Alfred E. Mann Institute for Biomedical Engineering at the University of Southern California , Los Angeles 90007 , California , United States.
ACS Appl Mater Interfaces. 2018 Jul 25;10(29):24876-24885. doi: 10.1021/acsami.8b08880. Epub 2018 Jul 10.
A simple method to rapidly customize and to also mass produce oral dosage forms is arguably a current bottleneck in the development of modern personalized medicine. Specifically, delayed-release mechanisms with well-controlled dosage profiles for combinations of traditional Chinese herbal extracts and Western medications are not well established. Herein, we demonstrate a novel multidrug-loaded membrane sandwich with structures infused with ibuprofen (IBU) and Ganoderma lucidum polysaccharide (GLP) using three-dimensional electrohydrodynamic printing and electrospinning techniques. The resulting flexible membrane consists of microscaled, multilayered cellulose acetate (CA) membranes loaded with IBU in the shape of either concentric squares or circles, as the top and bottom layers of a sandwich structure. In between the CA-IBU layers are randomly electrospun polyvinyl pyrrolidone (PVP) layers loaded with GLP. The complete fibrous membrane sandwich can be folded and embedded into a 0-size capsule to achieve oral compliance. Simulated in vitro testing of gastric and intestinal fluids demonstrated a triphasic release profile. There was an immediate release of GLP after gastric juices dissolved the capsule shell and the PVP, followed by the short-term release of 60% of the IBU within an hour afterward, and the remaining IBU was released in a sustained manner following a Fickian diffusion profile. In summary, this multidrug (both hydrophilic and/or hydrophobic) oral system with precision-designed structures should enable personalized therapeutic dosing.
一种快速定制和大规模生产口服剂型的简单方法,可以说是当前个性化医学发展的一个瓶颈。具体来说,对于中药提取物和西药的组合,具有良好控制剂量特征的延迟释放机制尚未得到很好的建立。在这里,我们展示了一种使用三维电动力学印刷和静电纺丝技术制备的新型多药物负载膜三明治,其中结构中注入了布洛芬(IBU)和灵芝多糖(GLP)。所得到的柔性膜由微尺度的多层醋酸纤维素(CA)膜组成,在顶、底层为同心正方形或圆形的形状,负载 IBU。在 CA-IBU 层之间是随机电纺的聚维酮(PVP)层,负载 GLP。完整的纤维膜三明治可以折叠并嵌入 0 号胶囊中,以实现口服顺应性。模拟的胃和肠液体外测试显示出三相释放特征。胶囊壳和 PVP 溶解后,GLP 立即释放,1 小时内释放 60%的 IBU,随后剩余的 IBU 以菲克扩散模式持续释放。总之,这种具有精确设计结构的多药物(亲水性和/或疏水性)口服系统应该能够实现个性化治疗剂量。