用设计元件组装的控释渗透给药系统的微细加工。

Bence Borbás, Nikolett Kállai-Szabó, Miléna Lengyel, Emese Balogh, Bálint Basa, Károly Süvegh, Romána Zelkó, István Antal
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引用次数: 0

摘要

背景:本研究探讨了如何将三维打印与传统压缩方法相结合,以开发一种多组分控释给药系统(DDS)。该系统使用渗透片层和半透膜来控制药物释放,类似于模块化乐高®结构:DDS 由两个直接压缩的片剂层(推拉)和一个半渗透膜组成,所有这些都包含在一个 3D 打印框架内。膜由醋酸纤维素和增塑剂(如甘油和丙二醇)制成。采用了包括正电子湮没寿命谱(PALS)在内的各种表征技术来评估微结构特性、润湿性、形态和药物溶解度:结果:甘油改善了膜的润湿性,PALS 证实了这一点。由于三维打印框架内的推拉片剂,该系统实现了零阶药物释放,不受搅拌速率的影响。释放曲线稳定,表明药物释放得到了有效控制:本研究成功开发了一种控释渗透式 DDS 原型,实现了盐酸奎宁 2 小时后的零阶释放动力学。这种模块化方法为人类和兽医的个性化疗法提供了潜力,可在护理点进行定制。
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Microfabrication of controlled release osmotic drug delivery systems assembled from designed elements.

Background: This study investigates combining 3D printing with traditional compression methods to develop a multicomponent, controlled-release drug delivery system (DDS). The system uses osmotic tablet layers and a semipermeable membrane to control drug release, similar to modular Lego® structures.

Methods: The DDS comprises two directly compressed tablet layers (push and pull) and a semipermeable membrane, all contained within a 3D-printed frame. The membrane is made from cellulose acetate and plasticizers like glycerol and propylene glycol. Various characterization techniques, including Positron Annihilation Lifetime Spectroscopy (PALS), were employed to evaluate microstructural properties, wettability, morphology, and drug dissolution.

Results: Glycerol improved the membrane's wettability, as confirmed by PALS. The system achieved zero-order drug release, unaffected by stirring rates, due to the push and pull tablets within the 3D-printed frame. The release profile was stable, demonstrating effective drug delivery control.

Conclusion: The study successfully developed a prototype for a controlled-release osmotic DDS, achieving zero-order release kinetics for quinine hydrochloride after 2 h. This modular approach holds potential for personalized therapies in human and veterinary medicine, allowing customization at the point of care.

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