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Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form

Liqui-pellet is a new dosage form stemming from pelletisation technology and concept from liquisolid technology. In spite of liqui-pellet overcoming a major hurdle in liquisolid technology through achieving excellent flow property with high liquid load factor, the formulation requires to be optimise...

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Detalles Bibliográficos
Autores principales: Lam, Matthew, Ghafourian, Taravat, Nokhodchi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978301/
https://www.ncbi.nlm.nih.gov/pubmed/31286452
http://dx.doi.org/10.1007/s13346-019-00659-6
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author Lam, Matthew
Ghafourian, Taravat
Nokhodchi, Ali
author_facet Lam, Matthew
Ghafourian, Taravat
Nokhodchi, Ali
author_sort Lam, Matthew
collection PubMed
description Liqui-pellet is a new dosage form stemming from pelletisation technology and concept from liquisolid technology. In spite of liqui-pellet overcoming a major hurdle in liquisolid technology through achieving excellent flow property with high liquid load factor, the formulation requires to be optimised in order to improve drug release rate. Liqui-pellets of naproxen containing Tween 80, Primojel, Avicel and Aerosil were extruded and spheronised. Flowability test confirmed that all liqui-pellet formulations have excellent-good flow property (Carr’s index between 3.9–11.17%), including liqui-pellets with a high liquid load factor of 1.52, where 38% of the total mass is co-solvent. This shows a relatively high liquid load factor can be achieved in liqui-pellet without compromising the flowability, which is one of the key novelty of this work. It was found that the improved drug release rate was due to the remarkably improved disintegration of the supposedly non-disintegrating microcrystalline-based pellet; the optimised liqui-pellet seems to explode into fragments in the dissolution medium. At pH 1.2, the optimised formulation had ~ 10% more drug release than non-optimised formulation after 2 h, and at pH 7.4, the drug release of the optimised pellet was nearing 100% at ~ 15 min, whereas the none-optimised pellet only achieved ~ 79% drug release after 2 h. DSC and XRPD indicated an increase in the dissolution rate could be due to molecularly dispersion of naproxen in the pellets. Overall results showed that liqui-pellet exhibited an enhanced drug release and the capacity for high liquid load factor whilst maintaining excellent flowability, rendering it a potentially commercially feasible drug delivery system.
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spelling pubmed-69783012020-02-03 Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form Lam, Matthew Ghafourian, Taravat Nokhodchi, Ali Drug Deliv Transl Res Original Article Liqui-pellet is a new dosage form stemming from pelletisation technology and concept from liquisolid technology. In spite of liqui-pellet overcoming a major hurdle in liquisolid technology through achieving excellent flow property with high liquid load factor, the formulation requires to be optimised in order to improve drug release rate. Liqui-pellets of naproxen containing Tween 80, Primojel, Avicel and Aerosil were extruded and spheronised. Flowability test confirmed that all liqui-pellet formulations have excellent-good flow property (Carr’s index between 3.9–11.17%), including liqui-pellets with a high liquid load factor of 1.52, where 38% of the total mass is co-solvent. This shows a relatively high liquid load factor can be achieved in liqui-pellet without compromising the flowability, which is one of the key novelty of this work. It was found that the improved drug release rate was due to the remarkably improved disintegration of the supposedly non-disintegrating microcrystalline-based pellet; the optimised liqui-pellet seems to explode into fragments in the dissolution medium. At pH 1.2, the optimised formulation had ~ 10% more drug release than non-optimised formulation after 2 h, and at pH 7.4, the drug release of the optimised pellet was nearing 100% at ~ 15 min, whereas the none-optimised pellet only achieved ~ 79% drug release after 2 h. DSC and XRPD indicated an increase in the dissolution rate could be due to molecularly dispersion of naproxen in the pellets. Overall results showed that liqui-pellet exhibited an enhanced drug release and the capacity for high liquid load factor whilst maintaining excellent flowability, rendering it a potentially commercially feasible drug delivery system. Springer US 2019-07-08 2020 /pmc/articles/PMC6978301/ /pubmed/31286452 http://dx.doi.org/10.1007/s13346-019-00659-6 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Lam, Matthew
Ghafourian, Taravat
Nokhodchi, Ali
Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title_full Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title_fullStr Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title_full_unstemmed Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title_short Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
title_sort optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978301/
https://www.ncbi.nlm.nih.gov/pubmed/31286452
http://dx.doi.org/10.1007/s13346-019-00659-6
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