Department of Pharmaceutics, National Institute of Pharmaceutical Education & Research, (NIPER)-Guwahati, Changsari, Assam 781101, India.
Department of Pharmaceutics, National Institute of Pharmaceutical Education & Research, (NIPER)-Guwahati, Changsari, Assam 781101, India.
Eur J Pharm Biopharm. 2024 Oct;203:114471. doi: 10.1016/j.ejpb.2024.114471. Epub 2024 Aug 24.
This study investigates the feasibility of fabrication of poly(1-vinyl-2-pyrrolidone) (Kollidon®25)-mediated filaments for producing tinidazole (TNZ)-loaded, customizable, child-friendly tablets (with varying shapes and sizes) using hot melt extrusion (HME) coupled with fused deposition modeling (FDM) technology. Kollidon®25, chosen for its ability to enhance the dissolution of TNZ (a BCS Class II drug), was evaluated for polymer-drug compatibility through Hansen solubility, polarity, and interaction parameter analyses, confirming good miscibility and affinity between TNZ and Kollidon®25. Placebo- and TNZ-loaded filaments were prepared in different ratios using HME, followed by the development of 3D-printed tablets via FDM. The fabricated batches of placebo and TNZ-loaded 3D tablets were characterized, and it was found that they had an average weight variation of 270.41 ± 7.44 mg and 270.87 ± 9.33 mg, hardness of 155.01 ± 11.79 N and 265.3 ± 7.62 N, and friability of 0.1583 ± 0.0011 % and 0.2254 ± 0.0013 %. Amorphization was confirmed by differential scanning calorimetry (DSC) and powder X-ray diffraction (PXRD) analysis. Scanning electron microscopy (SEM) revealed a layer-by-layer pattern with tiny fractures on the tablet surfaces, which enhanced media penetration, resulting in improved dissolution profiles. The TNZ release profile showed complete 100 % release within 2.0 h in a gastric acidic medium. These findings support the potential of Kollidon®25 to create customizable, child-friendly, 3D-printed dosage forms with different shapes and sizes for TNZ delivery, offering a unique approach to paediatric medications.
本研究探讨了通过热熔挤出(HME)与熔融沉积建模(FDM)技术相结合,制备聚(1-乙烯基-2-吡咯烷酮)(Kollidon®25)介导的纤维,以生产载有替硝唑(TNZ)、可定制、适合儿童的片剂(具有不同形状和大小)的可行性。选择 Kollidon®25 是因为它能够增强 TNZ(BCS 类 II 药物)的溶解度,通过 Hansen 溶解度、极性和相互作用参数分析评估聚合物-药物相容性,证实了 TNZ 和 Kollidon®25 之间良好的混溶性和亲和力。通过 HME 以不同比例制备载药和无载药纤维,然后通过 FDM 开发 3D 打印片剂。对制备的载药和无载药 3D 片剂批次进行了表征,结果发现它们的平均重量变异分别为 270.41±7.44mg 和 270.87±9.33mg,硬度分别为 155.01±11.79N 和 265.3±7.62N,脆碎度分别为 0.1583±0.0011%和 0.2254±0.0013%。差示扫描量热法(DSC)和粉末 X 射线衍射(PXRD)分析证实了非晶化。扫描电子显微镜(SEM)显示片剂表面有一层一层的图案和微小的裂缝,这增强了介质的渗透,从而改善了溶解曲线。TNZ 的释放曲线显示在胃酸性介质中 2.0 小时内完全释放 100%。这些发现支持 Kollidon®25 具有为 TNZ 传递创建可定制、适合儿童的、具有不同形状和大小的 3D 打印剂型的潜力,为儿科药物提供了一种独特的方法。