dissolution of oral medications for pediatric patients, considering their distinctive physiological characteristics. Overall, this study demonstrates the successful development of PEtOx-based 3D printed celecoxib sprinklets by coupling hot-melt extrusion and 3D printing technology. Future exploration holds the potential to revolutionize pharmaceutical production and advance personalized medication formulations.
为老年和儿科人群开发安全有效的配方是一项具有挑战性的任务,因为存在吞咽和口感问题。儿科配方缺乏标准化程序进一步使这一过程复杂化。将成人配方用于儿童可能会导致疗效和安全性不佳。为了克服这些挑战,由于其体积较小且剂量调整灵活,迷你片剂或小丸剂更适合老年和儿科人群。本研究的目的是开发一种使用热熔挤出技术的塞来昔布(一种非甾体抗炎药)3D 打印小丸剂配方,以解决传统制造方法的局限性。使用聚-2-乙基-四恶唑啉(Aquazol)和/或表面活性剂制备了三种不同的塞来昔布配方。随后,评估了载药长丝的机械性能和溶解度。固态表征证实药物在挤出过程中转化为无定形形式,计算机辅助设计软件有助于为熔融沉积建模设计小丸剂,扫描电子显微镜评估表面形态。槐糖脂比 TPGS 更好地塑化,从而降低了熔融挤出过程中的加工温度。体外药物释放表明成功增强了儿科患者口服药物的溶解度,考虑到他们独特的生理特征。总的来说,这项研究展示了通过结合热熔挤出和 3D 打印技术成功开发基于 PEtOx 的 3D 打印塞来昔布小丸剂。未来的探索有可能彻底改变药物生产并推进个性化药物配方。