3D Printing of Tunable Zero-Order Release Printlets

被引:40
|
作者
Fina, Fabrizio [1 ]
Goyanes, Alvaro [1 ,2 ,3 ]
Rowland, Martin [4 ]
Gaisford, Simon [1 ]
W. Basit, Abdul [1 ]
机构
[1] UCL, UCL Sch Pharm, Dept Pharmaceut, 29-39 Brunswick Sq, London WC1N 1AX, England
[2] Univ Santiago de Compostela, Dept Farmacol Farm & Tecnol Farmaceut, ID Farma GI 1645, Fac Farm, Santiago De Compostela 15782, Spain
[3] Univ Santiago de Compostela, Hlth Res Inst Santiago Compostela IDIS, Santiago De Compostela 15782, Spain
[4] Pfizer Ltd, Drug Prod Design, Discovery Pk,Ramsgate Rd, Sandwich CT13 9ND, Kent, England
基金
英国工程与自然科学研究理事会;
关键词
three dimensional printing; printing pharmaceuticals; personalized medicines; controlled release; 3D printed drug products; computer aided drug design and delivery; digital pharmaceutics; health and pharmaceutical sciences; gastrointestinal modified release drug delivery; DRUG-RELEASE; FLOATING TABLETS; MELT EXTRUSION; DOSAGE FORMS; DELIVERY; DESIGN; FABRICATION; IMMEDIATE; DEVICES; SYSTEM;
D O I
10.3390/polym12081769
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
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%w/wparacetamol) 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.
引用
收藏
页数:19
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