Influence of design parameters on sustained drug release properties of 3D-printed theophylline tablets

被引:1
|
作者
Pflieger, Thomas [1 ,4 ]
Venkatesh, Rakesh [1 ]
Dachtler, Markus [1 ]
Cooke, Karin [2 ]
Laufer, Stefan [3 ]
Lunter, Dominique [4 ,5 ]
机构
[1] DiHeSys Digital Hlth Syst GmbH, Marie Curie Str 19, D-73529 Schwabisch Gmund, Germany
[2] Gen Plus GmbH & Co KG, Staffelseestr 6, D-81477 Munich, Germany
[3] Eberhard Karls Univ Tubingen, Chair Pharmaceut Chem, Morgenstelle 8, D-72074 Tubingen, Germany
[4] Eberhard Karls Univ Tubingen, Chair Pharmaceut Technol, Morgenstelle 8, D-72074 Tubingen, Germany
[5] Univ Tubingen, Chair Pharmaceut Technol, Morgenstelle 8, D-72076 Tubingen, Germany
关键词
Pharmaceutical three-dimensional printing; (3DP); Theophylline; Individualized treatment; Pulmonary diseases; Sustained drug release; Oral dosage forms (ODF); 3D; PHARMACEUTICALS; DISSOLUTION;
D O I
10.1016/j.ijpharm.2024.124207
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The application of three-dimensional printing (3DP) in the pharmaceutical industry brings a broad spectrum of benefits to patients by addressing individual needs and improve treatment success. This study investigates the sustained release properties of 3DP tablets containing Theophylline (TPH), which is commonly used to treat respiratory diseases and recently having a comeback due to its potential in the treatment of conditions like Covid19. Since TPH is a narrow therapeutic window (NTW) drug with serious side effects in the event of overdose, the release properties must be observed particularly closely. We employed a state-of-the-art single screw extrusion 3D printer, which is fed with granules containing the drug. By employing a Taguchi orthogonal array design of experiments (DOE), tablet design parameters and factor related process stability were sought to be evaluated fundamentally. Following this, examinations regarding tailored TPH dosages were undertaken and a relationship between the real printed dose of selected tablet designs and their sustained drug release was established. The release profiles were analyzed using different mathematical model fits and compared in terms of mean dissolution times (MDT). Finally, in-vivo/in-vitro correlation (IVIVC) and physiologically based pharmacokinetic (PBPK) modeling showed that a paradigm patient group could be covered with the dosage forms produced.
引用
收藏
页数:11
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