Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil
This study reports the first case of an innovative drop-on-powder (DoP) three-dimensional (3D) printing technology to produce oral tablets (diameters of 10 mm and 13 mm) loaded with an anticancer model drug, 5-fluorouracil (FLU). For this study, a composition of the powder carrier containing CaSO<...
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doaj-cb61695fc49e4f86af3852a208e470022020-11-25T00:35:05ZengMDPI AGPharmaceutics1999-49232019-04-0111415010.3390/pharmaceutics11040150pharmaceutics11040150Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-FluorouracilKejing Shi0Deck K. Tan1Ali Nokhodchi2Mohammed Maniruzzaman3School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QJ, UKSchool of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QJ, UKSchool of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QJ, UKSchool of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QJ, UKThis study reports the first case of an innovative drop-on-powder (DoP) three-dimensional (3D) printing technology to produce oral tablets (diameters of 10 mm and 13 mm) loaded with an anticancer model drug, 5-fluorouracil (FLU). For this study, a composition of the powder carrier containing CaSO<sub>4</sub> hydrates, vinyl polymer, and carbohydrate was used as the matrix former, whereas 2-pyrrolidone with a viscosity like water was used as a binding liquid or inkjet ink. All tablets were printed using a commercial ZCorp 3D printer with modification. The resultant tablets were subject to coating with various polymeric solutions containing the drug. The composition of the polymeric solutions was adjusted at drug: polymer(s) 1:1 (<i>w</i>/<i>w</i>) ratio. Either Soluplus<sup>®</sup> (SOL) alone or in combination with polyethylene glycol (PEG) was used to develop the coating solution of 2.5% (<i>w</i>/<i>v</i>) concentration. The particle size analysis, flow test, and particle morphology studies revealed mono-modal narrow size distribution, good flow properties, and porous loosely bound texture (of the tablets), respectively. Moreover, the advanced application of the fluorescence microscopy showed a homogenous distribution of the drug throughout the surface of the 3D printed tablets. The <i>in vitro</i> dissolution studies showed that the tablet compositions, dimensions, and the coating solution compositions influenced the release of the drug from the tablets. It can be concluded that our innovative DoP 3D printing technology can be used to fabricate personalized dosage forms containing optimized drug content with high accuracy and shape fidelity. This is particularly suitable for those drugs that are highly unstable in thermal processing and cannot withstand the heat treatment, such as in fused deposition modeling (FDM) 3D printing.https://www.mdpi.com/1999-4923/11/4/1503D printingdrop-on-powderpowder-based 3D printingpersonalized medicine5-fluorouracilSoluplus |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kejing Shi Deck K. Tan Ali Nokhodchi Mohammed Maniruzzaman |
spellingShingle |
Kejing Shi Deck K. Tan Ali Nokhodchi Mohammed Maniruzzaman Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil Pharmaceutics 3D printing drop-on-powder powder-based 3D printing personalized medicine 5-fluorouracil Soluplus |
author_facet |
Kejing Shi Deck K. Tan Ali Nokhodchi Mohammed Maniruzzaman |
author_sort |
Kejing Shi |
title |
Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil |
title_short |
Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil |
title_full |
Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil |
title_fullStr |
Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil |
title_full_unstemmed |
Drop-On-Powder 3D Printing of Tablets with an Anti-Cancer Drug, 5-Fluorouracil |
title_sort |
drop-on-powder 3d printing of tablets with an anti-cancer drug, 5-fluorouracil |
publisher |
MDPI AG |
series |
Pharmaceutics |
issn |
1999-4923 |
publishDate |
2019-04-01 |
description |
This study reports the first case of an innovative drop-on-powder (DoP) three-dimensional (3D) printing technology to produce oral tablets (diameters of 10 mm and 13 mm) loaded with an anticancer model drug, 5-fluorouracil (FLU). For this study, a composition of the powder carrier containing CaSO<sub>4</sub> hydrates, vinyl polymer, and carbohydrate was used as the matrix former, whereas 2-pyrrolidone with a viscosity like water was used as a binding liquid or inkjet ink. All tablets were printed using a commercial ZCorp 3D printer with modification. The resultant tablets were subject to coating with various polymeric solutions containing the drug. The composition of the polymeric solutions was adjusted at drug: polymer(s) 1:1 (<i>w</i>/<i>w</i>) ratio. Either Soluplus<sup>®</sup> (SOL) alone or in combination with polyethylene glycol (PEG) was used to develop the coating solution of 2.5% (<i>w</i>/<i>v</i>) concentration. The particle size analysis, flow test, and particle morphology studies revealed mono-modal narrow size distribution, good flow properties, and porous loosely bound texture (of the tablets), respectively. Moreover, the advanced application of the fluorescence microscopy showed a homogenous distribution of the drug throughout the surface of the 3D printed tablets. The <i>in vitro</i> dissolution studies showed that the tablet compositions, dimensions, and the coating solution compositions influenced the release of the drug from the tablets. It can be concluded that our innovative DoP 3D printing technology can be used to fabricate personalized dosage forms containing optimized drug content with high accuracy and shape fidelity. This is particularly suitable for those drugs that are highly unstable in thermal processing and cannot withstand the heat treatment, such as in fused deposition modeling (FDM) 3D printing. |
topic |
3D printing drop-on-powder powder-based 3D printing personalized medicine 5-fluorouracil Soluplus |
url |
https://www.mdpi.com/1999-4923/11/4/150 |
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