Mechanical and Mechatronics Engineering Department, Faculty of Engineering and Information Technology, An-Najah National University, P.O. Box 7, Nablus P4110257, Palestine.
Medical and Health Sciences Research Center, An-Najah National University, P.O. Box 7, Nablus P4110257, Palestine.
ACS Biomater Sci Eng. 2024 Jun 10;10(6):3833-3841. doi: 10.1021/acsbiomaterials.4c00476. Epub 2024 May 15.
This study explores the realm of personalized medicine by investigating the utilization of 3D-printed dosage forms, specifically focusing on patient-specific enteric capsules designed for the modified release of ketoprofen, serving as a model drug. The research investigates two distinct scenarios: the modification of drug release from 3D-printed capsules crafted from hydroxypropyl methylcellulose phthalate:polyethylene glycol (HPMCP:PEG) and poly(vinyl alcohol) (PVA), tailored for pH sensitivity and delayed release modes, respectively. Additionally, a novel ketoprofen-loaded self-nanoemulsifying drug delivery system (SNEDDS) based on pomegranate seed oil (PSO) was developed, characterized, and employed as a fill material for the capsules. Through the preparation and characterization of the HPMCP:PEG based filament via the hot-melt extrusion method, the study thoroughly investigated its thermal and mechanical properties. Notably, the drug release analysis unveiled the intricate interplay between ketoprofen release, polymer type, and capsule thickness. Furthermore, the incorporation of ketoprofen into the SNEDDS exhibited an enhancement in its cylooxygenase-2 (COX-2) inhibitory activity. These findings collectively underscore the potential of 3D printing in shaping tailored drug delivery systems, thereby contributing significantly to the advancement of personalized medicine.
本研究通过调查 3D 打印剂型的利用,探索个体化医学领域,特别关注为特定患者设计的用于酮洛芬控释的肠溶胶囊,作为模型药物。该研究调查了两种不同情况:对基于邻苯二甲酸羟丙甲基纤维素-聚乙二醇(HPMCP:PEG)和聚乙烯醇(PVA)的 3D 打印胶囊中药物释放的修饰,分别针对 pH 敏感性和延迟释放模式进行设计。此外,还开发了一种基于石榴籽油(PSO)的新型酮洛芬载自乳化药物传递系统(SNEDDS),并将其用作胶囊的填充材料。通过熔融挤出法制备和表征基于 HPMCP:PEG 的长丝,全面研究了其热性能和机械性能。值得注意的是,药物释放分析揭示了酮洛芬释放、聚合物类型和胶囊厚度之间的复杂相互作用。此外,将酮洛芬纳入 SNEDDS 中,显示出其对环氧化酶-2(COX-2)抑制活性的增强。这些发现共同强调了 3D 打印在定制药物传递系统中的潜力,从而为个体化医学的发展做出了重要贡献。