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3D Printing of Tunable Zero-Order Release Printlets

机译:3D打印可调零级释放Printlet

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摘要

Zero-order release formulations are designed to release a drug at a constant rate over a prolonged time, thus reducing systemic side effects and improving patience adherence to the therapy. Such formulations are traditionally complex to manufacture, requiring multiple steps. In this work, fused deposition modeling (FDM) 3D printing was explored to prepare on-demand printlets (3D printed tablets). The design includes a prolonged release core surrounded by an insoluble shell able to provide zero-order release profiles. The effect of drug loading (10, 25, and 40% / paracetamol) on the mechanical and physical properties of the hot melt extruded filaments and 3D printed formulations was evaluated. Two different shell 3D designs (6 mm and 8 mm diameter apertures) together with three different core infills (100, 50, and 25%) were prepared. The formulations showed a range of zero-order release profiles spanning 16 to 48 h. The work has shown that with simple formulation design modifications, it is possible to print extended release formulations with tunable, zero-order release kinetics. Moreover, by using different infill percentages, the dose contained in the printlet can be infinitely adjusted, providing an additive manufacturing route for personalizing medicines to a patient.
机译:零级释放制剂设计用于在延长时间以恒定速率释放药物,从而减少全身副作用并改善耐心依从性。这种制剂传统上是复杂的制造,需要多个步骤。在这项工作中,探索了融合沉积建模(FDM)3D打印来准备按需选林(3D印刷片)。该设计包括由不溶性壳包围的长释放芯,能够提供零级释放型材。评估药物负载(10,25和40%/旁向戊酰胺)对热熔挤出长丝和3D印刷制剂的机械和物理性质的影响。两种不同的壳3D设计(6毫米和8毫米孔径)与三种不同的核心填充物(100,50和25%)一起制备。制剂显示了跨越16至48小时的一系列零级释放曲线。该工作表明,通过简单的配方设计修改,可以使用可调零释放动力学打印扩展释放配方。此外,通过使用不同的infill百分比,可以无限地调节印刷中包含的剂量,为患者提供个性化药物的添加剂制造路线。

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