3D打印技术在个性化给药系统中的应用

Bálint Basa, G. Jakab, E. Balogh, Bence Borbás, I. Antal
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引用次数: 0

摘要

考虑到个性化药物的配方,对增材制造的兴趣正在增长[1]。3D打印通常是一个附加过程,导致各种层逐层构建对象。除了3D打印之外,还有大量的方法可供使用,但其中只有少数方法可用于定制药物制造(例如光聚合、选择性激光烧结(SLS)和熔融沉积建模(FDM))[2]。在这些方法中,单元操作的数量被最小化,并且有机会根据个人的轮廓制造每个单独的打印件,而只需最少的人为干预,这可能是该领域研究活动增加的原因[3]。这种生产方式的额外好处是能够为儿科、老年医学和患有器官功能障碍的患者生产定制的药物,避免在他们体内达到有毒剂量的最小机会。以前有几种类型的剂型被微制,包括浮动系统、脉冲释放片剂和零级释放剂型[4]。2015年,第一个3D打印或分散片剂获得了FDA的批准。[5]我们研究的目的是设计和打印可生物降解的药物传递系统。筛选了市售长丝材料,并对打印设置进行了优化。此外,在模型药物的情况下,研究了壁厚、孔形态、孔数和孔大小等设计参数对药物传递的影响。此外,还研究了基质聚合物和胶凝剂在3D打印过程中的适用性。有一些配方旨在研究剂量比例,以扩大个性化用药的机会。2. 材料与方法
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The Application of 3D Printing in the Formulation of Personalized Drug Delivery Systems
the interest toward additive manufacturing is growing considering the formulation of personalized medicines [1]. 3D printing is commonly an additive process, which results in various layer-bylayer built objects. A vast number of methods are available beyond 3D Printing but there are only few of them which can be employed for tailored pharmaceutical manufacturing (e.g. Photopolymerization, Selective Laser Sintering (SLS) and Fused Deposition Modelling (FDM)) [2]. During these methods the number of unit operations is minimalized, and the opportunity to fabricate every single printlet shaped according to the individuals’ profile with only minimal human intervention can be the cause of the increased research activity in this field [3]. The additional benefit of this type of manufacturing is the capability of producing customized ways of medication for pediatrics, geriatrics and patients suffering from organ dsyfunctions, avoiding the slightest chance of reaching toxic doses in their body. Several types of dosage forms were previously microfabricated including floating systems, pulsatile drug release tablets and zero-order release forms [4]. The first 3D printed orodispersible tablet was approved by the FDA in 2015.[5] The objective of our study was to design and print biodegradable drug delivery systems. Commercially available filament materials were screened as well as the print settings were optimized. In addition, the influence of design parameters including wall thickness, morphology, number and size of pores on the drug delivery in case of model drugs was investigated. Moreover, the applicability of matrix polymers and gelling agents in the process of 3D printing was studied. There were some formulations aiming the study of dose proportionality, in order to expand the opportunities of personalized medication. 2. Materials and methods
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