FABRICATION OF A NOVEL HIGH-DENSITY THREE-DIMENSIONAL (3D)-PRINTED DEVICE FOR DOMPERIDONE TABLETS

Authors

  • Thapakorn Charoenying Pharmaceutical Development of the Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom
  • Prin Chaksmithanont Department of Industrial Pharmacy, Faculty of Pharmacy, Silpakorn University, Nakhon Pathom
  • Suwannee Panomsuk Pharmaceutical Development of the Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom
  • Nattawat Nattapulwat Department of Industrial Pharmacy, Faculty of Pharmacy, Silpakorn University, Nakhon Pathom
  • Samarwadee Plianwong Pharmaceutical Innovations of Natural Products Unit, Burapha university, Chonburi
  • Prasopchai Patrojanasophon Pharmaceutical Development of the Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom
  • Praneet Opanasopit Pharmaceutical Development of the Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom

DOI:

https://doi.org/10.14456/tbps.2023.8

Keywords:

high-density gastro-retentive drug delivery system, 3D-printing device, domperidone, tablet, iron powder-loaded polylactic acid, fused deposition modeling

Abstract

In conventional high-density tablets, a large amount of high-density material must be directly added to the tablets. Therefore, it may lead to undesired tablet properties. The aim of this study was to develop novel high-density three-dimensional (3D)-printed devices (HPDs) for a gastro-retentive drug delivery system (GRDDS). The HPDs were fabricated from iron powder-loaded polylactic acid (PLA) filaments using fused deposition modeling (FDM). A commercial domperidone (DOM) tablet was utilized as a model drug and placed into HPDs. To enable different drug release characteristics, the devices were fabricated with different hole diameters (1.0, 1.5, and 2.0 mm). The appearance, weight variation, and density of the HPDs were evaluated. In vitro dissolution of DOM from the HPDs was conducted to obtain the drug release characteristics. The kinetics of DOM release from HPDs was examined to elucidate the release mechanism. The printed HPDs had similar physical appearances to the designed 3D models. The HPDs had a density of more than or equal to 2.4 g/cm3 with a slightly rough texture due to the original texture of iron powder-loaded polylactic acid (PLA) filaments. The HPD with hole diameters of 1.5 mm showed an optimal sustained-release profile, with 98.8% of the drug released in 12 h because of the limit of the tablet’s surface area exposed to the medium. Moreover, zero-order kinetics was achieved from all HPDs. It can be concluded that HPDs successfully modified the drug release of regular DOM tablets to GRDDS without adding high-density excipients into the tablet directly and may be applied to other commercial drugs as a high-density drug delivery system.

References

Helliwell M, Taylor D. Solid oral dosage forms. Prof Nurse. 1993;8(5):313-7.

Charoenying T, Patrojanasophon P, Ngawhirunpat T, Rojanarata T, Akkaramongkolporn P, Opanasopit P. Fabrication of floating capsule-in- 3D-printed devices as gastro-retentive delivery systems of amoxicillin. J Drug Deliv Sci Technol. 2020;55.

Shin S, Kim TH, Jeong SW, Chung SE, Lee DY, Kim DH, et al. Development of a gastroretentive delivery system for acyclovir by 3D printing technology and its in vivo pharmacokinetic evaluation in Beagle dogs. PLoS One. 2019;14(5):e0216875.

Chawla G, Gupta P, Koradia V, Bansal KA. Gastroretention: a means to address regional variability in intestinal drug absorption. Pharmaceutical Technology. 2003;27(7):50-68.

Chai X, Chai H, Wang X, Yang J, Li J, Zhao Y, et al. Fused deposition modeling (FDM) 3D printed tablets for Intragastric floating delivery of domperidone. Sci Rep. 2017;7(1):2829.

Goyanes A, Fina F, Martorana A, Sedough D, Gaisford S, Basit AW. Development of modified release 3D printed tablets (printlets) with pharmaceutical excipients using additive manufacturing. Int J Pharm. 2017;527(1-2):21-30.

Ali Z, Türeyen EB, Karpat Y, Çakmakcı M. Fabrication of polymer micro needles for transdermal drug delivery system using DLP based projection stereo-lithography. Procedia CIRP. 2016;42:87-90.

Economidou SN, Pere CPP, Reid A, Uddin MJ, Windmill JFC, Lamprou DA, et al. 3D printed microneedle patches using stereolithography (SLA) for intradermal insulin delivery. Mater Sci Eng C Mater Biol Appl. 2019;102:743-55.

Charoenying T, Patrojanasophon P, Ngawhirunpat T, Rojanarata T, Akkaramongkolporn P, Opanasopit P. Three-dimensional (3D)-printed devices composed of hydrophilic cap and hydrophobic body for improving buoyancy and gastric retention of domperidone tablets. Eur J Pharm Sci. 2020;155:105555.

Li Q, Guan X, Cui M, Zhu Z, Chen K, Wen H, et al. Preparation and investigation of novel gastro-floating tablets with 3D extrusion-based printing. Int J Pharm. 2018;535(1-2):325-32.

Araujo MRP, Sa-Barreto LL, Gratieri T, Gelfuso GM, Cunha-Filho M. The digital pharmacies era: how 3D printing technology using fused deposition modeling can become a reality. Pharmaceutics. 2019;11(3).

Vaz VM, Kumar L. 3D printing as a promising tool in personalized medicine. AAPS PharmSciTech. 2021;22(1):49.

Sadia M, Arafat B, Ahmed W, Forbes RT, Alhnan MA. Channelled tablets: An innovative approach to accelerating drug release from 3D printed tablets. J Control Release. 2018;269:355-63.

Maroni A, Melocchi A, Parietti F, Foppoli A, Zema L, Gazzaniga A. 3D printed multi-compartment capsular devices for two-pulse oral drug delivery. J Control Release. 2017;268:10-8.

Goyanes A, Chang H, Sedough D, Hatton GB, Wang J, Buanz A, et al. Fabrication of controlled-release budesonide tablets via desktop (FDM) 3D printing. Int J Pharm. 2015;496(2):414-20.

Charoenying T, Patrojanasophon P, Ngawhirunpat T, Rojanarata T, Akkaramongkolporn P, Opanasopit P. Effects of thermal crosslinking on the properties and release profiles of three-dimensional (3D)-printed poly vinyl alcohol (PVA) tablets. Key Eng Mater. 2020;859:258-64.

Fu J, Yin H, Yu X, Xie C, Jiang H, Jin Y, et al. Combination of 3D printing technologies and compressed tablets for preparation of riboflavin floating tablet-in-device (TiD) systems. Int J Pharm. 2018;549(1-2):370-9.

Singpanna K, Charoenying T, Patrojanasophon P, Rojanarata T, Sukma M, Opanasopit P. Fabrication of a floating device of domperidone tablets using 3D-printing technologies. Key Eng Mater. 2020;859:289-94.

Kumar V, Vasa S, Banji D, et.al. Approaches for gastrotentive drug delivery systems. Int J of Appl Biol and Pharm Tech. 2010;1(2):589-601.

More S, Gavali K, Doke O, Kasgawade P. Gastroretentive drug delivery system. J Drug Deliv Ther. 2018;8(4).

Chareonying T, Akkaramongkolporn P, Opanasopit P. Development of floating 3D-printed devices for carvedilol tablet. Key Eng Mater. 2022;914:45-51.

British pharmacopoeia. Vol. 3. London: Health Ministers of the United Kingdom; 2019. Domperidone tablets; p. 538-9.

Mandal UK, Chatterjee B, Senjoti FG. Gastro-retentive drug delivery systems and their in vivo success: A recent update. Asian J Pharm Sci. 2016;11(5):575-84.

Bhandwalkar M, Dubal P, Tupe A, Mandrupkar S. Review on gastroretentive drug delivery system. Asian J Pharm Clin Res. 2020:38-45.

Hattori Y, Haruna Y, Otsuka M. Dissolution process analysis using model-free Noyes-Whitney integral equation. Colloids Surf. B: Biointerfaces. 2012;102:227-31.

Chai X, Chai H, Wang X, Yang J, Li J, Zhao Y, et al. Fused deposition modeling (FDM) 3D printed tablets for Intragastric floating delivery of domperidone. Sci Rep. 2017;7(1):2829.

Clark GM, Newton JM, Short MD. Gastrointestinal transit of pellets of differing size and density. Int J Pharm. 1993;100:81-92.

Desai N, Purohit R. Development of novel high density gastroretentive multiparticulate pulsatile tablet of clopidogrel bisulfate using quality by design approach. AAPS Pharm Sci Tech. 2017;18(8):3208-18.

Qi X, Ren Y, Wang X. New advances in the biodegradation of poly(lactic) acid. Int Biodeterior Biodegradation. 2017;117:215-23.

Downloads

Published

2023-01-24

Issue

Section

Original Research Articles