3D printing by fused deposition modeling (FDM) of a swellable/erodible capsular device for oral pulsatile release of drugs

被引:233
作者
Melocchi, Alice [1 ]
Parietti, Federico [2 ]
Loreti, Giulia [1 ]
Maroni, Alessandra [1 ]
Gazzaniga, Andrea [1 ]
Zema, Lucia [1 ]
机构
[1] Univ Milan, Dipartimento Sci Farmaceut, Sez Tecnol & Legislaz Farmaceut ME Sangalli, Via G Colombo 71, I-20133 Milan, Italy
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
关键词
3D printing; Fused deposition modeling; Capsular device; Pulsatile release; Real-time prototyping; Hydroxylpropyl cellulose filament; DELIVERY-SYSTEMS; FILM COATINGS; FABRICATION;
D O I
10.1016/j.jddst.2015.07.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present work was to explore the feasibility of fused deposition modeling (FDM) 3D printing in the manufacturing of capsular devices for oral pulsatile release based on a swellable/erodible polymer (hydroxypropyl cellulose, HPC). This involved an experimental evaluation of the possibility of fabricating hollow structures via FDM and the production of HPC filaments by hot melt extrusion (HME), which are not commercially available. Moreover, the set-up of appropriate computer aided design files had to be faced. A twin-screw extruder equipped with a rod-shaped die and a purposely designed pulling/calibrating device as well as a MakerBot Replicator 2 3D printer were employed for HME and FDM processing, respectively. Bodies and caps with satisfactory physico-technolcigical properties were obtained. The release test of assembled capsular devices pointed out a lag phase before rapid and quantitative liberation of the drug. The morphological changes undergone by the device when in contact with water and their release performance turned out comparable with those of analogous systems fabricated by injection molding. The possibility of manufacturing capsular devices for oral pulsatile release by FDM 3D printing starting from HPC filaments purposely prepared was thus demonstrated, and the real-time prototyping potential of FDM was assessed. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:360 / 367
页数:8
相关论文
共 31 条
[1]  
[Anonymous], 1994, STP PHARMA PRAT
[2]  
[Anonymous], 2001, AAPS PHARMSCITECH, DOI DOI 10.1208/PT020316
[3]  
Brent Stucker Ian Gibson DavidRosen., 2010, Additive manufacturing technologies, Vsecond, DOI [10.1007/978-1-4419-1120-9, DOI 10.1007/978-1-4419-1120-9]
[4]  
Chua CK, 2010, RAPID PROTOTYPING: PRINCIPLES AND APPLICATIONS, 3RD EDITION, DOI 10.1142/6665
[5]  
Gazzaniga A, 2011, AAPS PHARMSCITECH, V12, P295, DOI 10.1208/s12249-011-9581-6
[6]   Effect of geometry on drug release from 3D printed tablets [J].
Goyanes, Alvaro ;
Martinez, Pamela Robles ;
Buanz, Asma ;
Basit, Abdul W. ;
Gaisford, Simon .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 494 (02) :657-663
[7]   3D printing of modified-release aminosalicylate (4-ASA and 5-ASA) tablets [J].
Goyanes, Alvaro ;
Buanz, Asma B. M. ;
Hatton, Grace B. ;
Gaisford, Simon ;
Basit, Abdul W. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 89 :157-162
[8]   Levofloxacin implants with predefined microstructure fabricated by three-dimensional printing technique [J].
Huang, Weidong ;
Zheng, Qixin ;
Sun, Wangqiang ;
Xu, Huibi ;
Yang, Xiangliang .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 339 (1-2) :33-38
[9]   Oral dosage forms fabricated by Three Dimensional Printing™ [J].
Katstra, WE ;
Palazzolo, RD ;
Rowe, CW ;
Giritlioglu, B ;
Teung, P ;
Cima, MJ .
JOURNAL OF CONTROLLED RELEASE, 2000, 66 (01) :1-9
[10]   Desktop 3D printing of controlled release pharmaceutical bilayer tablets [J].
Khaled, Shaban A. ;
Burley, Jonathan C. ;
Alexander, Morgan R. ;
Roberts, Clive J. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2014, 461 (1-2) :105-111