3D Printed Pellets (Miniprintlets): A Novel, Multi-Drug, Controlled Release Platform Technology

被引:159
作者
Awad, Atheer [1 ]
Fina, Fabrizio [1 ]
Trenfield, Sarah J. [1 ]
Patel, Pavanesh [1 ]
Goyanes, Alvaro [2 ,3 ]
Gaisford, Simon [1 ,2 ]
Basit, Abdul W. [1 ,2 ]
机构
[1] UCL, UCL Sch Pharm, Dept Pharmaceut, 29-39 Brunswick Sq, London WC1N 1AX, England
[2] FabRx Ltd, 3 Romney Rd, Ashford TN24 0RW, Kent, England
[3] Univ Santiago de Compostela, R D Pharma Grp GI 1645, Dept Farmacol Farm & Tecnol Farmaceut, Santiago De Compostela 15782, Spain
关键词
three dimensional printing; additive manufacturing; 3D printed drug products; printlets; personalised medicines; personalized pharmaceuticals; multiple units; spheroids; beads; acetaminophen; INNOVATIVE APPROACH; DISSOLUTION; IBUPROFEN; PRODUCTS; DEVICES; TABLETS; PARACETAMOL; BICARBONATE; MANAGEMENT; BEHAVIOR;
D O I
10.3390/pharmaceutics11040148
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Selective laser sintering (SLS) is a single-step three-dimensional printing (3DP) process that can be leveraged to engineer a wide array of drug delivery systems. The aim of this work was to utilise SLS 3DP, for the first time, to produce small oral dosage forms with modified release properties. As such, paracetamol-loaded 3D printed multiparticulates, termed miniprintlets, were fabricated in 1 mm and 2 mm diameters. Despite their large surface area compared with a conventional monolithic tablet, the ethyl cellulose-based miniprintlets exhibited prolonged drug release patterns. The possibility of producing miniprintlets combining two drugs, namely paracetamol and ibuprofen, was also investigated. By varying the polymer, the dual miniprintlets were programmed to achieve customised drug release patterns, whereby one drug was released immediately from a Kollicoat Instant Release matrix, whilst the effect of the second drug was sustained over an extended time span using ethyl cellulose. Herein, this work has highlighted the versatility of SLS 3DP to fabricate small and intricate formulations containing multiple active pharmaceutical ingredients with distinct release properties.
引用
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页数:17
相关论文
共 57 条
[1]   Selective laser sintering of Mo-CuNi composite to be used as EDM electrode [J].
Amorim, Fred L. ;
Lohrengel, Armin ;
Neubert, Volkmar ;
Higa, Camila F. ;
Czelusniak, Tiago .
RAPID PROTOTYPING JOURNAL, 2014, 20 (01) :59-68
[2]   Tailored on demand anti-coagulant dosing: An in vitro and in vivo evaluation of 3D printed purpose-designed oral dosage forms [J].
Arafat, Basel ;
Qinna, Nidal ;
Cieszynska, Milena ;
Forbes, Robert T. ;
Alhnan, Mohamed A. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2018, 128 :282-289
[3]   Tablet fragmentation without a disintegrant: A novel design approach for accelerating disintegration and drug release from 3D printed cellulosic tablets [J].
Arafat, Basel ;
Wojsz, Magdalena ;
Isreb, Abdullah ;
Forbes, Robert T. ;
Isreb, Mohammad ;
Ahmed, Waqar ;
Arafat, Tawfiq ;
Alhnan, Mohamed A. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 118 :191-199
[4]   3D printed medicines: A new branch of digital healthcare [J].
Awad, Atheer ;
Trenfield, Sarah J. ;
Gaisford, Simon ;
Basit, Abdul W. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 548 (01) :586-596
[5]   Reshaping drug development using 3D printing [J].
Awad, Atheer ;
Trenfield, Sarah J. ;
Goyanes, Alvaro ;
Gaisford, Simon ;
Basit, Abdul W. .
DRUG DISCOVERY TODAY, 2018, 23 (08) :1547-1555
[6]  
Barnatt C., 2016, 3D printing
[7]  
Basit A.W., 2018, 3D Printing of Pharmaceuticals, DOI [10.1007/978-3-319-90755-0, DOI 10.1007/978-3-319-90755-0]
[8]   3D printed tablets loaded with polymeric nanocapsules: An innovative approach to produce customized drug delivery systems [J].
Beck, R. C. R. ;
Chaves, P. S. ;
Goyanes, A. ;
Vukosavljevic, B. ;
Buanz, A. ;
Windbergs, M. ;
Basit, A. W. ;
Gaisford, S. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 528 (1-2) :268-279
[9]   Paediatric and geriatric drug delivery [J].
Breitkreutz, Joerg ;
Boos, Joachim .
EXPERT OPINION ON DRUG DELIVERY, 2007, 4 (01) :37-45
[10]   A COMPARATIVE-STUDY OF THE GASTROINTESTINAL TRANSIT OF A PELLET AND TABLET FORMULATION [J].
DAVIS, SS ;
HARDY, JG ;
TAYLOR, MJ ;
WHALLEY, DR ;
WILSON, CG .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1984, 21 (02) :167-177