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定制按需抗凝血剂量:3D 打印定制口服剂型的体外和体内评价。

Tailored on demand anti-coagulant dosing: An in vitro and in vivo evaluation of 3D printed purpose-designed oral dosage forms.

机构信息

School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston, Lancashire, UK; Faculty of Medical Sciences and Public Health, Anglia Ruskin University, Chelmsford, UK.

Faculty of Pharmacy and Medical Sciences, University of Petra, Amman, Jordan.

出版信息

Eur J Pharm Biopharm. 2018 Jul;128:282-289. doi: 10.1016/j.ejpb.2018.04.010. Epub 2018 Apr 16.

Abstract

Coumarin therapy has been associated with high levels of inter- and intra-individual variation in the required dose to reach a therapeutic anticoagulation outcome. Therefore, a dynamic system that is able to achieve accurate delivery of a warfarin dose is of significant importance. Here we assess the ability of 3D printing to fabricate and deliver tailored individualised precision dosing using in-vitro and in-vivo models. Sodium warfarin loaded filaments were compounded using hot melt extrusion (HME) and further fabricated via fused deposition modelling (FDM) 3D printing to produce capsular-ovoid-shaped dosage forms loaded at 200 or 400 µg dose. The solid dosage forms and comparator warfarin aqueous solutions were administered by oral gavage to Sprague-Dawley rats. A novel UV imaging approach indicated that the erosion of the methacrylate matrix was at a rate of 16.4 and 15.2 µm/min for horizontal and vertical planes respectively. In vivo, 3D printed forms were as proportionately effective as their comparative solution form in doubling plasma exposure following a doubling of warfarin dose (184% versus 192% respectively). The 3D printed ovoids showed a lower C of warfarin (1.51 and 3.33 mg/mL versus 2.5 and 6.44 mg/mL) and a longer T (6 and 3.7 versus 4 and 1.5 h) in comparison to liquid formulation. This work demonstrates for the first time in vivo, the potential of FDM 3D printing to produce a tailored specific dosage form and to accurately titrate coumarin dose response to an individual patient.

摘要

香豆素治疗与达到治疗抗凝效果所需的剂量在个体内和个体间的高度变异性有关。因此,能够实现华法林剂量准确输送的动态系统具有重要意义。在这里,我们评估了 3D 打印在体外和体内模型中制造和输送定制个体化精准剂量的能力。使用热熔挤出(HME)将负载华法林的钠纤维复合,并通过熔融沉积建模(FDM)3D 打印进一步制造胶囊状卵形剂量形式,负载量为 200 或 400μg 剂量。将固体剂型和比较用华法林水溶液通过口服灌胃给予 Sprague-Dawley 大鼠。一种新的紫外成像方法表明,甲基丙烯酸酯基质的侵蚀速率分别为水平和垂直平面的 16.4 和 15.2μm/min。在体内,3D 打印的剂型在华法林剂量加倍后,其血浆暴露加倍的比例与比较溶液剂型一样有效(分别为 184%和 192%)。与液体制剂相比,3D 打印的卵形物的华法林 C 较低(分别为 1.51 和 3.33mg/mL 与 2.5 和 6.44mg/mL),T 较长(分别为 6 和 3.7h 与 4 和 1.5h)。这项工作首次在体内证明了 FDM 3D 打印在生产定制特定剂型和准确滴定个体患者香豆素剂量反应方面的潜力。

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