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Oral fast-dissolving DDD fabricated using 3DP

机译:使用3DP制成的口服速溶DDD

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摘要

A novel fast dissolving drug delivery device (DDD) with loose powders in it was designed and fabricated using the three dimensional printing (3DP) process. Based on computer-aided design models, the DDD containing the drug acetaminophen were prepared automatically by 3DP system. The inner powder regions were carried out by depositing the binder solutions onto selected regions during the layer-printing processes. The DDD exhibited standard-met mechanical performance with an acceptable hardness value of 56.45 N/cm2 and 3.65% total mass loss during the friability tests. Environmental scanning electron microscope image clearly showed that particles in the printed regions were diminished or even disappeared, and bound together, whereas the un-printed regions was incompact with cracks and fissures in them. All the DDD were disintegrated and wetted rapidly in the in vitro tests. The average disintegration time of DDD was 17.9s and the average wetting time was 56.6 s. The in vitro dissolution tests informed that 96.3% of the drug was released in the initial two minutes. 3DP is capable of offering strategies for the research and development of novel fast dissolving DDD.
机译:使用三维打印(3DP)工艺设计和制造了一种新型的具有松散粉末的快速溶解药物输送装置(DDD)。基于计算机辅助设计模型,通过3DP系统自动制备含有对乙酰氨基酚的DDD。通过在层印刷过程中将粘合剂溶液沉积到所选区域上来进行内部粉末区域。 DDD具有标准的机械性能,在脆性测试过程中可接受的硬度值为56.45 N / cm2,总质量损失为3.65%。环境扫描电子显微镜图像清楚地表明,印刷区域中的颗粒减少甚至消失,并结合在一起,而未印刷区域中的裂纹和裂缝则不紧密。在体外测试中,所有的DDD都迅速崩解并润湿。 DDD的平均崩解时间为17.9s,平均润湿时间为56.6s。体外溶出度测试表明在最初的两分钟内释放了96.3%的药物。 3DP能够为新型快速溶解DDD的研发提供策略。

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